Next Article in Journal
Tetrel Bonding in Anion Recognition: A First Principles Investigation
Next Article in Special Issue
Synthesis, Biological Evaluation, DNA Binding, and Molecular Docking of Hybrid 4,6-Dihydrazone Pyrimidine Derivatives as Antitumor Agents
Previous Article in Journal
Thermal and Mechanical Characterization of Yarn Samples from Flemish Tapestry of the Sixteenth Century
Previous Article in Special Issue
Dihydrotanshinone I Inhibits the Proliferation and Growth of Oxaliplatin-Resistant Human HCT116 Colorectal Cancer Cells
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 27
Issue 23
10.3390/molecules27238451
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents

by
Sandra Fernandes
1,
Shea T. Meyer
2,
Jigisha P. Shah
2,
Arijit A. Adhikari
2,
William G. Kerr
1 and
John D. Chisholm
2,*
1
Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA
2
Department of Chemistry, Syracuse University, Syracuse, NY 13244, USA
*
Author to whom correspondence should be addressed.
Molecules 2022, 27(23), 8451; https://doi.org/10.3390/molecules27238451
Submission received: 29 September 2022 / Revised: 28 November 2022 / Accepted: 30 November 2022 / Published: 2 December 2022
(This article belongs to the Special Issue Novel Anti-cancer Lead Compounds)
Browse Figures
Versions Notes

Abstract

:
Inhibition of phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase (SHIP) with small molecule inhibitors leads to apoptosis in tumor cells. Inhibitors that target both SHIP1 and SHIP2 (pan-SHIP1/2 inhibitors) may have benefits in these areas since paralog compensation is not possible when both SHIP paralogs are being inhibited. A series of tryptamine-based pan-SHIP1/2 inhibitors have been synthesized and evaluated for their ability to inhibit the SHIP paralogs. The most active compounds were also evaluated for their effects on cancer cell lines.

Graphical Abstract

1. Introduction

The PI3K pathway is a major cell signaling pathway in eukaryotic cells, having been shown to have a strong influence on cell division and cell survival. The pathway is named for the phosphoinositide 3-kinase (PI3K) enzyme (in this case referring specifically to the PIK3CA isoform) [1], which phosphorylates the membrane-anchored inositol phospholipid PI(4,5)P2 to form PI(3,4,5)P3. These membrane-anchored inositol phospholipids function as secondary messengers in the PI3K pathway. The diverse phosphorylation patterns present on the inositol ring of these lipids are recognized by PH domains present in signaling molecules such as serine/threonine kinases (such as Akt) which are typically activated upon binding to the inositol phospholipids and also by subsequent phosphorylation by other protein kinases (e.g., 3-phosphoinositide-dependent protein kinase-1, PDK1). This activation initiates a signaling cascade that transduces signals from the membrane to the cell nucleus. Signals from this pathway influence many cellular events, including cell division and survival. Modulating the concentration of the different inositol phospholipids on the interior of the plasma membrane has become a focus in the treatment of cancer, as controlling the amounts of these molecules may be used to curtail undesired cell division or survival. Inhibition of PI3K has been heavily investigated [2,3,4], with a number of clinically relevant PI3K inhibitors having been developed. Resistance to PI3K inhibitors has now been reported under some circumstances [5,6,7], so investigations into alternative approaches to influence PI3K signaling have been initiated. Modulation of the SH2-containing 5‘-inositol phosphatases SHIP1 and/or SHIP2, inositol phosphatases that degrade PI(3,4,5)P3, may provide another approach to sway PI3K pathway signaling. While SHIP is often considered as reversing signals initiated from PI3K phosphorylation, such as the well-known tumor promoter phosphatase and tensin homolog protein (PTEN) [8], the situation is more complex, with significant evidence pointing to SHIP1/2 facilitating tumor cell survival [9,10,11,12,13,14,15]. The primary difference between PTEN and the SHIP paralogs can be attributed to PTEN hydrolyzing the 3′ phosphate to generate PI(4,5)P2 from PI(3,4,5)P3, while SHIP1 and SHIP2 are 5′ phosphatases which convert PI(3,4,5)P3 to PI(3,4)P2. Therefore, SHIP and PTEN exert distinct effects on downstream signaling. Additionally, recent results show that the Akt2 isoform binds with greater affinity to PI(3,4)P2 [16], the product of the SHIP enzymes, instigating selective activation of Akt2 instead of activation of Akt1/Akt3 as is observed with PI(3,4,5)P3, the product of PI3K [17,18]. Therefore, the products of both SHIP1/2 and PI3K, PI(3,4)P2 and PI(3,4,5)P3, respectively, may be required to boost signals which lead to excessive cell division and promote survival in certain neoplasms. This has been termed the “Two PIP Hypothesis” where abnormal signaling from an imbalance in the amounts of both PI(3,4,5)P3 and PI(3,4)P2 may promote the development of the malignant state (Figure 1).
Consistent with the “Two PIP Hypothesis”, levels of the SHIP1 product PI(3,4)P2 are increased in several leukemia cells lines [19], while increased amounts of PI(3,4)P2 in inositol polyphosphate 4-phosphatase type II (INPP4A/B) knockout mice are implicated in promoting tumor formation [20,21]. We have also shown that the SHIP1 inhibitor 3α-aminocholestane (3AC) reduces Akt activation and promotes apoptosis of human blood cell cancers that express SHIP1, further supporting the hypothesis [9,14]. The key role of PI(3,4)P2 in cancer cell signaling was confirmed in these studies by demonstrating that the addition of PI(3,4)P2 onto leukemia cells is protective from apoptosis by SHIP1 inhibition in a dose-dependent fashion [9]. Related studies have shown that a SHIP1 agonist also slows the growth of multiple myeloma cells in vitro [22]. The observation that both agonists and antagonists of SHIP1 are cytotoxic to multiple myeloma cells highlights the delicate balance of PI(3,4,5)P3 and PI(3,4)P2 a cancer cell must maintain in order to develop and perpetuate the malignant state. Altogether a number of different breakdowns in PI3K signaling are possible in order for a cancer cell to reach a malignant state that satisfies the “Two PIP Hypothesis”.
There may also be applications for pan-SHIP1/2 inhibitors in the treatment of several types of cancer. As stated previously, a SHIP1 inhibitor showed cytotoxic effects on leukemia cells [9]. Other cancers may be more sensitive to SHIP2 inhibition, as SHIP2 expression is increased in breast cancer and promotes survival signals from epidermal growth factor receptor (EGF-R) in these tumors [11,13]. Further studies from our groups have shown that pan-SHIP1/2 inhibitors are also quite effective at slowing the growth of tumor cells [14,23]. Even though small molecule inhibitors are available for Akt [24], SHIP modulation provides a different molecular mechanism to influence PI3K signaling. This is advantageous for treating tumors that have become resistant to Akt inhibitors. The ability to produce a pan-SHIP1/2 inhibitor could prevent tumors from developing a resistance to inhibition of one SHIP paralog leading them to then utilize the other SHIP paralog to produce PI(3,4)P2. Such SHIP paralog compensation was in fact observed in vivo in a xenogeneic multiple myeloma model treated with the SHIP1-selective inhibitor 3α-aminocholestane (3AC). While 3AC was found to be effective in protecting the majority of mice from multiple myeloma growth; however, in those where there was relapse the tumor had up-regulated endogenous SHIP2 expression [14].
A number of groups have reported the identification of small molecules that modulate SHIP activity [25,26,27]. Our own work in the area began with a high-throughput screen (HTS) used to identify molecules that inhibit recombinant SHIP1, which identified a number of lead compounds [9,14,28]. One inhibitor found from this screen was tryptamine K103 (1) (Figure 2), a close analog of the serotonin antagonist benanserin 2 [29,30].
K103 showed inhibition of both SHIP paralogs, marking it as a pan-SHIP1/2 inhibitor, but the molecule showed no effect on OCRL, another 5′ inositol phosphatase [14]. In line with the “Two PIP Hypothesis” the molecule demonstrated significant antitumor effects on several cell lines, especially on breast cancer cells [14,23]. Additional studies on K103 showed that inhibition of SHIP1/2 in multiple myeloma cells resulted in a G2/M cell cycle arrest, followed by caspase cascade activation leading to extensive apoptosis [14]. Tryptamine 1 is compliant with commonly used measures of druglike small molecule properties [31,32], but during the course of this work, it was discovered that 1 induced a psychotropic effect in mice which limited the usefulness of the molecule in vivo. Therefore, some synthetic studies on this tryptamine were initiated to define what features of the molecule were needed to maintain pan-SHIP1/2 inhibition so that an inhibitor with good pharmacodynamic properties and an improved side effect profile could be designed.

