Introduction Coumarin is a fragrant organic chemical com- pound in the benzopyrone chemical class isolated from different plant sources (Geissman 1962; Har- borne, 1988a; Harborne 1988b) and has various pharmacological activities. For example, the couma- rin nucleus is present in a number of potential drug molecules such as nonpeptidic HIV protease inhibi- tors, (Thaisrivongs et al., 1996) topoisomerase II (Rappa et al., 2000) and tyrosine kinase inhibitors (Yang 1999). Alternatively quinolines and their derivatives are known to have several applications in drugs and pharmaceuticals. A combination of benzopyran or chromen with a quinoline moiety in a single mole- cule, for example, 6H-chromeno[4,3-b]quinoline (Vu et al., 2007; Hegab et al., 2007 ) or 1-benzopyrano[3,4 -f]quinoline (Tabakovic et al., 1983) have also been identified for the promising bioactive molecules. The combination of quinoline and coumarin in a single molecule, for example, 6H-1-benzopyrano[4,3- b]quinolin-6-one (Tabakovic et al., 1987; Mulakayala et al., 2012) is acknowledged as a separate class of heterocycle. It can be used as a model for the detec- tion of bioactive molecules is not common. By know- ing the cytotoxicities of coumarins and chromeno [4,3-b]quinoline derivatives (Ajdini et al., 1984), we hypothesized that design of small molecules based on 6H-1-benzopyrano[4,3-b]quinolin-6-one might show anticancer properties. Herein we report the synthesis of a number of 6H-1- benzopyrano[4,3-b]quinolin-6-one derivatives along A Journal of the Bangladesh Pharmacological Society (BDPS) Bangladesh J Pharmacol 2015; 10: 660-671 Journal homepage: www.banglajol.info Abstracted/indexed in Academic Search Complete, Agroforestry Abstracts, Asia Journals Online, Bangladesh Journals Online, Biological Abstracts, BIOSIS Previews, CAB Abstracts, Current Abstracts, Directory of Open Access Journals, EMBASE/Excerpta Medica, Google Scholar, HINARI (WHO), International Pharmaceutical Abstracts, Open J-gate, Science Citation Index Expanded, SCOPUS and Social Sciences Citation Index; ISSN: 1991-0088 Abstract A convenient synthesis of 6H-1-benzopyrano[4,3-b]quinolin-6-one derivatives was reported using 4-chloro-2-oxo-2H-chromene-3-carbaldehyde with differ- ent aromatic amines using silica sulfuric acid. The compounds were tested for their anticancer activity against colon (HCT-116 and S1-MI-80), prostate (PC3 and DU-145), breast (MCF-7 and MDAMB-231) cancer cells. These com- pounds showed more selectivity and potent cytotoxic activity against colon cancer cells. 3c was tested against five other colon cancer cell lines (HT-29, HCT-15, LS-180, LS-174, and LoVo), which had similar cytotoxicity and selectivity. 3c did not induce PXR-regulated ABCB1 or ABCG2 transporters. In fact, 3c induced cytotoxicity in HEK293 cells over expressing ABCB1 or ABCG2 to the same extent as in normal HEK293 cells. It was cytotoxic approximately 3- and 5-fold to resistant colon carcinoma S1-MI-80 cells. 3c also produced concentration-dependent changes in HCT-116 colon cancer cells, in mitochondrial membrane potential, leading to apoptosis, and sub- micromolar concentrations caused chromosomal DNA fragmentation. Article Info Received: 12 June 2015 Accepted: 2 July 2015 Available Online: 2 August 2015 DOI: 10.3329/bjp.v10i3.23645 Cite this article: Li TL, Guo HF, Li FJ, Sun ZG, Zhang HC. Synthesis and biological evalua- tion of 6H-1-benzopyrano[4,3-b] quinolin-6-one derivatives as inhibi- tors of colon cancer cell growth. Bangladesh J Pharmacol. 2015; 10: 660 -71. Synthesis and biological evaluation of 6H-1-benzopyrano[4,3-b] quinolin-6-one derivatives as inhibitors of colon cancer cell growth Tie-Ling Li1, Hai-Feng Guo2, Fu-Juan Li3, Zhi-Guo Sun2 and Heng-Chun Zhang2 1Department of Pathology, MuDanJiang Medical University, Mudanjiang 157 011, China; 2Department of General Surgery, The affiliated Red Hospital of Mudanjiang Medical University, Mudanjiang 157 011, China; 3Department of Pathogenic Biology and Immunology Laboratory，MuDanJiang Medical University, Mudanjiang 157 011, China. with the in vitro anticancer properties of the com- pounds synthesized. Materials and Methods Chemistry Chemicals and reagents were purchased either from Sigma or Merck, and all reagents were of analytical reagent grade. Thin-layer chromatography (TLC) was performed on Merck silica gel 60 F254 plates and visualized under UV light. 1H NMR spectra were recorded with Varian Mercury Plus 400 MHz instrument. 13C NMR spectra were recorded with a Varian Gemini 100 MHz instrument. All the chemical shifts are reported in µ (ppm) using TMS as an internal standard. Multiplicity is indicated by one or more of the following abbreviations: s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), br (broad); the coupling constants (J) correspond to the order of the multiplicity assign- ment. Mass spectra were recorded with a PE Sciex model API 3000 instrument. All the reactions were carried out under nitrogen atmosphere. General procedure for the preparation of 6H-chromeno [4,3- b]quinolin-6-one (3a–j) A solution of 4-chloro-2-oxo-2H-chromene-3-carb- aldehyde (1 mmol) (Bairagi et al., 2009) and aroma- tic amine (1.5 mmol) in ethanol (5 mL) was added to amberlyst 15 (10 mol%). The reaction was refluxed for 2 hours and after completion of the reaction the reaction mixture was filtered to remove the catalyst. The filtrate was concentrated and the residue was purified by flash chromatography (n-hexane/ethyl- acetate 3:1) to afford the desired product. 6H-Chromeno[4,3-b]quinolin-6-one (3a) white solid; mp 224–227ºC; 1H NMR (400 MHz, DMSO-d6): µ 9.34 (s, 1H), 8.65 (dd, J = 7.5 and 1.5 Hz, 1H), 8.30 (d, J = 8.1 Hz, 1H), 8.21 (d, J = 8.7 Hz, 1H), 8.03–8.05 (m, 1H), 7.64–7.74 (m, 2H), 7.45–7.49 (m, 2H); 13C NMR (100 MHz, DMSO-d6): µ 160.7, 152.7, 150.4, 149.4, 141.2, 134.1, 133.0, 130.2, 129.0, 128.0, 127.3, 125.2, 125.0, 119.6, 117.6, 116.4; MS (ES mass): m/z 248 (M+1, 100%); HRMS: calcd for C16H10NO2: 248.0702, found 248.0701. 11-Methoxy-6H-chromeno[4,3-b]quinolin-6-one (3b) white solid; mp 234–236ºC; 1H NMR (400 MHz, DMSO-d6):  9.1 (s, 1H), 8.85 (dd, J = 7.5 and 1.3 Hz, 1H), 7.56–7.62 (m, 3H), 7.38–7.45 (m,2H), 7.24 (d, J = 5.7 Hz, 1H), 4.15 (s, 3H); 13C NMR (100 MHz,CDCl3):  160.6, 153.2, 152.3, 150.0, 136.1, 129.7, 129.6, 127.7, 127.1, 126.5, 125.8, 124.3, 122.0, 110.1, 114.8, 112.2, 56.1; MS (ES mass):m/z 278 (M+1, 10%); HRMS: calcd for C17H12NO3: 278.0815, found278.0817. 9,10-Difluoro-6H-chromeno[4,3-b]quinolin-6-one (3c) white solid; mp 252–255ºC; 1H NMR (400 MHz, CDCl3): µ 9.23 (s, 1H), 8.84 (dd, J = 8.1 and 1.5 Hz, 1H), 7.83–7.87 (m, 1H), 7.63–7.67 (m, 1H), 7.41–7.56 (m, 3H); 13C NMR (100 MHz, CDCl3): µ 160.9, 152.8, 150.1, 140.2,140.1, 132.8, 125.3, 125.2, 119.2, 117.5, 115.9, 115.7, 114.5, 114.4, 114.3, 114.2; MS(ES mass): m/z 284 (M+1, 100%). HRMS: calcd for C16H8F2NO2:284.0465, found: 284.04653. 10,11-Difluoro-6H-chromeno[4,3-b]quinolin-6-one (3d) white solid; mp 257–260ºC; 1H NMR (400 MHz, DMSO-d6): µ 9.46 (s, 1H), 8.62 (dd, J = 7.5 and 1.3 Hz, 1H), 8.24–8.28 (m, 1H), 7.84–7.91 (m, 1H), 7.75– 7.70 (m, 1H), 7.41–7.50 (m, 2H); 13C NMR (100 MHz, CDCl3): µ 160.7, 152.8, 150.5, 141.0, 133.1, 125.6, 125.4, 125.3 (2C), 125.2, 125.1, 124.8, 119.0, 118.7, 118.5, 117.3; MS (ES mass): m/z 284 (M+1, 100%); HRMS: calcd for C16H7F2NO2: 284.0486, found 284.0478. 10-Bromo-6H-chromeno[4,3-b]quinolin-6-one (3e) Bangladesh J Pharmacol 2015; 10: 660-671 661 White solid; mp 245–247ºC; 1H NMR (400 MHz, CDCl3): µ: 9.21 (s, 1H), 8.74 (dd, J = 8 and 1.5 Hz, 1H), 8.44 (s, 1H), 7.88 (d, J = 8.7 Hz, 1H), 7.72 (dd, J = 8.7 and 1.5 Hz, 1H), 7.61–7.65 (m, 1H),7.38–7.47 (m, 2H); 13C NMR (100 MHz, DMSO-d6): µ 161.1, 152.9, 150.5, 141.2, 132.9, 132.7, 131.9, 131.8, 131.3, 130.4, 125.9, 125.5, 125.2, 117.5, 115.9, 110.1; MS (ES mass):m/z 327.1 (M+2, 100%); HRMS: calcd for C16H9BrNO2: 327.2545,found 327.2541. 10-Fluoro-6H-chromeno[4,3-b]quinolin-6-one (3f) white solid; mp 234–237ºC; 1H NMR (400 MHz, CDCl3): µ 9.20 (s, 1H), 8.76 (dd, J = 8.1 and 1.5 Hz, 1H), 8.01–8.05 (m, 1H), 7.85 (dd, J = 9.8 and 2.3 Hz,1H), 7.58–7.65 (m, 1H), 7.38–7.48 (m, 3H); 13CNMR (100 MHz,DMSO-d6): µ 160.6, 153.1, 151.5, 150.6, 141.6, 133.5, 125.5, 125.2, 124.9, 119.5, 118.9, 118.6, 117.8, 116.1, 112.8, 112.6; MS (ES mass): m/z 266.2 (M+1, 10%); HRMS: calcd for C16H9FNO2: 266.2021, found 266.2018. 9-Fluoro-6H-chromeno[4,3-b]quinolin-6-one (3g) white solid; mp 224–226ºC; 1H NMR (400 MHz, CDCl3): µ 9.18 (s, 1H), 8.78 (dd, J = 8.1 and 1.5 Hz, 1H), 8.26–8.27 (m, 1H), 7.58–7.73 (m, 3H), 7.41–7.46 (m, 2H); 13C NMR (100 MHz, DMSO-d6): µ 160.9, 152.8, 150.3, 149.4, 141.3, 134.1, 133.0, 130.2, 129.1, 127.8, 127.4, 125.2, 125.1, 119.6, 117.6, 116.3; m/z 266.4 (M+1, 100%); HRMS: calcd for C16H9FNO2: 266.3032, found 266.3028. 9-Methoxy-6H-chromeno[4,3-b]quinolin-6-one (3h) white solid; mp 229–231ºC; 1H NMR (400 MHz, CDCl3): µ 9.2 (s, 1H), 8.77 (dd, J = 9.9 and 1.5 Hz, 1H), 8.13 (d, J = 9.1 Hz, 1H), 7.54–7.60 (m, 2H), 7.38– 7.44 (m, 2H), 7.22 (d, J = 2.7 Hz, 1H), 3.98 (s, 3H); 13C NMR (100 MHz, TFA): µ 159.5, 153.7, 151.5, 147.5, 142.1, 138.8, 134.6, 134.5, 127.1, 124.7, 124.1, 122.0, 121.7, 118.8, 105.8, 105.5, 58.5; MS (ES mass): m/z 278.1 (M+1, 10%); HRMS: calcd for C17H12NO3: 278.0815, found 278.0813. 9-Methyl-6H-chromeno[4,3-b]quinolin-6-one (3i) white solid; mp 234–236ºC; 1H NMR (400 MHz, CDCl3): µ 9.11 (s, 1H), 8.76 (dd, J = 8.1 and 1.5 Hz, 1H), 8.13 (d, J = 8.3 Hz, 1H), 7.73–7.75 (m, 2H), 7.55– 7.57 (m, 1H), 7.37–7.44 (m, 2H), 2.58 (s, 3H); 13C NMR (100 MHz, DMSO-d6): µ 160.8, 152.7, 150.7, 149.5, 145.0, 140.8, 132.88, 130.2, 129.8, 128.1, 125.7, 125.2, 124.5, 119.7, 117.6, 115.5, 22.2; MS (ES mass): m/z 262;2 (M+1, 100%); HRMS: calcd, for C17H12NO2: 262.0869, found 262.0867. 9-Chloro-6H-chromeno[4,3-b]quinolin-6-one (3j) white solid; mp 242–244ºC; 1H NMR (400 MHz, CDCl3): µ 9.0 (s, 1H), 8.75 (dd, J = 7.5 and 1.5 Hz, 1H), 8.17–8.21 (d, J = 9.3 Hz 1H), 8.1 (s, 1H), 7.86 (dd, J = 9.1 and 2.5 Hz, 1H), 7.58–7.63 (m, 1H), 7.38– 7.45 (m, 2H); 13C NMR (100 MHz, CDCl3): µ 160.8, 152.4, 149.6, 149.1, 139.8, 134.1,133.2, 132.5, 131.1, 127.6, 127.5, 125.1, 125.0, 119.1, 117.3, 116.3; MS (ES mass): m/z 282.2 (M+1, 100%); HRMS: calcd for C16H9ClNO2, 282.0244, found 282.0242. 662 Bangladesh J Pharmacol 2015; 10: 660-671 10-Chloro-6H-chromeno[4,3-b]quinolin-6-one (3k) White solid; m.p. 243 -245ºC; 1 H NMR (400 MHz, CDCl3): δ 9.05 (s, 1H), 8.70 (d, J = 6.7 Hz, 1H), 8.12 (d, J = 9.1 Hz, 1H), 7.93 (d, J = 1.8 Hz, 1H), 7.82 (dd, J = 8.9 Hz and 2.1, 1H), 7.55 – 7.60 (m, 1H), 7.34 – 7.42 (m, 1H); 13C NMR (100 MHz, CDCl3); δ 161.0, 152.8, 150.6, 149.5, 140.0, 134.3, 133.6, 132.7, 131.2, 127.8, 127.7, 125.3, 125.1, 119.4, 117.5, 116.5; MS (ES mass): m/z 282.2 (M+1, 100%); HRMS calcd for C16H8O2NCl, 281.0242 found 281.0246 9,10-Dimethoxy-6H-chromeno[4,3-b]quinolin-6-one (3l) Yellow solid; mp 291-294 oC, 1 H NMR (400 MHz, CDCl3): δ 8.94 (s, 1H), 8.66 (d, J = 7.7 Hz, 1H), 7.53 (t, J = 7.5 Hz, 1H), 7.47 (s, 1H) 7.37 (dd, J = 7.8 and 14.3 Hz, 2H), 7.11 (s, 1H), 4.10 (s, 3H), 4.03 (s, 3H); 13C NMR (100 MHz, CDCl3); δ 161.7, 156.1, 152.5, 150.8, 149.3, 148.1, 137.8, 131.7, 124.8, 124.7, 123.6, 120.1, 117.4, 114.2, 107.6, 105.6, 56.6, 56.4; MS (ES mass): m/z 307.2 (M+1, 100%); HRMS calcd for C18H13O4N, 307.0840found 307.0834. Biology DMEM media, 0.25% trypsin, propidium iodide, paclitaxel, buffers, and reagents were purchased from VWR (VWR International Inc., Suwanee, GA). MitoTracker Red and Alexa Fluor 488 annexin V kits for flow cytometry were purchased from Life Sciences (Molecular Probes Inc., Invitrogen, Eugene, OR). DMSO and RIF were purchased from Sigma. Cell culture Colon carcinoma cell lines [HCT-116, HCT-15, HT- 29, Lovo, LS-180, LS-174, S1 (a clone of LS174T cells)] and prostatic cancer cell lines [DU-145 and PC -3] and breast carcinoma cells [MDA-MB-231 and MCF-7] were grown as adherent monolayers in flasks with Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) in a humidified incubator containing 5% CO2 at 37ºC. A G482 mutant ABCG2-overexpressing, drug-resistant colon cancer cell line, S1-M1-80, was maintained in medium with 80 µM mitoxantrone (Miri et al., 2011; Robey