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Molecules 2012, 17(4), 4252-4265; doi:10.3390/molecules17044252
Published: 10 April 2012
Abstract: We report the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives as probes for imaging β-amyloid (Aβ) plaques. These derivatives showed binding affinities for Aβ1–40 aggregates with Ki values varying from 4.1 to 288.4 nM. (E)-5-(4-iodostyryl)-1H-indole (8) clearly stained Aβ plaques in the brain sections of Alzheimer’s disease (AD) model mice (APP/PS1). Furthermore, autoradiography for [125I]8 displayed intense and specific labeling of Aβ plaques in the brain sections mentioned above with low background. In biodistribution experiments using normal mice [125I]8 showed high initial brain uptake followed by rapid washout (4.27 and 0.64% ID/g at 2 and 30 min post injection, respectively). These findings suggests that [123I]8 may be a potential SPECT imaging agent for detecting Aβ plaques in AD brain.
Alzheimer’s disease (AD) is a kind of irreversible, progressive brain disease characterized by dementia, cognitive impairment and memory loss. Although currently the pathogenesis of AD is not completely understood, it is generally accepted that β-amyloid (Aβ) plaques is considered to be one of the biomarkers for early diagnosis of AD [1,2,3]. Therefore, in vivo imaging agent for Aβ plaques applicable for PET (positron emission tomography) or SPECT (single photon emission computed tomography) would be very useful for early diagnosis of AD and provide significant information to evaluate the efficacy of AD therapies [4,5].
To date, several radiolabeled ligands have been developed as imaging probes for Aβ plaques . For example, [11C]SB-13 [7,8], [18F]BAY94-9172  and [18F]AV-45 [10,11] derived from Congo Red (CR), [11C]PIB [12,13], [18F]GE-067  and [123I]IMPY [15,16,17] derived from thioflavin T (ThT) (Figure 1). However, [123I]IMPY, the only SPECT tracer tested in human studies, has failed because of its low in vivo stability and its insufficient target-to-background ratio. In comparison with PET, SPECT is a more widely accessible and cost-effective technique in terms of routine diagnostic use. Consequently, the development of more useful imaging agents for Aβ plaques labeled with 123I (T1/2, 13 h, 159 keV) or 99mTc (T1/2, 6 h, 140 keV) for SPECT has been a critical issue.
Previously, we successfully developed a series of novel imaging agents for β-amyloid plaques based on the N-benzoylindole core which showed high binding affinities with Ki values in the nM range . The brain uptake of these derivatives was encouraging, but their washout from the brain in normal mice appeared to be relatively slow. Qu et al. have developed indolylphenylacetylenes as potential Aβ plaques imaging agent, and the use of indolyl groups may improve the brain kinetics for β-amyloid imaging agents . Recently, Watanabe et al. have developed phenylindoles for image β-amyloid in brain, these derivatives demonstrated high binding affinities to Aβ1–42aggregates . Following these successful results, we applied highly conjugated (E)-5-styryl-1H-indole as a core structure for Aβ imaging agents to explore more useful candidates with favorable pharmacokinetics as Aβ imaging probes, and developed (E)-6-styrylquinoline derivatives for further studies (Figure 2). Reported herein are the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives and especially, two radioiodinated derivatives as potential SPECT tracers for imaging β-amyloid plaques in the brain.
2. Results and Discussion
2.1. Chemistry and Radiochemistry
The synthetic route to the (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives is shown in Scheme 1.
The key step was the base-catalyzed Wittig reaction between substituted triphenyl phosphonium ylides 2a–g and 1H-indole-5-carbaldehyde or quinoline-6-carbaldehyde. The tributyltin derivatives 11, 19 were prepared in yields of 22.3% and 28.6%, respectively, from the bromo-precursors 7, 16using an exchange reaction catalyzed by Pd(0). [125I]8 and [125I]17 were prepared via a iodo-destannylation reaction using hydrogen peroxide as the oxidant. The products were purified by radio-HPLC using a reverse-phase column and mobile phase consisting of acetonitrile with a flow rate of 1 mL/min. In order to identify the radiotracer, the non-radioactive 8 and 17 were co-injected and co-eluted with the corresponding radioactive product, respectively. Their HPLC profiles using acetonitrile and water (90:10 v/v) as mobile phase at a flow rate of 1 mL/min are present in Figure 3.
