U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H36O3
Molecular Weight 360.5301
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DROMOSTANOLONE PROPIONATE

SMILES

[H][C@@]12CC[C@H](OC(=O)CC)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])CC(=O)[C@H](C)C[C@]34C

InChI

InChIKey=NOTIQUSPUUHHEH-UXOVVSIBSA-N
InChI=1S/C23H36O3/c1-5-21(25)26-20-9-8-17-16-7-6-15-12-19(24)14(2)13-23(15,4)18(16)10-11-22(17,20)3/h14-18,20H,5-13H2,1-4H3/t14-,15+,16+,17+,18+,20+,22+,23+/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H36O3
Molecular Weight 360.5301
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Dromostanolone Propionate (known by the brand names Masteron and Drolban) was invented by Syntex in 1959. About 10 years later it was released on the American market by Lilly as brand name Drolban. The drug was first approved in the USA for use as a treatment of female breast cancer. However, the profile of side-effects included pronouncement of male characteristics in women and when more effective breast cancer treatments came to market drostanolone was gradually phased out. No longer used clinically dromostanolone propionate became very popular in the bodybuilding community. Today dromostanolone propionate remains on the list of approved medications, but it is not being manufactured or sold by pharmaceutical companies. It is still produced illegally by underground labs for use in the bodybuilding community.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Drolban

Approved Use

Unknown
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
2 day
single, intramuscular
DROMOSTANOLONE plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
100 mg 4 times / day multiple, oral
Dose: 100 mg, 4 times / day
Route: oral
Route: multiple
Dose: 100 mg, 4 times / day
Sources:
unhealthy, adult
n = 9
Health Status: unhealthy
Age Group: adult
Sex: M+F
Population Size: 9
Sources:
Disc. AE: Hypertriglyceridemia...
AEs leading to
discontinuation/dose reduction:
Hypertriglyceridemia (5 patients)
Sources:
AEs

AEs

AESignificanceDosePopulation
Hypertriglyceridemia 5 patients
Disc. AE
100 mg 4 times / day multiple, oral
Dose: 100 mg, 4 times / day
Route: oral
Route: multiple
Dose: 100 mg, 4 times / day
Sources:
unhealthy, adult
n = 9
Health Status: unhealthy
Age Group: adult
Sex: M+F
Population Size: 9
Sources:
PubMed

PubMed

TitleDatePubMed
Systematic review of the clinical effect of glucocorticoids on nonhematologic malignancy.
2008 Mar 28
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Intramuscular
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:00:44 GMT 2023
Edited
by admin
on Fri Dec 15 15:00:44 GMT 2023
Record UNII
X20UZ57G4O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DROMOSTANOLONE PROPIONATE
MI   ORANGE BOOK   USAN  
USAN  
Official Name English
DROMOSTANOLONE PROPIONATE [ORANGE BOOK]
Common Name English
NSC-1298
Code English
17β-Hydroxy-2α-methyl-5α-androstan-3-one propionate
Common Name English
DROSTANOLONE PROPIONATE [JAN]
Common Name English
32379
Code English
DROSTANOLONE PROPIONATE
JAN   MART.   WHO-DD  
Common Name English
NSC-12198
Code English
DROLBAN
Brand Name English
DROMOSTANOLONE PROPIONATE [USAN]
Common Name English
MASTERON
Brand Name English
PERMASTRIL
Brand Name English
ANDROSTAN-3-ONE, 2-METHYL-17-(1-OXOPROPOXY)-, (2.ALPHA.,5.ALPHA.,17.BETA
Common Name English
MASTERID
Brand Name English
DROSTANOLONE PROPIONATE [MART.]
Common Name English
DROMOSTANOLONE PROPIONATE [MI]
Common Name English
Drostanolone propionate [WHO-DD]
Common Name English
Classification Tree Code System Code
DEA NO. 4000
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
NCI_THESAURUS C243
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
Code System Code Type Description
IUPHAR
6947
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
NSC
12198
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
DRUG CENTRAL
965
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
EVMPD
SUB118291
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
FDA UNII
X20UZ57G4O
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
PUBCHEM
224004
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-303-1
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
MESH
C007561
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
ChEMBL
CHEMBL1201048
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
CAS
521-12-0
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
NCI_THESAURUS
C1077
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
CHEBI
31523
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
DRUG BANK
DB14655
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
NSC
1298
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
SMS_ID
100000143068
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
MERCK INDEX
m4767
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
DROSTANOLONE PROPIONATE
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
RXCUI
23683
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID1022972
Created by admin on Fri Dec 15 15:00:44 GMT 2023 , Edited by admin on Fri Dec 15 15:00:44 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY