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ASBT

Apical sodium-dependent bile acid transporter (ASBT, SLC10A2) is a key membrane transporter encoded by the SLC10A2 gene. It is primarily expressed on the apical membrane of terminal ileal epithelial cells and is responsible for the active reabsorption of bile acids. It utilises the sodium ion gradient to transport bile acids back to the liver from the intestinal lumen at a 2:1 coupling ratio, thereby maintaining the homeostasis of bile acids and cholesterol in the body. ASBT preferentially binds conjugated bile acids such as glycocholic acid and taurocholate. Its expression is regulated by multiple factors, including transcription factors and nuclear receptors. ASBT dysfunction or genetic mutations can disrupt bile acid metabolism, leading to disorders such as hypercholesterolaemia and primary bile acid malabsorption syndrome.

Maralixibat Chloride
T32873228113-66-4In house
Maralixibat Chloride (LUM001 chloride), an apical, sodium-dependent, bile acid transport inhibitor, prevents enterohepatic bile acid recirculation.
  • $263
In Stock
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Odevixibat
T16376501692-44-0
Odevixibat (A4250) is an effective, selective and orally active ileal bile acid transporter inhibitor. Odevixibat has the potential for the treatment of primary biliary cirrhosis. Odevixibat reduces cholestatic liver and bile duct injury in mice model.
  • $31
In Stock
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TargetMol | Inhibitor Sale
S 0960
T70688142974-51-4In house
S 0960 is a dimeric bile acid analog, a specific inhibitor of the sodium-dependent bile salt transporter in the ileum, used in metabolic disease research.
  • $758
In Stock
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Linerixibat
T39781345982-69-5
Linerixibat (GSK2330672) is a highly effective, nonabsorbable ASBT inhibitor (IC50: 42 ± 3 nM) that can lower glucose in an animal model of type 2 diabetes and demonstrates excellent developability properties.
  • $76
In Stock
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Elobixibat
T15209439087-18-0In house
Elobixibat (A 3309) is an inhibitor of the ileal bile acid transporter (IC50: 0.13 nM, 0.53 nM, and 5.8 nM for mouse, human, and canine IBAT). Elobixibat can be used in studies about chronic idiopathic constipation.
  • $98
In Stock
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(S)-Elobixibat
T88374439087-68-0
(S)-Elobixibat is the S-isomer of Elobixibat. It is an orally active inhibitor of Apical Sodium-Dependent Bile (IBAT) and can reduce LDL cholesterol, increase serum GLP-1, and promote colonic motility. This compound shows potential for treating metabolic syndrome and can be studied for constipation, dyslipidemia, non-alcoholic hepatitis, and liver tumors.
  • $1,660
6-8 weeks
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264W94
T10090178961-24-5
264W94 is a robust inhibitor of the ileal bile acid transporter (IBAT) and a novel agent for reducing cholesterol levels. It exhibits CYP7A1 induction and demonstrates significant antilipemic activity.
  • Inquiry Price
3-6 months
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Ritivixibat
T696222460667-52-9
Ritivixibat is an ileal bile acid transporter (IBAT) inhibitor and bile acid modulator. It is utilized in research related to cardiovascular diseases, fatty acid metabolism disorders, glucose utilization abnormalities, gastrointestinal conditions, and liver diseases.
  • $1,970
8-10 weeks
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Elobixibat hydrate
T725151633824-78-8
Elobixibat hydrate, a potent inhibitor of the ileal bile acid transporter (IBAT), exhibits IC50 values of 0.53 ± 0.17 nM, 0.13 ± 0.03 nM, and 5.8 ± 1.6 nM for human, mouse, and canine IBAT, respectively. It is utilized in the research of chronic idiopathic constipation (CIC).
  • $1,970
1-2 weeks
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S-8921
T16818151165-96-7
S-8921 is an inhibitor of ileal Na+ bile acid cotransporter.
  • $1,520
6-8 weeks
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Volixibat
T172361025216-57-2
Volixibat is a highly selective and competitive apical sodium-dependent bile acid transporter inhibitor. Volixibat has the potential for treatment for non-alcoholic steatohepatitis.
  • $1,520
Backorder
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SC-435 mesylate
T28700289037-67-8
SC-435 is an ileal apical sodium co-dependent bile acid transporter (ASBT). SC-435 inhibits plasma cholesterol.
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3-6 months
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