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1392487-51-2

1392487-51-2 structure
1392487-51-2 structure
  • Name: G36
  • Chemical Name: (3aS,4R,9bR)-4-(6-Bromo-1,3-benzodioxol-5-yl)-8-isopropyl-3a,4,5, 9b-tetrahydro-3H-cyclopenta[c]quinoline
  • CAS Number: 1392487-51-2
  • Molecular Formula: C22H22BrNO2
  • Molecular Weight: 412.320
  • Catalog: Research Areas Endocrinology
  • Create Date: 2017-04-09 21:34:15
  • Modify Date: 2024-01-08 11:47:10
  • G-36 is a cell permeable non-steroidal antagonist of G-protein-coupled estrogen receptor (GPER/GPR30) which selectively inhibits estrogen-mediated activation of PI3K by GPER, but not by ERα. G-36 also inhibits estrogen-mediated calcium mobilization (IC50=112 nM)[1].

Name (3aS,4R,9bR)-4-(6-Bromo-1,3-benzodioxol-5-yl)-8-isopropyl-3a,4,5, 9b-tetrahydro-3H-cyclopenta[c]quinoline
Synonyms CaCCinh-A01
(3aS,4R,9bR)-4-(6-Bromo-1,3-benzodioxol-5-yl)-8-isopropyl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline
3H-Cyclopenta[c]quinoline, 4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-8-(1-methylethyl)-, (3aS,4R,9bR)-
G-36
Description G-36 is a cell permeable non-steroidal antagonist of G-protein-coupled estrogen receptor (GPER/GPR30) which selectively inhibits estrogen-mediated activation of PI3K by GPER, but not by ERα. G-36 also inhibits estrogen-mediated calcium mobilization (IC50=112 nM)[1].
Related Catalog
References

[1]. Dennis MK, Field AS, Burai R, Ramesh C, Petrie WK, Bologa CG, Oprea TI, Yamaguchi Y, Hayashi S, Sklar LA, Hathaway HJ, Arterburn JB, Prossnitz ER. Identification of a GPER/GPR30 antagonist with improved estrogen receptor counterselectivity. J Steroid Biochem Mol Biol. 2011 Nov;127(3-5):358-66.

Density 1.4±0.1 g/cm3
Boiling Point 478.4±45.0 °C at 760 mmHg
Molecular Formula C22H22BrNO2
Molecular Weight 412.320
Flash Point 243.1±28.7 °C
Exact Mass 411.083374
PSA 30.49000
LogP 5.83
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.619
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