C[C@H]1CCC\C(C)=C/C[C@H](NC(=O)C[C@H](O)C(C)(C)C(=O)[C@H](C)[C@H]1O)C(\C)=C\C1=CSC(CO)=N1

InChIKey=ANCRVOJZHVMMOG-IVSQCGTASA-N

C27H42N2O5S

506.7

Organic compounds

Phenylpropanoids and polyketides

Macrolides and analogues

Epothilones and analogues

Not available

Epothilones and analogues

Macrolactams 2,4-disubstituted thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Azacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives Aromatic alcohols

Aromatic heteromonocyclic compounds

Epothilone - Macrolactam - 2,4-disubstituted 1,3-thiazole - Azole - Heteroaromatic compound - Thiazole - Carboxamide group - Ketone - Lactam - Cyclic ketone - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Aromatic alcohol - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as epothilones and analogues. These are macrolides consisting of a 16-member lactone ring conjugated at the carbon 16 with a 1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl group. Some epothilone analogues containing a lactam ring instead of the lactone ring.

Not available