Metabolite Card
Formula: C22H32O3 (344.2351)
SMILES: [H][C@@]12CC[C@H](OC(=O)CC)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12C
Synonyms [en]
testosterone propionate; 17-propionyl-17beta-hydroxyandrost-4-en-3-one; Virormone; Agovirin; CAS-57-85-2; Testrex
Last reviewed on 2024-06-28.
Cite this Page
Testosterone propionate. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000018343). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Testosterone Propionate is only found in individuals that have used or taken this drug. It is an ester of testosterone with a propionate substitution at the 17-beta position. [PubChem]The effects of testosterone in humans and other vertebrates occur by way of two main mechanisms: by activation of the androgen receptor (directly or as DHT), and by conversion to estradiol and activation of certain estrogen receptors. Free testosterone (T) is transported into the cytoplasm of target tissue cells, where it can bind to the androgen receptor, or can be reduced to 5α-dihydrotestosterone (DHT) by the cytoplasmic enzyme 5α-reductase. DHT binds to the same androgen receptor even more strongly than T, so that its androgenic potency is about 2.5 times that of T. The T-receptor or DHT-receptor complex undergoes a structural change that allows it to move into the cell nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects.
DBLinks
- CAS Registry Number: 57-85-2
- PubChem CID: 5995
- ChEBI: 9466
- HMDB: HMDB0015489
- LipidMaps: LMST02020076
- KEGG: C08158
- BioCyc:
- NCBI MeSH: Testosterone Propionate
- Wikipedia: Testosterone propionate
Other DBLinks
- CAS Registry Number: 35271-40-0
- CAS Registry Number: 57-85-2
- PubChem: 5995
- ChEBI: ChEBI:290629
- ChEBI: ChEBI:9466
- HMDB: HMDB0015489
- LipidMaps: LMST02020076
- KEGG: C08158
- KEGG: D00959
- NCBI MeSH: Testosterone Propionate
- Wikipedia: Testosterone propionate
- Wikipedia: Testosterone_propionate
- DrugBank: DB01420
- RefMet: RM0194362
- MoNA: LU139101
- MoNA: LU139102
- MoNA: LU139103
- MoNA: LU139104
- MoNA: LU139105
- MoNA: LU139106
- Metlin: METLIN_2783
- Coconut NaturalProduct: CNP0315797.1
- Coconut NaturalProduct: CNP0315797.3
Class / Ontology
- WishartLab ClassyFire: [Steroid esters] Steroid esters
- RefMet: [C19 steroids] C19 steroids
- LipidMaps: [C19 steroids (androgens) and derivatives [ST0202]] C19 steroids (androgens) and derivatives [ST0202]
- ChEBI: [CHEBI:9466] Testosterone propionate
- Coconut NaturalProduct: [Androstane steroids] Androstane steroids