Novel Sulfonamide Derivatives Carrying a Biologically Active 3,4-Dimethoxyphenyl Moiety as VEGFR-2 Inhibitors

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorMohammed Ghorab, Mostafa
dc.contributor.authorSulaiman Alsaid, Mansour
dc.contributor.authorElbadawy Ashour, Abdelkader
dc.contributor.authorAbdulalrahman Al-Mishari, Abdullah
dc.contributor.authorKumar, Ashok
dc.contributor.authorFayaz Ahmedd, Sheikh
dc.date.accessioned2019-10-22T09:16:03Z
dc.date.available2019-10-22T09:16:03Z
dc.date.issued2016
dc.description.abstractNovel sulfonamides 3–19 with a biologically active 3,4-dimethoxyphenyl moiety were designed and synthesized. The structures of the synthesized compounds were established using elemental analyses, IR, 1H-NMR, 13C-NMR spectral data and mass spectroscopy. All the synthesized compounds were evaluated for their in vitro anticancer activity against four cancer cell lines, namely human hepatocellular carcinoma (HepG2), human medulloblastoma (Daoy), human cervical cancer (HeLa), and human colon cancer (HT-29), by using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and dasatinib as the reference drug. Among the tested derivatives, compounds 4, 10, 16, and 19 showed good activity as cytotoxic agents. The most active derivatives were evaluated for their ability to inhibit vascular endothelial growth factor receptor (VEGFR)-2. Compounds Z-4-(3-(3,4-dimethoxyphenyl)-3-oxoprop-1-enylamino)-N- (5-methyl-1,3,4-thiadiazol-2-yl)-benzenesulfonamide 10 and Z-4-(3-(3,4-dimethoxyphenyl)-3-oxoprop-1- enylamino)-N-(1H-indazol-6-yl)-benzenesulfonamide 19 were more active as VEGFR-2 inhibitors than dasatinib. Molecular docking of the most active derivatives on the active site of VEGFR-2 revealed that compound 19 exhibited favorable and promising results.en_US
dc.description.sponsorshipChemical and Pharmaceutical Bulletinen_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=22769&tip=sid&clean=0
dc.identifier.citation1) Jemal A., Bray F., Center M. M., Ferlay J., Ward E. F. D., Forman D., Cancer J. Clin., 61, 69–90 (2011). 2) Thun M. J., DeLancey J. O., Center M. M., Jemal A., Ward E. M., Carcinogenesis, 31, 100–110 (2010). 3) Heffeter P., Jakupec M. A., Körner W., Wild S., von Keyserlingk N. G., Elbling L., Zorbas H., Korynevska A., Knasmüller S., Sutterlüty H., Micksche M., Keppler B. K., Berger W., Biochem. Pharmacol., 71, 426–440 (2006). 4) Zwick E., Bange J., Ullrich A., Endocr. Relat. Cancer, 8, 161–173 (2001). 5) Peng F.-W., Xuan J., Wu T.-T., Xue J.-Y., Ren Z.-W., Liu D.-K., Wang X.-Q., Chen X.-H., Zhang J.-W., Xu Y.-G., Shi L., Eur. J. Med. Chem., 109, 1–12 (2016). 6) Sun L., Tran N., Liang C., Tang F., Rice A., Schreck R., Waltz K., Shawver L. K., McMahon G., Tang C., J. Med. Chem., 42, 5120– 5130 (1999). 7) Kubo K., Shimizu T., Ohyama S., Murooka H., Iwai A., Nakamura K., Hasegawa K., Kobayashi Y., Takahashi N., Takahashi K., Kato S., Izawa T., Isoe T., J. Med. Chem., 48, 1359–1366 (2005). 