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BAR 501

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Products Intro: Product Name:BAR 501
CAS:1632118-69-4
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: ANHUI WITOP BIOTECH CO., LTD
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Products Intro: Product Name:BAR 501
CAS:1632118-69-4
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Products Intro: Product Name:(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
CAS:1632118-69-4
Purity:98% Package:1g,10g,25g,100g,500g,1kg
Company Name: BOC Sciences
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Products Intro: Product Name:BAR-501
CAS:1632118-69-4
Package:10 mg Remarks:Please reach out to us for more information about custom solutions.
Company Name: Zhejiang J&C Biological Technology Co.,Limited
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Products Intro: Product Name:BAR 501
CAS:1632118-69-4
Purity:99% Package:5KG;1KG Remarks:BAR 501
BAR 501 Basic information
Product Name:BAR 501
Synonyms:BAR 501;CPDD0945;BAR501, 98%, a potent and selective agonist of GPBAR1;BAR 501; BAR-501;(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;Inhibitor,GPBAR1,TGR5,GPCR19,G-protein coupled receptor 19,BAR-501,BAR501,G protein-coupled Bile Acid Receptor 1,inhibit;Cholane-3,7,24-triol, 6-ethyl-, (3α,5β,6β,7β)-;BAR501, 10 mM in DMSO
CAS:1632118-69-4
MF:C26H46O3
MW:406.64
EINECS:
Product Categories:APIs
Mol File:1632118-69-4.mol
BAR 501 Structure
BAR 501 Chemical Properties
Boiling point 527.6±25.0 °C(Predicted)
density 1.047±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:65.5(Max Conc. mg/mL);161.07(Max Conc. mM)
DMF:20.0(Max Conc. mg/mL);49.18(Max Conc. mM)
Ethanol:34.33(Max Conc. mg/mL);84.42(Max Conc. mM)
form A crystalline solid
pka14.82±0.70(Predicted)
color White to off-white
Safety Information
MSDS Information
BAR 501 Usage And Synthesis
UsesBAR501 is a potent and selective agonist of GPBAR1 with an EC50 of 1 μM.
in vivo

Pretreating rats for 6 days with BAR501, 15 mg/kg, reduces basal portal pressure and blunts the vasoconstriction activity of norepinephrine. Pretreatment with BAR501 attenuates the hepatic vasomotor activity induced by shear stress and methoxamine. Administration of BAR501 exerts a direct vasodilatory activity in the CCl4 model. Treating mice with BAR501 at the dose of 15 mg/Kg reduces portal pressure and AST plasma levels. BAR501 attenuates endothelial dysfunction by regulating CSE expression/activity[1].

References[1] 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. PLoS One. 2015 Nov 5;10(11):e0141082. DOI:10.1371/journal.pone.0141082
BAR 501 Preparation Products And Raw materials
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