| Primary information |
|---|
| ID | 20497 |
| Pubchem ID | 247020 |
| Name | 21-Hydroxypregnenolone |
| Description | 21-hydroxypregnenolone is an essential intermediate in corticosterone synthesis. The hydrolysis of 21-hydroxypregnenolone of fetal origin by steryl-sulfatase (SOS; EC 3.1.6.2); may be important in the biosynthesis of deoxycorticosterone |
| Synonym | (3beta)-3;21-Dihydroxypregn-5-en-20-one;(3b)-3;21-Dihydroxypregn-5-en-20-one;(3Β)-3;21-dihydroxypregn-5-en-20-one;(3b)-3;21-Dihydroxy-pregn-5-en-20-one;3b;21-Dihydroxy-5-pregnen-20-one;3b;21-Dihydroxy |
| Molecular Weight | 332.477 |
| Formula | C21H32O3 |
| IUPAC | 2-hydroxy-1-[(1S;2R;5S;10S;11S;14S;15S)-5-hydroxy-2;15-dimethyltetracyclo[8.7.0.0²;⁷.0¹¹;¹⁵]heptadec-7-en-14-yl]ethan-1-one |
| SMILE | [H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |
| PDB ID | NA |
| KEGG | C05485 |
| HMDB ID | HMDB0004026 |
| Melting Point (Degree C) | NA |
| Water Solubility | NA |
| Drugbank ID | NA |
| Receptor | NA |
| Reference | HMDB
|