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1-Testosterone

1-Testosterone (abbreviated and nicknamed as 1-Testo, 1-T), also known as δ1-dihydrotestosterone (δ1-DHT), as well as dihydroboldenone, is a synthetic anabolic–androgenic steroid (AAS) and a 5α-reduced derivative of boldenone (Δ1-testosterone). It differs from testosterone by having a 1(2)-double bond instead of a 4(5)-double bond in its A ring.[1] It was legally sold online in the United States until 2005, when it was reclassified as a Schedule III drug.

1-Testosterone
Clinical data
Other names1-Testo; 1-T; δ1-Dihydrotestosterone; δ1-DHT; Dihydroboldenone
Drug classAndrogen; Anabolic steroid
Legal status
Legal status
Pharmacokinetic data
MetabolismLiver
ExcretionUrine
Identifiers
  • (5S,8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
CAS Number
  • 65-06-5 N
PubChem CID
  • 579094
DrugBank
  • DB01481 Y
ChemSpider
  • 206590 Y
UNII
  • Y984BV1Q0G
ChEBI
  • CHEBI:59714 Y
CompTox Dashboard (EPA)
  • DTXSID80215312
ECHA InfoCard100.164.058
Chemical and physical data
FormulaC19H28O2
Molar mass288.431 g·mol−1
3D model (JSmol)
  • Interactive image
  • O=C4\C=C/[C@]1([C@@H](CC[C@@H]2[C@@H]1CC[C@@]3([C@@H](O)CC[C@@H]23)C)C4)C
  • InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h7,9,12,14-17,21H,3-6,8,10-11H2,1-2H3/t12-,14-,15-,16-,17-,18-,19-/m0/s1 Y
  • Key:OKJCFMUGMSVJBG-ABEVXSGRSA-N Y
 NY (what is this?)  (verify)

Side effects edit

Pharmacology edit

Pharmacodynamics edit

A 2006 study determined that 1-testosterone has a high androgenic and anabolic potency even without being metabolized, so it can be characterized as a typical anabolic steroid. 1-Testosterone binds in a manner that is highly selective to the androgen receptor (AR) and has a high potency to stimulate AR-dependent transactivation. In vivo, an equimolar dose of 1-testosterone has the same potency to stimulate the growth of the prostate, the seminal vesicles and the androgen-sensitive levator ani muscle as the reference anabolic steroid testosterone propionate, but, unlike testosterone propionate, 1-testosterone also increases liver weight.[2]

Chemistry edit

1-Testosterone, IUPAC name 17β-hydroxy-5α-androst-1-en-3-one, also known as 4,5α-dihydro-δ1-testosterone (Δ1-DHT) or as 5α-androst-1-en-17β-ol-3-one, is a synthetic androstane steroid and a derivative of dihydrotestosterone (DHT).

Derivatives edit

Two prohormones of 1-testosterone are 1-androstenediol and 1-androstenedione, the latter of which may be synthesized from stanolone acetate.[3]

Mesabolone is a ketal made from 1-testosterone.

1-Testosterone also is known to be used to synthesize mestanolone and metenolone.[citation needed]

Methyl-1-testosterone is the 17α-methyl derivative of 1-testosterone.

Detection in body fluids edit

Doping with 1-testosterone can be detected in urine samples using gas chromatography.[4]

References edit

  1. ^ William Llewellyn (2009). Anabolics (9 ed.). Molecular Nutrition. p. 22,135. ISBN 978-0-9679304-7-3.
  2. ^ Friedel A, Geyer H, Kamber M, Laudenbach-Leschowsky U, Schänzer W, Thevis M, Vollmer G, Zierau O, Diel P (August 2006). "17beta-hydroxy-5alpha-androst-1-en-3-one (1-testosterone) is a potent androgen with anabolic properties". Toxicol. Lett. 165 (2): 149–55. doi:10.1016/j.toxlet.2006.03.001. PMID 16621347.
  3. ^ Zhang H, Qiu Z (December 2006). "An efficient synthesis of 5α-androst-1-ene-3,17-dione". Steroids. 71 (13–14): 1088–90. doi:10.1016/j.steroids.2006.09.008. PMID 17123559. S2CID 53258890.
  4. ^ S. Jain, A. Beotra and T. Kaur (2005). (PDF). Recent Advances in Doping Analysis. 13: 407–410. Archived from the original (PDF) on 2011-08-25. Retrieved 2011-06-18.