2. Results and Discussion

The synthesis of K103 and related tryptamines was undertaken as shown in Scheme 1. The tryptamine core was accessed from a Fischer indole synthesis [33] with ketone 3 and hydrazine 4 as previously reported [34]. The indole nitrogen was then alkylated with benzyl bromides or benzyl chlorides using cesium carbonate in refluxing acetonitrile using the method of Fink [35]. Removal of the phthalimide protecting group with hydrazine and formation of the HCl salt of the resulting amine resulted in K103 1 as well as the analogs 7b–7e. A 5-thiomethyltryptamine with no benzyl group on the indole nitrogen (7f) was also prepared by deprotection of the phthalimide of 5 with hydrazine followed by the formation of the HCl salt.
Analogs without the thiomethyl group on the tryptamine were also prepared (Scheme 2). The synthesis of these compounds employs phenylhydrazine hydrochloride 8 and ketone 3 in the Fischer indole reaction. Alkylation of the indole nitrogen in compound 9 with benzyl bromide or 2-chlorobenzylbromide gave the alkylated indoles 10a and 10b, respectively. These compounds were then deprotected leading to 11a and 11b after HCl salt formation.
Substitution on the tryptamine primary amine was also briefly explored (Scheme 3). The primary amine was converted to methylsulfonamide 15 and acetamide 16 to determine if a basic nitrogen was needed for SHIP inhibition. Reduction of the amide 16 led to the ethylamine derivative 17, while treatment of the parent compound with excess paraformaldehyde under reductive amination conditions gave the dimethylamino derivative 14. The methylamine analog was also accessed by the formation of the Boc-protected amine 12, followed by reduction to the methylamine with LiAlH4 and then the formation of the HCl salt 13. This method provided more consistent results than reductive amination methods, which usually led to a mixture of starting material, methylamine and dimethylamine when one equivalent of paraformaldehyde was used.
These compounds were then tested for their activity against the two SHIP paralogs, SHIP1 and SHIP2 in the colorimetric malachite green phosphatase assay [36]. The malachite green assay detects the amount of free phosphate produced from enzymatic reactions with SHIP and an inositol phospholipid substrate [9]. The Malachite assay is useful for ruling out compounds that are fluorescent or have aggregation issues and is inexpensive, so it was utilized as the primary screen even though it is not as sensitive as other assays. Compounds that showed significant inhibition of SHIP in the Malachite had their IC50 against SHIP1 determined using a Fluorescence Polarization (FP) assay that we have previously described [9,14]. The FP assay is significantly more sensitive than the Malachite assay, and so this assay was used to determine IC50 of inhibitors that appeared active in the Malachite assay.
Testing of these tryptamines indicated that the halogen on the N-benzyl group seemed to improve inhibition of SHIP, as compounds 1, 7b–7d and 11b showed significant activity while 7f and 11a showed virtually no activity against SHIP1 or SHIP2 (Table 1). Deletion of the thiomethyl group did allow for an active compound (11b), but the determination of the IC50 showed that there was some loss of activity when compared to 1. Interestingly, returning the thiomethyl group to the 5-position of the indole along with the addition of an unsubstituted benzyl group did provide an active analog (7e), appearing to indicate that the thiomethyl is more responsible for activity than the halogen on the N-benzyl group. Modification of the N-benzyl group by moving the chloride to the 4-positon (7b) or using a 2,3-dichlorbenzyl (7d) provided analogs with significant activity, while the addition of a 4-bromobenzyl group gave less active analog.
Compounds with modifications of the primary amine of the tryptamine were also tested. Acylation was first explored, but acetamide 16 proved to be difficult to test, as it tended to precipitate when mixed with buffer. The methylsulfonamide 15 oddly proved to be a weak agonist of SHIP1. While SHIP1 agonists may have applications as anti-inflammatories [39,40], the agonist activity of 15 was weak and therefore was not further pursued. The addition of two methyl groups to the amine was also explored, with the tertiary amine salt 14 being inactive. Monoalkylation with either a methyl (13) or ethyl group (17) did lead to analogs with activity against SHIP2; however, no inhibition of SHIP1 was observed. While these analogs may present a path towards selective inhibitors of SHIP2, these compounds will not be useful in determining the effects of pan-SHIP inhibition in tumor models.
The most active pan-SHIP1/2 inhibitors (1, 7b, 7d, and 7e) were then evaluated for cytotoxicity on several cancer cell lines using the MTT colorimetric assay for cell metabolic activity (Figure 3) [41]. The assay monitors the ability of NADPH-dependent cellular oxidoreductases to reduce the dye MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide), which when reduced produces a purple color that can be easily quantified. This assay is often used to determine cell viability [42]. Initially, the three new tryptamines and the parent compound 1 were evaluated on a number of leukemia cell lines (NB4, HSB2, K562 and 697-Pre-B) as well as the multiple myeloma cell line OPM-2. All of these cell lines express SHIP1 due to their hematopoietic origin, as SHIP1 is selectively expressed in blood and bone marrow cells [43]. Cytotoxicity was also found on the breast cancer cell lines MBA-MD-231 and MCF-7, which is likely due to the inhibition of SHIP2. SHIP2 is known to be overexpressed in breast cancer cells [11,13], and inhibition of SHIP2 has been shown to be cytotoxic to these cells previously [14,23]. Unexpectedly, the compound that exerted the greatest effect on these cell lines was 7d, which in nearly every cell line exerted the greatest cytotoxicity. While not quite as active as 1 in the FP assay, 7d is more hydrophobic with a ClogP of 4.6 vs. the ClogP of 4.11 for 1. Being more hydrophobic, tryptamine 7d may spend more time associated with the plasma membrane where SHIP activity is most important in signal transduction, and this may explain the greater influence on cells in the MTT assay.

3. Conclusions

In summary, an initial evaluation of some tryptamine pan-SHIP1/2 inhibitors has been conducted. The parent tryptamine and some analogous tryptamines have been synthesized and evaluated for activity against both SHIP paralogs in the Malachite Green assay. Several of these analogs showed significant activity against these inositol phosphatase enzymes. The most active analogs all contained chlorinated benzyl groups on the indole N1 nitrogen and a thiomethyl group at the 5-position on the indole. Some alkyl substitution was tolerated on the primary amine of the tryptamine, but disubstitution with alkyl groups or conversion to an amide or sulfonamide led significantly to reduced SHIP inhibition. The most active analogs showed good activity against a number of cancer cell lines. The analog that was best at killing cancer cells was not the most potent SHIP inhibitor, but this may be due to the lipophilicity of the compounds, as the most lipophilic compound was the most potent on cells and SHIP is known to be recruited the cell membrane. Future work will include efforts to further differentiate the structure from the tryptamine scaffold to avoid any psychotropic side effects.

4. Experimental

4.1. General Experimental Information

All anhydrous reactions were run under a positive pressure of argon. Dichloromethane (DCM) was dried by passage through an alumina column. 1,2-Dichloroethane (DCE) was freshly distilled from calcium hydride before use. Tetrahydrofuran (THF) was freshly distilled from Na/benzophenone still before use. Ethyl acetate (EA) and hexanes were purchased from commercial sources and used as received. Silica gel column chromatography was performed using 60 Å silica gel (230−400 mesh). Melting points are uncorrected. The 4-oxo-1-phthalimidopentane (1) [44] and the 4-(methylthio)phenylhydrazine hydrochloride (2) used in the indole synthesis were prepared as reported previously [45].

4.2. Synthesis of Protected Tryptamines 5 and 9

2-(2-(2-Methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (5). 4-(Methylthio)phenylhydrazine hydrochloride 2 (1.96 g, 10.3 mmol) and 4-oxo-1-phthalimidopentane 3 (2.66 g, 11.5 mmol) were dissolved in ethanol (40 mL, 0.3 M). p-Toluenesulfonic acid monohydrate (3.51 g, 46.3 mmol) was added and the mixture was heated to reflux for 18 h. The mixture was then allowed to cool to room temperature and poured into 1 M aq. NaOH solution. The mixture was then extracted with DCM, and the organic extracts were dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by precipitating the desired tryptamine with EA yielding a yellow solid (3.100 g, 86%). TLC Rf = 0.34 (20% EA/80% hexanes); IR (ATR) 3337, 1706, 1394, 717 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 10.79 (s, 1H), 7.79–7.84 (m, 4H), 7.37 (d, J = 1.8 Hz, 1H), 7.15 (d, J = 8.4 Hz, 1H), 6.94 (dd, J = 8.3, 1.8 Hz, 1H), 3.73 (t, J = 7.6 Hz, 2H), 2.94 (t, J = 7.3 Hz, 2H), 2.38 (s, 3H), 2.25 (s, 3H); 13C NMR (100 MHz, DMSO-d6) δ 168.3, 134.8, 134.3, 133.8, 132.0, 129.5, 126.1, 123.4, 121.9, 117.8, 111.6, 106.7, 38.5, 23.0, 18.3, 11.5. This compound has been previously reported [34].
2-(2-(2-Methyl-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (9). Phenylhydrazine hydrochloride 8 (0.76 g, 7.72 mmol) and 4-oxo-1-phthalimidopentane 3 (2.00 g, 8.65 mmol) were dissolved in ethanol (3 mL, 0.3 M). p-Toluenesulfonic acid monohydrate (6.61 g, 34.75 mmol) was added to the mixture and heated to reflux for 18 h. The mixture was then allowed to cool to room temperature and poured into 1 M NaOH. The mixture was then extracted with DCM, and the combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by precipitating the desired tryptamine with EA yielding an orange powder (2.15 g, 92%). TLC Rf = 0.36 (30% EA/70% hexanes); IR (ATR) 3377, 3349, 2941, 1761, 1697, 1395, 711 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 10.72 (s, 1H), 7.80–7.85 (m, 4H), 7.42 (d, J = 7.4 Hz, 1H), 7.21 (d, J = 7.8 Hz, 1H), 6.96 (d, J = 7.0 Hz, 1H), 6.90 (d, J = 7.6 Hz, 1H), 3.74 (t, J = 7.2 Hz, 2H), 2.96 (t, J = 7.3 Hz, 2H), 2.27 (s, 3H); 13C NMR (100 MHz, DMSO) δ 168.2, 135.6, 134.8, 132.8, 132.1, 128.6, 123.4, 120.5, 118.7, 117.4, 110.9, 106.8, 38.5, 23.2, 11.5. This compound has been previously reported [46].