et al., 2001). The assay media for PXR transactivation assays included phenol red-free DMEM (Lonza) supplemented with 5% charcoal/dextran-treated FBS (HyClone) and the other additives. PXR transactivation assay HepG2 cells were transfected with pcDNA3-hPXR and CYP3A4-luc plasmids using FuGENE 6 (Pro- mega). After 24 hours of transfection in growth media, 10,000 cells were plated into wells of 96-well culture plates (PerkinElmer), and treated with DMSO, RIF, or 3c for an additional 24 hours. At 48 hours of transfection, a luciferase assay was perfor- med to measure luminescence using the Neolite Reporter Gene Assay System (PerkinElmer) and a FLUOstar Optima microplate reader (BMG Labtech). Normalized CYP3A4 promoter activity was express- ed as fold induction over the DMSO control. Cell viability was measured in parallel by CellTiter-Glo luminescent assays (Promega), which determine the number of metabolically active cells by quantifying the ATP present. Luminescence was measured with a FLUOstar Optima plate reader (BMG Labtech). Cell cytotoxicity as determined by MTT assays and morphological analysis The MTT assay (Carmichael et al., 1987) was used to determine cytotoxicity of the compounds to the follow- ing cells: HCT-116, HCT-15, HT-29, LS-180, LS-174, Lovo, S1, DU-145, PC-3, MDA-MB-231 and MCF-7. Briefly, the cells were harvested with trypsin and suspended at a final concentration of 5 X 103 cells/well. Cells were seeded (180 µL/well) into 96-well multi- plates. Different concentrations of 6H-1-benzopyrano [4,3-b]quinolin-6-one derivatives (20 µL/well) were added. After 72 hours of incubation, 20 µL of MTT solution (4 mg/mL) was added in each well, and the plates were incubated further 4 hours, allowing the viable cells to convert the yellow-colored MTT into dark -blue formazan crystals. Subsequently, the medium was removed, and DMSO (100 µL) was added in each well to dissolve the formazan crystals. The absorbance was determined at 570 nm with an OPSYS microplate Reader (DYNEX Technologies, Inc., Chantilly, VA, USA). The means ± SD concentrations were calculated from at least three experiments performed in triplicate. The IC50 values were calculated from survival curves using the Bliss method. At 68 hours, cells with or without treatment were photographed by use of an inverted microscope (Olympus, BX53F) with fluores- cent lamps and digital cameras. The data were acquired and analyzed by CellSens software. Mitochondrial membrane potential and DNA fragmentation analysis Mitochondrial membrane potential and apoptosis N O O Cl N O O MeO MeO Bangladesh J Pharmacol 2015; 10: 660-671 663 were measured for colon cancer HCT-116 cells using MitoTracker Red and Alexa Fluor 488 annexin V kits for flow cytometry (Molecular) Probes Inc., Invitrogen, Eugene, OR). Briefly, apoptosis was induced by exposing HCT-116 cells (seeded in 6 well -plates) with or without 3C at 1 or 10 µM concentra- tions for 4 hours. Equal amounts of cells were harvested, and, to each mL of cells, 4 µL of 10 µM working solution of MitoTracker Red was added. Cells were stained at 37ºC for 30 min in an atmos- phere of 5% CO2. The cells were washed with PBS and suspended in 100 µL of 1X annexin-binding buffer, to which 5 µL of Alexa Fluor 488 annexin V was added. Cells were incubated for an additional 15 min, after which 400 µL of 1X annexin-binding buffer was added. The stained cells were counted by flow cytometry, measuring the fluorescence at 530 nm and 585 nm (BD FACSCalibur Flow Cytometer using FlowJo FACS data analysis software). A characteristic feature of apoptosis is induction of oligonucleosomal DNA fragmentation by cytotoxic compounds, which activate nucleases that degrade the higher-order chromatin structure of DNA into mono- and oligonucleosomal DNA fragments (Hen- kels and Turchi, 1999; Wu et al., 2005). To establish the mode of action of 3C in colon cancer cytotoxi- city, a DNA fragmentation assay was performed. Apoptotic degradation of DNA was analyzed by agarose gel electrophoresis. Briefly, HCT-116 cells were cultured in the presence of 3c (2.5 µM) for 6 hours. Genomic DNA was extracted from the cells by use of Promega Wizard Genomic DNA purifica- tion kits (Promega Corporation, Madison, WI) and resolved on 1% agarose gels at 40V for 4 hours. DNA was visualized by ethidium bromide staining and photographed. Results and Discussion Chemistry To find the convenient procedure we investigated the cylclization of 4-chloro-2-oxo-2H-chromene-3- carbaldehyde (1) with aniline (2) using Amberlyst-15 resin as catalyst in ethanol under reflux (Scheme-1) for 2 hours which yielded 6H-1-benzopyrano[4,3-b] quinolin-6-one 3a in 91% (Table I). Several amines were used for checking the compatibility of this method. All the amines including aromatic and substituted aromatic amines were well tolerated with the current methodology to yield the required products in good to excellent yields. Thus, the structures of the synthesized compounds are shown in Table I. Biological evaluation Growth curves, cell cytotoxicity, and morphological analysis for 6H-1-benzopyrano [4,3-b]quinolin-6- one derivative derivatives (3a–3l) 6H-1-benzopyrano[4,3-b]quinolin-6-one derivatives (3a–3l) were evaluated for cytotoxic effects on threetypes of cancer cells, that is, colon (HCT-116 and S1), prostate (PC3 and DU-145), breast (MCF-7 and MDAMB-231) cell lines. The 3-(4,5- dimethylthiazol-2-yl) -2,5 -diphenyltetrazolium bromide (MTT) assay was used. All compounds were tested at concentrations ranging from 0.1 µM to 100 µM. The 50% minimum inhibitory concentra- tions (IC50) are summarized in Table I. 6H-1-benzopyrano [4,3-b]quinolin-6-one derivatives (3a–3l) were exhibited variable degrees of growth inhibitory activity towards the three human cancer cell lines (Table I). Compound 3d, showed only a modest inhibitory activity (IC50 >40 µM) on the tested cells. Other compounds, with the exception of 3d, showed moderately more or less cytotoxic activity relative to 3c. Compound 3c with a 9,10-difluoro substitution, was most effective against breast (MDAMB-231) cancer cells, with IC50 values ranging between 44 and 50 µM. A similar cytotoxic profile against colon cancer (HCT-116 and S1) and breast cancer cells was observed for 3f, which has a 10-fluoro substitution. Among the eight compounds studied, 3C, with a difluoro substitution on the 9 and 10 position of the 6H-1-benzopyrano [4,3-b]quinolin-6-one ring, show- ed selective and potent growth inhibition against colon cancer cells. The IC50 values of 3c against HCT -116 and S1 cells were 0.6 lM and 0.8 lM, respectively. Prostate cancer cells (PC-3 and DU-145) were also inhibited by 3c, with an IC50 values ranging from 0.8 lM to 1.2 lM. Further, 3c showed moderate growth inhibitory activity (IC50 >10 lM) against breast (MCF-7 and MDAMB-231) cancer cells. Overall, these results established that the 9,10- difluoro substitution is significant to the anticancer activity of 6H-1-benzopyrano [4,3-b]quinolin-6-one and that compound 3c was a promising candidate for further studies with colon cancer cells. 3c exhibits potent and selective cytotoxic activity on various colon cancer cells results of compound 3c on colon carcinoma cells encouraged us to expand our Scheme I: Synthetic scheme of 6H-1-benzopyrano[4,3-b] quinolin-6-one derivatives from 4-chloro-2-oxo-2H- chromene-3-carbaldehyde 664 Bangladesh J Pharmacol 2015; 10: 660-671 Table I Synthesis of a novel series of substituted 5-(aminomethylene)thiazolidine-2,4-dionesa Entry Amine (2) Product Yield (%)b 1 3a 92 2 3b 93 3 3c 81 4 3d 78 5 3e 84 6 3f 87 7 3g 82 8 3h 85 9 3i 92 Bangladesh J Pharmacol 2015; 10: 660-671 665 Table II Activity of 6H-1-benzopyrano [4,3-b]quinolin-6-one derivatives against various cell lines Colon Prostate Breast Compound HCT-116 S1 PC3 DU-145 MCF-7 MDAMB-231 3a 48.6 ± 8.6 54.2 ± 9.8 65.2 ± 13.2 69.4 ± 12.4 76.5 ± 16.4 78.5 ± 14.2 3b 56.2 ± 11.3 61.2 ± 10.6 71.3 ± 11.2 71.9 ± 12.9 86.2 ± 14.3 82.1 ± 12.3 3c 1.6 ± 0.1 1.7 ± 0.1 0.9 ± 0.2 1.6 ± 0.6 7.6 ± 0.8 6.6 ± 0.4 3d 4.6 ± 0.4 3.8 ± 0.3 5.2 ± 0.5 6.4 ± 0.4 11.2 ± 1.1 13.2 ± 1.6 3e 82.5 ± 14.3 86.5 ± 