Guanidine Derivatives Containing the Chalcone Skeleton Are Potent Antiproliferative Compounds against Human Leukemia Cells

In this study, we investigated the effects of eleven synthetic guanidines containing the 1,3-diphenylpropenone core on the viabilities of six human cancer cells. The most cytotoxic compound against human cancer cells of this series contains a N-tosyl group and a N-methylpiperazine moiety 6f. It was cytotoxic against leukemia cells (U-937, HL-60, MOLT-3, and NALM-6) with significant effects against Bcl-2-overexpressing U-937/Bcl-2 cells as well as the human melanoma SK-MEL-1 cell line. It exhibited low cytotoxicity against quiescent or proliferating human peripheral blood mononuclear cells. The IC50 value for the leukemia U-937 cells was 1.6 ± 0.6 µM, a similar value to that in the antineoplastic agent etoposide. The guanidine containing a N-phenyl substituent 6i was also as cytotoxic as the guanidine containing the N-tosyl substituent and the N-methylpiperazine group 6f against human U-937 leukemia cells and both synthetic guanidines were potent apoptotic inducers. Cell death was mediated by the activation of the initiator caspase-9 and the executioner caspase-3, and associated with the release of cytochrome c. These synthetic guanidines are potent cytotoxic compounds against several human leukemia cells and even the human melanoma cell line SK-MEL-1 and might be useful in the development of new strategies in the fight against cancer.


Introduction
The development of new hybrid cancer drugs by the combination of two or more biologically relevant "parent" molecules can improve bioactivity, specificity, and help overcome drug resistance. Incorporating a natural product's privileged structure such as chalcone as one of the parent molecules is an excellent starting point to develop new drugs [1]. Chalcones, consisting of a diaryl propenone system, are the major precursors for the biosynthesis of flavonoids and can interact with several cancer drug targets, exhibiting promising in vitro and in vivo activities against both drug-susceptible and drug-resistant cancers [2]. The chalcone core is considered an appropriate chemical entity to implement rational fragment-based drug discovery strategies in the search of novel anticancer agents [3]. These chemical entities are highly suitable for further optimization based on systematic functionalization of the starting fragment core, taking into account their pharmacological and physicochemical properties. Recently, numerous chalcone hybrids have been prepared 2 of 15 and evaluated as potential anticancer agents. Some of them have shown excellent potency against tumor cells in vitro and in vivo, indicating that these compounds may have therapeutic value [3,4].
Guanidines are versatile organosuperbases and are able to bind to carboxylates, phosphates, and metals. The guanidinium cation participates in special interactions between ligands and receptors or enzymes and substrates and may have important biological properties and chemical and pharmaceutical implications. They are of great interest in medicinal chemistry and constitute a key motif of many clinical drugs including the anti-diabetic drug dimethyldiguanide and the peptic ulcer drug cimetidine. Guanidine derivatives are also widely distributed in nature and have attracted a lot of attention due to their chemical diversity and broad biological activities [5,6].
The aim of this study was (i) to synthesize a series of benzyloxychalcones containing a trisubstituted guanidine functional group and (ii) to explore the effects of different substituents on the cytotoxic effects of guanidine functionality against six human cancer cell lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl moiety on one of the nitrogen atoms of the guanidine functional group and (ii) the presence of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on another nitrogen atom of the guanidine functional group. In addition, we explored whether the most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guanidine-chalcone hybrids on viability of six human cancer cell lines. These compounds were prepared in an efficient one-pot process in which three reactions were carried out in the same solvent through the sequential addition of three reagents as indicated below. This atom-economy procedure incorporates almost all atoms of starting materials and reagents into the final product by the attachment of chemical building blocks. The azidochalcone 3 was prepared in a straightforward manner by a standard aldolic condensation procedure combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocyanate was then added to the iminophosphorane compound to produce carbodiimide 5, which was immediately transformed into guanidine 6 by adding different amines (Scheme 1). This synthesis is based on a similar one described previously by Foster et al. [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrids 6a-6k and the starting reagents. Table 1. Azidochalcone, isocyanates, and amines as starting reagents to generate the corresponding guanidine-chalcone hybrids.

