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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H30O3
Molecular Weight 330.4611
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TESTOSTERONE ACETATE

SMILES

[H][C@@]12CC[C@H](OC(C)=O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CCC4=CC(=O)CC[C@]34C

InChI

InChIKey=DJPZSBANTAQNFN-PXQJOHHUSA-N
InChI=1S/C21H30O3/c1-13(22)24-19-7-6-17-16-5-4-14-12-15(23)8-10-20(14,2)18(16)9-11-21(17,19)3/h12,16-19H,4-11H2,1-3H3/t16-,17-,18-,19-,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H30O3
Molecular Weight 330.4611
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Testosterone acetate, a testosterone ester, is an androgen. It is a steroid lipid molecule considered to be practically insoluble (in water) and basic. It is an anabolic steroid and testosterone prodrug. Testosterone acetate has a faster rate of absorption in the body then other esters. In combination with two other testosterone esters, testosterone valerate and testosterone undecanoate, it is a part of Deposterona, an injectable veterinary blend steroid preparation marketed in Mexico. With its blend of slow and fast-acting esters, Deposterona is essentially a low dosed alternative to Sustanon and is used primarily to treat impotence, weakness, fatigue, and hypogonadism in male breeding animals (cows, pigs, canines, and sheep), and also as a general protein-sparing anabolic. Testosterone acetate is classified as a Schedule III drug by the United States Drug Enforcement Agency and is only legal with a prescription due to his potential for misuse and abuse.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Deposterona

Approved Use

To treat impotence, weakness, fatigue and hypogonadism in male breeding animals (cows, pigs, canines, sheep)
PubMed

PubMed

TitleDatePubMed
[The influence of pregnancy and hormone on the lymphatic stomata in guinea pig's ovary bursa].
2003 Feb
Induction of androgen receptor activity by norgestimate and norelgestromin in MDA-MB 231 breast cancer cells.
2004 Jul
Androgen-induced vocal transformation in adult female African clawed frogs.
2005 Jul
Comparison of crystal structures of human type 3 3alpha-hydroxysteroid dehydrogenase reveals an "induced-fit" mechanism and a conserved basic motif involved in the binding of androgen.
2005 Jun
An unusual ring--a opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila.
2009 Sep
3alpha-androstanediol, but not testosterone, attenuates age-related decrements in cognitive, anxiety, and depressive behavior of male rats.
2010
Patents

Patents

Sample Use Guides

For bodybuilding purposes, Deposterona (12mg of testosterone acetate, 12mg of testosterone valerate, and 36mg of testosterone undecanoate per milliliter of oil) is injected on at least a weekly basis, in a dosage of 120-360 mg (2-6 ml). Dividing the weekly dosage into two or more smaller applications can reduce injection volume. Cycles are generally between 6 and 12 weeks in length. This level is sufficient to provide noticeable gains in muscle size and strength.
Route of Administration: Intravascular
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:41:40 GMT 2023
Edited
by admin
on Fri Dec 15 19:41:40 GMT 2023
Record UNII
5652105Y6S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TESTOSTERONE ACETATE
MI   WHO-DD  
Common Name English
TESTOSTERONE ACETATE IMPURITY A [EP IMPURITY]
Common Name English
TESTOSTERONE IMPURITY E [EP IMPURITY]
Common Name English
Testosterone acetate [WHO-DD]
Common Name English
TESTOSTERONE 17-ACETATE
Common Name English
3-OXOANDROST-4-EN-17.BETA.-YL ACETATE
Systematic Name English
17.BETA.-ACETOXY-4-ANDROSTEN-3-ONE
Systematic Name English
TESTOSTERONE ACETATE [MI]
Common Name English
NSC-523836
Code English
Code System Code Type Description
MERCK INDEX
m10594
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY Merck Index
EVMPD
SUB130904
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
ECHA (EC/EINECS)
213-876-6
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
CAS
1045-69-8
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
NSC
523836
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
SMS_ID
100000156833
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID80909007
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
CHEBI
16524
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
PUBCHEM
92145
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
WIKIPEDIA
Testosterone acetate
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
FDA UNII
5652105Y6S
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
MESH
C040594
Created by admin on Fri Dec 15 19:41:40 GMT 2023 , Edited by admin on Fri Dec 15 19:41:40 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP