1-Testosterone Explained

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.

Pharmacology

Pharmacodynamics

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

See also: List of androgens/anabolic steroids.

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

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

Detection in body fluids

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

Notes and References

  1. Book: William Llewellyn. Anabolics. 9. 2009. Molecular Nutrition. 978-0-9679304-7-3. 22,135.
  2. Friedel A, Geyer H, Kamber M, Laudenbach-Leschowsky U, Schänzer W, Thevis M, Vollmer G, Zierau O, Diel P . 17beta-hydroxy-5alpha-androst-1-en-3-one (1-testosterone) is a potent androgen with anabolic properties . Toxicol. Lett. . 165 . 2 . 149–55 . 16621347 . 10.1016/j.toxlet.2006.03.001. August 2006.
  3. Zhang H, Qiu Z . An efficient synthesis of 5α-androst-1-ene-3,17-dione . Steroids . 71 . 13–14 . 1088–90 . 17123559 . 10.1016/j.steroids.2006.09.008. December 2006. 53258890 .
  4. S. Jain, A. Beotra and T. Kaur . A Case Study: Detection of 1-Testosterone in Urine by GC-MSD . Recent Advances in Doping Analysis . 13 . 2005 . 407–410 . 2011-06-18 . https://web.archive.org/web/20110825032543/http://proceedings.live-record.de/proceedings_13_pdf/13_407.pdf . 2011-08-25 . dead .