From Figure 3, the retention times of non-radioactive 8 and [125I]8 were observed to be 6.45 min and 6.89 min, respectively. The retention times of non-radioactive 17 and [125I]17 were observed to be 19.56 min and 19.94 min, respectively. The differences in retention time were in good agreement with the time lag which corresponds with the volume and flow rate within the distance between the UV and radioactive detector of our HPLC system. After purification by HPLC, the radiochemical purities of both [125I]8 and [125I]17 were greater than 98%. The radiochemical yields of [125I]8 and [125I]17 were 48–67% and 61–78%, respectively. The log D values of [125I]8 and [125I]17 were 2.52 ± 0.04 and 2.73 ± 0.03, respectively, which are in the appropriate range for brain imaging agents indicative of good permeability through the blood-brain barrier (BBB).
2.2. In Vitro Binding Studies Using the Aggregated Aβ1–40
The affinity of (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives for Aβ1–40 aggregates was determined by competition binding assay using [125I]TZDM as radio-ligand. TZDM was also screened using the same competition assay for comparison. The Ki values shown in Table 1 were varied from 4.1 to 288.4 nM suggesting that all these compounds share the same binding site with ThT. The Ki value of TZDM was 4.2 nM, which is comparable to that of previously reported in the literature (Ki = 0.9 nM) . (E)-5-styryl-1H-indole (4) without any substituents showed moderate binding affinity (Ki = 25.1 nM). Introducing a F, Cl or OCH3 group at the para-position of the phenyl ring decreased the binding affinity (Ki = 89.3, 51.5 and 32.4 nM for compounds 5, 6 and 10, respectively), while introducing a Br or CH3 group at the same position increased the affinity (Ki = 16.3 and 15.8 nM for compounds 7 and 9, respectively). It is noteworthy that compound 8 with a iodo group showed Ki value of 4.1 nM, which is comparable with that of TZDM. In general, (E)-5-styryl-1H-indole derivatives showed slightly better potency in binding to Aβ1–40 aggregates than (E)-6-styrylquinoline derivatives. Since derivatives 8 and 17 with iodine at the para-position of the phenyl ring displayed nanomolar affinities for Aβ1–40 aggregates, we prepared [125I]8 and [125I]17 for further evaluation as potential ligands for 123I-labeled SPECT imaging agents.
|Table 1. Ki values of (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives for Aβ1–40 aggregates against [125I]TZDM.|
|Compound||Ki (nM) a||Compound||Ki (nM) a|
|4||25.1 ± 2.1||10||32.4 ± 1.9|
|5||89.3 ± 2.6||14||270.4 ± 1.5|
|6||51.5 ± 1.0||15||45.0 ± 1.3|
|7||16.3 ± 1.7||16||23.5 ± 1.3|
|8||4.1 ± 0.2||17||8.6 ± 1.2|
|9||15.8 ± 1.5||18||288.4 ± 1.3|
|TZDM||4.2 ± 0.4||TZDM b||0.9 ± 0.2|
a Measured in triplicate with results given as the mean ± SD; b Data from .
2.3. In Vitro Fluorescent Staining of Amyloid Plaques in Brain Sections from Transgenic Mouse
To confirm the binding affinities of these derivatives for Aβ plaques in the brain, in vitro fluorescent staining of brain sections (8 µm) from a transgenic model mouse (APP/PS1, 12 months, male) was carried out with compound 8. As shown in Figure 4, many fluorescence spots were observed in the brain sections of transgenic mice (Figure 4B). The fluorescent labeling pattern was consistent with that observed with thioflavin-S (Figure 4A). These results suggested that 8 show specific binding to Aβplaques in the transgenic model mouse brain.
2.4. In Vitro Labeling of Brain Sections from Transgenic Mouse by Autoradiography
The results of in vitro autoradiography of [125I]8 in the brain sections of a transgenic model mouse (APP/PS1, 12 months, male) are shown in Figure 5. [125I]8 showed excellent labeling of Aβ plaques in the cortex region of the brain sections, and no remarkable accumulation of radioactivity were observed in white matter. The same sections were also stained with thioflavin-S and the localizations of Aβ plaques were in accord with the results of autoradiography. These results demonstrated that [125I]8 was specific for Aβ plaques, which were consistent with the high binding affinity of compound 8 to Aβ1–40 aggregates.
