Structure via PubChem · Public domain (PubChem)
melengestrol acetate
Sign in to saveAlso known as 17alpha-Acetoxy-6-methyl-16-methylenepregna-4,6-diene-3,20-dione, 17-Hydroxy-6-methyl-16-methylenepregna-4,6-diene-3,20-dione acetate
chemical compound
In the Vinony graph
Within Vinony's link graph, melengestrol acetate is referenced by 386 other articles, and connects out to mometasone furoate, 17α-hydroxyprogesterone and segesterone acetate.
It sits within the topics Acetate esters, Antineoplastic drugs and Drugs not assigned an ATC code.
Its subject is documented across 6 Wikipedia language editions.
Chemical data
- Formula
- C25H32O4
- Molecular weight
- 396.5 g/mol
- IUPAC name
- [(8R,9S,10R,13S,14S,17R)-17-acetyl-6,10,13-trimethyl-16-methylidene-3-oxo-1,2,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-yl] acetate
- SMILES
- CC1=C[C@@H]2[C@H](CC[C@]3([C@H]2CC(=C)[C@@]3(C(=O)C)OC(=O)C)C)[C@@]4(C1=CC(=O)CC4)C
- InChIKey
- UDKABVSQKJNZBH-DWNQPYOZSA-N
- XLogP
- 3.1
- Polar surface area
- 60.4 Ų
- H-bond donors
- 0
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
336 papers- [Analytical Method for Melengestrol Acetate in Livestock Products Using LC-MS/MS].Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan · 2024
- Melengestrol Acetate (Veterinary Medicinal Products).Food safety (Tokyo, Japan) · 2017
- Fungal mediated biotransformation of melengestrol acetate, and T-cell proliferation inhibitory activity of biotransformed compounds.Bioorganic chemistry · 2020
- Control of the bovine estrous cycle with melengestrol acetate (MGA): a review.Journal of animal science · 1989
- Safety and pharmacologic evaluations of melengestrol acetate in cattle and other animals: A review.Journal of the American Veterinary Medical Association · 1970
via PubMed
Wikidata facts
- Mass
- 396.23006
Show 6 more facts
- chemical formula
- C₂₅H₃₂O₄
- canonical SMILES
- CC1=CC2C(CCC3(C2CC(=C)C3(C(=O)C)OC(=O)C)C)C4(C1=CC(=O)CC4)C
- isomeric SMILES
- CC1=C[C@@H]2[C@H](CC[C@]3([C@H]2CC(=C)[C@@]3(C(=O)C)OC(=O)C)C)[C@@]4(C1=CC(=O)CC4)C
- subject has role
- glucocorticoid
- different from
- megestrol acetate
- Commons category
- Melengestrol acetate
via Wikidata · CC0
Connections
mometasone furoate
Entity
17α-hydroxyprogesterone
Entity
segesterone acetate
Entity
United States
Country
Canada
Country
Animalia
Entity
cattle
Entity
International Standard Book Number
Entity
alcohols
Entity
uterus
Entity
birth control
Entity
public domain
Entity
digital object identifier
Entity
chemical formula
Entity
organic compound
Entity
ester
Entity
steroid
Entity
rhesus macaque
Entity
molar mass
Entity
PubMed
Entity