4.3. General Procedure for N-Alkylation of Indoles

The indole (1 equiv) was dissolved in acetonitrile (0.1 M). Cs2CO3 (6 equiv) and the benzyl halide (3 equiv) were added and the mixture was heated to 80 °C for 18 h. The mixture was cooled to rt, and then filtered to remove the remaining Cs2CO3 and other salts. The filtrate was poured into brine and extracted with DCM. The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated. Silica gel chromatography then provided the desired products.

4.4. Tabulated Spectral Data for Protected Tryptamines 6a–6e, 10a–10b

2-(2-(1-(2-Chlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (6a). The crude oil was purified via silica gel chromatography with 100% chloroform yielding a yellow powder (2.65 g, 65%). TLC Rf = 0.43 (100% CHCl3); IR (ATR) 2936, 2929, 1707, 716 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.79–7.82 (m, 2H), 7.67–7.69 (m, 2H), 7.64 (s, 1H), 7.39 (d, J = 8.0 Hz, 1H), 7.17 (t, J = 7.6 Hz, 1H), 7.07 (dd, J = 1.4, 8.4 Hz, 1H), 7.02 (t, J = 8.5 Hz, 2H), 6.19 (d, J = 8.5 Hz, 1H), 5.30 (s, 2H), 3.93 (t, J = 7.4 Hz, 2H), 3.12 (t, J = 7.4 Hz, 2H), 2.49 (s, 3H), 2.27 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.3, 135.1, 135.0, 134.3, 133.8, 132.1, 131.8, 129.3, 128.8, 128.5, 127.7, 127.4, 126.9, 123.1, 123.0, 118.5, 109.5, 108.0, 44.4, 38.4, 23.5, 18.6, 10.0; Anal. Calcd for C27H23ClN2O2S: C, 68.27; H, 4.88; N, 5.90. Found: C, 68.34; H, 4.51; N, 6.18.
2-(2-(1-(4-Chlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (6b). The crude oil was purified via silica gel chromatography with 100% DCM yielding a yellow oil (0.470 g, 35%). TLC Rf = 0.63 (100% DCM); IR (ATR) 3038, 2920, 1702, 1027, 717 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.77–7.79 (m, 2H), 7.66–7.69 (m, 2H), 7.63 (s, 1H), 7.21 (d, J = 7.7 Hz, 2H), 7.08 (d, J = 8.4 Hz, 1H), 7.03 (d, J = 8.4 Hz, 1H), 6.83 (d, J = 8.1 Hz, 2H), 5.20 (s, 2H), 3.90 (t, J = 7.4 Hz, 2H), 3.10 (t, J = 7.4 Hz, 2H), 2.49 (s, 3H), 2.26 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.2, 136.2, 135.1, 134.2, 133.8, 133.1, 132.1, 128.9, 128.7, 127.7, 127.3, 123.1, 123.0, 118.6, 109.4, 108.0, 46.0, 38.4, 23.5, 18.7, 10.2. This compound has been reported previously [47].
2-(2-(1-(4-Bromobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (6c). The crude residue was purified via silica gel chromatography with 30% EA: 70% hexanes yielding an orange oil (0.780 g, 53%). TLC Rf = 0.43 (30% EA: 70% hexanes); IR (ATR) 2919, 2857, 1705, 1010, 715 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.77–7.80 (m, 2H), 7.67–7.69 (m, 2H), 7.62 (s, 1H), 7.36 (d, J = 8.4 Hz, 2H), 7.08 (dd, J = 1.2, 8.4 Hz, 1H), 7.03 (d, J = 8.4 Hz, 1H), 6.76 (d, J = 8.3 Hz, 2H), 5.18 (s, 2H), 3.90 (t, J = 8.0 Hz, 2H), 3.10 (t, J = 8.0 Hz, 2H), 2.49 (s, 3H), 2.26 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.2, 136.7, 135.0, 134.2, 133.8, 132.1, 131.9, 128.7, 127.7, 127.7, 123.1, 123.0, 121.1, 118.6, 109.4, 108.0, 46.0, 38.4, 23.5, 18.7, 10.1. This compound has been reported previously [47].
2-(2-(1-(2,4-Dichlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (6d). The crude oil was purified via silica gel column chromatography (80% hexanes: 20% EA) yielding a yellow solid (5.18 g, 60%). TLC Rf = 0.48 (80% hexanes: 20% EA), 1H NMR (400 MHz, CDCl3) δ 7.78–7.80 (m, 2H), 7.67–7.69 (m, 2H), 7.60 (d, J = 1.5 Hz, 1H), 7.40 (d, J = 2.0 Hz, 1H), 7.38 (d, J = 2.0 Hz, 1H), 7.02–7.09 (m, 2H), 6.10 (d, J = 8.4 Hz, 1H), 5.25 (s, 2H), 3.92 (t, J = 7.2 Hz, 2H), 3.12 (t, J = 7.3 Hz, 2H), 2.47 (s, 3H), 2.24 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 168.3, 134.9, 134.0, 133.9, 133.7, 133.6, 132.3, 132.1, 131.8, 129.1, 128.8, 128.0, 127.9, 127.7, 123.1, 118.5, 109.3, 108.4, 44.0, 38.4, 23.5, 18.5, 10.0. HRMS (ESI) m/z calcd for C27H23Cl2N2O4S [M+H] 509.0851, found: 509.0850.
2-(2-(1-Benzyl-2-methyl-5-(methylthio)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (6e). The crude oil was purified via silica gel chromatography with 30% EA: 70% hexanes yielding a yellow oil (1.04 g, 83%). TLC Rf = 0.50 (30% EA: 70% hexanes); IR (ATR) 3028, 2917, 1703 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.97–8.00 (m, 2H), 7.84–7.86 (m, 2H), 7.83 (s, 1H), 7.37–7.45 (m, 4H), 7.26 (s, 1H), 7.09 (d, J = 7.0 Hz, 2H), 5.43 (s, 2H), 4.08 (t, J = 7.9 Hz, 2H), 3.28 (t, J = 7.9 Hz, 2H), 2.68 (s, 3H), 2.48 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.3, 137.7, 135.2, 134.4, 133.8, 132.1, 128.8, 128.7, 127.4, 127.3, 125.9, 123.1, 122.9, 118.6, 109.6, 107.7, 46.6, 38.4, 23.6, 18.7, 10.2. This compound has been reported previously [34].
2-(2-(1-(2-Chlorobenzyl)-2-methyl-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (10a). The crude oil was purified via silica gel chromatography with 20% EA: 80% hexanes yielding a yellow solid (0.670 g, 48%). TLC Rf = 0.47 (20% EA: 80% hexanes); IR (ATR) 3300, 2918, 2860, 1704, 1042, 742 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.81–7.83 (m, 2H), 7.68–7.72 (m, 3H), 7.39 (d, J = 8.2 Hz, 1H), 7.16 (t, J = 7.7 Hz, 1H), 7.08–7.11 (m, 3H), 7.02 (t, J = 7.7 Hz, 1H), 6.21 (d, J = 7.7 Hz, 1H), 5.34 (s, 2H), 3.95 (t, J = 8.2 Hz, 2H), 3.16 (t, J = 7.7 Hz, 2H), 2.26 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.3, 136.3, 135.3, 133.8, 133.5, 132.2, 131.8, 129.3, 128.4, 128.0, 127.3, 126.9, 123.1, 121.2, 119.6, 118.1, 108.9, 108.2, 44.3, 38.5, 23.7, 9.9. This compound has been reported previously [47].
2-(2-(1-Benzyl-2-methyl-1H-indol-3-yl)ethyl)isoindoline-1,3-dione (10b). The crude oil was purified via silica gel chromatography with 20% EA: 80% hexanes yielding a yellow-white solid (0.310 g, 24%). TLC Rf = 0.26 (20% EA: 80% hexanes); IR (ATR) 3028, 2920, 2854, 1704, 714, 695 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.81–7.83 (m, 2H), 7.68–7.70 (m, 3H), 7.16–7.25 (m, 4H), 7.08–7.10 (m, 2H), 6.93 (d, J = 7.0 Hz, 2H), 5.29 (s, 2H), 3.91 (t, J = 8.1 Hz, 2H), 3.12 (t, J = 8.1 Hz, 2H), 2.32 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 168.3, 137.9, 136.5, 133.8, 133.6, 132.2, 128.7, 127.9, 127.2, 125.9, 123.1, 121.0, 119.3, 118.0, 109.0, 107.9, 46.5, 38.5, 23.7, 10.1. This compound has been reported previously [34].

