mesterolone 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
androgens/anabolic steroids 3342 1424-00-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • mesterolone
  • androviron
  • mesteranum
  • mestoranum
17 beta-Hydroxy-1 alpha-methyl-5 alpha-androstan-3-one. A synthetic steroid with anabolic and androgenic activities.
  • Molecular weight: 304.47
  • Formula: C20H32O2
  • CLOGP: 4.07
  • LIPINSKI: 0
  • HAC: 2
  • HDO: 1
  • TPSA: 37.30
  • ALOGS: -4.68
  • ROTB: 0

Drug dosage:

DoseUnitRoute
50 mg O

ADMET properties:

PropertyValueReference
BA (Bioavailability) 3 % Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H

Approvals:

None

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC G03BB01 GENITO URINARY SYSTEM AND SEX HORMONES
SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM
ANDROGENS
5-androstanon (3) derivatives
MeSH PA D045930 Anabolic Agents
MeSH PA D006728 Hormones

Drug Use | Suggest Off label Use Form| |View source of the data|

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Sex hormone-binding globulin Secreted Kd 9.60 CHEMBL
Androgen receptor Transcription factor IC50 4.74 CHEMBL

External reference:

IDSource
N0000167465 NUI
D04947 KEGG_DRUG
C0025503 UMLSCUI
CHEBI:135293 CHEBI
CHEMBL258918 ChEMBL_ID
DB13587 DRUGBANK_ID
D008655 MESH_DESCRIPTOR_UI
15020 PUBCHEM_CID
1965 INN_ID
0SRQ75X9I9 UNII
6781 RXNORM
004004 NDDF
126166005 SNOMEDCT_US
96346001 SNOMEDCT_US

Pharmaceutical products:

None