Chalcone
Isocyanate Amine Product  [3]. These chemical entities are highly suitable for further optimization based on systematic functionalization of the starting fragment core, taking into account their pharmacological and physicochemical properties. Recently, numerous chalcone hybrids have been prepared and evaluated as potential anticancer agents. Some of them have shown excellent potency against tumor cells in vitro and in vivo, indicating that these compounds may have therapeutic value [3,4]. Guanidines are versatile organosuperbases and are able to bind to carboxylates, phosphates, and metals. The guanidinium cation participates in special interactions between ligands and receptors or enzymes and substrates and may have important biological properties and chemical and pharmaceutical implications. They are of great interest in medicinal chemistry and constitute a key motif of many clinical drugs including the antidiabetic drug dimethyldiguanide and the peptic ulcer drug cimetidine. Guanidine derivatives are also widely distributed in nature and have attracted a lot of attention due to their chemical diversity and broad biological activities [5,6].
The aim of this study was (i) to synthesize a series of benzyloxychalcones containing a trisubstituted guanidine functional group and (ii) to explore the effects of different substituents on the cytotoxic effects of guanidine functionality against six human cancer cell lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl moiety on one of the nitrogen atoms of the guanidine functional group and (ii) the presence of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on another nitrogen atom of the guanidine functional group. In addition, we explored whether the most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guanidine-chalcone hybrids on viability of six human cancer cell lines. These compounds were prepared in an efficient one-pot process in which three reactions were carried out in the same solvent through the sequential addition of three reagents as indicated below. This atom-economy procedure incorporates almost all atoms of starting materials and reagents into the final product by the attachment of chemical building blocks. The azidochalcone 3 was prepared in a straightforward manner by a standard aldolic condensation procedure combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocyanate was then added to the iminophosphorane compound to produce carbodiimide 5, which was immediately transformed into guanidine 6 by adding different amines (Scheme 1). This synthesis is based on a similar one described previously by Foster et al. [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrids 6a-6k and the starting reagents.  [3]. These chemical entities are highly suitable for further optimization based on systematic functionalization of the starting fragment core, taking into account their pharmacological and physicochemical properties. Recently, numerous chalcone hybrids have been prepared and evaluated as potential anticancer agents. Some of them have shown excellent potency against tumor cells in vitro and in vivo, indicating that these compounds may have therapeutic value [3,4]. Guanidines are versatile organosuperbases and are able to bind to carboxylates, phosphates, and metals. The guanidinium cation participates in special interactions between ligands and receptors or enzymes and substrates and may have important biological properties and chemical and pharmaceutical implications. They are of great interest in medicinal chemistry and constitute a key motif of many clinical drugs including the antidiabetic drug dimethyldiguanide and the peptic ulcer drug cimetidine. Guanidine derivatives are also widely distributed in nature and have attracted a lot of attention due to their chemical diversity and broad biological activities [5,6].
The aim of this study was (i) to synthesize a series of benzyloxychalcones containing a trisubstituted guanidine functional group and (ii) to explore the effects of different substituents on the cytotoxic effects of guanidine functionality against six human cancer cell lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl moiety on one of the nitrogen atoms of the guanidine functional group and (ii) the presence of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on another nitrogen atom of the guanidine functional group. In addition, we explored whether the most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guanidine-chalcone hybrids on viability of six human cancer cell lines. These compounds were prepared in an efficient one-pot process in which three reactions were carried out in the same solvent through the sequential addition of three reagents as indicated below. This atom-economy procedure incorporates almost all atoms of starting materials and reagents into the final product by the attachment of chemical building blocks. The azidochalcone 3 was prepared in a straightforward manner by a standard aldolic condensation procedure combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocyanate was then added to the iminophosphorane compound to produce carbodiimide 5, which was immediately transformed into guanidine 6 by adding different amines (Scheme 1). This synthesis is based on a similar one described previously by Foster et al. [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrids 6a-6k and the starting reagents.  [3]. These chemical entities are highly suitable for further optimization based on syste atic functionalization of the starting fragment core, taking into account their pharmac logical and physicochemical properties. Recently, numerous chalcone hybrids have be prepared and evaluated as potential anticancer agents. Some of them have shown exc lent potency against tumor cells in vitro and in vivo, indicating that these compounds m have therapeutic value [3,4]. Guanidines are versatile organosuperbases and are able to bind to carboxylat phosphates, and metals. The guanidinium cation participates in special interactions b tween ligands and receptors or enzymes and substrates and may have important biolo cal properties and chemical and pharmaceutical implications. They are of great interest medicinal chemistry and constitute a key motif of many clinical drugs including the an diabetic drug dimethyldiguanide and the peptic ulcer drug cimetidine. Guanidine der atives are also widely distributed in nature and have attracted a lot of attention due their chemical diversity and broad biological activities [5,6].
The aim of this study was (i) to synthesize a series of benzyloxychalcones containi a trisubstituted guanidine functional group and (ii) to explore the effects of different su stituents on the cytotoxic effects of guanidine functionality against six human cancer c lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl m ety on one of the nitrogen atoms of the guanidine functional group and (ii) the presen of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on anoth nitrogen atom of the guanidine functional group. In addition, we explored whether t most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted gua idine-chalcone hybrids on viability of six human cancer cell lines. These compounds we prepared in an efficient one-pot process in which three reactions were carried out in t same solvent through the sequential addition of three reagents as indicated below. Th atom-economy procedure incorporates almost all atoms of starting materials and reagen into the final product by the attachment of chemical building blocks. The azidochalcon was prepared in a straightforward manner by a standard aldolic condensation procedu combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treat with triphenylphosphine until the complete formation of iminophosphorane 4. The isoc anate was then added to the iminophosphorane compound to produce carbodiimide which was immediately transformed into guanidine 6 by adding different amin (Scheme 1). This synthesis is based on a similar one described previously by Foster et [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybri 6a-6k and the starting reagents.  [3]. These chemical entities are highly suitable for further optimization based on system atic functionalization of the starting fragment core, taking into account their pharmaco logical and physicochemical properties. Recently, numerous chalcone hybrids have been prepared and evaluated as potential anticancer agents. Some of them have shown excel lent potency against tumor cells in vitro and in vivo, indicating that these compounds may have therapeutic value [3,4]. Guanidines are versatile organosuperbases and are able to bind to carboxylates phosphates, and metals. The guanidinium cation participates in special interactions be tween ligands and receptors or enzymes and substrates and may have important biologi cal properties and chemical and pharmaceutical implications. They are of great interest in medicinal chemistry and constitute a key motif of many clinical drugs including the anti diabetic drug dimethyldiguanide and the peptic ulcer drug cimetidine. Guanidine deriv atives are also widely distributed in nature and have attracted a lot of attention due to their chemical diversity and broad biological activities [5,6].
The aim of this study was (i) to synthesize a series of benzyloxychalcones containing a trisubstituted guanidine functional group and (ii) to explore the effects of different sub stituents on the cytotoxic effects of guanidine functionality against six human cancer cel lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl moi ety on one of the nitrogen atoms of the guanidine functional group and (ii) the presenc of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on anothe nitrogen atom of the guanidine functional group. In addition, we explored whether th most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guan idine-chalcone hybrids on viability of six human cancer cell lines. These compounds wer prepared in an efficient one-pot process in which three reactions were carried out in th same solvent through the sequential addition of three reagents as indicated below. Thi atom-economy procedure incorporates almost all atoms of starting materials and reagent into the final product by the attachment of chemical building blocks. The azidochalcone was prepared in a straightforward manner by a standard aldolic condensation procedur combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocy anate was then added to the iminophosphorane compound to produce carbodiimide 5 which was immediately transformed into guanidine 6 by adding different amine (Scheme 1). This synthesis is based on a similar one described previously by Foster et al [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrid 6a-6k and the starting reagents. Table 1. Azidochalcone, isocyanates, and amines as starting reagents to generate the correspondin guanidine-chalcone hybrids.

