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Ralaniten

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ralaniten
Clinical data
Other namesEPI-002
Drug classNonsteroidal antiandrogen
Identifiers
  • (2R)-3-[4-[2-[4-[(2S)-3-Chloro-2-hydroxypropoxy]phenyl]propan-2-yl]phenoxy]propane-1,2-diol
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC21H27ClO5
Molar mass394.89 g·mol−1
3D model (JSmol)
  • CC(C)(C1=CC=C(C=C1)OC[C@@H](CO)O)C2=CC=C(C=C2)OC[C@@H](CCl)O
  • InChI=1S/C21H27ClO5/c1-21(2,15-3-7-19(8-4-15)26-13-17(24)11-22)16-5-9-20(10-6-16)27-14-18(25)12-23/h3-10,17-18,23-25H,11-14H2,1-2H3/t17-,18-/m1/s1
  • Key:HDTYUHNZRYZEEB-QZTJIDSGSA-N

Ralaniten (developmental code nameEPI-002) is anN-terminal domain antiandrogen which was never marketed.[1] It is aderivative ofbisphenol A[2] and one of the fourstereoisomers ofEPI-001.[1] Aprodrug of ralaniten,ralaniten acetate (EPI-506), was under development for the treatment ofprostate cancer.[3]

See also

[edit]

References

[edit]
  1. ^abMyung JK, Banuelos CA, Fernandez JG, Mawji NR, Wang J, Tien AH, et al. (July 2013)."An androgen receptor N-terminal domain antagonist for treating prostate cancer".The Journal of Clinical Investigation.123 (7):2948–2960.doi:10.1172/JCI66398.PMC 3696543.PMID 23722902.
  2. ^Monaghan AE, McEwan IJ (2016)."A sting in the tail: the N-terminal domain of the androgen receptor as a drug target".Asian Journal of Andrology.18 (5):687–694.doi:10.4103/1008-682X.181081.PMC 5000789.PMID 27212126.
  3. ^Maughan BL, Antonarakis ES (December 2015). "Clinical Relevance of Androgen Receptor Splice Variants in Castration-Resistant Prostate Cancer".Current Treatment Options in Oncology.16 (12): 57.doi:10.1007/s11864-015-0375-z.PMID 26537882.S2CID 30398927.
ARTooltip Androgen receptor
Agonists
SARMsTooltip Selective androgen receptor modulator
Antagonists
GPRC6A
Agonists
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