Основные атрибуты  химическое свойство химические свойства, назначение, производство поставщик
 структурированное изображение

Epothilone C

  • русский язык имя
  • английское имяEpothilone C
  • CAS №186692-73-9
  • CBNumberCB71214331
  • ФормулаC26H39NO5S
  • мольный вес477.66
  • номер MDLMFCD02102104
  • файл Mol186692-73-9.mol
химическое свойство
Температура кипения 657.7±55.0 °C(Predicted)
плотность 1.097
пка 13.47±0.70(Predicted)
ИнЧИКей BEFZAMRWPCMWFJ-QJKGZULSSA-N
SMILES O1[C@H](/C(/C)=C/C2=CSC(C)=N2)CC=CCCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC1=O |c:13|
FDA UNII 18T00XLN7E

Epothilone C химические свойства, назначение, производство

Описание

Epothilone C: a tubulin inhibitor
Epothilones are 16-membered bacterial macrolides isolated from the bacterium Sorangium cellulosum by H?fle et al., who reported that epothilone A and B had antifungal and cytotoxic activity in 1993. After that, it was reported that epothilones could promote the microtubule polymerization with characteristics and a dynamic mechanism similar to paclitaxel and be bound to tubulin on the paclitaxel microtubule binding site. Other epothilone analogues, such as epothilone C, D, E, and F, have been discovered. Epothilone C is a cytotoxic antitumour natural product. It is produced by the combined action of one nonribosomal peptide synthetase (NRPS) and nine polyketide synthase (PKS) modules in a multienzyme system[1-2].

Использование

Epothilone C is a related compound of Epothilones, which are a novel class of antineoplastic agents with antitubulin activity. In addition, Epothilones utilize a similar mechanism of action to that of taxanes and are less susceptible to multidrug resistance caused by P-glycoprotein. Studies showed that Epothilones exhibit antitumor activity against human cancer cells that are taxane-resistant.

Epothilone C поставщик

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