2.5. In Vivo Biodistribution Studies
In vivo biodistribution studies of [125I]8 and [125I]17 were performed in normal mice. The uptake of radiotracer in the organs of interest at different time points after intravenous administration of [125I]8 and [125I]17 is summarized in Table 2. [125I]8 showed high initial brain uptake followed by rapid clearance (4.27 and 0.28% ID/g at 2 and 60 min post injection, respectively). On the other hand, [125I]17 showed relatively low brain uptake and slow washout (2.05 and 0.55% ID/g at 2 and 60 min post injection, respectively). As compared with previously reported radioiodinated N-benzoylindole derivatives , radioiodinated (E)-5-styryl-1H-indole derivative [125I]8 showed greatly improved brain uptake. Because there are no plaques in normal brain, potential Aβ-specific probe should possess high brain uptake followed by fast washout in normal mice. The brain2min/brain60min ratio has been used as an index to compare the washout rate from normal brain and select candidate tracers with appropriate kinetics in vivo. It was reported that [123I]IMPY showed a high initial brain uptake and fast washout in normal mice (2.88% ID/organ and 0.21% ID/organ at 2 min and 60 min postinjection, respectively) . The brain2min/brain60min ratio of [125I]8 (15.3) is higher than that of [123I]IMPY (13.7), indicating [125I]8 may possess suitable pharmacokinetic properties for imaging Aβ plaques in AD brain. Accordingly, [125I]8 may be comparable or even better for detecting Aβ plaques. Therefore, (E)-5-styryl-1H-indole derivative [125I]8, with nanomolar affinity to Aβ1–40 aggregates, excellent BBB permeability as well as fast washout from the normal brain, may be suitable for development as a novel Aβ imaging agent.
|Table 2. Biodistribution in normal mice after iv injection of [125I]8 and [125I]17 (% ID/g, avg of 5 mice ± SD) and its partition coefficient (D).|
|Organ||2 min||15 min||30 min||60 min||120 min||240 min|
|[125I]8 (log D = 2.52 ± 0.04)|
|Blood||11.91 ± 0.62||12.29 ± 1.30||7.64 ± 0.62||4.49 ± 0.28||2.93 ± 0.30||1.50 ± 0.13|
|Brain||4.27 ± 0.49||1.37 ± 0.16||0.64 ± 0.11||0.28 ± 0.06||0.20 ± 0.08||0.10 ± 0.02|
|Heart||5.76 ± 0.38||3.70 ± 0.40||2.55 ± 0.52||1.59 ± 0.28||1.47 ± 0.48||0.65 ± 0.16|
|Liver||14.73 ± 0.66||10.66 ± 0.31||7.14 ± 1.13||4.45 ± 0.23||4.19 ± 0.61||3.06 ± 0.36|
|Spleen||4.38 ± 0.33||4.21 ± 0.26||3.44 ± 0.21||2.44 ± 0.12||1.87 ± 0.28||1.37 ± 0.09|
|Lung||10.76 ± 0.63||8.22 ± 0.88||5.39 ± 0.83||3.28 ± 0.10||2.30 ± 0.20||1.43 ± 0.52|
|Kidney||11.66 ± 1.52||14.89 ± 4.23||9.46 ± 1.95||4.65 ± 0.98||1.93 ± 0.76||1.34 ± 0.36|
|Stomach a||1.23 ± 0.56||4.82 ± 0.46||3.50 ± 0.19||1.72 ± 0.21||3.48 ± 0.79||2.31 ± 1.44|
|Muscle||2.64 ± 0.40||2.01 ± 0.24||1.25 ± 0.04||0.81 ± 0.12||0.61 ±0.24||0.35 ± 0.09|
|[125I]17 (log D = 2.73 ± 0.03)|
|Blood||11.39 ± 1.56||6.31 ± 0.51||5.80 ± 0.37||3.86 ± 0.74||1.97 ± 0.35||1.38 ± 0.24|
|Brain||2.05 ± 0.25||1.18 ± 0.17||0.93 ± 0.13||0.55 ± 0.11||0.26 ± 0.03||0.14 ± 0.02|
|Heart||7.70 ± 0.86||3.80 ± 0.12||3.21 ± 0.11||2.55 ± 0.21||1.33 ± 0.06||0.80 ± 0.19|
|Liver||22.45 ± 1.79||9.95 ± 0.18||9.12 ± 0.53||6.97 ± 0.28||3.93 ± 0.46||2.96 ± 0.28|
|Spleen||5.88 ± 0.30||5.91 ± 0.58||4.66 ± 0.52||4.71 ± 0.97||2.25 ± 0.36||1.59 ± 0.17|
|Lung||13.56 ± 1.71||6.42 ± 0.47||5.64 ± 0.41||4.55 ± 0.49||2.01 ± 0.18||1.43 ± 0.28|
|Kidney||15.01 ± 1.56||7.47 ± 1.01||6.57 ± 0.50||4.72 ± 0.69||2.20 ± 0.34||1.64 ± 0.23|
|Stomach a||4.05 ± 0.09||15.84 ± 0.78||8.11 ± 1.21||6.75 ± 0.43||11.12 ± 2.48||7.03 ± 1.51|
|Muscle||2.78 ± 0.42||1.68 ± 0.20||2.30 ± 0.32||1.40 ± 0.34||0.72 ± 0.21||0.61 ± 0.08|
a Expressed as % ID/organ.
