Design, Synthesis, and Biological Activity of Sulfonamide Analogues of Antofine and Cryptopleurine as Potent and Orally Active Antitumor Agents
DC Field | Value | Language |
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dc.contributor.author | Kwon, Yongseok | - |
dc.contributor.author | Song, Jayoung | - |
dc.contributor.author | Lee, Honggu | - |
dc.contributor.author | Kim, Eun-Yeong | - |
dc.contributor.author | Lee, Kiho | - |
dc.contributor.author | Lee, Sang Kook | - |
dc.contributor.author | Kim, Sanghee | - |
dc.date.accessioned | 2021-09-04T11:33:59Z | - |
dc.date.available | 2021-09-04T11:33:59Z | - |
dc.date.created | 2021-06-10 | - |
dc.date.issued | 2015-10-08 | - |
dc.identifier.issn | 0022-2623 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/92205 | - |
dc.description.abstract | Due to their profound antiproliferative activity and unique mode of action, phenanthroindolizidine and phenanthroquinolizidine alkaloids, represented by antofine and cryptopleurine, have attracted attention recently as potential therapeutic agents. We have designed, synthesized, and evaluated the methanesulfonamide analogues of these natural alkaloids with the hope of improving their druglikeness. The analogues showed enhanced growth inhibition of human cancer cells compared with the parent natural products. In particular, a methanesulfonamide analogue of cryptopleurine (513) exhibited improved bioavailability and significant antitumor activity, which suggests that 5b is a promising new anticancer agent. Our studies suggest that the inhibition of cancer cell growth by 5b is associated with the induction of G0/G1 cell cycle arrest via nicotinamide N-methyltransferase-dependent JNK activation in Cain-1 renal cancer cells. In addition, compound 5b significantly inhibited the migration and invasion of Cain-1 cancer cells by modulating the p38 MAPK signaling pathway. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | NICOTINAMIDE N-METHYLTRANSFERASE | - |
dc.subject | PHENANTHROINDOLIZIDINE ALKALOIDS PERGULARININE | - |
dc.subject | RELEVANT CHEMICAL SPACE | - |
dc.subject | RENAL-CELL CANCER | - |
dc.subject | NATURAL-PRODUCTS | - |
dc.subject | ANTICANCER AGENTS | - |
dc.subject | DRUG DISCOVERY | - |
dc.subject | COLORECTAL-CANCER | - |
dc.subject | TUMOR-MARKER | - |
dc.subject | PROTEIN | - |
dc.title | Design, Synthesis, and Biological Activity of Sulfonamide Analogues of Antofine and Cryptopleurine as Potent and Orally Active Antitumor Agents | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Kiho | - |
dc.identifier.doi | 10.1021/acs.jmedchem.5b00764 | - |
dc.identifier.scopusid | 2-s2.0-84943766941 | - |
dc.identifier.wosid | 000362701600010 | - |
dc.identifier.bibliographicCitation | JOURNAL OF MEDICINAL CHEMISTRY, v.58, no.19, pp.7749 - 7762 | - |
dc.relation.isPartOf | JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.title | JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.volume | 58 | - |
dc.citation.number | 19 | - |
dc.citation.startPage | 7749 | - |
dc.citation.endPage | 7762 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.subject.keywordPlus | NICOTINAMIDE N-METHYLTRANSFERASE | - |
dc.subject.keywordPlus | PHENANTHROINDOLIZIDINE ALKALOIDS PERGULARININE | - |
dc.subject.keywordPlus | RELEVANT CHEMICAL SPACE | - |
dc.subject.keywordPlus | RENAL-CELL CANCER | - |
dc.subject.keywordPlus | NATURAL-PRODUCTS | - |
dc.subject.keywordPlus | ANTICANCER AGENTS | - |
dc.subject.keywordPlus | DRUG DISCOVERY | - |
dc.subject.keywordPlus | COLORECTAL-CANCER | - |
dc.subject.keywordPlus | TUMOR-MARKER | - |
dc.subject.keywordPlus | PROTEIN | - |
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