15.6 93.2 ± 17.6 91.4 ± 16.3 74.6 ± 12.6 72.6 ± NA 3f 12.1 ± 3.2 12.9 ± 2.8 15.3 ± 5.3 16.2 ± 4.8 18.3 ± 5.3 17.6 ± NA 3g 13.5 ± 2.9 14.6 ± NA 21.6 ± 4.3 25.3 ± 4.3 17.6 ± 4.3 18.3 ± 5.3 3h 91.6 ± 12.4 93.5 ± 4.2 120.3 ± 18.3 114.6 ± 17.2 93.2 ± 14.2 91.3 ± 7.5 3i 86.3 ± 14.3 84.3 ± 15.2 95.6 ± 15.6 92.3 ± 14.3 72.3 ± NA 75.8 ± 12.9 3j 89.5 ± NA 95.8 ± 18.2 44.6 ± NA 87.3 ± 11.2 106.7 ± 19.4 110.5 ± 18.6 3k 85.4 ± 14.2 83.4 ± 7.4 111.4 ± 18.3 94.5 ± 14.6 58.4 ± 6.9 62.4 ± 4.6 3l 91.6 ± 12.7 72.8 ± 11.6 57.3 ± 15.8 53.7 ± 17.8 78.6 ± 16.2 71.6 ± 12.4 Cell survival assay was determined by the MTT assay. IC50 values are represented as means ± SD of three independent experiments performed in triplicate. A mean IC50 value of 100 mM was the cut off. NA, not assessed aAll the reactions were performed using 4-chloro-2-oxo-2H-chromene-3-carbaldehyde 1 (1.0 mmol), aniline 2 (1.1 mmol) and amberlyst-15 (15 mol%), ethanol (10 vol.), reflux, 2-3 hours; b Isolated yields Table I Synthesis of a novel series of substituted 5-(aminomethylene)thiazolidine-2,4-dionesa (Cont.) Entry Amine (2) Product Yield (%)b 10 3j 96 11 3k 96 12 3l 97 666 Bangladesh J Pharmacol 2015; 10: 660-671 studies to different types of colon cancer cells (HCT-15, HT-29, Lovo, LS-180, and LS-174). All these cancer cells were sensitive to 3c at concentrations ranging from µ0.6 to 1.0 µM (Table II, Figure 1A and B). Notably, 3c was 10–15 fold more selective for inhibition of colon cancer cells relative to HEK293 cells (Figure 1A and B); 10–30 Figure 1: Cytotoxic effects of 3c A) Survival of colon cancer cells S1, HCT-116, HCT-15, HT-29, Lovo, and LS-180 compared to that of human embryonic kidney cells, EK293/ pcDNA3.1; B) IC50 values of 3c for colon cancer cells S1, HCT-116, HCT-15, HT-29, Lovo, and LS-180 relative to human embryonic kidney cells (HEK293/pcDNA3.1). Cell survival was determined by the MTT assay. IC50 values are represented as means ± SD of three independent experiments performed in triplicate. Statistically, *p<0.05; **p<0.01, colon cancer cells versus the HEK293/pcDNA3.1; C) Morphological analysis of the cytotoxic effects of 3c (0, 0.5, 2 and 10 M) on colon cancer cells, HCT-116 and HCT-15; prostate cancer cells, DU-145; and human embryonic kidney cells HEK- 293, exposed for 68 hours, was made by microscopy at 20x. The cells were photographed for each triplicate treatment with an inverted microscope (Olympus, BX53F) with fluorescent lamps and digital cameras. A representative figure is shown for each treatment. The data were acquired and analyzed with Cell Sens software Bangladesh J Pharmacol 2015; 10: 660-671 667 fold more selective for other cancer cells. (breast, prostate) (Table I); After 68 hours of treatment of HCT- 116, HCT-15, and HEK293 cells with 0, 0.5, 2, or 10 µM 3c, morphological changes, complementing the cytoto- xicity data, were evident in all the cells (Figure 1c shows representative images). In sum, the cytotoxic effect of 3c on colon cancer cells is particularly notable because of its selectivity and its IC50 values of <1 µM. 3C does not activate pregnane X receptor (PXR), is not a substrate of ABCB1 or ABCG2 transporters, and is cytotoxic to chemoresistant colon cancer cells {PXR is a ligand-dependent nuclear receptor involved in regulating the expression of ATP-binding cassette (ABC) transporters, including ABCB1 (a.k.a. P- glycoprotein) and ABCG2 (a.k.a. breast cancer esistance protein, BCRP) (Pondugula et al., 2009, Pondugula and Mani, 2013). Activation of PXR by xenobiotics leads to chemoresistance, concern in drug development and clinical therapy. The possible activation of PXR by3C was examined with HepG2 cell-based reporter gene assays. Although rifampicin (RIF), an agonist of human Table II IC50 values for IND-2 inhibition of various colon cancer cell lines Colon cancer cells IC50 ± SD (nM) 3c HCT-15 670.6 ± 48.9 HCT-116 634.5 ± 120.1 HT-29 790.8 ± 103.5 LS-180 1023.5 ± 230.6 LS-174 874.6 ± 89.7 S1 798.3 ± 137.4 Lovo 993.8 ± 142.6 Figure 2: 3c does not induce human PXR transactivation of CYP3A4 promoter