Unless otherwise indicated, all chemicals used in synthesis were commercial products and were used without further puriﬁcation. Na125I (2200 Ci/mmol) was obtained from PerkinElmer Life and Analytical Sciences, USA. The double transgenic (APP/PS1) AD model mouse was obtained from Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Comparative Medicine Center of Peking Union Medical College (Beijing, China). 1H-NMR spectra were obtained on Bruker (400 MHz) NMR spectrometer at room temperature with TMS as an internal standard. Chemical shifts are reported as δ values relative to internal TMS. Coupling constants are reported in hertz. The multiplicity is deﬁned by s (singlet), d (doublet), t (triplet), and m (multiplet). Mass spectra were acquired using the Surveyor MSQ Plus (ESI) (Waltham, MA, USA) instrument. HPLC was performed on a Shimadzu SCL-10AVP system (Shimadzu Corporation, Kyoto, Japan) which consisted of a binary pump with on-line degasser, a model SPD-10AVP UV-VIS detector operating at a wavelength of 254 nm, and a Packard 500TR series flow scintillation analyzer (Packard BioScience Co., Wallingford, CT, USA) with a Alltech Alltima RPC-18 column (5 μm, ID = 4.6 mm, length = 250 mm). The samples were analyzed using acetonitrile and water (90:10 v/v) as mobile phase at a flow rate of 1 mL/min. The sample was separated using acetonitrile as mobile phase at a flow rate of 1 mL/min. All key compounds were proven by analytical HPLC analysis to show ≥95% purity (Supporting information).
3.1.1. General Procedure for Preparing Substituted Triphenyl Phosphonium Ylide 2 (2a–g)
The suitable 4-substituted-1-(bromomethyl)benzene 1a–g (1 mmol) and triphenylphosphine (1 mmol) was heated to reflux in xylene (10 mL) for about 6 h. The mixture was filtered and crude materials were purified by recrystallization with toluene.
3.1.2. General Procedure for Preparing 4–11, 13
The appropriate substituted compounds 2a–g (1 mmol), 1H-indole-5-carbaldehyde (3, 1 mmol), and CH3ONa (1 mmol) was heated to reflux in CH3OH (12 mL) for about 5 h. The organic solvent was removed under vacuum. Crude materials were purified by column chromatography on silica gel (petroleum ether/AcOEt, 4/1).
(E)-5-Styryl-1H-indole (4). Yield 53.6%, 1H-NMR (DMSO-d6) δ: 7.73 (1H, s), 7.58 (2H, d, J = 7.5 Hz), 7.43–7.38 (5H, m), 7.32 (1H, d, J = 16.5 Hz), 7.22 (1H, t, J = 7.2 Hz), 7.12 (1H, d, J = 16.4 Hz), 6.44 (1H, d, J = 3.0 Hz). HRMS m/z C16H13N found 220.1120/calcd 220.1126 ([M+H]+). m.p. 162–163 °C.
(E)-5-(4-Fluorostyryl)-1H-indole (5). Yield 71.4%, 1H-NMR (DMSO-d6) δ: 7.72 (1H, s), 7.62 (2H, dd, J1 = 8.6 Hz, J2 =5.7 Hz), 7.40 (2H, dd, J1 = 11.4 Hz, J2 = 8.6 Hz), 7.34 (1H, d, J = 3.0 Hz), 7.27 (1H, d, J = 16.4 Hz), 7.19 (2H, t, J = 8.8 Hz), 7.12 (1H, d, J = 16.4 Hz), 6.44 (1H, d, J = 3.0 Hz). HRMS m/z C16H12FN found 238.0878/calcd 238.0876 ([M+H]+). m.p. 179–180 °C.
