Compound
16alpha,17alpha-dihydroxyprogesterone
A synthetic progestational dihydroxy derivative of progesterone. Its acetonide possesses anti-inflammatory properties.
Structure
- Class
- Organic compound
- Formula
- C21H30O4
- Mass
- 346.467 g/mol
- Charge
- 0
- InChIKey
- CXDWHYOBSJTRJU-SRWWVFQWSA-N
- SMILES
- [H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@@]1(C)[C@@]2([H])C[C@@H](O)[C@]1(O)C(C)=O
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
2 statements
2 statements · 1 reference database · Subject: 16alpha,17alpha-dihydroxyprogesterone · Sources: Rhea
- 16alpha,17alpha-dihydroxyprogesterone is metabolised by CYP17A1ProteinRhea RHEA:53216Inferred only
- 16alpha,17alpha-dihydroxyprogesterone is metabolised by CYP17A1ProteinRhea RHEA:53220Inferred only
Reactions
2 reactions
17alpha-hydroxyprogesterone+reduced [NADPH--hemoprotein reductase]+dioxygen16alpha,17alpha-dihydroxyprogesterone+oxidized [NADPH--hemoprotein reductase]+water+hydron
Catalysed by CYP17A1
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:53216CC BY 4.0Reference data
16alpha,17alpha-dihydroxyprogesterone+reduced [NADPH--hemoprotein reductase]+dioxygen6beta,16alpha,17alpha-trihydroxyprogesterone+oxidized [NADPH--hemoprotein reductase]+water+hydron
Catalysed by CYP17A1
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:53220CC BY 4.0Reference data
Other names
7 names
Resolves to: 16alpha,17alpha-dihydroxyprogesterone
- Also called
- 16 alpha,17 alpha-dihydroxyprogesteronealgestonaAlgestoneAlphasoneST 21:3;O4
- Systematic name
- 16alpha,17-dihydroxypregn-4-ene-3,20-dione16α,17-dihydroxypregn-4-ene-3,20-dione