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Prinaberel

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Prinaberel
Clinical data
ATC code
  • None
Identifiers
  • (4Z)-2-Fluoro-4-(5-hydroxy-7-vinyl-1,3-benzoxazol-2(3H)-ylidene)-2,5-cyclohexadien-1-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.222.969Edit this at Wikidata
Chemical and physical data
FormulaC15H10FNO3
Molar mass271.247 g·mol−1
3D model (JSmol)
  • O=C3\C=C/C(=C2/Oc1c(cc(O)cc1N2)\C=C)/C=C3/F
  • InChI=1S/C15H10FNO3/c1-2-8-5-10(18)7-12-14(8)20-15(17-12)9-3-4-13(19)11(16)6-9/h2-7,17-18H,1H2/b15-9-
  • Key:FCXYSEXZEGPLGG-DHDCSXOGSA-N

Prinaberel (INN,USAN) (developmental code namesERB-041,WAY-202041) is asynthetic,nonsteroidal, and highlyselectiveagonist of theERβsubtype of theestrogen receptor.[1] It is used inscientific research to elucidate the role of the ERβ receptor.[2] Studies have indicated that selective ERβ agonists like prinaberel could be useful in the clinical treatment of a variety ofmedical conditions includinginflammatory bowel disease,rheumatoid arthritis,endometriosis, andsepsis.[3] Accordingly, prinaberel either was or still is under investigation byWyeth for the treatment of some of these conditions.[4]

See also

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References

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  1. ^Harris HA, Albert LM, Leathurby Y, et al. (October 2003)."Evaluation of an estrogen receptor-beta agonist in animal models of human disease".Endocrinology.144 (10):4241–9.doi:10.1210/en.2003-0550.PMID 14500559.
  2. ^Koehler KF, Helguero LA, Haldosén LA, Warner M, Gustafsson JA (May 2005)."Reflections on the discovery and significance of estrogen receptor beta".Endocrine Reviews.26 (3):465–78.doi:10.1210/er.2004-0027.PMID 15857973.
  3. ^Harris HA (2006). "Preclinical characterization of selective estrogen receptor beta agonists: new insights into their therapeutic potential".Ernst Schering Foundation Symposium Proceedings. 2006/1 (1):149–61.doi:10.1007/2789_2006_021.ISBN 978-3-540-49547-5.PMID 17824176.
  4. ^"Prinaberel - Wyeth phase change II, USA (endometriosis)".R & D Focus Drug News. 2006-06-05. Archived fromthe original on 2016-03-07. Retrieved2012-05-20.

External links

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ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


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