(E)-5-(4-Chlorostyryl)-1H-indole (6). Yield 70.2%, 1H-NMR (DMSO-d6) δ: 7.74 (1H, s), 7.60 (2H, d, J = 8.5 Hz), 7.44–7.38 (4H, m), 7.35 (1H, d, J = 3.0 Hz), 7.34 (1H, d, J = 16.4 Hz), 7.12 (1H, d, J = 16.4 Hz), 6.44 (1H, d, J = 3.0 Hz). HRMS m/z C16H12ClN found 254.0733/calcd 254.0737 ([M+H]+). m.p. 205–206 °C.
(E)-5-(4-Bromostyryl)-1H-indole (7). Yield 68.3%, 1H-NMR (DMSO-d6) δ: 7.74 (1H, s), 7.54 (4H, s), 7.43–7.40 (2H, m), 7.36 (1H, d, J = 16.4 Hz), 7.35 (1H, d, J = 3.1 Hz), 7.11 (1H, d, J = 16.4 Hz), 6.44 (1H, d, J = 3.0 Hz). HRMS m/z C16H12BrN found 298.0235/calcd 298.0231 ([M+H]+). m.p. 215–216 °C.
(E)-5-(4-Iodostyryl)-1H-indole (8). Yield 55.3%, 1H-NMR (DMSO-d6) δ: 7.73 (1H, s), 7.70 (2H, d, J = 8.4 Hz), 7.43–7.39 (4H, m), 7.36 (1H, d, J = 16.4 Hz), 7.34 (1H, d, J = 3.1 Hz), 7.08 (1H, d, J = 16.5 Hz), 6.44 (1H, d, J = 2.9 Hz). HRMS m/z C16H12IN found 246.1283/calcd 246.1299 ([M+H]+). m.p. 211–212 °C.
(E)-5-(4-Methoxystyryl)-1H-indole (9). Yield 67.7%, 1H-NMR (DMSO-d6) δ: 7.70 (1H, s), 7.47 (2H, d, J = 8.0 Hz), 7.39 (2H, dd, J1 = 11.5 Hz, J2 = 8.6 Hz), 7.33 (1H, d, J = 3.0 Hz), 7.25 (1H, d, J = 16.4 Hz), 7.17 (2H, d, J = 8.0 Hz), 7.08 (1H, d, J = 16.4 Hz), 6.44 (1H, d, J = 3.0 Hz), 2.31 (3H, s). HRMS m/z C17H15N found 234.1126/calcd 234.1126 ([M+H]+). m.p. 176–177 °C.
(E)-5-(4-Methoxystyryl)-1H-indole (10). Yield 65.2%, 1H-NMR (DMSO-d6) δ: 7.68 (1H, s), 7.51 (2H, d, J = 8.6 Hz), 7.40–7.35 (2H, m), 7.33 (1H, d, J = 3.0 Hz), 7.16 (1H, d, J = 16.4 Hz), 7.06 (1H, d, J = 16.4 Hz), 6.93 (2H, d, J = 8.5 Hz), 6.42 (1H, d, J = 3.0 Hz), 3.77 (3H, s). HRMS m/z C17H15NO found 250.1241/calcd 250.1232 ([M+H]+). m.p. 163–164 °C.
(E)-5-(4-(Tributylstannyl)styryl)-1H-indole (11). A mixture of 7 (29.8 mg, 0.1 mmol), bis(tributyltin) (290 mg, 0.5 mmol), and Pd(Ph3P)4 (12.0 mg, 0.01 mmol) in toluene (15 mL) was stirred at 110 °C overnight. After removing the solvent in vacuo, the crude products were purified by column chromatography (petroleum ether/AcOEt, 20/1) to give 11 as a light-yellow-colored solid with a yield of 22.3%. 1H-NMR (CDCl3) δ: 8.87 (1H, d, J = 2.8 Hz), 8.15 (1H, d, J = 8.1 Hz), 8.08 (1H, d, J = 8.7 Hz), 7.98 (1H, dd, J1 = 8.9 Hz, J2 = 1.6 Hz), 7.82 (1H, s), 7.52 (4H, dd, J1 = 19.6 Hz, J2 = 8.5 Hz), 7.40 (1H, dd, J1 = 8.2 Hz, J2 = 4.2 Hz),7.28 (2H, dd, J1 = 16.4 Hz, J2 = 8.0 Hz), 1.64–1.55 (6H, m), 1.40–1.35 (6H, m), 1.16–1.11 (6H, m), 0.97–0.90 (9H, m). ESI-MS m/z C28H39NSn found 510.4/calcd 509.2 ([M+H]+).