4.5. General Procedure for Deprotection of the Phthalamide

To a solution of phthalimide-protected tryptamine (1 equiv) dissolved in methanol (0.3 M) was added hydrazine hydrate (5 equiv). The reaction mixture was brought to reflux at 75 °C for 30 min. The mixture was then allowed to cool, filtered, and concentrated under vacuum. The residue was purified via silica gel column chromatography using a 95% DCM: 5% methanol: 1% conc. aq. NH4OH. The resulting tryptamine was then dissolved in ethyl ether and added to a solution ethyl ether-hydrochloric acid (1 M) and allowed to stir for 30 min. The mixture was concentrated under vacuum and purified via recrystallization from ether/methanol.
2-(1-(2-Chlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (1). Recovered as white crystals (0.130 g, 74%). mp = 187–190 °C; IR (ATR) 2990, 2870, 2794, 1467, 1037, 752 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.60 (s, 1H), 7.46 (d, J = 8.0 Hz, 2H), 7.23 (t, J = 7.8 Hz, 1H), 7.14 (s, 1H), 7.07 (t, J = 7.5 Hz, 1H), 6.23 (d, J = 7.5 Hz, 1H), 5.44 (s, 2H), 3.11–3.16 (m, 4H), 2.49 (s, 3H), 2.31 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 135.5, 135.1 135.0, 131.6, 129.2, 128.5, 128.2, 128.2, 127.0, 126.5, 123.1, 118.1, 109.6, 105.7, 43.9, 39.8, 22.2, 17.4, 8.6; Anal. Calcd for C19H22Cl2N2S: C, 59.84; H, 5.81; N, 7.35. Found: C, 59.82; H, 5.71; N, 7.30.
2-(1-(4-Chlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (7b). Recovered as an off-white solid (0.047 g, 15%). IR (ATR) 2911, 2137, 1608, 1577, 1489, 1012, 794 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.58 (s, 1H), 7.23–7.27 (m, 3H), 7.13 (d, J = 9.2 Hz, 1H), 6.94 (d, J = 7.4 Hz, 2H), 5.36 (s, 2H), 3.12 (bs, 4H), 2.48 (s, 3H), 2.34 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 136.9, 135.5, 135.0, 132.7, 128.4, 128.2, 127.9, 127.4, 123.0, 118.1, 109.7, 105.5, 45.4, 39.8, 22.2, 17.4, 8.8. HRMS (ESI) m/z calcd for C19H22ClN2S [M+H] 345.1186, found: 345.1184.
2-(1-(4-Bromobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (7c). Recovered as an off-white solid (0.0113 g, 40%). IR (ATR) 2964, 2914, 2854, 1606, 1577, 1469, 1009, 791 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.48 (d, J = 1.7 Hz, 1H), 7.30 (d, J = 8.4 Hz, 2H), 7.12 (d, J = 8.4 Hz, 1H), 7.03 (dd, J = 8.5, 1.8 Hz, 1H), 6.78 (d, J = 8.4 Hz, 2H), 5.24 (s, 2H), 2.97–3.06 (m, 4H), 2.38 (s, 3H), 2.23 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 137.4, 135.5, 135.0, 131.4, 128.2, 127.9, 127.8, 123.0, 120.6, 118.1, 109.7, 105.5, 45.5, 39.8, 22.2, 17.4, 8.9. HRMS (ESI) m/z calcd for C19H22BrN2S [M+H] 389.0681, found: 389.0680.
2-(1-(2,4-Dichlorobenzyl)-2-methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (7d). Recovered as an off-white solid (0.403 g, 28%). IR (ATR) 2981, 2878, 2811, 1610, 1587, 1564, 1415 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.82 (s, 3H), 7.71 (d, J = 2.0 Hz, 1H), 7.57 (s, 1H), 7.24–7.28 (m, 2H), 7.05 (dd, J = 1.2, 8.2 Hz, 1H), 6.19 (d, J = 8.5 Hz, 1H), 5.41 (s, 2H), 2.94–3.01 (m, 4H), 2.49 (s, 3H), 2.25 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 135.4, 134.9, 134.2, 133.5, 132.4, 128.9, 128.4, 128.2, 127.8, 127.3, 123.2, 118.1, 109.6, 105.9, 43.6, 39.8, 22.2, 17.3, 8.6; Anal. Calcd for C19H22Cl2N2S: C, 59.84; H, 5.81; N, 7.35. Found: C, 59.82; H, 5.71; N, 7.30.
2-(1-Benzyl-2-methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (7e). Recovered as an off-white solid (0.0443 g, 36%). IR (ATR) 2965, 2908, 1605, 1578, 1470, 1020, 717 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.57 (s, 1H), 7.21–7.28 (m, 4H), 7.14 (dd, J = 2.1, 8.5 Hz, 1H), 6.97 (d, J = 7.1 Hz, 2H), 5.38 (s, 2H), 3.107–3.16 (m, 4H), 2.48 (s, 3H), 2.34 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 138.0, 135.6, 135.1, 128.3, 128.1, 127.7, 126.9, 125.8, 123.0, 118.1, 109.8, 105.2, 46.0, 39.9, 22.2, 17.5, 8.8. This compound has been reported previously [34].
2-(2-Methyl-5-(methylthio)-1H-indol-3-yl)ethanaminium chloride (7f). Recovered as a brown plate-like solid (0.124 g, 66%). IR (ATR) 2980, 2915, 2162,1458, 1432, 1294, 797 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.52 (d, J = 1.6 Hz, 1H), 7.22 (d, J = 8.4 Hz, 1H), 7.04 (dd, J = 8.4, 1.6 Hz, 1H), 3.05–3.11 (m, 4H), 2.44 (s, 3H), 2.38 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 134.6, 133.9, 128.8, 126.8, 122.5, 117.9, 111.0, 104.4, 39.9, 21.9, 17.7, 10.2. This compound has been reported previously [34].
2-(1-(2-Chlorobenzyl)-2-methyl-5-1H-indol-3-yl)ethanaminium chloride (11a). Recovered as an off-white solid (0.130 g, 25%). IR (ATR) 2980, 2970, 1736, 1591, 1570, 1469, 743 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.58–7.60 (m, 1H), 7.45 (d, J = 7.7 Hz, 1H), 7.16–7.25 (m, 2H), 7.03–7.10 (m, 3H), 6.22 (d, J = 7.2 Hz, 1H), 5.45 (s, 2H), 3.17 (bs, 4H), 2.32 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 140.6, 139.2, 137.9, 135.6, 133.1, 132.3, 131.4, 130.9, 130.5, 125.1, 123.3, 121.1, 112.8, 109.8, 47.7, 43.8, 26.2, 12.5. HRMS (ESI) m/z calcd for C18H20ClN2 [M+H] 299.1309, found: 299.1308.
2-(1-Benzyl-2-methyl-1H-indol-3-yl) ethanaminium chloride (11b). Recovered as an off-white solid (0.1080 g, 46%). IR (ATR) 3026, 2913, 1604, 1568, 1467, 733 cm−1; 1H NMR (400 MHz, CD3OD) δ 7.53 (d, J = 6.8 Hz, 1H), 7.20–7.30 (m, 4H), 7.04–7.12 (m, 2H), 6.97 (d, J = 7.2 Hz, 2H), 5.40 (s, 2H), 3.12–3.15 (m, 4H), 2.35 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 138.2, 136.8, 134.1, 128.3, 127.3, 126.8, 125.8, 120.9, 119.1, 116.9, 109.1, 105.4, 45.9, 39.9, 22.3, 8.8. HRMS (ESI) m/z calcd for C18H21N2 [M+H] 265.1699, found: 265.1697.

