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Furazabol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Furazabol
Skeletal formula of furazabol
Space-filling model of the furazabol molecule
Clinical data
Trade namesFrazalon, Miotalon, Qu Zhi Shu
Other namesAndrofurazanol; DH-245; Furazalon; Frazalon; Pirzalon; 17α-Methyl-5α-androsta[2,3-c]furazan-17β-ol; 17β-Hydroxy-17α-methyl-5α-androstano[2,3-c]-1',2',5'-oxadiazole; 17α-Methyl-5α-androstano[2,3-c][1,2,5]oxadiazol-17β-ol
Routes of
administration
By mouth
Drug classAndrogen;Anabolic steroid
ATC code
Legal status
Legal status
Pharmacokinetic data
Eliminationhalf-life4 hours[citation needed]
ExcretionUrine
Identifiers
  • (1S,2S,10S,13R,14S,17S,18S)-2,17,18-Trimethyl-6-oxa-5,7-diazapentacyclo[11.7.0.02,10.04,8.014,18]icosa-4,7-dien-17-ol
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.013.621Edit this at Wikidata
Chemical and physical data
FormulaC20H30N2O2
Molar mass330.472 g·mol−1
3D model (JSmol)
  • O[C@@]5([C@@]4([C@H]([C@H]3[C@@H]([C@]2(Cc1nonc1C[C@@H]2CC3)C)CC4)CC5)C)C
  • InChI=1S/C20H30N2O2/c1-18-11-17-16(21-24-22-17)10-12(18)4-5-13-14(18)6-8-19(2)15(13)7-9-20(19,3)23/h12-15,23H,4-11H2,1-3H3/t12-,13+,14-,15-,18-,19-,20-/m0/s1 checkY
  • Key:RGLLOUBXMOGLDQ-IVEVATEUSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Furazabol (INNTooltip International Nonproprietary Name,JANTooltip Japanese Accepted Name) (brand namesFrazalon,Miotalon,Qu Zhi Shu), also known asandrofurazanol, is asynthetic,orally activeanabolic-androgenic steroid which has been marketed inJapan since 1969.[1][2][3][4] It is a17α-alkylatedderivative ofdihydrotestosterone (DHT) and is closely related structurally tostanozolol, differing from it only by having afurazanring system instead ofpyrazole.[5] Furazabol has a relatively high ratio ofanabolic toandrogenic activity.[4] As with other 17α-alkylated AAS, it may have a risk ofhepatotoxicity.[6] The drug has been described as anantihyperlipidemic and is claimed to be useful in the treatment ofatherosclerosis andhypercholesterolemia,[5] but according to William Llewellyn, such properties of furazabol are a myth.[7]

Doping

[edit]

Previously a relatively unknown drug to North American athletes, Furazabol gained notoriety in theCommission of Inquiry into the Use of Drugs and Banned Practices Intended to Increase Athletic Performance (known colloquially as theDubin inquiry). After winning the 100m gold at the1988 Summer Olympics in Seoul, Canadian sprinterBen Johnson tested positive for the anabolic steroidStanozolol, was later stripped of his gold medal, and banned from competition for two years.[8] Johnson initially denied the allegations, asserting he had never taken banned substances. He later claimed the positive finding was the result of sabotage, and that he had actually taken Furazabol, which at the time could not be detected by theGas Chromatography-Mass Spectrometry assay used to analyze samples at the Games. Contrariwise, Stanozolol had been widely used in elite athlete circles since the 1970s, and as of 1988, could be reliably identified by conventional testing procedures.[9]

Testifying before the Dubin Inquiry, Johnson's physicianGeorge "Jamie" Astaphan claimed that he had been administering Furazabol (which he termed Estragol) to Johnson since the mid-1980s, and that Johnson likely self-administered Stanozolol within a month of the Games opening in Seoul.

In later testimony, Johnson's training mateAngella Issajenko told the Commission that she too had obtained Furazabol from Astaphan, or so she thought. The former-Canadian record holder revealed that, after Johnson's positive test, she had an analysis done on a leftover vial of what she thought contained Furazabol, and was informed it was identified as Stanozolol. Issajenko, and later the Commission's Chief Justice Charles Dubin, concluded Astaphan had been peddling Stanozolol to Johnson, Issajenko, and other Canadian team members all along, and that Furazabol was either a figment of his imagination, or an outright lie.[10]

References

[edit]
  1. ^J. Elks (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 585–.ISBN 978-1-4757-2085-3.
  2. ^Index Nominum 2000: International Drug Directory. Taylor & Francis. 2000. pp. 475–.ISBN 978-3-88763-075-1.
  3. ^William Andrew Publishing (22 October 2013).Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 1725–.ISBN 978-0-8155-1856-3.
  4. ^abProgress in Medicinal Chemistry. Elsevier. 1 January 1979. pp. 62–63.ISBN 978-0-08-086264-4.
  5. ^abFragkaki AG, Angelis YS, Koupparis M, Tsantili-Kakoulidou A, Kokotos G, Georgakopoulos C (2009). "Structural characteristics of anabolic androgenic steroids contributing to binding to the androgen receptor and to their anabolic and androgenic activities. Applied modifications in the steroidal structure".Steroids.74 (2):172–97.doi:10.1016/j.steroids.2008.10.016.PMID 19028512.S2CID 41356223.
  6. ^Abbate V, Kicman AT, Evans-Brown M, McVeigh J, Cowan DA, Wilson C, Coles SJ, Walker CJ (2015). "Anabolic steroids detected in bodybuilding dietary supplements - a significant risk to public health".Drug Test Anal.7 (7):609–18.doi:10.1002/dta.1728.PMID 25284752.
  7. ^William Llewellyn (2007).Anabolics 2007: Anabolic Steroids Reference Manual. Body of Science.ISBN 978-0967930466.
  8. ^Mann, Andrea."September 27, 1988: Ben Johnson is stripped of his Olympic gold medal after failing drugs test".BT. BT Group. Retrieved24 March 2020.
  9. ^Masse, Robert (1989). "Studies on anabolic steroids. III. Detection and characterization of stanozolol urinary metabolites in humans by gas chromatography-mass spectrometry".Journal of Chromatography.497:17–37.PMID 2625454.
  10. ^Harvey, Randy (March 17, 1989)."Milky White Substance: Is It a Solution?".Los Angeles Times. Retrieved24 March 2020.


Androgens
(incl.AASTooltip anabolic–androgenic steroid)
ARTooltip Androgen receptoragonists
Progonadotropins
Antiandrogens
ARTooltip Androgen receptorantagonists
Steroidogenesis
inhibitors
5α-Reductase
Others
Antigonadotropins
Others
ARTooltip Androgen receptor
Agonists
SARMsTooltip Selective androgen receptor modulator
Antagonists
GPRC6A
Agonists
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