Quinoline-6-carbaldehyde (13). Quinoline-6-carbaldehyde (13) was prepared from 6-methylquinoline (12) according to the previously reported procedure . 6-Methylquinoline (12, 4.0 g, 27.6 mmol) was heated to 160 °C and selenium dioxide (2.0 g, 18.4 mmol) was added. The mixture was stirred for 16 h, cooled to room temperature, and diluted with ethyl acetate (30 mL). The solution was decanted, and the residue was extracted with ethylacetate (20 mL × 2). The combined organic phase was concentrated, and the residue was purified by column chromatography on silica gel (petroleum ether/AcOEt, 4/1) to give 13 as a light gray solid (1.3 g, 30%). 1H-NMR (CDCl3) δ: 10.21 (1H, s), 9.06 (1H, dd, J1 = 4.2 Hz, J2 = 1.6 Hz), 8.38–8.35 (2H, m), 8.27–8.24 (2H, m), 7.55 (1H, dd, J1 = 8.3 Hz, J2 = 4.3 Hz).
3.1.3. General procedure for preparing 14–19
The suitable substituted compounds 2b–f (1 mmol), 13 (1 mmol), CH3ONa (1 mmol) was heated to reflux in CH3OH (12 mL) for about 6 h. The organic solvent was removed under vacuum. Crude materials were washed by water and purified by column chromatography on silica gel (petroleum ether/AcOEt, 6/1).
(E)-6-(4-Fluorostyryl)quinoline (14). Yield 66.8%, 1H-NMR (DMSO-d6) δ: 8.86 (1H, dd, J1 = 8.9 Hz, J2 = 1.4 Hz), 8.35 (1H, d, J = 8.0 Hz), 8.11 (1H, dd, J1 = 8.8 Hz, J2 = 1.5 Hz), 8.07 (1H, s), 8.01 (1H, d, J = 8.8 Hz), 7.73(2H, dd, J1 = 8.7 Hz, J2 = 5.7 Hz), 7.54 (1H, dd, J1 = 8.2 Hz, J2 = 4.2 Hz), 7.45 (2H, dd, J1 = 16.5 Hz, J2 = 7.7 Hz), 7.26 (1H, t, J = 8.8 Hz). HRMS m/z C17H12FN found 250.1039/calcd 250.1032 ([M+H]+). m.p. 120–121 °C.
(E)-6-(4-Chlorostyryl)quinoline (15). Yield 72.3%, 1H-NMR (DMSO-d6) δ: 8.86 (1H, d, J = 3.4 Hz), 8.35 (1H, d, J = 7.9 Hz), 8.12 (1H, d, J = 8.8 Hz), 8.08 (1H, s), 8.01 (1H, d, J = 8.7 Hz), 7.70 (2H, d, J = 8.2 Hz), 7.53 (2H, dd, J1 = 8.4 Hz, J2 = 4.1 Hz), 7.49–7.47 (4H, m). HRMS m/z C17H12ClN found 266.0732/calcd 266.0737 ([M+H]+). m.p. 129–130 °C.
(E)-6-(4-Bromostyryl)quinoline (16). Yield 73.9%, 1H-NMR (DMSO-d6) δ: 8.87 (1H, dd, J1 = 4.1 Hz, J2 = 1.5 Hz), 8.36 (1H, d, J = 8.0 Hz), 8.14 (1H, dd, J1 = 8.8 Hz, J2 = 1.6 Hz), 8.09 (1H, s), 8.01 (1H, d, J = 8.8 Hz), 7.63(4H, dd, J1 = 13.3 Hz, J2 = 8.8 Hz), 7.54 (1H, dd, J1 = 8.1 Hz, J2= 4.2 Hz), 7.48 (2H, dd, J1 = 16.6 Hz, J2 = 13.3 Hz). HRMS m/z C17H12BrN found 310.0217/calcd 310.0231 ([M+H]+). m.p. 143–144 °C.
(E)-6-(4-Iodostyryl)quinoline (17). Yield 70.2%, 1H-NMR (DMSO-d6) δ: 8.87 (1H, d, J = 4.1 Hz), 8.35 (1H, d, J = 8.0 Hz), 8.12 (1H, d, J = 8.9 Hz), 8.09 (1H, s), 8.01 (1H, d, J = 8.9 Hz), 7.78 (2H, d, J = 8.0 Hz), 7.56–7.40 (5H, m). HRMS m/z C17H12IN found 358.0100/calcd 358.0093 ([M+H]+). m.p. 173–174 °C.