activity A) CYP3A4 prompter activity was determined in HepG2 cells after transient cotransfection with pGL3-CYP3A4-luc reporter and pcDNA3-hPXR plasmids for 24 hours, followed by treatment with DMSO, RIF, or 3c for an additional 24 hours. The induction of CYP3A4 promoter activity was normalized as fold increase over the DMSO control. Data represent means ± SD from three different experiments. Statistical significance (*p<0.05) was determined with Student’s t test by comparing the effects of RIF or 3c with DMSO; B) Effect of 3c on HepG2 cell viability. During the PXR trans- activation studies, viability of HepG2 cells was determined simultaneously in parallel experiments with the Cell Titer-Glo luminescent cell viability assay kit and the data are expressed as luminescence units. Data represent the means ± SD of triplicate determinations. Statistical significance (*p<0.05) was determined with Student’s t test by comparing the effects of RIF or 3c with DMSO; C) Effect of 3c on the survival of cells overexpress- ing ABCB1 or ABCG2.32 Effects of 3c, topotecan, and SN-38 on S1 and S1-M1-80 cells. MTT cytotoxicity assays were used to measure survival of HEK293/pcDNA3.1, HEK293/R2, HEK293/ABCB1, S1, and S1-M1-80 cells. Data points represent the means ± SD of triplicate determinations. Rep- resentative results from three independent experiments, each performed in triplicate, are shown 668 Bangladesh J Pharmacol 2015; 10: 660-671 Figure 3: Effects of 3c on mitochondrial membrane potential and DNA fragmentation A) HCT-116 cells in complete medium were expose to 3c (0, 1, or 10 mM) for 4 hours. Cells were then treated with the reagents of the MitoTracker Red and Alexa Fluor 488 annexin V kits for flow cytometry. Representative results from two independent experiments, each performed in triplicate, are shown; B) 3c induced DNA damage in HCT-116 cells. Chromosomal DNA was extracted from HCT-116 cells and resolved on a 1% agarose gel at 40 V for 6 hours. Lane 1: ‘M’, Marker; lanes 2 and 3: untreated HCT cells, 500 ng and 1 lg, respectively; lanes 4 and 5: HCT cells incubated with 3c (2.5 mM) for 6 hours Bangladesh J Pharmacol 2015; 10: 660-671 669 PXR, induced PXR transactivation of CYP3A4 promoter activity, 3c at 1 or 10 µM did not affect PXR transactivation (Figure 2A), showing that 3c does not activate PXR at concentrations cytotoxic to colon cancer cells and indicating that 3c does not induce PXR- mediated drug resistance in cancer cells. Similar to RIF, 3c at 10 µM was marginally cytotoxic, although 3c at 1 µM was non-cytotoxic (Figure 2B), showing that the lack of effect of 3c on PXR was not due to cytotoxicity. Multi-drug resistance (MDR) factors, such as ABCB1 and ABCG2 transporters, present limitations for the development of anticancer agents. (Perin et al., 2011) These transporters are expressed in a variety of solid and hematological malignancies, where they are involved in the efflux of various therapeutic drugs, leading to MDR. Ideally, drugs that are not substrates for these transporters are preferred as anticancer agents. 3c was screened against ABCB1- and ABCG2-over-expressing cells, and its effects were compared with positive controls paclitaxel and mitoxantrone, respectively. There was no substantial resistance to 3c in ABCB1- or ABCG2-overexpress- ing cells, as all the cells were sensitive at similar concentrations of 3c (Figure 2C), indicating that 3c is not a substrate for ABCB1 and ABCG2 transporters. These results support our PXR analysis (Figure 2A). Additionally, the cytotoxic potential of 3c was evaluated for a G482 mutant ABCG2-over- expressing, drug-resistant colon cancer cell line, S1- M1-80. S1-M1-80 cells showed significant resistance (p<0.001) to SN-38, an active metabolite of irino- tecan and topotecan (Figure 2D). 