Compound Identification
SMILES
CNC1=NC(=CS1)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
InChIKey
InChIKey=CCTLCFZVECFAME-KVLFQYKSSA-N
Formula
C23H34N2O2S
Mass
402.6
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Lipids and lipid-like molecules
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Class
Steroids and steroid derivatives
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Subclass
Androstane steroids
- Level 5 Androgens and derivatives
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Subclass
Androstane steroids
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Class
Steroids and steroid derivatives
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Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Androstane steroids
Intermediate Tree Nodes
Not available
Direct Parent
Androgens and derivatives
Alternative Parents
3-hydroxy delta-4-steroids 3-beta-hydroxysteroids 17-hydroxysteroids Delta-4-steroids Secondary alkylarylamines 2,4-disubstituted thiazoles 2-amino-1,3-thiazoles Tertiary alcohols Heteroaromatic compounds Secondary alcohols Cyclic alcohols and derivatives Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Androgen-skeleton - 3-hydroxy-delta-4-steroid - 3-hydroxysteroid - Hydroxysteroid - 3-beta-hydroxysteroid - 17-hydroxysteroid - Delta-4-steroid - 2,4-disubstituted 1,3-thiazole - Secondary aliphatic/aromatic amine - 1,3-thiazol-2-amine - Thiazole - Tertiary alcohol - Azole - Cyclic alcohol - Heteroaromatic compound - Secondary alcohol - Azacycle - Organoheterocyclic compound - Secondary amine - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Alcohol - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.
External Descriptors
Not available