(E)-6-(4-Methylstyryl)quinoline (18). Yield 71.7%, 1H-NMR (DMSO-d6) δ: 8.85 (dd, J1 = 4.0 Hz, J2 = 1.4 Hz, 1H), 8.36 (d, J = 8.1 Hz, 1H), 8.11 (dd, J1 = 8.8 Hz, J2 = 1.6 Hz, 1H), 8.06 (s, 1H), 8.01 (d, J = 8.8 Hz, 1H), 7.57(d, J = 8.0 Hz, 2H), 7.54 (dd, J1 = 8.3 Hz, J2 = 4.3 Hz, 1H), 7.41 (s, 2H), 7.23 (d, J = 7.9 Hz, 2H). HRMS m/z C17H12IN found 246.1299/calcd 246.1283 ([M+H]+). m.p. 125–126 °C.
(E)-6-(4-(Tributylstannyl)styryl)quinolin (19). The same reaction described above to prepare 11 was used, and a primrose yellow-colored solid of 19 was obtained in a yield of 28.6% from 16. 1H-NMR (CDCl3) δ: 8.87 (1H, d, J = 2.8 Hz), 8.15 (1H, d, J = 8.1 Hz), 8.08 (1H, d, J = 8.7 Hz), 7.98 (1H, dd, J1 = 8.9 Hz, J2 = 1.6 Hz), 7.82 (1H, s), 7.52 (4H, dd, J1 = 19.6 Hz, J2 = 8.5 Hz), 7.40 (1H, dd, J1 = 8.2 Hz, J2 = 4.2 Hz),7.28 (2H, dd, J1 = 16.4 Hz, J2 = 8.0 Hz), 1.64–1.55 (6H, m), 1.40–1.34 (6H, m), 1.16–1.13 (6H, m), 0.96–0.91 (9H, m). ESI-MS m/z C29H39NSn found 522.6/calcd 521.2 ([M+H]+).
3.1.4. Preparation of Radioiodinated Ligands
The radioiodinated compounds [125I]8 and [125I]17 were prepared from the corresponding tributyltin derivatives by an iododestannylation according to the procedure described previously . Brieﬂy, H2O2 (3%, 100 µL) was added to a mixture of a tributyltin derivative (0.1 mg/100 µL in ethanol), sodium [125I]iodide (speciﬁc activity 2,200 Ci/mmol), and 1 M HCl (100 µL) in a sealed vial. The reaction was allowed to proceed at room temperature for 15 min and then quenched by addition of saturated NaHSO3 solution (50 µL). The reaction mixture, after neutralization with 1 M NaOH, was puriﬁed by HPLC using a Alltech Alltima RPC-18 column (250 mm × 4.6 mm, 5 µm) and mobile phase consisting of acetonitrile with a flow rate of 1.0 mL/min. Finally, the radiochemical identity of the radioiodinated ligands were verified by co-injection and co-elution with non-radioactive 8 and 17 from HPLC profiles (Alltech Alltima RPC-18 column, 250 × 4.6 mm, 5 μm, CH3CN/H2O = 9/1 at the flow rate of 1.0 mL/min). The desired fractions containing the product were collectd and evaporated to dryness and redissolved in 100% ethanol. The ﬁnal products were stored at −20 °C for further studies.
3.2. Partition Coefﬁcient Determination
The determination of partition coefﬁcients of [125I]8 and [125I]17 was performed according to the procedure previously reported with some modifications . Ligand [125I]8 or [125I]17 (~5 μCi) was mixed with 3 mL each of n-octanol and PBS (0.02 M, pH 7.4) in a test tube. The test tube was vortexed for 5 min at room temperature, followed by centrifugation for 10 min at 3,000 rpm. Two weighed samples from the n-octanol (50 µL) and buffer layers (400 µL) were counted in a γ-counter. The partition coefﬁcient was expressed as the logarithm of the ratio of the counts per gram from n-octanol versus that of PBS. Samples from the n-octanol layer were repartitioned until consistent partition coefﬁcient values were obtained. The measurements were done in triplicate and repeated three times.