4.6. Modification of the Tryptamine Primary Amine

tert-Butyl-N-(2{1-[(2-chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl)-1H-indol-3-yl}ethyl)carbamate (12). Tryptamine 1 (0.200 g, 0.530 mmol) was dissolved in 3 mL of 2:1 methanol/THF. Triethylamine (0.081 mL, 0.53 mmol) and di-tert-butyl dicarbonate (0.108 g, 0.57 mmol) were added to the mixture. After 4 h at rt the solvent was removed via rotary evaporation and the residue was taken up in EA. The solution was washed with sat. NaHCO3 (3 × 15 mL). The organic layer was collected, dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified via silica gel chromatography using a 90% hexanes: 10% EA eluent yielding carbamate 12 as a foamy white solid (0.120 g, 51%). TLC Rf = 0.25 (10% EA: 90% hexanes); IR (ATR) 3350, 2975, 1692, 1162 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.57 (s, 1H), 7.40 (d, J = 8.0 Hz, 1H), 7.13–7.19 (m, 2H), 7.01–7.08 (m, 2H), 6.21 (d, J = 7.7 Hz, 1H), 5.33 (s, 2H), 4.56 (bs, 1H), 3.37 (bs, 2H), 2.94 (t, J = 6.5 Hz, 2H), 2.52 (s, 3H), 2.27 (s, 3H), 1.43 (s, 9H); 13C NMR (100 MHz, CD3CN) δ 156.4, 136.2, 135.7, 135.5, 132.2, 129.9, 129.7, 129.3, 128.0, 127.9, 127.4, 122.8, 119.1, 110.2, 109.6, 78.5, 44.7, 41.5, 28.2, 25.2, 18.2, 9.9. HRMS (ESI) m/z calcd for C24H30ClN2O2S [M+H] 445.1711, found: 445.1708.
(2{1-[(2-Chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl-1H-indol-3-yl}ethyl)methylaminium chloride (13). Carbamate 12 (0.200 g, 0.450 mmol) was dissolved in dry THF (5 mL, 0.1 M) and cooled to 0 °C. LiAlH4 solution (1 M in THF, 1.92 mL, 1.92 mmol) was added slowly to the mixture at 0 °C. The reaction was allowed to warm to rt and then heated to reflux for 4h. After cooling the reaction to rt, the mixture was diluted with 10 mL of ethyl ether and quenched by the sequential addition of 80 µL of water, 240 µL of 15% aq. NaOH solution, and 80 µL of water. Approximately 1 g of anhydrous MgSO4 was then added and, after stirring for 15 min, the mixture filtered through celite with ethyl ether and concentrated. The residue was purified via silica gel chromatography using a solvent gradient of 100% EA to 95% EA: 5% NH4OH yielding the methylamine derivative. This was then added to a 1:1 ether-hydrochloric acid solution (1 mL, 2 M) and allowed to stir for 30 min. The mixture was concentrated under vacuum and purified via recrystallization from ether/methanol yielding 13 as a red solid (0.124 g, 70% from 12). IR (ATR) 2917, 2696, 2431, 1466, 1441, 1038, 751 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.64 (s, 1H), 7.42 (d, J = 7.8 Hz, 1H), 7.19 (d, J = 7.8 Hz, 1H), 7.07 (s, 1H), 7.02 (t, J = 7.8 Hz, 1H), 6.20 (d, J = 7.4 Hz, 1H), 5.36 (s, 2H), 3.11–3.23 (m, 4H), 2.74 (s, 3H), 2.47 (s, 3H), 2.29 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 135.5, 135.1, 131.7, 129.2, 128.5, 128.2, 128.1, 127.0, 126.5, 123.1, 118.1, 111.4, 109.6, 105.3, 49.4, 43.9, 32.4, 21.1, 17.4, 8.6. HRMS (ESI) m/z calcd for C20H24ClN2S [M+H] 359.1343, found: 359.1340.
(2{1-[(2-Chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl-1H-indol-3-yl}ethyl) dimethylaminium chloride (14). Tryptamine 1 (0.175 g, 0.460 mmol) was dissolved in 0.60 mL of acetic acid. Sodium cyanoborohydride (0.289 g, 4.6 mmol) dissolved in 1 mL of methanol was added to the reaction followed by the addition of formalin (37%, 1.8 mL, 23 mmol). The mixture was stirred at rt for 18 h, followed by solvent removal in vacuo. The residue was dissolved in DCM and the mixture was washed using 2 M aq. NaOH solution (3 × 5 mL). The organic layer was then dried over anhydrous Na2SO4, filtered, and concentrated. The crude oil was purified via silica gel chromatography using a 90% DCM: 10% MeOH eluent yielding a clear oil that was then added to a 1:1 ether-hydrochloric acid solution (1 mL, 2 M) and allowed to stir for 30 min. The mixture was concentrated under vacuum and purified via recrystallization from ether/methanol yielding 14 a red solid (0.040 g, 21% over 2 steps). IR (ATR) 2917, 2780, 2665, 2469, 1466, 1441, 1413, 1048, 750 cm−1; 1H NMR (400 MHz, CDCl3) δ 12.94 (bs, 1H), 7.55 (s, 1H), 7.41 (d, J = 7.8 Hz, 1H), 7.15–7.21 (m, 2H), 7.01–7.09 (m, 2H), 6.17 (d, J = 7.5 Hz, 1H), 5.33 (s, 2H), 3.38–3.42 (m, 2H), 3.20 (m, 2H), 2.91 (s, 3H), 2.89 (s, 3H), 2.55 (s, 3H), 2.36 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 135.3, 135.2, 134.6, 131.9, 129.5, 128.7, 128.3, 127.8, 127.3, 126.6, 123.4, 118.2, 110.0, 105.3, 58.1, 44.5, 42.9, 20.2, 18.8, 10.3. HRMS (ESI) m/z calcd for C21H26ClN2S [M+H] 373.1499, found: 373.1496.
N-(2{1-[(2-Chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl)-1H-indol-3-yl}ethyl) methanesulfonamide (15). Tryptamine 1 (0.250 g, 0.530 mmol) was dissolved in 0.6 mL of DCM and cooled to −78 °C. Triethylamine (0.074 mL, 0.527 mmol) was added to the mixture and, after 5 min, methanesulfonyl chloride (0.041 mL, 0.527 mmol) dissolved in 0.6 mL of DCM was added. The mixture was kept at −78 °C for 2 h, and then warmed to rt and diluted with water. The mixture was extracted using DCM (3 × 5 mL) and the combined organic layers were washed with sat. aq. NaCl solution. The organic layer was then dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified via silica gel chromatography (30% EA: 70% hexanes) yielding sulfonamide 15 a white powder (0.091 g, 46%). TLC Rf = 0.22 (30% EA: 70% hexanes); IR (ATR) 3659, 3287, 2980, 2919, 1463, 1440, 1313, 1145, cm−1; 1H NMR (400 MHz, CDCl3) δ 7.59 (s, 1H), 7.43 (d, J = 7.3 Hz, 1H), 7.16–7.20 (m, 2H), 7.06–7.11 (m, 2H), 6.24 (d, J = 7.3 Hz, 1H), 5.36 (s, 2H), 4.42 (bs, 1H), 3.43–3.41 (m, 2H), 3.09–3.05 (m, 2H), 2.89 (s, 3H), 2.55 (s, 3H), 2.33 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 135.3, 135.0, 134.9, 131.9, 129.5, 128.7, 128.4, 128.0, 127.4, 126.7, 123.3, 118.6, 109.8, 107.3, 44.5, 43.6, 40.4, 25.7, 18.7, 10.2. HRMS (ESI) m/z calcd for C20H24ClN2O2S2 [M+H] 423.0962, found: 423.0960.
N-(2{1-[(2-Chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl-1H-indol-3-yl}ethyl) acetamide (16). Tryptamine 1 (0.120 g, 0.314 mmol) was dissolved in 1.5 mL of 2:1 methanol/THF and cooled to 0 °C. Triethylamine (0.086 mL, 0.692 mmol) was added to the mixture and stirred 5 min. Acetic anhydride (0.033 mL, 0.346 mmol) was added and the reaction was brought to rt and stirred for 2 h. The mixture was then diluted in EA and washed with sat. aq. NaHCO3 (3 × 15 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified via silica gel chromatography (40% EA: 60% hexanes) yielding acetamide 16 as a red foamy solid (0.110 g, 98%). TLC Rf = 0.33 (40% EA: 60% hexanes); IR (ATR) 3249, 3067, 2919, 1630, 1468,1368, 752 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.57 (s, 1H), 7.40 (d, J = 8.0 Hz, 1H), 7.12–7.19 (m, 2H), 7.00–7.07 (m, 2H), 6.19 (d, J = 7.7 Hz, 1H), 5.79 (bs, 1H), 5.32 (s, 2H), 3.50 (q, J = 6.3 Hz, 2H), 2.96 (t, J = 6.8 Hz, 2H), 2.51 (s, 3H), 2.26 (s, 3H), 1.92 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 170.2, 135.3, 135.0, 134.5, 131.9, 129.5, 128.7, 128.6, 127.7, 127.3, 126.7, 123.2, 118.9, 109.7, 108.7, 44.5, 40.3, 24.5, 23.3, 18.8, 10.0. HRMS (ESI) m/z calcd for C21H24ClN2OS [M+H] 387.1292, found: 387.1290.
(2{1-[(2-Chlorophenyl)methyl]-2-methyl-5-(methylsulfanyl-1H-indol-3-yl}ethyl) ethylaminium chloride (17). Acetamide 16 (0.37 mmol, 150 mg) was dissolved in dry THF (5 mL, 0.1 M) and cooled to 0 °C. LiAlH4 (1 M in THF, 2.0 mL, 2.0 mmol) was added slowly to the mixture at 0 °C. The reaction was warmed to rt and then heated to reflux for 4h. After cooling the reaction to rt, the mixture was diluted with 10 mL of ethyl ether and quenched by the sequential addition of 100 µL of water, 300 µL of 15% aq. NaOH solution, and 100 µL of water. Approximately 1 g of anhydrous MgSO4 was then added and, after stirring for 15 min, the mixture filtered through celite with ethyl ether and concentrated. The residue was then purified via silica gel chromatography using (90% DCM: 9% methanol: 1% conc. aq. NH4OH) to provide the corresponding ethylamine as a yellow oil (63%). This oil was then added to a 1:1 ether-HCl acid solution (1 mL, 2 M) and allowed to stir for 30 min. The mixture was concentrated under vacuum and purified via recrystallization from ether/methanol yielding 17 as a white solid. mp = 196–198 °C (MeOH). IR (thin film) 3443, 2908, 2900, 1551, 1375, 1242 cm−1; 1H NMR (300 MHz, CDCl3) δ 7.61 (s. 1H), 7.38 (m, 1H), 7.11–7.19 (m, 2H), 6.98–7.06 (m, 2H), 6.18 (d, J = 7.6 Hz, 1H), 5.31 (s, 2H), 3.10 (bs, 2H), 3.03 (t, J = 6.5 Hz, 2H), 2.93 (t, J = 6.2 Hz, 2H), 2.75 (q, J = 7.1 Hz, 2H), 2.52 (s, 3H), 2.28 (s, 3H), 1.11–1.04 (t, 3H); 13C NMR (75 MHz, CDCl3) δ 135.4, 135.2, 134.7, 134.5, 132.0, 129.6, 128.9, 128.6, 127.9, 127.6, 126.9, 123.3, 118.6, 110.0, 52.9, 46.6, 44.6, 29.9, 21.0, 19.0, 10.5. HRMS (ESI) m/z calcd for C21H26ClN2S [M+H] 373.1499, found: 373.1495.

