BAR-501 - CAS 1632118-69-4
Catalog number: B0084-482211
Category: Inhibitor
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C26H46O3
Molecular Weight:
406.651
COA:
Inquire
Targets:
GABA Receptor
Description:
BAR-501, a UDCA derivative, is a selective GPBAR1 agonist devoid of any FXR agonistic activity. BAR-501 effectively transactivates GPBAR1 in HEK293 cells overexpressing a CRE along with GPBAR1, with a EC50 of 1 μM. Besides, protects against development of portal hypertension in rodent models of liver injury and endothelial dysfunction.
Ordering Information
Catalog Number Size Price Stock Quantity
B0084-482211 10 mg $198 In stock
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Brife Description:
A selective GPBAR1 agonist
Appearance:
Solid powder
Synonyms:
3R,5S,6S,7S,8S,9S,10S,13R,14S,17R)-6-ethyl-17-((R)-5-hydroxypentan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol; BAR-501; BAR 501; BAR501
Solubility:
Soluble in DMSO
Storage:
Store in a cool and dry place and at 0 - 4℃ for short term (days to weeks) or -42℃ for long term (months to years).
MSDS:
Inquire
Shelf Life:
2 years
Boiling Point:
527.6±25.0 °C | Condition: Press: 760 Torr
Density:
1.047±0.06 g/cm3
InChIKey:
DQBAHTQWQZRMFH-CRPAWOMZSA-N
InChI:
1S/C26H46O3/c1-5-18-22-15-17(28)10-12-26(22,4)21-11-13-25(3)19(16(2)7-6-14-27)8-9-20(25)23(21)24(18)29/h16-24,27-29H,5-15H2,1-4H3/t16-,17-,18+,19-,20+,21+,22+,23+,24+,25-,26-/m1/s1
Canonical SMILES:
C[C@H](CCCO)[C@H]1CC[C@@]2([H])[C@]3([H])[C@@H](O)[C@@H](CC)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C
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