3.3. In Vitro Binding Studies Using the Aggregated Aβ1–40
The lyophilized white powder of β-amyloid(1–40) were purchased from AnaSpec (San Jose, CA, USA). After reconstituted by adding basic buffer (1% NH4OH. 60–70 μL) to β-amyloid (1–40) (1 mg) aggregation of Aβ1–40 was carried out by gently dissolving Aβ1–40 (0.25 mg/mL) in a PBS buffer (pH 7.4). The solution was incubated at 37 °C for 72 h with gentle and constant shaking. Binding studies were carried out according to the procedure described previously with some modifications using [125I]TZDM as the radiolabeled standard . Briefly, the competition binding assays were performed by mixing Aβ1–40 aggregates (100 µL), and [125I]TZDM (100 µL) in appropriate concentration (0.02 nM, diluted in 10% EtOH), test ligand (10−5–10−10 M, 100 µL) and PBS (0.02 M, pH 7.4, 700 µL) in a ﬁnal volume of 1 mL. The mixture was incubated at 37 °C for 2 h. Then the bound and free radioactivities were separated by vacuum ﬁltration through Whatman GF/B glass ﬁlters via a Brandel Mp-48T cell harvester followed by 3 × 4 mL washes with PBS (0.02 M, pH 7.4, 4 °C) containing 10% ethanol at room temperature. Filters containing the bound 125I ligand were counted in a γ-counter (WALLAC Wizard 1470, PerkinElmer Life Sciences, Waltham, MA, USA) with 75% counting efﬁciency. The IC50 values were determined using GraphPad Prism 5.0, and those for the inhibition constant (Ki) were calculated using the Cheng Prusoff equation: Ki = IC50/(1 + [L]/Kd) .
3.4. In Vitro Fluorescent Staining of Amyloid Plaques in Brain Sections from Transgenic Mouse
Parafﬁn-embedded brain sections of transgenic model mouse (8 µm, APP/PS1, 12 months, male) were used for the in vitro fluorescent staining of amyloid plaques. The brain sections were deparafﬁnized with xylene, ethanol and distilled water. After immersion in PBS (0.02 M, pH 7.4) for 30 min, the brain sections were incubated with 20% ethanol solution (1 µM) of compound 8 for 10 min. The localization of plaques was confirmed by staining with thioﬂavin-S on the adjacent sections. Finally, the sections were washed with 40% ethanol and PBS (0.02 M, pH 7.4). Fluorescent observation was performed by a Stereo Discovery V12 instrument (Zeiss, Oberkochen, Germany) equipped with a LP 505 filter set (excitation, 405 nm).
3.5. In Vitro Labeling of Brain Sections from Transgenic Mouse by Autoradiography
The brain sections mentioned above were incubated with [125I]8 (5 µCi/100µL) for about 20 min at room temperature. Then the sections were washed with saturated Li2CO3 in 40% EtOH for 3 min and 40% EtOH for 3 min, followed by rinsing with water for 30 s. After drying, the 125I-labeled sections were exposed to phosphorus ﬁlm for 8 h and then scanned with the phosphor imaging system (Cyclone, Packard) at the resolution of 600 dpi. The presence and localization of plaques were confirmed by the ﬂuorescent staining with thioﬂavin-S on the same sections using a Stereo Discovery V12 (Zeiss) instrument equipped with a LP 505 filter set (excitation: 405 nm).
3.6. In Vivo Biodistribution in Normal Mice
In vivo biodistribution studies were performed in KunMing normal mice (female, average weight 18–22 g) and in accordance with the national laws related to the care and experiments on laboratory animal. A saline solution (100 µL) containing [125I]8 or [125I]17 (1 µCi) was injected directly into the tail vein of mice. The mice (n = 5 for each time point) were sacriﬁced at designated time points post-injection. The organs of interest were removed and weighed, and the radioactivity was counted with an automatic γ-counter (WALLAC Wizard 1470).
A series of (E)-5-styryl-1H-indole and (E)-6-styrylquinoline based compounds have been synthesized and evaluated as novel imaging probes for Aβ plaques. Compound 8 was found to possess nanomolar affinity for β-amyloid plaques. In autoradiography, [125I]8 clearly labeled amyloid plaques in the cortex region of AD model mice. Moreover, [125I]8 displayed high initial brain uptake and fast clearance in biodistribution studies in normal mice. The findings suggest that the (E)-5-styryl-1H-indole derivative [123I]8 may be a potential probe for detecting β-amyloid plaques in the AD brain.
Supplementary materials can be accessed at: http://www.mdpi.com/1420-3049/17/4/4252/s1.
This work was funded by NSFC (20871021 and 21071023). The authors thank Mengchao Cui (College of Chemistry, Beijing Normal University, Beijing, China) for his kindness in providing the paraffin-embedded brain sections of AD model mice. The authors also thank Jin Liu (College of Life Science, Beijing Normal University) for providing the Zeiss Oberver Z1 equipment.
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- Sample Availability: Samples of the compounds are available from the authors.
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