Chalcone
Isocyanate Amine Product their chemical diversity and broad biological activities [5,6]. The aim of this study was (i) to synthesize a series of benzyloxychalcones containing a trisubstituted guanidine functional group and (ii) to explore the effects of different substituents on the cytotoxic effects of guanidine functionality against six human cancer cell lines. These substituents included (i) the presence of a p-tosylsulfonamide or phenyl moiety on one of the nitrogen atoms of the guanidine functional group and (ii) the presence of different groups such as the isopropyl, diisopropyl, phenyl, or a heterocycle on another nitrogen atom of the guanidine functional group. In addition, we explored whether the most cytotoxic compounds induce cell death by apoptosis in leukemia cells.

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guanidine-chalcone hybrids on viability of six human cancer cell lines. These compounds were prepared in an efficient one-pot process in which three reactions were carried out in the same solvent through the sequential addition of three reagents as indicated below. This atom-economy procedure incorporates almost all atoms of starting materials and reagents into the final product by the attachment of chemical building blocks. The azidochalcone 3 was prepared in a straightforward manner by a standard aldolic condensation procedure combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocyanate was then added to the iminophosphorane compound to produce carbodiimide 5, which was immediately transformed into guanidine 6 by adding different amines (Scheme 1). This synthesis is based on a similar one described previously by Foster et al. [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrids 6a-6k and the starting reagents. Table 1. Azidochalcone, isocyanates, and amines as starting reagents to generate the corresponding guanidine-chalcone hybrids.

Chalcone
Isocyanate Amine Product

Synthesis
In the present study, we explored the effects of a collection of 11 trisubstituted guanidine-chalcone hybrids on viability of six human cancer cell lines. These compounds were prepared in an efficient one-pot process in which three reactions were carried out in the same solvent through the sequential addition of three reagents as indicated below. This atom-economy procedure incorporates almost all atoms of starting materials and reagents into the final product by the attachment of chemical building blocks. The azidochalcone 3 was prepared in a straightforward manner by a standard aldolic condensation procedure combining the acetophenone 1 with the benzaldehyde 2. The azidochalcone 3 was treated with triphenylphosphine until the complete formation of iminophosphorane 4. The isocyanate was then added to the iminophosphorane compound to produce carbodiimide 5, which was immediately transformed into guanidine 6 by adding different amines (Scheme 1). This synthesis is based on a similar one described previously by Foster et al. [1]. Table 1 shows the chemical structures of the synthesized guanidine-chalcone hybrids 6a-6k and the starting reagents. Table 1. Azidochalcone, isocyanates, and amines as starting reagents to generate the corresponding guanidine-chalcone hybrids.

