GSK2330672 free base · Synonyms: Linerixibat
GSK2330672 is an inhibitor of the apical sodium-dependent bile acid transporter.
For research use only. Not for human or veterinary use.
GSK2330672 structure
CAS No.: 1345982-69-5
Pack sizes & pricing
| Size | Price | SKU | Stock | |
|---|---|---|---|---|
| 50 mg | USD 450.00 | BP-01872-50mg | In stock | Get quote |
| 100 mg | USD 750.00 | BP-01872-100mg | In stock | Get quote |
| 250 mg | USD 1,250.00 | BP-01872-250mg | In stock | Get quote |
| 500 mg | USD 1,950.00 | BP-01872-500mg | In stock | Get quote |
| 1 g | Inquire | BP-01872-1g | In stock | Inquire |
Need another size or custom synthesis? Request a quote.
Description
GSK2330672 (Linerixibat) is an inhibitor of the apical sodium-dependent bile acid transporter (ASBT; IC50s = 42, 2.1, and 1.9 nM for human, mouse, and rat ASBT, respectively).
Biological activity
In Vitro The zwitterionic, nonhygroscopic, crystalline salt form of Linerixibat (Compound 56) shows good aqueous solubility at pH 7.4 (>7 mg/mL), excellent thermal stability, and did not generate reactive or humanspecific metabolite, characteristics. In Vivo Linerixibat (GSK2330672; 0.05-10 mg/kg; oral gavage; twice daily; for 14 days; male ZDF rat) treatment lowers glucose in an animal model of type 2 diabetes.
Identifiers
- SMILES
-
CCCC[C@]1(CC)CS(=O)(=O)C2=CC(CNC(CC(O)=O)CC(O)=O)=C(OC)C=C2[C@H](N1)C1=CC=CC=C1 - InChIKey
-
CZGVOBIGEBDYTP-VSGBNLITSA-N
Specifications
- MW (average)
- 546.6760
- Formula
- C28H38N2O7S
- CAS No.
- 1345982-69-5
- Physical state
- Solid
- Color
- White to off-white
- Shipping
- Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
- Storage
- Powder -20℃ 3 years; In solvent -20℃ 1 month;
Solubility
Soluble in DMSO
Documents
References
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