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BAR 502

Product Name
BAR 502
CAS No.
1612191-86-2
Chemical Name
BAR 502
Synonyms
181945;BAR 502;BAR502 ,S0033;CID 101886309;BAR 502;BAR-502;BAR502;BAR 502, 98%, a dual FXR and GPBAR1 agonist;6α-ethyl-3α,7α-dihydroxy-24-nor-5β-cholan-23-ol;24-Norcholane-3,7,23-triol, 6-ethyl-, (3α,5β,6α,7α)-;(3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)-6-ethyl-17-((R)-4-hydroxybutan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol;GPCR19,BAR 502,G protein-coupled Bile Acid Receptor 1,BAR-502,BAR502,Autophagy,GPBAR1,NR1H4,Inhibitor,G-protein coupled receptor 19,inhibit,FXR,TGR5
CBNumber
CB33155146
Molecular Formula
C25H44O3
Formula Weight
392.62
MOL File
1612191-86-2.mol
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BAR 502 Property

Boiling point:
516.0±25.0 °C(Predicted)
Density 
1.055±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMSO:35.0(Max Conc. mg/mL);89.14(Max Conc. mM)
Ethanol:51.0(Max Conc. mg/mL);129.89(Max Conc. mM)
form 
A crystalline solid
pka
14.81±0.70(Predicted)
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
22462
Product name
BAR502
Purity
≥95%
Packaging
1mg
Price
$33
Updated
2024/03/01
Cayman Chemical
Product number
22462
Product name
BAR502
Purity
≥95%
Packaging
5mg
Price
$143
Updated
2024/03/01
Cayman Chemical
Product number
22462
Product name
BAR502
Purity
≥95%
Packaging
10mg
Price
$254
Updated
2024/03/01
Cayman Chemical
Product number
22462
Product name
BAR502
Purity
≥95%
Packaging
25mg
Price
$553
Updated
2024/03/01
ChemScene
Product number
CS-6892
Product name
BAR502
Purity
>98.0%
Packaging
1mg
Price
$132
Updated
2021/12/16
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BAR 502 Chemical Properties,Usage,Production

Uses

BAR-502 3-O-Sulfate is an impurity of BAR-502 (B161220), which can be used to treat hepatitis D virus infection.

in vivo

Treatment with BAR502 causes a 10% reduction of b.w., increases insulin sensitivity and circulating levels of HDL, while reduces steatosis, inflammatory and fibrosis scores and liver expression of SREPB1c, FAS, PPARγ, CD36 and CYP7A1 mRNA. BAR502 increases the expression of SHP and ABCG5 in the liver and SHP, FGF15 and GLP1 in intestine. BAR502 promotes the browning of epWAT and reduces liver fibrosis induced by CCl4[2]. In models of non-obstructive cholestasis, BAR502 attenuates liver injury without causing itching. Co-treatment with BAR502 increases survival, attenuates serum alkaline phosphatase levels and robustly modulates the liver expression of canonical FXR target genes including OSTα, BSEP, SHP and MDR1, without inducing pruritus[3].

BAR 502 Preparation Products And Raw materials

Raw materials

Preparation Products

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1612191-86-2, BAR 502Related Search:


  • (3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)-6-ethyl-17-((R)-4-hydroxybutan-2-yl)-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol
  • 6α-ethyl-3α,7α-dihydroxy-24-nor-5β-cholan-23-ol
  • BAR 502
  • BAR 502, 98%, a dual FXR and GPBAR1 agonist
  • 181945
  • 24-Norcholane-3,7,23-triol, 6-ethyl-, (3α,5β,6α,7α)-
  • BAR 502;BAR-502;BAR502
  • GPCR19,BAR 502,G protein-coupled Bile Acid Receptor 1,BAR-502,BAR502,Autophagy,GPBAR1,NR1H4,Inhibitor,G-protein coupled receptor 19,inhibit,FXR,TGR5
  • CID 101886309
  • BAR502 ,S0033
  • 1612191-86-2