Hybrid Compounds Inhibit the Viability of Human Cancer Cells
The potential cytotoxicity of hybrid compounds containing the chalcone skeleton a a guanidine group was evaluated using several human cancer cells (Table 2). These can cells included the histiocytic lymphoma U-937, the acute promyelocytic leukemia HLthe acute lymphoblastic leukemia MOLT-3, the pre-B NALM-6, the cell line over-expre ing the human Bcl-2 protein (U-937/Bcl-2), and the melanoma SK-MEL-1 cell line.

Hybrid Compounds Inhibit the Viability of Human Cancer Cells
The potential cytotoxicity of hybrid compounds containing the chalcone skeleton and a guanidine group was evaluated using several human cancer cells (Table 2). These cancer cells included the histiocytic lymphoma U-937, the acute promyelocytic leukemia HL-60, the acute lymphoblastic leukemia MOLT-3, the pre-B NALM-6, the cell line over-expressing the human Bcl-2 protein (U-937/Bcl-2), and the melanoma SK-MEL-1 cell line.
The studies of the effect on cell viability of this series of compounds revealed that in the case of hybrid compounds containing the p-tosylsulfonyl group, the cytotoxicity was dependent on the corresponding amine. As shown in Table 2, the isopropylamino derivative 6a and the phenylmethylamino derivative 6c were more potent than the corresponding diisopropylamino derivative 6b. The cytotoxicity increased in the following order: diisopropylamino 6b < isopropylamino 6a~phenylmethylamino 6c, except for MOLT-3 cells, in which the three compounds showed similar IC 50 values and for NALM-6 in which the most cytotoxic compound was the isopropylamino derivative 6a. There was an important change in cytotoxicity for compounds with a heterocycle structure as a substituent, according to whether the amino group was from a piperidine 6d, a morpholine 6e, or a N-methylpiperazine 6f. In these experiments, etoposide and doxorubicin were used as positive controls. In general, the most cytotoxic compound was the hybrid compound 6f. The greatest differences in cytotoxicity were observed in U-937 cells in which the order of cytotoxicity was: 6f > 6e > 6d. In MOLT-3 cells, these three derivatives were almost equally potent with IC 50 values between 1.5 µM and 3.3 µM, and in U-937/Bcl-2 cells, the morpholine derivative 6e showed similar potency to the piperazine derivative 6f. As shown in Table 2, the N-methylpiperazine derivative 6f was the most cytotoxic compound in all cell lines assayed including the melanoma cell line SK-MEL-1. The IC 50 values were between 1.5 µM and 4.5 µM, similar to the antineoplastic etoposide, which showed IC 50 values of 1.8 ± 0.2 µM, 0.6 ± 0.2 µM, and 0.2 ± 0.1 µM for U-937, HL-60 and MOLT-3, respectively. However, the substitution of the cyclic amine 6f for an amine containing a long (C18) aliphatic chain yielded a compound (hybrid compound 6g) which was not cytotoxic against the cancer cell lines assayed, probably due to its low solubility.
Among the N-phenyl derivatives, compound 6i containing a piperidine ring was, in general, the most cytotoxic compound with IC 50 values that were either less than (U-937, HL-60, MOLT-3, and U-937/Bcl-2) or close to (NALM-6, SK-MEL-1) 10 µM. The substitution of the piperidine 6i ring by a N-methylpiperazine 6k ring determined a decrease in cytotoxicity. In contrast, the substitution of the piperidine 6i by a morpholine 6j increased the cytotoxicity against MOLT-3, NALM-6, and SK-MEL-1.
In general, over expression of Bcl-2 did not confer protection against hybrid compoundsinduced cytotoxicity since the IC 50 values were similar or even lower than that for the parental U-937 cells. In U-937/Bcl-2 cells, the p-tosyl derivatives containing the morpholine ring 6e, the phenyl group 6c, and N-methylpiperazine 6f were equally potent showing IC 50 values between 2.2 ± 0.8 µM and 4.2 ± 1.2 µM. In these cells, the N-phenyl guanidine derivative containing the piperidine ring 6i was equally cytotoxic as it was against the parental U-937 cell line. Most compounds assayed in MOLT-3 cells were equally potent, showing IC 50 values below 10 µM. The exceptions were the p-tosyl derivative containing an octadecyl substituent 6g and the N-phenylguanidine containing the N-methylpiperazine ring 6k. A similar trend was observed in NALM-6 cells since most compounds showed similar IC 50 values. The exception was the p-tosyl derivative 6b, which showed low cytotoxicity against NALM-6. The substitution of the p-tosyl-sulfonyl group 6b by a phenyl group 6h increased the cytotoxicity five-fold (IC 50 = 27.0 ± 0.8 µM vs. IC 50 = 5.4 ± 0.2 µM). The piperidine derivative (compound 6i) was more potent than the p-tosylsulfonyl derivative (compound 6d) in U-937, U-937/Bcl-2, HL-60, and SK-MEL-1 cells.