testosterone, confused, with, boldenone, abbreviated, nicknamed, testo, also, known, dihydrotestosterone, well, dihydroboldenone, synthetic, anabolic, androgenic, steroid, reduced, derivative, boldenone, testosterone, differs, from, testosterone, having, doubl. Not to be confused with Boldenone 1 Testosterone abbreviated and nicknamed as 1 Testo 1 T also known as d1 dihydrotestosterone d1 DHT as well as dihydroboldenone is a synthetic anabolic androgenic steroid AAS and a 5a reduced derivative of boldenone D1 testosterone It differs from testosterone by having a 1 2 double bond instead of a 4 5 double bond in its A ring 1 It was legally sold online in the United States until 2005 when it was reclassified as a Schedule III drug 1 TestosteroneClinical dataOther names1 Testo 1 T d1 Dihydrotestosterone d1 DHT DihydroboldenoneDrug classAndrogen Anabolic steroidLegal statusLegal statusUS Schedule IIIPharmacokinetic dataMetabolismLiverExcretionUrineIdentifiersIUPAC name 5S 8R 9S 10R 13S 14S 17S 17 hydroxy 10 13 dimethyl 4 5 6 7 8 9 11 12 14 15 16 17 dodecahydrocyclopenta a phenanthren 3 oneCAS Number65 06 5 NPubChem CID579094DrugBankDB01481 YChemSpider206590 YUNIIY984BV1Q0GChEBICHEBI 59714 YCompTox Dashboard EPA DTXSID80215312ECHA InfoCard100 164 058Chemical and physical dataFormulaC 19H 28O 2Molar mass288 431 g mol 13D model JSmol Interactive imageSMILES O C4 C C C 1 C H CC C H 2 C H 1CC C 3 C H O CC C H 23 C C4 CInChI InChI 1S C19H28O2 c1 18 9 7 13 20 11 12 18 3 4 14 15 5 6 17 21 19 15 2 10 8 16 14 18 h7 9 12 14 17 21H 3 6 8 10 11H2 1 2H3 t12 14 15 16 17 18 19 m0 s1 YKey OKJCFMUGMSVJBG ABEVXSGRSA N Y N Y what is this verify Contents 1 Side effects 2 Pharmacology 2 1 Pharmacodynamics 3 Chemistry 3 1 Derivatives 3 2 Detection in body fluids 4 ReferencesSide effects editSee also Anabolic steroid Adverse effectsPharmacology editPharmacodynamics edit A 2006 study determined that 1 testosterone has a high androgenic and anabolic potency even without being metabolized so it can be characterized as a typical anabolic steroid 1 Testosterone binds in a manner that is highly selective to the androgen receptor AR and has a high potency to stimulate AR dependent transactivation In vivo an equimolar dose of 1 testosterone has the same potency to stimulate the growth of the prostate the seminal vesicles and the androgen sensitive levator ani muscle as the reference anabolic steroid testosterone propionate but unlike testosterone propionate 1 testosterone also increases liver weight 2 Chemistry editSee also List of androgens anabolic steroids 1 Testosterone IUPAC name 17b hydroxy 5a androst 1 en 3 one also known as 4 5a dihydro d1 testosterone D1 DHT or as 5a androst 1 en 17b ol 3 one is a synthetic androstane steroid and a derivative of dihydrotestosterone DHT Derivatives edit Two prohormones of 1 testosterone are 1 androstenediol and 1 androstenedione the latter of which may be synthesized from stanolone acetate 3 Mesabolone is a ketal made from 1 testosterone 1 Testosterone also is known to be used to synthesize mestanolone and metenolone citation needed Methyl 1 testosterone is the 17a methyl derivative of 1 testosterone Detection in body fluids edit Doping with 1 testosterone can be detected in urine samples using gas chromatography 4 References edit William Llewellyn 2009 Anabolics 9 ed Molecular Nutrition p 22 135 ISBN 978 0 9679304 7 3 Friedel A Geyer H Kamber M Laudenbach Leschowsky U Schanzer W Thevis M Vollmer G Zierau O Diel P August 2006 17beta hydroxy 5alpha androst 1 en 3 one 1 testosterone is a potent androgen with anabolic properties Toxicol Lett 165 2 149 55 doi 10 1016 j toxlet 2006 03 001 PMID 16621347 Zhang H Qiu Z December 2006 An efficient synthesis of 5a androst 1 ene 3 17 dione Steroids 71 13 14 1088 90 doi 10 1016 j steroids 2006 09 008 PMID 17123559 S2CID 53258890 S Jain A Beotra and T Kaur 2005 A Case Study Detection of 1 Testosterone in Urine by GC MSD PDF Recent Advances in Doping Analysis 13 407 410 Archived from the original PDF on 2011 08 25 Retrieved 2011 06 18 Retrieved from https en wikipedia org w index php title 1 Testosterone amp oldid 1184634584, wikipedia, wiki, book, books, library,

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