A-4250

For research use only. Not for therapeutic Use.

  • CAT Number: I000257
  • CAS Number: 501692-44-0
  • Molecular Formula: C37H48N4O8S2
  • Molecular Weight: 740.93
  • Purity: 98%
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A-4250(Cat No.:I000257)(also known as Odevixibat) is a potent, selective ileal bile acid transporter (IBAT) inhibitor used for the treatment of progressive familial intrahepatic cholestasis (PFIC) and other cholestatic liver diseases. By inhibiting IBAT, A-4250 reduces the reabsorption of bile acids in the intestines, leading to decreased bile acid accumulation in the liver and circulation. This alleviates liver damage and reduces symptoms such as severe itching (pruritus) associated with cholestasis. A-4250 offers a novel, non-surgical approach to managing rare pediatric liver disorders, improving patient outcomes and quality of life.


Catalog Number I000257
CAS Number 501692-44-0
Synonyms

A-4250; A4250; A 4250;(S)-2-((R)-2-(2-((3,3-dibutyl-7-(methylthio)-1,1-dioxido-5-phenyl-2,3,4,5-tetrahydrobenzo[f][1,2,5]thiadiazepin-8-yl)oxy)acetamido)-2-(4-hydroxyphenyl)acetamido)butanoic acid

Molecular Formula C37H48N4O8S2
Purity 98%
Target Apical Sodium-Dependent Bile Acid Transporter
Target Protein

Q12908

Solubility Soluble in DMSO
Appearance Solid
Storage Dry, dark and at 2 - 8 °C for six months or -20°C for two years.
IC50 IC50: IBAT
IUPAC Name (2S)-2-[[(2R)-2-[[2-[(3,3-dibutyl-7-methylsulfanyl-1,1-dioxo-5-phenyl-2,4-dihydro-1λ6,2,5-benzothiadiazepin-8-yl)oxy]acetyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]butanoic acid
InChI InChI=1S/C37H48N4O8S2/c1-5-8-19-37(20-9-6-2)24-41(26-13-11-10-12-14-26)29-21-31(50-4)30(22-32(29)51(47,48)40-37)49-23-33(43)39-34(25-15-17-27(42)18-16-25)35(44)38-28(7-3)36(45)46/h10-18,21-22,28,34,40,42H,5-9,19-20,23-24H2,1-4H3,(H,38,44)(H,39,43)(H,45,46)/t28-,34+/m0/s1
InChIKey XULSCZPZVQIMFM-IPZQJPLYSA-N
SMILES CCCCC1(CN(C2=CC(=C(C=C2S(=O)(=O)N1)OCC(=O)N[C@H](C3=CC=C(C=C3)O)C(=O)N[C@@H](CC)C(=O)O)SC)C4=CC=CC=C4)CCCC
Reference

<br />
1: Graffner H, Gillberg PG, Rikner L, Marschall HU. The ileal bile acid
transporter inhibitor A4250 decreases serum bile acids by interrupting the
enterohepatic circulation. Aliment Pharmacol Ther. 2016 Jan;43(2):303-10. doi:
10.1111/apt.13457. PubMed PMID: 26527417.<br />
2: Baghdasaryan A, Fuchs CD, &#214;sterreicher CH, Lemberger UJ, Halilbasic E, P&#229;hlman
I, Graffner H, Krones E, Fickert P, Wahlstr&#246;m A, St&#229;hlman M, Paumgartner G,
Marschall HU, Trauner M. Inhibition of intestinal bile acid absorption improves
cholestatic liver and bile duct injury in a mouse model of sclerosing
cholangitis. J Hepatol. 2016 Mar;64(3):674-81. doi: 10.1016/j.jhep.2015.10.024.
PubMed PMID: 26529078.<br />
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