The structure-activity relationship (SAR) reveals that the introduction of the guanidine group enhances the cytotoxicity of the chalcone skeleton in comparison with the azidochalcone 3, and the results of the cytotoxicity assays of p-tosylsulfonyl derivatives revealed that the most potent compound contains a N-methylpiperazine ring and the order of potency was N-methylpiperazine > morpholine > piperidine.
The cytotoxicity assays of the N-phenyl derivatives series revealed that: (i) the hybrid compound 6i containing a piperidine ring was, in general, the most cytotoxic compound showing IC 50 values below 10 µM, except in NALM-6 (IC 50 = 10.8 ± 0.5 µM) and SK-MEL-1 (IC 50 = 13.8 ± 1.2 µM) cells; (ii) the substitution of the piperidine 6i by a morpholine ring 6j decreased the cytotoxicity against human U-937, HL-60, and U-937/Bcl-2 cells; and (iii) the substitution of the piperidine ring 6i by a N-methylpiperazine ring 6k decreased the cytotoxicity against all cell lines assayed.
The SAR against U-937 and HL-60 leukemia cells of this series of hybrid compounds containing the chalcone skeleton and a guanidine group is displayed graphically in Figure 1.
The structure-activity relationship (SAR) reveals that the introduction of the g dine group enhances the cytotoxicity of the chalcone skeleton in comparison with th idochalcone 3, and the results of the cytotoxicity assays of p-tosylsulfonyl derivativ vealed that the most potent compound contains a N-methylpiperazine ring and the of potency was N-methylpiperazine > morpholine > piperidine.
The cytotoxicity assays of the N-phenyl derivatives series revealed that: (i) the h compound 6i containing a piperidine ring was, in general, the most cytotoxic comp showing IC50 values below 10 µM, except in NALM-6 (IC50 = 10.8 ± 0.5 µM) and SK-1 (IC50 = 13.8 ± 1.2 µM) cells; (ii) the substitution of the piperidine 6i by a morpholin 6j decreased the cytotoxicity against human U-937, HL-60, and U-937/Bcl-2 cells; an the substitution of the piperidine ring 6i by a N-methylpiperazine ring 6k decrease cytotoxicity against all cell lines assayed.
The SAR against U-937 and HL-60 leukemia cells of this series of hybrid compo containing the chalcone skeleton and a guanidine group is displayed graphically in F 1.
Combination of phenyl group with diisopropyl or cyclic amines enhances the activity Combination of tosyl group with isopropyl, phenyl or cyclic amines enhances activity The results suggest that the main determinant of cytotoxicity in hybrid compo containing the p-toluensulfonyl group is the presence of a N-methylpiperazine rin the most cytotoxic compound was the hybrid compound 6f in the six cell lines ass As shown in Table 2, compound 6f showed similar IC50 values for U-937 and HL-60 values obtained with etoposide, which was included as a positive control. The h leukemia MOLT-3 cells and the cell line overexpressing Bcl-2 (U-937/Bcl-2) were als sitive to these hybrid compounds. Compound 6i was also as cytotoxic as compound both U-937 and HL-60 cells. Representative concentration-dependent inhibition of c ability curves of compounds 6f and 6i against U-937 are shown in Figure 2a. As visua by phase-contrast microscopy, these compounds induced significant morpholo changes and an important reduction in the number of cells (Figure 2b). To determin potential selectivity of hybrid compounds 6f and 6i against human leukemia cell compared the effect against human mononuclear cells (PBMC) obtained from health nors. Proliferating and quiescent lymphocytes showed lower cytotoxicity even at 1 hybrid compounds for 24 h. Fresh and proliferating PBMC were more resistant to th totoxic effects of these compounds (Figure 2c). The results suggest that the main determinant of cytotoxicity in hybrid compounds containing the p-toluensulfonyl group is the presence of a N-methylpiperazine ring and the most cytotoxic compound was the hybrid compound 6f in the six cell lines assayed. As shown in Table 2, compound 6f showed similar IC 50 values for U-937 and HL-60 to the values obtained with etoposide, which was included as a positive control. The human leukemia MOLT-3 cells and the cell line overexpressing Bcl-2 (U-937/Bcl-2) were also sensitive to these hybrid compounds. Compound 6i was also as cytotoxic as compound 6f in both U-937 and HL-60 cells. Representative concentration-dependent inhibition of cell viability curves of compounds 6f and 6i against U-937 are shown in Figure 2a. As visualized by phase-contrast microscopy, these compounds induced significant morphological changes and an important reduction in the number of cells (Figure 2b). To determine the potential selectivity of hybrid compounds 6f and 6i against human leukemia cells, we compared the effect against human mononuclear cells (PBMC) obtained from healthy donors. Proliferating and quiescent lymphocytes showed lower cytotoxicity even at 10 µM hybrid compounds for 24 h. Fresh and proliferating PBMC were more resistant to the cytotoxic effects of these compounds (Figure 2c).

