Compound Identification
SMILES
COC(=O)C1=C(C)O[C@]2(C)[C@H](C[C@H]3[C@](C)(CO[Si](C)(C)C)[C@H](CC[C@]3(C)[C@H]2C1=O)O[Si](C)(C)C)O[Si](C)(C)C
InChIKey
InChIKey=UVPRXZVVRFUAKD-KWKMUCFVSA-N
Formula
C29H54O7Si3
Mass
598.999
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Steroids and steroid derivatives
Alternative Parents
Naphthopyrans Naphthalenes Dihydropyranones Vinylogous esters Trialkylheterosilanes Methyl esters Enoate esters Silyl ethers Ketones Oxacyclic compounds Organic metalloid salts Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Steroid - Naphthopyran - Naphthalene - Dihydropyranone - Pyran - Trialkylheterosilane - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Carboxylic acid ester - Ketone - Silyl ether - Carboxylic acid derivative - Organoheterosilane - Monocarboxylic acid or derivatives - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organic metalloid moeity - Organooxygen compound - Carbonyl group - Organic oxide - Organosilicon compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as steroids and steroid derivatives. These are compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred.
External Descriptors
Not available