MedKoo Cat#: 563350 | Name: G-1 GPER inhibitor
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

G-1 is a selective agonist for GPER. It acts by blocking tubulin polymerization.

Chemical Structure

G-1 GPER inhibitor
G-1 GPER inhibitor
CAS#881639-98-1

Theoretical Analysis

MedKoo Cat#: 563350

Name: G-1 GPER inhibitor

CAS#: 881639-98-1

Chemical Formula: C21H18BrNO3

Exact Mass: 411.0470

Molecular Weight: 412.28

Elemental Analysis: C, 61.18; H, 4.40; Br, 19.38; N, 3.40; O, 11.64

Price and Availability

Size Price Availability Quantity
10mg USD 285.00 2 Weeks
25mg USD 550.00 2 Weeks
50mg USD 850.00 2 Weeks
100mg USD 1,250.00 2 Weeks
200mg USD 1,850.00 2 Weeks
500mg USD 2,650.00 2 Weeks
1g USD 3,650.00 2 Weeks
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Synonym
G-1; G 1; G1; G-1 GPER inhibitor; GPR30 Agonist, G-1; GPR30 inhibitor G1
IUPAC/Chemical Name
1-((3aS,4R,9bR)-4-(6-bromobenzo[d][1,3]dioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-8-yl)ethan-1-one
InChi Key
VHSVKVWHYFBIFJ-HKZYLEAXSA-N
InChi Code
InChI=1S/C21H18BrNO3/c1-11(24)12-5-6-18-15(7-12)13-3-2-4-14(13)21(23-18)16-8-19-20(9-17(16)22)26-10-25-19/h2-3,5-9,13-14,21,23H,4,10H2,1H3/t13-,14+,21-/m1/s1
SMILES Code
[H][C@]12CC=C[C@@]1([H])C1=C(C=CC(C(C)=O)=C1)N[C@H]2C1=CC2=C(C=C1Br)OCO2
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 412.28 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Thomas P. Rapid steroid hormone actions initiated at the cell surface and the receptors that mediate them with an emphasis on recent progress in fish models. Gen Comp Endocrinol. 2012 Feb 1;175(3):367-83. doi: 10.1016/j.ygcen.2011.11.032. Epub 2011 Nov 29. Review. PubMed PMID: 22154643; PubMed Central PMCID: PMC3264783. 2: Revankar CM, Mitchell HD, Field AS, Burai R, Corona C, Ramesh C, Sklar LA, Arterburn JB, Prossnitz ER. Synthetic estrogen derivatives demonstrate the functionality of intracellular GPR30. ACS Chem Biol. 2007 Aug 17;2(8):536-44. Epub 2007 Jul 27. PubMed PMID: 17655271. 3: Song RX, Fan P, Yue W, Chen Y, Santen RJ. Role of receptor complexes in the extranuclear actions of estrogen receptor alpha in breast cancer. Endocr Relat Cancer. 2006 Dec;13 Suppl 1:S3-13. Review. PubMed PMID: 17259556. 4: Revankar CM, Cimino DF, Sklar LA, Arterburn JB, Prossnitz ER. A transmembrane intracellular estrogen receptor mediates rapid cell signaling. Science. 2005 Mar 11;307(5715):1625-30. Epub 2005 Feb 10. PubMed PMID: 15705806.