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Propylpyrazoletriol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Propylpyrazoletriol
Identifiers
  • 4-[2,3-bis(4-hydroxyphenyl)-4-propyl-1H-pyrazol-5-ylidene]cyclohexa-2,5-dien-1-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC24H22N2O3
Molar mass386.451 g·mol−1
3D model (JSmol)
  • CCCC1=C(N(NC1=C2C=CC(=O)C=C2)C3=CC=C(C=C3)O)C4=CC=C(C=C4)O
  • InChI=1S/C24H22N2O3/c1-2-3-22-23(16-4-10-19(27)11-5-16)25-26(18-8-14-21(29)15-9-18)24(22)17-6-12-20(28)13-7-17/h4-15,25,28-29H,2-3H2,1H3
  • Key:UOSWGERPQQOSHS-UHFFFAOYSA-N

Propylpyrazoletriol (PPT) is asynthetic,nonsteroidalagonist ofERα with 400-fold selectivity overERβ[1] that is used widely inscientific research to study the function ofERα.[2][3][4] Though originally thought to be highly selective for ERα, PPT has subsequently been found to also act as anagonist of theGPER (GPR30).[5]

See also

[edit]

References

[edit]
  1. ^Weatherman RV (8 September 2008). "Untangling the Estrogen Receptor Web: Tools to Selectively Study Estrogen-Binding Receptors". In Ottow E, Weinmann H (eds.).Nuclear Receptors as Drug Targets. Methods and Principles in Medicinal Chemistry. John Wiley & Sons. pp. 47–64 (50).doi:10.1002/9783527623297.ch3.ISBN 978-3-527-62330-3.
  2. ^Pfaus JG, Jones SL, Flanagan-Cato LM, Blaustein JD (15 November 2014)."Female sexual behavior: Hormonal Priming and Control". In Plant TM, Zeleznik AJ (eds.).Knobil and Neill's Physiology of Reproduction: Two-Volume Set. Vol. 2. Academic Press. pp. 2287–2370 (2311).ISBN 978-0-12-397769-4.
  3. ^Aguirre C, Jayaraman A, Pike C, Baudry M (December 2010)."Progesterone inhibits estrogen-mediated neuroprotection against excitotoxicity by down-regulating estrogen receptor-β".Journal of Neurochemistry.115 (5):1277–87.doi:10.1111/j.1471-4159.2010.07038.x.PMC 3010223.PMID 20977477.
  4. ^Mann MK (2008).Synthesis of Non-steroidal Estrogen Receptor Proteolysis Targeting Chimeric Molecules (PROTACS) (Ph.D. thesis). University of Illinois at Urbana-Champaign. pp. 11–.
  5. ^Prossnitz ER, Barton M (May 2014)."Estrogen biology: new insights into GPER function and clinical opportunities".Molecular and Cellular Endocrinology.389 (1–2):71–83.doi:10.1016/j.mce.2014.02.002.PMC 4040308.PMID 24530924.
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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