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RU-56187

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
RU-56187
Clinical data
Drug classNonsteroidal antiandrogen
Identifiers
  • 2-(Trifluoromethyl)-4-(3,4,4-trimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl)benzonitrile
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H12F3N3OS
Molar mass327.33 g·mol−1
3D model (JSmol)
  • CC1(C(=O)N(C(=S)N1C)C2=CC(=C(C=C2)C#N)C(F)(F)F)C
  • InChI=1S/C14H12F3N3OS/c1-13(2)11(21)20(12(22)19(13)3)9-5-4-8(7-18)10(6-9)14(15,16)17/h4-6H,1-3H3
  • Key:HLBUAKQNKJTEIU-UHFFFAOYSA-N

RU-56187 is anonsteroidal antiandrogen which was never marketed.[1][2][3][4][5] It shows 92% of theaffinity oftestosterone for theandrogen receptor and negligible affinity for othersteroid hormone receptors.[1][2] The medication is asilent antagonist of the androgen receptor.[5] RU-56187 is 3- to 10-fold morepotent as an antiandrogen thanbicalutamide ornilutamide in animals.[1] Both RU-56187 andRU-58841 appear to beprodrugs ofcyanonilutamide (RU-56279)in vivo in animals.[3]

See also

[edit]

References

[edit]
  1. ^abcSingh SM, Gauthier S, Labrie F (February 2000). "Androgen receptor antagonists (antiandrogens): structure-activity relationships".Curr. Med. Chem.7 (2):211–47.doi:10.2174/0929867003375371.PMID 10637363.
  2. ^abTeutsch G, Goubet F, Battmann T, Bonfils A, Bouchoux F, Cerede E, Gofflo D, Gaillard-Kelly M, Philibert D (January 1994). "Non-steroidal antiandrogens: synthesis and biological profile of high-affinity ligands for the androgen receptor".J. Steroid Biochem. Mol. Biol.48 (1):111–9.doi:10.1016/0960-0760(94)90257-7.PMID 8136296.S2CID 31404295.
  3. ^abCousty-Berlin D, Bergaud B, Bruyant MC, Battmann T, Branche C, Philibert D (October 1994). "Preliminary pharmacokinetics and metabolism of novel non-steroidal antiandrogens in the rat: relation of their systemic activity to the formation of a common metabolite".J. Steroid Biochem. Mol. Biol.51 (1–2):47–55.doi:10.1016/0960-0760(94)90114-7.PMID 7947350.S2CID 29752252.
  4. ^Matias JR, Gaillard M (June 1995). "Local inhibition of sebaceous gland growth by topically applied RU 58841".Ann. N. Y. Acad. Sci.761 (3):56–65.Bibcode:1995NYASA.761...56M.doi:10.1111/j.1749-6632.1995.tb31369.x.PMID 7625751.S2CID 45086788.
  5. ^abKemppainen JA, Langley E, Wong CI, Bobseine K, Kelce WR, Wilson EM (March 1999)."Distinguishing androgen receptor agonists and antagonists: distinct mechanisms of activation by medroxyprogesterone acetate and dihydrotestosterone".Mol. Endocrinol.13 (3):440–54.doi:10.1210/mend.13.3.0255.PMID 10077001.
ARTooltip Androgen receptor
Agonists
SARMsTooltip Selective androgen receptor modulator
Antagonists
GPRC6A
Agonists


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