اپوتیلون
Sign in to saveAlso known as epothilone
{| class="toccolours" border="1" style="float: right; clear: right; margin: 0 0 1em 1em; border-collapse: collapse;" ! | Epothilones |- | align="center" colspan="2" bgcolor="#ffffff"| 250px|Epothilones A (R = H) and B (R = Me) Epothilones A (R = H) and B (R = CH3) |- | Chemical formulae | A: C26H39NO6S B: C27H41NO6S |- | Molecular masses | A: 493.66 g/mol B: 507.68 g/mol |- | CAS numbers | A: 152044-53-6 B: 152044-54-7 |- | PubChem | A: 448799 B: 448013 |- | align="center" colspan="2" bgcolor="#ffffff"| 250px|Epothilones C (R = H) and D (R = Me) Epothilones C (R = H) and D (R = CH3) |- | Chemi
Research
1,440 papers- Epothilones as Natural Compounds for Novel Anticancer Drugs Development.International journal of molecular sciences · 2023
- Epothilones: clinical update and future directions.Oncology (Williston Park, N.Y.) · 2008
- Epothilones: a novel class of non-taxane microtubule-stabilizing agents.Current pharmaceutical design · 2002
- Epothilones in the treatment of cancer.Expert opinion on investigational drugs · 2006
- Synthesis & antitumor activity of epothilones B and D and their analogs.Future medicinal chemistry · 2018
via PubMed
Wikidata facts
- Subclass of
- macrolides
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- Commons category
- Epothilones
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