8) Hennequin L. F., Stokes E. S. E., Thomas A. P., Johnstone C., Plé P. A., Ogilvie D. J., Dukes M., Wedge S. R., Kendrew J., Curwen J. O., J. Med. Chem., 45, 1300–1312 (2002). 9) Tripathy R., Reiboldt A., Messina P. A., Iqbal M., Singh J., Bacon E. R., Angeles T. S., Yang S. X., Albom M. S., Robinson C., Chang H., Ruggeri B. A., Mallamo J. P., Bioorg. Med. Chem. Lett., 16, 2158–2162 (2006). 10) Munchhof M. J., Beebe J. S., Casavant J. M., Cooper B. A., Doty J. L., Higdon R. C., Hillerman S. M., Soderstrom C. I., Knauth E. A., Marx M. A., Rossi A. M. K., Sobolov S. B., Sun J., Bioorg. Med. Chem. Lett., 14, 21–24 (2004). 11) Mendel D. B., Laird A. D., Smolich B. D., Blake R. A., Liang C., Hannah A. L., Shaheen R. M., Ellis L. M., Weitman S., Shawver L. K., Cherrington J. M., Anticancer Drug Des., 15, 29–41 (2000). 12) Scott R. W., Neville S. N., Urbina A., Camp D., Stankovic N., Org. Process Res. Dev., 10, 296–303 (2006). 13) Semenza G. L., N. Engl. J. Med., 358, 2066–2067 (2008). 14) Hicklin D. J., Ellis L. M., J. Clin. Oncol., 23, 1011–1027 (2005). 15) Ferrara N., Endocr. Rev., 25, 581–611 (2004). 16) Guo S., Colbert L. S., Fuller M., Zhang Y., Gonzalez-Perez R. R., Biochim. Biophys. Acta, 1806, 108–121 (2010). 17) Partanen T. A., Alitalo K., Miettinen M., Cancer, 86, 2406–2412 (1999). 18) Folkman J., N. Engl. J. Med., 285, 1182–1186 (1971). 19) Jain R. K., Duda D. G., Willett C. G., Sahani D. V., Zhu A. X., Loeffler J. S., Batchelor T. T., Sorensen A. G., Nat. Rev. Clin. Oncol., 6, 327–338 (2009). 20) Baka S., Clamp A. R., Jayson G. C., Expert Opin. Ther. Targets, 10, 867–876 (2006). 21) Gupta K., Zhang J., Postgrad. Med. J., 81, 236–242 (2005). 22) Sternberg C. N., Davis I. D., Mardiak J., Szczylik C., Lee E., Wagstaff J., Barrios C. H., Salman P., Gladkov O. A., Kavina A., Zarbá J. J., Chen M., McCann L., Pandite L., Roychowdhury D. F., Hawkins R. E., J. Clin. Oncol., 28, 1061–1068 (2010). 23) van der Graaf W. T., Blay J.-Y., Chawla S. P., Kim D.-W., Bui- Nguyen B., Casali P. G., Schöffski P., Aglietta M., Staddon A. P., Beppu Y., Le Cesne A., Gelderblom H., Judson I. R., Araki N., Ouali M., Marreaud S., Hodge R., Dewji M. R., Coens C., Demetri G. D., Fletcher C. D., Dei Tos A. P., Hohenberger P.; EORTC Soft Tissue and Bone Sarcoma Group, PALETTE study group, Lancet, 379, 1879–1886 (2012). 24) Bukowski R. M., Yasothan U., Kirkpatrick P., Nat. Rev. Drug Discov., 9, 17–18 (2010). 25) Fukuoka K., Usuda J., Iwamoto Y., Fukumoto H., Nakamura T., Yoneda T., Narita N., Saijo N., Nishio K., Invest. New Drugs, 19, 219–227 (2001). 26) Supuran C. T., Scozzafava A., Expert Opin. Ther. Pat., 10, 575–600 (2000). 27) Payne J. E., Bonnefous C., Hassig C. A., Symons K. T., Guo X., Nguyen P.-M., Annable T., Wash P. L., Hoffman T. Z., Rao T. S., Shiau A. K., Malecha J. W., Noble S. A., Hager J. H., Smith N. D., Bioorg. Med. Chem. Lett., 18, 6093–6096 (2008). 