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| | vinzolidine Basic information |
| Product Name: | vinzolidine | | Synonyms: | vinzolidine;2H-3,7-Methanoazacycloundecino[5,4-b]indole-9-carboxylic acid, 9-[(2β,3β,4β,5α,12R,19α)-4-(acetyloxy)-3'-(2-chloroethyl)-6,7-didehydro-16-methoxy-1-methyl-2',4'-dioxospiro[aspidospermidine-3,5'-oxazolidin]-15-yl]-5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-, methyl ester, (3R,5S,7R,9S)- (9CI) | | CAS: | 67699-40-5 | | MF: | C48H58ClN5O9 | | MW: | 884.46 | | EINECS: | 266-915-4 | | Product Categories: | | | Mol File: | 67699-40-5.mol |  |
| | vinzolidine Chemical Properties |
| | vinzolidine Usage And Synthesis |
| Uses | Vinzolidine is a semisynthetic derivative of the catharanthus alkaloid. Vinzolidine exerts its cytotoxic effect on tumor cells by interfering with microtubulin polymerization, thereby inhibiting cell division. Vinzolidine can be utilized in research to investigate synergistic effects when combined with other chemotherapeutic agents or biologic therapies, as well as to study cancer cells' tolerance or resistance to these treatments, and to explore approaches to overcome such obstacles[1]. | | References | [1] Aapro M S, et al. Interactions of human leukocyte interferon with vinca alkaloids and other chemotherapeutic agents against human tumors in clonogenic assay[J]. Cancer Chemotherapy and Pharmacology, 1983, 10: 161-166. DOI:10.1007/BF00255753 |
| | vinzolidine Preparation Products And Raw materials |
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