Hybrid Compounds Induce Changes in Cell Cycle in Human U-937 Leukaemia Cells
Although the compounds 6f and 6i were the most cytotoxic against human can cells, we were interested in knowing whether other compounds of this series were ab affect the cell cycle. To explore this, U-937 cells were incubated with 10 µM of sele compounds 6c, 6e, 6f, 6h, 6i, and 6j for 24 h, and analyzed by flow cytometry after pidium iodide staining. As shown in Table 3, guanidine 6e induced an arrest at the G phase of the cell cycle. The percentage of control cells in G2-M phase was approxima 14%, which increased to 27% and this was accompanied by a significant decrease in c in the G1 phase. This suggests that the effects on viability may be caused at least in by an arrest of the cell cycle. The percentage of sub-G1 (i.e., apoptotic cells) increased u

Hybrid Compounds Induce Changes in Cell Cycle in Human U-937 Leukaemia Cells
Although the compounds 6f and 6i were the most cytotoxic against human cancer cells, we were interested in knowing whether other compounds of this series were able to affect the cell cycle. To explore this, U-937 cells were incubated with 10 µM of selected compounds 6c, 6e, 6f, 6h, 6i, and 6j for 24 h, and analyzed by flow cytometry after propidium iodide staining. As shown in Table 3, guanidine 6e induced an arrest at the G 2 -M phase of the cell cycle. The percentage of control cells in G 2 -M phase was approximately 14%, which increased to 27% and this was accompanied by a significant decrease in cells in the G 1 phase. This suggests that the effects on viability may be caused at least in part by an arrest of the cell cycle. The percentage of sub-G 1 (i.e., apoptotic cells) increased until 23.5% (~10-fold), 11.9% (~5-fold), 25.1% (~10-fold), and 31.6% (~13-fold) by compounds 6c, 6e,  6f, and 6i, respectively (Figure 3a). Representative histograms of flow cytometry after propidium iodide labelling are shown in Figure 3b. To confirm that the decrease in viability triggered by 6f and 6i was caused by apoptosis induction, treated cells were double stained with annexin V-FITC and propidium iodide and subjected to flow cytometry. The number of annexin V-FITC positive cells increased 11-fold (3.5% vs. 38%) and 10-fold (3.5% vs. 36%) for compounds 6f and 6i, respectively, in U-937 cells confirming that these specific guanidines are potent apoptosis inducers (Figure 3c). Interestingly, dose-response studies revealed that PBMC were more resistant toward compounds 6f and 6i. The number of annexin V-FITC positive cells hardly increased with respect to control after treatment with 3 µM of compounds 6f and 6i, but increased 3-fold (9.3% vs. 27%) and 1.4-fold (9.3% vs. 13%) with respect to control after treatment with 10 µM compounds 6f and 6i, respectively (Figure 3d). 23.5% (~10-fold), 11.9% (~5-fold), 25.1% (~10-fold), and 31.6% (~13-fold) by compound 6e, 6f, and 6i, respectively (Figure 3a). Representative histograms of flow cytometry propidium iodide labelling are shown in Figure 3b. To confirm that the decrease in vi ity triggered by 6f and 6i was caused by apoptosis induction, treated cells were do stained with annexin V-FITC and propidium iodide and subjected to flow cytometry number of annexin V-FITC positive cells increased 11-fold (3.5% vs. 38%) and 10 (3.5% vs. 36%) for compounds 6f and 6i, respectively, in U-937 cells confirming that t specific guanidines are potent apoptosis inducers (Figure 3c). Interestingly, dose-resp studies revealed that PBMC were more resistant toward compounds 6f and 6i. The n ber of annexin V-FITC positive cells hardly increased with respect to control after t ment with 3 µM of compounds 6f and 6i, but increased 3-fold (9.3% vs. 27%) and 1.4 (9.3% vs. 13%) with respect to control after treatment with 10 µM compounds 6f an respectively (Figure 3d).

Hybrid Compounds Induce Caspase Activation, PARP Cleavage, and Cytochrome c Release in Human U-937 Leukemia Cells
To determine whether the mechanism of cell death triggered by compounds 6f and 6i was associated with caspase activation, the enzyme activities of caspases-3/7, -8, and -9 were determined in lysates using tetrapeptide substrates. As shown in Figure 4a, maximal caspase-3/7 and -9 activities were detected after 24 h of treatment with 10 µM of both guanidines in U-937 cells, while caspase-8 was less activated. Caspase-3/7 and caspase-9 activities increased approximately three-fold and two-fold after treatment with guanidines 6f and 6i, respectively.