28) Kawai M., BaMaung N. Y., Fidanze S. D., Erickson S. A., Tedrow J. S., Sanders W. J., Vasudevan A., Park C., Hutchins C., Comess K. M., Kalvin D., Wang J., Zhang Q., Lou P., Tucker-Garcia L., Bouska J., Bell R. L., Lesniewski R., Henkin J., Sheppard G. S., Bioorg. Med. Chem. Lett., 16, 3574–3577 (2006). 29) Supuran C. T., Scozzafava A., Expert Opin. Ther. Pat., 12, 217–242 (2002). 30) Villar R., Encio I., Migliaccio M., Gil M. J., Martinez-Merino V., Bioorg. Med. Chem., 12, 963–968 (2004). 31) Huang S., Connolly P. J., Lin R., Emanuel S., Middleton S. A., Bioorg. Med. Chem. Lett., 16, 3639–3641 (2006). 32) Hande K. R., Hagey A., Berlin J., Cai Y., Meek K., Kobayashi H., Lockhart A. C., Medina D., Sosman J., Gordon G. B., Rothenberg M. L., Clin. Cancer Res., 12, 2834–2840 (2006). 33) Nakamura K., Yamamoto A., Kamishohara M., Takahashi K., Taguchi E., Miura T., Kubo K., Shibuya M., Isoe T., Mol. Cancer Ther., 3, 1639–1649 (2004). 34) Al-Dosari M. S., Ghorab M. M., Al-Said M. S., Nissan Y. M., Chem. Pharm. Bull., 61, 50–58 (2013). 35) Al-Said M. S., Ghorab M. M., Nissan Y. M., Chem. Cent. J., 6, 64 (2012). 36) Ghorab M. M., Ragab F. A., Heiba H. I., Agha H. M., Nissan Y. M., Arch. Pharm. Res., 35, 59–68 (2012). 37) Al-Dosari M. S., Ghorab M. M., Alsaid M. S., Nissan Y. M., Ahmed A. B., Eur. J. Med. Chem., 69, 373–383 (2013). 38) Ghorab M. M., Ceruso M., Alsaid M. S., Nissan Y. M., Arafa R. K., Supuran C. T., Eur. J. Med. Chem., 87, 186–196 (2014). 39) Ghorab M. M., Alsaid M. S., Ceruso M., Nissan Y. M., Supuran C. T., Bioorg. Med. Chem., 22, 3684–3695 (2014). 40) Ghorab M. M., Alsaisd M. S., Nissan Y. M., Acta Pol. Pharm., 72, 65–78 (2015). 41) Ghorab M. M., Alsaid M. S., Al-Dosari M. S., Nissan Y. M., Al- Mishari A. A., Chem. Cent. J., 10, 18 (2016). 42) Wan J.-P., Cao S., Liu Y., J. Org. Chem., 80, 9028–9033 (2015). 43) Al-Salahi M. M. R., Ashour A. E., Alswaidan I., Asian J. Chem., 26, 2173–2176 (2014). 44) Lombardo L. J., Lee F. Y., Chen P., Norris D., Barrish J. C., Behnia K., Castaneda S., Cornelius L. A. M., Das J., Doweyko A. M., Fairchild C., Hunt J. T., Inigo I., Johnston K., Kamath A., Kan D., Klei H., Marathe P., Pang S., Peterson R., Pitt S., Schieven G. L., Schmidt R. J., Tokarski J., Wen M.-L., Wityak J., Borzilleri R. M., J. Med. Chem., 47, 6658–6661 (2004). 45) Biovendor kit. Human VEGF-R2/KDR ELISA. Cat. No.: RBMS2019Ren_US
dc.identifier.doihttps://doi.org/
dc.identifier.otherhttps://doi.org/
dc.identifier.urihttp://central-library.msa.edu.eg:8009/xmlui/handle/123456789/476
dc.language.isoenen_US
dc.publisherChemical and Pharmaceutical Bulletinen_US
dc.relation.ispartofseriesChem. Pharm. Bull.;Vol. 64, No. 12, 1747–1754
dc.subjectgrowth factor receptoren_US
dc.subjectbenzenesulfonamideen_US
dc.subject3,4-dimethoxyphenyl; anticanceren_US
dc.titleNovel Sulfonamide Derivatives Carrying a Biologically Active 3,4-Dimethoxyphenyl Moiety as VEGFR-2 Inhibitorsen_US
dc.typeArticleen_US

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