| 词条 | Testosterone phenylpropionate |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (1S,2R,10R,11S,14S,15S)-2,15-dimethyl-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-6-en-14-yl 3-phenylpropanoate | image = Testosterone phenpropionate.svg | width = 250px | image2 = Testosterone phenylpropionate molecule ball.png | width2 = 250px | tradename = Testolent, Sustanon, Omnadren | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = Intramuscular injection | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = | CAS_number = 1255-49-8 | CAS_supplemental = | ATC_prefix = | ATC_suffix = | PubChem = 14743 | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = 14062 | UNII = 8GN84GWX51 | ChEMBL = 2356993 | KEGG = D08574 | C=28 | H=36 | O=3 | molecular_weight = 420.58364 g/mol | smiles = C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OC(=O)CCC4=CC=CC=C4)CCC5=CC(=O)CC[C@]35C | StdInChI_Ref = | StdInChI = 1S/C28H36O3/c1-27-16-14-21(29)18-20(27)9-10-22-23-11-12-25(28(23,2)17-15-24(22)27)31-26(30)13-8-19-6-4-3-5-7-19/h3-7,18,22-25H,8-17H2,1-2H3/t22-,23-,24-,25-,27-,28-/m0/s1 | StdInChIKey_Ref = | StdInChIKey = HHSXYDOROIURIP-FEZCWRLCSA-N | synonyms = }}Testosterone phenylpropionate (BAN) (brand name Testolent), or testosterone phenpropionate, also known as testosterone hydrocinnamate, is a synthetic anabolic-androgenic steroid (AAS) and an androgen ester – specifically, the C17β phenylpropionate ester of testosterone – which was formerly marketed in Romania.[1][2][3][4] It was first reported in the scientific literature in 1955 and was an ingredient of several isolated AAS commercial products, but was never widely used.[4] Testosterone phenylpropionate was also notably a component of Sustanon and Omnadren.[4][5] See also
References1. ^{{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA641|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=641–642}} {{Androgens and antiandrogens}}{{Androgen receptor modulators}}{{genito-urinary-drug-stub}}{{steroid-stub}}2. ^{{cite book|title=Index Nominum 2000: International Drug Directory|url=https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA976|date=January 2000|publisher=Taylor & Francis|isbn=978-3-88763-075-1}} 3. ^{{cite book|author1=I.K. Morton|author2=Judith M. Hall|title=Concise Dictionary of Pharmacological Agents: Properties and Synonyms|url=https://books.google.com/books?id=tsjrCAAAQBAJ&pg=PA270|date=6 December 2012|publisher=Springer Science & Business Media|isbn=978-94-011-4439-1}} 4. ^1 2 {{cite book|author=William Llewellyn|title=Anabolics|url=https://books.google.com/books?id=afKLA-6wW0oC&pg=PT697|year=2011|publisher=Molecular Nutrition Llc|isbn=978-0-9828280-1-4|pages=583,697}} 5. ^{{cite book|author=Kenneth L. Becker|title=Principles and Practice of Endocrinology and Metabolism|url=https://books.google.com/books?id=FVfzRvaucq8C&pg=PA1185|year=2001|publisher=Lippincott Williams & Wilkins|isbn=978-0-7817-1750-2|pages=1185–}} 3 : Androgens and anabolic steroids|Androstanes|Testosterone esters |
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