4.7. Malachite Green Phosphatase Release Assays

Malachite green assays to monitor phosphatase release (Echelon Biosciences) were performed with recombinant human truncated SHIP1 (tSHIP1) [48] and SHIP2 (Echelon Biosciences). Serial dilutions of the compounds dissolved in DMSO were added to the recombinant enzymes diluted in reaction buffer Rx (50 mM Hepes pH 7.4, 150 mM NaCl, 1 mM MgCl2, 0.25 mM EDTA) in triplicate reaction wells in 96-well plates. After incubation for 2 min at room temperature, 2.5 µL of 1 mM phosphatidylinositol 3,4,5-trisphosphate diC8 (PI(3,4,5)P3-diC8, Echelon Biosciences) was added to each reaction to a final concentration of 100 µM in a final volume of 25 µL /well. Following a 20 min incubation at 37 °C, 100 µL of Malachite Green solution (Echelon Biosciences) was added to each well and the plates were incubated at room temperature in the dark for 15 min. Plates were then read at 620 nm on a plate reader (Synergy 2, BioTek, Santa Clara, CA, USA). In addition, 3α-Aminocholestane, a known SHIP1 inhibitor, and AS1949490, a known SHIP2 inhibitor, were used as positive controls.

4.8. Fluorescence Polarization (FP) Assays for the Detection of PI(3,4)P2

The FP Assay [49] for the detection of PI(3,4)P2 (Echelon Biosciences) was performed using tSHIP1 [48] with serial dilutions of the tryptamines in DMSO according to the manufacturer’s recommendation as previously described [14]. Briefly, serial dilution of the compounds and control with 2.5% solvent only (0 µM) is added to the enzyme in a volume of 40 µL of enzyme-specific reaction buffer (Rx) (S1 Reaction buffer for tSHIP1: 20 mM Tris pH 7.5, 150 mM NaCl, 0.05% Tween 20, 10 mM MgCl2), (S2 reaction buffer for tSHIP1 or SHIP2-Enz: 50 mM Hepes pH 7.4, 150 mM NaCl, 1mM MgCl2, 0.25 mM EDTA). 40 µL of 4 µM PIP3 (PI(3,4,5)P3-diC8) in Rx buffer is added to each reaction and incubated at 37 °C for 20 min, followed by heat inactivation for 3 min at 95 °C. Reactions were spun down briefly and 10 µL of each reaction was added in 6 replicate wells to a black 384-well plate provided with the FP kit. 10 µL of 1X reconstituted Detector (a phosphoinositide binding protein) in PBS is then added to each well, followed by 5 µL of 1X freshly diluted Probe (in PBS, a fluorophore-labeled phosphoinositide) protected from light. Assay plates are gently tapped to mix, the plate is sealed and spun down briefly and the reaction is allowed to equilibrate for 60 min at room temperature protected from light. Control wells are included with each assay (no enzyme control (NE): 5µL Rx buffer with 2.5% solvent + 5 µL PIP3 (4 µM), 10 µL Detector, 5 µL Probe, Probe Alone (PA) control (10 µL enzyme buffer, 10 µL PBS, 5 µL Probe). Fluorescence polarization is then read on a Bio-Tek Synergy 2 (BioTek, Santa Clara, CA, USA) plate reader and is expressed in milli Polarization (mP) units. 3α-Aminocholestane, a known SHIP1 inhibitor, and AS1949490, a known SHIP2 inhibitor, were used as positive controls.

4.9. MTT Cell Viability Assay

Cells were treated in triplicate or more with increasing concentrations of the compound. Cell viability was determined with a Cell Counting Kit (Dojindo Molecular Technologies, Rockville, MD, USA) per the manufacturer’s instructions. The odds density (OD) of compound-treated cells was divided by the OD of their vehicle control, and the viability was expressed as a percentage of untreated cells. Results are expressed as mean ± standard error of the mean (SEM) of three individual experiments. HSB2 (ATCC CCL-120.1), K562 (ATCC CCL-243), MBA-MD-231 (ATCC HTB-26), and MCF-7 (ATCC HTB-22) cell lines were obtained from the ATCC (American Type Culture Collection, Manassas, VA, USA), while the 697 Pre-B (ACC 42), NB-4 (ACC 207), and OPM-2 (ACC-50) cell lines were obtained from the DSMZ (German Collection of Microorganisms and Cell Cultures, Göttingen, Germany). Both the ATCC and DSMZ perform genetic validation on deposited cell lines.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27238451/s1, copies of 1H NMR and 13C NMR spectra; Table S1: Predicted Physiochemical Properties and Lipophilicity for the Tested Tryptaminesa; Table S2: Predicted Pharmacokinetic Properties for the Tested Tryptaminesa.

Author Contributions

Conceptualization, W.G.K. and J.D.C.; investigation, S.F., S.T.M. and J.P.S.; A.A.A.; formal analysis, S.F., S.T.M. and J.P.S.; A.A.A., W.G.K. and J.D.C.; writing—original draft preparation, J.D.C. and S.T.M.; writing—review and editing, J.D.C., W.G.K., S.F. and S.T.M.; supervision, W.G.K. and J.D.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the U.S. National Institutes of Health under award number RF1AG059717.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable, no human subjects involved.

Data Availability Statement

Not applicable.

Conflicts of Interest

S.F., W.G.K. and J.D.C. have patents, pending and issued, concerning the analysis and targeting of SHIP1 and SHIP2 in disease. The other authors have no conflicts to disclose.

Sample Availability

Samples of the compounds can be obtained from the authors subject to availability.

References

  1. Balla, T. Phosphoinositides: Tiny lipids with giant impact on cell regulation. Physiol. Rev. 2013, 93, 1019–1137. [Google Scholar] [CrossRef] [PubMed]
  2. Liu, P.; Cheng, H.; Roberts, T.M.; Zhao, J.J. Targeting the phosphoinositide 3-kinase pathway in cancer. Nat. Rev. Drug Discov. 2009, 8, 627–644. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Wu, P.; Hu, Y. Small molecules targeting phosphoinositide 3-kinases. MedChemComm 2012, 3, 1337–1355. [Google Scholar] [CrossRef]
  4. Marone, R.; Cmiljanovic, V.; Giese, B.; Wymann, M.P. Targeting phosphoinositide 3-kinase-Moving towards therapy. Biochim. Biophys. Acta 2008, 1784, 159–185. [Google Scholar] [CrossRef]
  5. Elkabets, M.; Vora, S.; Juric, D.; Morse, N.; Mino-Kenudson, M.; Muranen, T.; Tao, J.; Campos, A.B.; Rodon, J.; Ibrahim, Y.H.; et al. mTORC1 inhibition is required for sensitivity to PI3K p110α inhibitors in PIK3CA-mutant breast cancer. Sci. Transl. Med. 2013, 5, 196ra99. [Google Scholar] [CrossRef] [Green Version]
  6. Brown, K.K.; Toker, A. The phosphoinositide 3-kinase pathway and therapy resistance in cancer. F1000Prime Rep. 2015, 7, 13. [Google Scholar] [CrossRef]
  7. Park, S.; Kim, Y.S.; Kim, D.Y.; So, I.; Jeon, J.-H. PI3K pathway in prostate cancer: All resistant roads lead to PI3K. Biochim. Biophys. Acta Rev. Cancer 2018, 1870, 198–206. [Google Scholar] [CrossRef]
  8. Song, M.S.; Salmena, L.; Pandolfi, P.P. The functions and regulation of the PTEN tumour suppressor. Nat. Rev. Mol. Cell Biol. 2012, 13, 283–296. [Google Scholar] [CrossRef]
  9. Brooks, R.; Fuhler, G.M.; Iyer, S.; Smith, M.J.; Park, M.-Y.; Paraiso, K.H.T.; Engelman, R.W.; Kerr, W.G. SHIP1 Inhibition Increases Immunoregulatory Capacity and Triggers Apoptosis of Hematopoietic Cancer Cells. J. Immunol. 2010, 184, 3582–3589. [Google Scholar] [CrossRef] [Green Version]
  10. Prasad, N.K.; Decker, S.J. SH2-containing 5’-inositol phosphatase, SHIP2, regulates cytoskeleton organization and ligand-dependent down-regulation of the epidermal growth factor receptor. J. Biol. Chem. 2005, 280, 13129–13136. [Google Scholar] [CrossRef]
  11. Prasad, N.K.; Tandon, M.; Badve, S.; Snyder, P.W.; Nakshatri, H. Phosphoinositol phosphatase SHIP2 promotes cancer development and metastasis coupled with alterations in EGF receptor turnover. Carcinogenesis 2008, 29, 25–34. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Prasad, N.K.; Tandon, M.; Handa, A.; Moore, G.E.; Babbs, C.F.; Snyder, P.W.; Bose, S. High Expression of Obesity-Linked Phosphatase SHIP2 in Invasive Breast Cancer Correlates with Reduced Disease-Free Survival. Tumor Biol. 2008, 29, 330–341. [Google Scholar] [CrossRef]
  13. Prasad, N.K. SHIP2 phosphoinositol phosphatase positively regulates EGFR-Akt pathway, CXCR4 expression, and cell migration in MDA-MB-231 breast cancer cells. Int. J. Oncol. 2009, 34, 97–105. [Google Scholar] [CrossRef] [PubMed]
  14. Fuhler, G.M.; Brooks, R.; Toms, B.; Iyer, S.; Gengo, E.A.; Park, M.Y.; Gumbleton, M.; Viernes, D.R.; Chisholm, J.D.; Kerr, W.G. Therapeutic potential of SH2 domain-containing inositol-5′-phosphatase 1 (SHIP1) and SHIP2 inhibition in cancer. Mol. Med. 2012, 18, 65–75. [Google Scholar] [CrossRef] [PubMed]
  15. Blunt, M.D.; Ward, S.G. Targeting PI3K isoforms and SHIP in the immune system: New therapeutics for inflammation and leukemia. Curr. Opin. Pharmacol. 2012, 12, 444–451. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Liu, S.-L.; Wang, Z.-G.; Hu, Y.; Xin, Y.; Singaram, I.; Gorai, S.; Zhou, X.; Shim, Y.; Min, J.-H.; Gong, L.-W.; et al. Quantitative Lipid Imaging Reveals a New Signaling Function of Phosphatidylinositol-3,4-Bisphophate: Isoform- and Site-Specific Activation of Akt. Mol. Cell 2018, 71, 1092–1104. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Franke, T.F.; Kaplan, D.R.; Cantley, L.C.; Toker, A. Direct regulation of the Akt proto-oncogene product by phosphatidylinositol-3,4-bisphosphate. Science 1997, 275, 665–668. [Google Scholar] [CrossRef]
  18. Ma, K.; Cheungb, S.M.; Marshallb, A.J.; Duronio, V. PI(3,4,5)P3 and PI(3,4)P2 levels correlate with PKB/akt phosphorylation at Thr308 and Ser473, respectively; PI(3,4)P2 levels determine PKB activity. Cell Signal. 2008, 20, 684–694. [Google Scholar] [CrossRef]
  19. Jain, S.K.; Susa, M.; Keeler, M.L.; Carlesso, N.; Druker, B.; Varticovski, L. PI 3-kinase activation in BCR/abl-transformed hematopoietic cells does not require interaction of p85 SH2 domains with p210 BCR/abl. Blood 1996, 88, 1542–1550. [Google Scholar] [CrossRef]
  20. Gewinner, C.; Wang, Z.C.; Richardson, A.; Teruya-Feldstein, J.; Etemadmoghadam, D.; Bowtell, D.; Barretina, J.; Lin, W.M.; Rameh, L.; Salmena, L.; et al. Evidence that inositol polyphosphate 4-phosphatase type II is a tumor suppressor that inhibits PI3K signaling. Cancer Cell 2009, 16, 115–125. [Google Scholar] [CrossRef]
  21. Ivetac, I.; Gurung, R.; Hakim, S.; Horan, K.A.; Sheffield, D.A.; Binge, L.C.; Majerus, P.W.; Tiganis, T.; Mitchell, C.A. Regulation of PI(3)K/Akt signalling and cellular transformation by inositol polyphosphate 4-phosphatase-1. EMBO Rep. 2009, 10, 487–493. [Google Scholar] [CrossRef]
  22. Kennah, M.; Yau, T.Y.; Nodwell, M.; Krystal, G.; Andersen, R.J.; Ong, C.J.; Mui, A.L.F. Activation of SHIP via a small molecule agonist kills multiple myeloma cells. Exp. Hematol. 2009, 37, 1274–1283. [Google Scholar] [CrossRef] [PubMed]
  23. Hoekstra, E.; Willemsen, M.; van der Woude Christien, J.; Bruno Marco, J.; Peppelenbosch Maikel, P.; Fuhler Gwenny, M.; Das Asha, M.; Ten Hagen Timo, L.M.; Swets, M.; Kuppen Peter, J.K.; et al. Lipid phosphatase SHIP2 functions as oncogene in colorectal cancer by regulating PKB activation. Oncotarget 2016, 7, 73525–73540. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Hillmann, P.; Fabbro, D. PI3K/mTOR pathway inhibition: Opportunities in oncology and rare genetic diseases. Int. J. Mol. Sci. 2019, 20, 5792. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Suwa, A.; Kurama, T.; Shimokawa, T. SHIP2 and its involvement in various diseases. Expert Opin. Ther. Targets 2010, 14, 727–737. [Google Scholar] [CrossRef]
  26. Thomas, M.P.; Erneux, C.; Potter, B.V.L. SHIP2: Structure, Function and Inhibition. ChemBioChem 2017, 18, 233–247. [Google Scholar] [CrossRef] [Green Version]
  27. Pedicone, C.; Meyer, S.T.; Chisholm, J.D.; Kerr, W.G. Targeting SHIP1 and SHIP2 in cancer. Cancers 2021, 13, 890. [Google Scholar] [CrossRef]
  28. Russo, C.M.; Adhikari, A.A.; Wallach, D.R.; Fernandes, S.; Balch, A.N.; Kerr, W.G.; Chisholm, J.D. Synthesis and initial evaluation of quinoline-based inhibitors of the SH2-containing inositol 5’-phosphatase (SHIP). Bioorg. Med. Chem. Lett. 2015, 25, 5344–5348. [Google Scholar] [CrossRef] [Green Version]
  29. Woolley, D.W.; Shaw, E. An antiserotonin which is active when fed. J. Pharmacol. Exp. Ther. 1953, 108, 87–93. [Google Scholar]
  30. Shaw, E.; Woolley, D.W. Synthesis and demonstration of antiserotonin activity of 1-benzyl-2-methyl-5-hydroxytryptamine (BAS-phenol). Proc. Soc. Exp. Biol. Med. 1957, 96, 439–442. [Google Scholar] [CrossRef]
  31. Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 1997, 23, 3–25. [Google Scholar] [CrossRef]
  32. Hughes, J.P.; Rees, S.; Kalindjian, S.B.; Philpott, K.L. Principles of early drug discovery. Br. J. Pharmacol. 2011, 162, 1239–1249. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Hughes, D.L. Progress in the Fischer indole reaction. A review. Org. Prep. Proced. Int. 1993, 25, 607–632. [Google Scholar] [CrossRef]
  34. Sosic, I.; Anderluh, M.; Sova, M.; Gobec, M.; Mlinaric Rascan, I.; Derouaux, A.; Amoroso, A.; Terrak, M.; Breukink, E.; Gobec, S. Structure-Activity Relationships of Novel Tryptamine-Based Inhibitors of Bacterial Transglycosylase. J. Med. Chem. 2015, 58, 9712–9721. [Google Scholar] [CrossRef]
  35. Fink, D.M. Cesium carbonate-promoted N-alkylation of indoles. Synlett 2004, 15, 2394–2396. [Google Scholar] [CrossRef]
  36. Cogan, E.B.; Birrell, G.B.; Griffith, O.H. A Robotics-Based Automated Assay for Inorganic and Organic Phosphates. Anal. Biochem. 1999, 271, 29–35. [Google Scholar] [CrossRef] [Green Version]
  37. Moriguchi, I.; Hirono, S.; Nakagome, I.; Hirano, H. Comparison of reliability of log P values for drugs calculated by several methods. Chem. Pharm. Bull. 1994, 42, 976–978. [Google Scholar] [CrossRef] [Green Version]
  38. Daina, A.; Michielin, O.; Zoete, V.; Michielin, O.; Michielin, O. SwissADME: A free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci. Rep. 2017, 7, 42717. [Google Scholar] [CrossRef] [Green Version]
  39. Dungan, O.M.; Dormann, S.; Fernandes, S.; Duffy, B.C.; Effiong, D.G.; Kerr, W.G.; Chisholm, J.D. Synthetic studies on the indane SHIP1 agonist AQX-1125. Org. Biomol. Chem. 2022, 20, 4016–4020. [Google Scholar] [CrossRef]
  40. Pedicone, C.; Fernandes, S.; Matera, A.; Meyer, S.T.; Loh, S.; Ha, J.-H.; Bernard, D.; Chisholm, J.D.; Paolicelli, R.C.; Kerr, W.G. Discovery of a novel SHIP1 agonist that promotes degradation of lipid-laden phagocytic cargo by microglia. iScience 2022, 25, 104170. [Google Scholar] [CrossRef]
  41. Mosmann, T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55–63. [Google Scholar] [CrossRef]
  42. Stockert, J.C.; Horobin, R.W.; Colombo, L.L.; Blázquez-Castro, A. Tetrazolium salts and formazan products in Cell Biology: Viability assessment, fluorescence imaging, and labeling perspectives. Acta Histochem. 2018, 120, 159–167. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Kerr, W.G.; Pedicone, C.; Dormann, S.; Pacherille, A.; Chisholm, J.D. Small Molecule Targeting of SHIP1 and SHIP2. Biochem. Soc. Trans. 2020, 48, 291–300. [Google Scholar] [CrossRef] [PubMed]
  44. Eriks, J.C.; Van der Goot, H.; Sterk, G.J.; Timmerman, H. Histamine H2-receptor agonists. Synthesis, in vitro pharmacology, and qualitative structure-activity relationships of substituted 4- and 5-(2-aminoethyl)thiazoles. J. Med. Chem. 1992, 35, 3239–3246. [Google Scholar] [CrossRef] [PubMed]
  45. Ahlström, M.M.; Ridderström, M.; Zamora, I.; Luthman, K. CYP2C9 Structure−Metabolism Relationships:  Optimizing the Metabolic Stability of COX-2 Inhibitors. J. Med. Chem. 2007, 50, 4444–4452. [Google Scholar] [CrossRef]
  46. Righi, M.; Topi, F.; Bartolucci, S.; Bedini, A.; Piersanti, G.; Spadoni, G. Synthesis of Tryptamine Derivatives via a Direct, One-Pot Reductive Alkylation of Indoles. J. Org. Chem. 2012, 77, 6351–6357. [Google Scholar] [CrossRef] [PubMed]
  47. Archer, S. 5-Methylthio-1-Benzyl Tryptamines. U.S. Patent 3074960, 22 January 1963. [Google Scholar]
  48. Brooks, R.; Iyer, S.; Akada, H.; Neelam, S.; Russo, C.M.; Chisholm, J.D.; Kerr, W.G. Coordinate Expansion of Murine Hematopoietic and Mesenchymal Stem Cell Compartments by SHIPi. Stem Cells 2015, 33, 848–858. [Google Scholar] [CrossRef]
  49. Drees, B.E.; Weipert, A.; Hudson, H.; Ferguson, C.G.; Chakravarty, L.; Prestwich, G.D. Competitive fluorescence polarization assays for the detection of phosphoinositide kinase and phosphatase activity. Comb. Chem. High Throughput Screen. 2003, 6, 321–330. [Google Scholar] [CrossRef]
Molecules 27 08451 g001 550
Figure 1. Malignancy and the “Two PIP Hypothesis”. Signaling an imbalance in the amounts of both PI(3,4,5)P3 and PI(3,4)P2 may lead to the development of a malignancy.
Figure 1. Malignancy and the “Two PIP Hypothesis”. Signaling an imbalance in the amounts of both PI(3,4,5)P3 and PI(3,4)P2 may lead to the development of a malignancy.
Molecules 27 08451 g001
Molecules 27 08451 g002 550
Figure 2. Structure of the pan-SHIP1/2 inhibitor K103 and Benanserin HCl.
Figure 2. Structure of the pan-SHIP1/2 inhibitor K103 and Benanserin HCl.
Molecules 27 08451 g002
Molecules 27 08451 sch001 550
Scheme 1. Synthesis of K103 and analogs.
Scheme 1. Synthesis of K103 and analogs.
Molecules 27 08451 sch001
Molecules 27 08451 sch002 550
Scheme 2. Synthesis of sulfur-free K103 analogs.
Scheme 2. Synthesis of sulfur-free K103 analogs.
Molecules 27 08451 sch002
Molecules 27 08451 sch003 550
Scheme 3. Modifications of the primary amine.
Scheme 3. Modifications of the primary amine.
Molecules 27 08451 sch003
Molecules 27 08451 g003 550
Figure 3. Activity of pan-SHIP1/2 Inhibitors against leukemia, multiple myeloma, and breast cancer cell lines. MTT assays show that some tryptamines kill tumor cell lines. Results are shown with connecting lines for clarity and expressed as mean ± standard error of the mean (SEM) of three individual experiments.
Figure 3. Activity of pan-SHIP1/2 Inhibitors against leukemia, multiple myeloma, and breast cancer cell lines. MTT assays show that some tryptamines kill tumor cell lines. Results are shown with connecting lines for clarity and expressed as mean ± standard error of the mean (SEM) of three individual experiments.
Molecules 27 08451 g003
Table
Table 1. In Vitro Evaluation of Tryptamines.
Table 1. In Vitro Evaluation of Tryptamines.
Molecules 27 08451 i001
EntryCmpdR1XYCLogP bMalachite
(500 µM)
% Inhib.
SHIP1		Malachite
(250 µM)
% Inhib.
SHIP1		IC50
SHIP1
(Via FP)		Malachite
(500 µM)
% Inhib.
SHIP2		Malachite
(250 µM)
% Inhib.
SHIP2		IC50
SHIP2
(via FP)
112-chlorobenzylNH3+ Cl−SMe4.1151%7%5 µM59%7%10 µM
27b4-chlorobenzylNH3+ Cl−SMe4.1133%0%11 µM49%18%14 µM
37c4-bromobenzylNH3+ Cl−SMe4.2347%3%51 µM38%30%58 µM
47d2,4-dichlorobenzylNH3+ Cl−SMe4.6052%32%30 µM58%50%30 µM
57ebenzylNH3+ Cl−SMe2.1040%0%13 µM39%28%12 µM
67fHNH3+ Cl−SMe3.620%0%-2%0%-
711abenzylNH3+ Cl−H3.120%0%-10%2%-
811b2-chlorobenzylNH3+ Cl−H3.6258%30%55 µM50%11%62 µM
9132-chlorobenzylMeNH2+ Cl−SMe4.349%0%-38%14%-
10142-chlorobenzylMe2NH+ Cl−SMe4.565%0%-6%0%-
11152-chlorobenzylNHSO2MeSMe3.27−27%−10%-ndnd-
12162-chlorobenzylNHAcSMe4.010% a25% a-0%0%-
13172-chlorobenzylEtNH2+ Cl−SMe4.5621%1%-47%13%-
a Compound was precipitating due to poor solubility. b CLogP calculated for the free amine using the MLOGP method [31,37] with SwissADME [38]. A list of calculated physiochemical and pharmokinetic properties can be found in the Supplementary Material.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Fernandes, S.; Meyer, S.T.; Shah, J.P.; Adhikari, A.A.; Kerr, W.G.; Chisholm, J.D. N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents. Molecules 2022, 27, 8451. https://doi.org/10.3390/molecules27238451

AMA Style

Fernandes S, Meyer ST, Shah JP, Adhikari AA, Kerr WG, Chisholm JD. N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents. Molecules. 2022; 27(23):8451. https://doi.org/10.3390/molecules27238451

Chicago/Turabian Style

Fernandes, Sandra, Shea T. Meyer, Jigisha P. Shah, Arijit A. Adhikari, William G. Kerr, and John D. Chisholm. 2022. "N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents" Molecules 27, no. 23: 8451. https://doi.org/10.3390/molecules27238451

APA Style

Fernandes, S., Meyer, S. T., Shah, J. P., Adhikari, A. A., Kerr, W. G., & Chisholm, J. D. (2022). N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents. Molecules, 27(23), 8451. https://doi.org/10.3390/molecules27238451

Article Metrics

Back to TopTop