3c, however, inhibited the resistant S1-M1-80 cells 3–5 fold more potently (p<0.001) than SN-38 and topotecan (Figure 2D). This could be because: (a) 3c did not interact with ABCG2 transporters, was not effluxed by resistant S1-M1-80 cells, and maintained its cytotoxic concentration, or (b) 3c blocked the ABCG2 transporters and retained its cytotoxic potential in resistant S1-M1-80 cells. If the second reason is true, 3c may be beneficial in combination chemotherapy against colorectal and other tumors with agents that are substrates of ABCG2 transporters. However, further mechanistic experiments including ATPase, photo-affinity labeling assays, and combination chemotherapy are necessary to confirm the interactions of 3c with ABCB1 and ABCG2 transporters. 3c induces reduces mitochondrial membrane potential and causes apoptosis and DNA fragmentation in coloncancer cells Inappropriately regulated apoptosis is implicated in cancer. Whereas, mitochondrial dysfunction is involved in signaling processes that initiate apoptotic events, loss of membrane asymmetry, cytochrome c, and other apoptogenic factors released from mitochondria initiate apoptotic cell death. In the process of apoptosis, phospha- tidylserine (PS), otherwise located on the cyto- plasmic surface, is displaced from the inner to the outer leaflet of the plasma membrane. The extracellular exposed PS has high affinity for binding to the human vascular anticoagulant, annexin V, a 35–36 kDa, Ca2+-dependent, phospho- lipid-binding protein. This principle is used to determine the binding of annexin V, labeled with a fluorophore or biotin, to exposed PS on the outer leaflet and thereby to identify apoptotic cells. (Koopman et al., 1994) Live cells, 63.11% of untreated HCT-116 cells with intact mitochondrial membranes, are seen in quadrant I of Figure 3A. Of these cells, 27.6% had a loss in mitochondrial membrane potential and had started the process of apoptosis. Treatment with 3c, even at 1 µM, for 4 hours produced a significant loss (p<0.01) of membrane potential in 68.46% of the cells, as seen in quadrant II of Figure 3A. At 10 µM, 3c treatment for 4 h showed that almost all the cells (98.36%) had no or low mitochondrial membrane potential and thus were primed to undergo apoptosis (quadrant II of Figure 3A). These data show that 3c produces concentration-dependent decreases in mitochondrial potential of HCT-116 colon cancer cells, leading to apoptosis. The extent of 3c-induced DNA damage in HCT-116 colon cancer cells was assessed by chromosomal DNA fragmentation.Treatment with 2.5 µM 3c for 6 h led to fragmentation of chromosomal DNA (Figure 3B). In contrast, chromosomal DNA of untreated cells was intact. These results indicate that 3c induces DNA breakage at multiple positions across chromosomal DNA, leading to apoptosis. Conclusion The present study describes the synthesis of 6H-1- b e n z o py ra n o [4 ,3 - b ] q u ino l i n -6 - on e de r i va - tives derivatives (3a–3l). The synthesized analogues 3a-3l was evaluated their anti-cancer activity. 9,10- difluoro-6H-chromeno[4,3-b]quinolin-6-one 3c was shown potent inhibition against colon cancer cells. References Ajdini N, Leci O, Tabakovic I, Tabakovic K. Chemistry of coumarin, phase-transfer catalysis in the C-alkylation of 4-arylaminocoumarins. Bull Soc Chim.1984; 49: 495-500. Bairagi S, Bhosale A, Deodhar MN. 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Bangladesh J Pharmacol 2015; 10: 660-671 671 https://scholar.google.co.in/citations?view_op=view_citation&hl=en&user=YYgYTCAAAAAJ&citation_for_view=YYgYTCAAAAAJ:9yKSN-GCB0IC https://scholar.google.co.in/citations?view_op=view_citation&hl=en&user=YYgYTCAAAAAJ&citation_for_view=YYgYTCAAAAAJ:9yKSN-GCB0IC https://scholar.google.co.in/citations?view_op=view_citation&hl=en&user=YYgYTCAAAAAJ&citation_for_view=YYgYTCAAAAAJ:9yKSN-GCB0IC https://scholar.google.co.in/citations?view_op=view_citation&hl=en&user=YYgYTCAAAAAJ&citation_for_view=YYgYTCAAAAAJ:9yKSN-GCB0IC Introduction: Materials and Methods: Results and Discussion: were sensitive to 3c at concentrations ranging from 06: 226911 I: IV: Alexa Fluor 488 dye fluorescence: Control: 3c 25 M: Conclusion: References: Author Info HaiFeng Guo Principal contact email guohaifeng07gmailcom: Text1: DatePrinted: This article was downloaded by you on: Aug 26, 2016