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BAR 501 impurity

BAR 501 impurity

Item no.	TMO-T8752-50mg
Manufacturer	TargetMol
CASRN	1632118-70-7
Amount	50 mg
Quantity options	100 mg 1 mL x 10 mM (in DMSO) 10 mg 1 mg 200 mg 25 mg 50 mg 5 mg
Category	Reagents & Chemicals Molecules
Type	Molecules
Specific against	other
Purity	99.97%
Citations	Renga B, et al. Reversal of Endothelial Dysfunction by GPBAR1 Agonism in Portal Hypertension Involves a AKT/FOXOA1 Dependent Regulation of H2S Generation and Endothelin-1.
Smiles	C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3)[C@@]([C@@H](CCCO)C)(CC4)[H])[H])([C@H](O)[C@@H](CC)[C@@]1(C[C@H](O)CC2)[H])[H])[H]
ECLASS 10.1	32169090
ECLASS 11.0	32169090
UNSPSC	12000000
Alias	1632118-70-7,GPCR19
Shipping Condition	Cool pack
Available
Manufacturer - Targets	GPCR19
Shipping Temperature	Cool pack
Storage Conditions	-20
Molecular Weight	406.64
Description	BAR501 impurity is an impurity found in the preparation of BAR501 that acts as an agonist of the G protein-coupled bile acid-activated receptor (GP-BAR1). BAR501 impurity (10 μM) induces a 150% increase in luciferase activity in a GP-BAR1 reporter gene assay
Pathways	GPCR/G Protein

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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