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1161002-05-6

1161002-05-6 Structure

1161002-05-6 Structure
IdentificationBack Directory
[Name]

(3aS*,4R*,9bR*)-4-(6-Bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-3H-cyclopenta[c]quinoline
[CAS]

1161002-05-6
[Synonyms]

H37
G-15
RMB5
AGPAT1
LUCA15
1-AGPAT1
LPAAT-alpha
G15;G-15;G 15;1161002-05-6
RNA binding motif protein 5
Compound G15 - GPR30 antagonist
Anti-AGPAT1 antibody produced in rabbit
(3aS*,4R*,9bR*)-4-(6-Bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-3H-cyclopenta[c]quinoline
(3aR,4R,9bS)-4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline
(3aS,4R,9bR)-4-(6-BroMo-1,3-benzodioxol-5-yl)-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-, (3aS,4R,9bR)-
(3aS,4R,9bR)-4-(6-Bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline (G-15)
[Molecular Formula]

C19H16BrNO2
[MDL Number]

MFCD16618401
[MOL File]

1161002-05-6.mol
[Molecular Weight]

370.24
Chemical PropertiesBack Directory
[Melting point ]

178-180 °C
[Boiling point ]

462.7±45.0 °C(Predicted)
[density ]

1.472±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

insoluble in H2O; insoluble in EtOH; ≥37 mg/mL in DMSO
[form ]

solid
[pka]

3.98±0.40(Predicted)
[color ]

White to off-white
[biological source]

rabbit
Hazard InformationBack Directory
[Description]

G protein-coupled estrogen receptor (GPER), or GPR30, specifically binds natural and man-made estrogens. It is thought to be involved in estrogen-sensitive cancers. GPER knockout mice are fertile, although they exhibit thymic atrophy, impaired glucose tolerance, and altered bone growth. G-15 is a cell-permeable non-steroidal antagonist of GPER (Ki = 20 nM). It displays low affinity cross-reactivity with the classical estrogen receptor (ER), ERα, so that at doses greater than 1 μM it is capable of mediating limited ER-dependent transcriptional activity. G-15 antagonizes the anti-depressive effects of estrogen in vivo.
[Uses]

(3aS,4R,9bR)-4-(6-Bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline is also known as “G-15”, a G-protein-coupled estrogen receptor antagonist designed for the treatment of estrogen-sensitive cancers.
[in vivo]

G15 (1.46 mg/kg; i.h.; twice a week for 14 weeks) decreases the number of tumor nodules and tumor index increased by the E2 or G1 group in urethane-induced adenocarcinoma mice[1].

Animal Model:Four-week-old female Kunming mice (Urethane-induced adenocarcinoma)[1]
Dosage:1.46 mg/kg (combination with E2, 0.09 mg/kg and fulvestrant (Ful), 2.4 mg/kg)
Administration:Subcutaneous injection; twice a week for 14 weeks
Result:The number of tumor nodules decreased in the E2+Ful+G15 group.
[storage]

-20°C, protect from light
[References]

[1] dennis mk, burai r, ramesh c, et al. in vivo effects of a gpr30 antagonist. nat chem biol, 2009, 5 (6): 421-427.
[2] g-protein-coupled estrogen receptor and the gper-antagonist g-15 inhibits proliferation in endometriotic cells. fertil steril, 2013, 100 (3): 770-776.
[3] hammond r, nelson d, kline e, et al. chronic treatment with a gpr30 antagonist impairs acquisition of a spatial learning task in young female rats. horm behav, 2012, 62 (4): 367-374.
Spectrum DetailBack Directory
[Spectrum Detail]

(3aS*,4R*,9bR*)-4-(6-Bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-3H-cyclopenta[c]quinoline(1161002-05-6)1HNMR
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