Methoxy-activated indole-7-carbohydrazides; synthesis, antioxidant, and anticancer properties
dc.authorscopusid | 55326408200 | |
dc.authorscopusid | 57240814700 | |
dc.authorscopusid | 57880074500 | |
dc.authorscopusid | 56572574200 | |
dc.authorscopusid | 57542417200 | |
dc.authorscopusid | 57201682024 | |
dc.authorscopusid | 55308985300 | |
dc.contributor.author | Kandemir, Hakan | |
dc.contributor.author | Izgi, Samet | |
dc.contributor.author | Çınar, İrfan | |
dc.contributor.author | Cebeci, Fatma | |
dc.contributor.author | Dirican, Ebubekir | |
dc.contributor.author | Sağlam, Mehmet F. | |
dc.contributor.author | Şengül, İbrahim F. | |
dc.date.accessioned | 2023-04-20T08:02:28Z | |
dc.date.available | 2023-04-20T08:02:28Z | |
dc.date.issued | 2022 | |
dc.department | Fakülteler, Fen Edebiyat Fakültesi, Kimya Bölümü | |
dc.description.abstract | Indole has been known as a key heterocyclic motif in the development of new structures for both chemical and biological properties. In this current study, a new range of indole-7-carbohydrazides has been successfully synthesized starting from the readily available 3-phenyl and 2,3-diphenyl 4,6-dimethoxyindoles. The structures of the novel compounds were confirmed by utilizing H-1 NMR, C-13 NMR, FT-IR, high-resolution mass spectrometry, and single crystal X- ray diffraction techniques. In addition, the indole-7-carbohydrazides showed promising antioxidant results in preliminary screens. Some of the new compounds generated from dimethoxy indoles were also screened for their anticancer activity against SH-SHY5Y (human neuroblastoma), AGS (human gastric adenocarcinoma), and MDA-MB-231 (human breast adenocarcinoma) cell lines. The results revealed that the compound 12 was the promising candidate, showing cytotoxic effects on both neuroblastoma, stomach, and breast cancer cells. | |
dc.description.sponsorship | Turkiye Bilimsel ve Teknolojik Arastirma Kurumu; Tekirdag Namik Kemal University [NKUBAP.01, 19.220]; Scientific and Technological Research Council of Turkey [120Z116] | |
dc.description.sponsorship | NAMIK KEMAL UNIVERSITESI; Turkiye Bilimsel ve Teknolojik Arastirma Kurumu; Tekirdag Namik Kemal University, Grant/Award Number: NKUBAP.01. GA.19.220; The Scientific and Technological Research Council of Turkey, Grant/Award Number: 120Z116 | |
dc.identifier.doi | 10.1002/jhet.4562 | |
dc.identifier.issn | 0022-152X | |
dc.identifier.issn | 1943-5193 | |
dc.identifier.scopus | 2-s2.0-85137568357 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.uri | https://doi.org/10.1002/jhet.4562 | |
dc.identifier.uri | https://hdl.handle.net/20.500.11776/10951 | |
dc.identifier.wos | WOS:000852569600001 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.institutionauthor | Kandemir, Hakan | |
dc.language.iso | en | |
dc.publisher | Wiley | |
dc.relation.ispartof | Journal of Heterocyclic Chemistry | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Antiinflammatory Activity | |
dc.subject | Indole Alkaloids | |
dc.subject | Inhibitors | |
dc.title | Methoxy-activated indole-7-carbohydrazides; synthesis, antioxidant, and anticancer properties | |
dc.type | Article |
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