Discussion
In the present report, we synthesized a series of chalcone hybrids containing trisubstituted guanidines and explored the potential effects on human cancer cell viability. We found that the p-tosyl derivative containing a N-methylpiperazine 6f was the most potent cytotoxic compound against the six cell lines assayed. It seems that the main determinant of this cytotoxicity is the nature of the heterocycle since the N-methylpiperazine derivative An indicator of caspase activation is the cleavage of poly(ADP-ribose)polymerase (PARP). This enzyme is involved in DNA repair and PARP cleavage is considered a hallmark of cell death. To explore whether guanidines 6f and 6i induced PARP cleavage, lysates of treated cells were analyzed by immunoblotting. As shown in Figure 4b, the full-length PARP protein dramatically decreased after 24 h of treatment with 10 µM of both guanidines indicating the processing of this protein. In accordance with PARP cleavage, the executioner caspase-3 was processed, as detected by the generation of a fragment of 18-20 kDa in the immunoblots. In a similar way as the enzymatic assays, the immunoblot experiments also revealed pro-caspase-9 processing suggesting that PARP cleavage might be attributable to pro-caspase-9 cleavage followed by caspase-3 activation.
Since caspase-9 activation is dependent on the release of cytochrome c from the intermembrane space of mitochondria to cytosol, we explored whether the cell death induced by selected guanidines involves cytochrome c release. To this end, dose-response experiments were performed and cytosolic fractions were analyzed by Western blot after 24 h of treatment with increasing concentrations of guanidines. As shown (Figure 4b), the level of cytochrome c increased in the cytosolic fraction in accordance with the processing and activation of pro-caspase-9. These results indicate that guanidines induce cytochrome c release and the processing and activation of caspases.

Discussion
In the present report, we synthesized a series of chalcone hybrids containing trisubstituted guanidines and explored the potential effects on human cancer cell viability. We found that the p-tosyl derivative containing a N-methylpiperazine 6f was the most potent cytotoxic compound against the six cell lines assayed. It seems that the main determinant of this cytotoxicity is the nature of the heterocycle since the N-methylpiperazine derivative was more potent than the morpholine or piperidine derivatives. The second most potent inhibitor of cell viability, at least against leukemia cells, was the N-phenyl derivative 6i. Interestingly, dose-response studies revealed that quiescent PBMC and proliferating PBMC were more resistant than the human leukemia U-937 cell line against the cytotoxicity triggered by the most potent guanidines. It is a remarkable finding that PBMC show increased apoptosis resistance toward guanidines 6f and 6i since the increases in the percentages of annexin V-FITC positive cells compared with the control were lower than in U-937 cells. The effects on cell viability and the mechanisms involved in cell death induction of these specific compounds have not been investigated to date. Our results demonstrated that at least one of the guanidines, compound 6e containing a N-tosyl group and a morpholine ring, blocks proliferation of leukemia cells by arresting the cells in the G 2 -M phase of the cell cycle. This suggests that compound 6e might target cyclin-dependent kinase 1 (CDK1) which is a stimulator of cell cycle progression. CDK1 inhibition induces cell cycle arrest in the G 2 -M phase and apoptosis and targeting CDK1 has showed promising results for cancer treatment in different preclinical models [7]. Another possibility might be that compound 6e can bind tubulin and therefore interfere with the mitotic process as described for chalcone derivatives [8]. Further research is needed to confirm the specific target/s of this compound.
Cell cycle analysis revealed that inhibition of cell viability by the other hybrid compounds (compounds 6c, 6f, 6h, and 6i) was not caused by a significant cell cycle arrest in any phase. The experiments presented here, using U-937 cells as a model, supported apoptosis as the main cytotoxicity pathway induced by two specific guanidines, 6f and 6i, containing the chalcone skeleton. This was supported by an increase in the percentage of sub-G 1 and annexin V-FITC positive cells, caspase activation, and PARP cleavage. During apoptosis, caspases cause PARP cleavage and inactivation [9]. PARP protein is normally involved in DNA repair and is a known substrate for caspase-3. Moreover, these guanidines induced a concentration-dependent release of mitochondrial cytochrome c and this was in accordance with the activation of caspase-9 and caspase-3 determined by the enzymatic analysis and the immunoblots experiments. Mitochondrial outer membrane permeabilization is the critical step for the intrinsic pathway of apoptosis [10]. This pathway involves the cytosolic release of apoptogenic factors that normally reside in the mitochondrial intermembrane space such as cytochrome c [11]. These results suggest that cell death induction triggered by these specific compounds occurs via the intrinsic apoptotic pathway.
It is known that overexpression of Bcl-2 protein protects the cells because it prevents the release of the pro-apoptotic protein cytochrome c from the mitochondria to the cytosol, apoptosome formation, and the consequent activation of caspase-9 [12]. Bcl-2 is frequently overexpressed in lymphomas and leukemias [13]. Therefore, this protein is a potential target in therapy. Previous reports have shown that multisite Bcl-2 phosphorylation induced by anti-mitotic drugs may inhibit Bcl-2 [14]. For example, helenalin, a naturally occurring sesquiterpene lactone, is able to induce cell death in cells overexpressing Bcl-2 and this effect could be due to the inactivation of Bcl-2 protein or, alternatively, this compound could trigger a pathway that bypasses mitochondria [15]. In addition, etoposide, but not staurosporine, bypasses the chemoresistance conferred by Bcl-2 in Hep3B hepatoma cells [16]. Our experiments demonstrate that guanidines are cytotoxic against human leukemia U-937 cells that overexpress Bcl-2. These results strongly suggest that selected guanidines kill cancer cells mainly through induction of apoptotic cell death. Future studies will be necessary to determine whether additional pathways of cell death are involved in U-937 cells.

Assay of Caspase Activity
Caspase activity was determined by measuring proteolytic cleavage of specific chromogenic substrates as previously described [22]. Briefly, cells were treated with the specified guanidines for 24 h, harvested by centrifugation (1000× g for 5 min at 4 • C), washed twice with PBS, resuspended in lysis buffer (50 mM HEPES, pH 7.4, 0.1 mM EDTA, 1 mM dithiothreitol, and 0.1% Chaps), spun (17,000× g for 10 min at 4 • C) and the supernatants were normalized by protein concentration and used to determine enzyme activity. The net increase in absorbance at 405 nm after incubation at 37 • C was indicative of caspase activity. The colorimetric substrates were DEVD-pNA (for caspase-3 like protease activity), IETD-pNA (for caspase-8 activity), and LEHD-pNA (for caspase-9 activity).

Western Blot Analysis
For whole cell lysates, cells were harvested by centrifugation (500× g, 10 min, 4 • C), washed twice with PBS, and pellets were resuspended in lysis buffer (1% Triton X-100, 10 mM sodium fluoride, 2 mM EDTA, 20 mM Tris-HCl (pH 7.4), 2 mM tetrasodium pyrophosphate, 10% glycerol, 137 mM NaCl, and 20 mM sodium β-glycerophosphate), with the protease inhibitors phenylmethylsulfonyl fluoride (PMSF, 1 mM), aprotinin, leupeptin, and pepstatin A (5 µg/mL each) and kept on ice for 15 min. Cells were sonicated on ice 5 times (5 s each, with intervals between each sonication of 5 s) with a Braun Labsonic 2000 microtip sonifier and centrifuged (11,000× g, 10 min, 4 • C). For subcellular fractionation, cells were washed twice with PBS and then resuspended in ice-cold buffer (20 mM HEPES (pH 7.5), 250 mM sucrose, 10 mM KCl, 1.5 mM MgCl 2 , 1 mM EDTA, 1 mM EGTA, and 1 mM dithiothreitol containing protease inhibitors (0.1 mM PMSF and 1 µg/mL leupeptin, aprotinin, and pepstatin A)). After 15 min on ice, cells were lysed by pushing them several times through a 29-gauge needle, and the lysate was centrifuged at 1000× g for 5 min at 4 • C. The resulting supernatant fraction was centrifuged at 15,000× g for 20 min at 4 • C, and the resulting supernatant was used as the cytosolic fraction. The Bradford method was used to determine protein concentration. The samples loaded in sodium dodecyl sulfatepolyacrylamide gel (from 7.5 to 15% depending on the molecular weight of interest) were prepared with the same protein amount and boiled for 5 min. The proteins were transferred to poly(vinylidene difluoride) membranes for 20 h at 20 V. The membranes were blocked with 10% nonfat milk in Tris-buffered saline (50 mM Tris-HCl (pH 7.4), 150 mM NaCl) containing 0.1% Tween-20 (TBST) for 1 h, followed by incubation with specific antibodies against caspase-3, PARP, caspase-9, β-actin, tubulin, and cytochrome c overnight at 4 • C. Membranes were washed three times with TBST and incubated for 1 h with the specific secondary antibody and the antigen-antibodies complexes were visualized by enhanced chemiluminescence using the manufacturer's protocol.

Statistical Analysis
Statistical differences between means were tested using (i) Student's t-test (two samples) or (ii) one-way analysis of variance (ANOVA) (three or more samples) with a posteriori pairwise comparisons of means carried out using Tukey's test. A significance level of p < 0.05 was used.

Conclusions
In summary, we designed and synthesized a series of trisubstituted guanidines containing a 1,3-diphenylpropenone core and different substituents on the guanidine functional group taking advantage of a one-pot procedure involving three sequential reactions. The SARs revealed that (i) the presence of a piperazine ring in p-toluensulfonyl guanidines generated a more cytotoxic response than the corresponding isopropylamino, diisopropylamino, piperidine, morpholine, or phenylamino derivatives and (ii) the presence of a piperidine ring in N-phenylguanidines enhanced the cytotoxicity in comparison with the corresponding diisopropylamino, morpholine, and N-methylpiperazine derivatives. The most cytotoxic compounds were the p-toluensulfonylguanidine containing a N-methylpiperazine and the N-methyl-N-phenylguanidine containing a piperidine ring against the human leukemia cells. Both compounds showed less cytotoxicity against human peripheral blood mononuclear cells, suggesting that they may have potential therapeutic value. These compounds induce cell death by apoptosis, which was associated with cytochrome c release, caspase activation, and PARP cleavage while the over-expression of the anti-apoptotic protein Bcl-2 did not block cell viability inhibition.
Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/ijms232415518/s1. The following are available online, spectral and analytical data for hybrid compounds.