898537-18-3
Chemical Structure
Luseogliflozin
Synonym(s): TS 071
- CAS No.: 898537-18-3
- Formula:C23H30O6S
- Molecular Weight:434.55
IUPAC Name: (2S,3R,4R,5S,6R)-2-(5-(4-ethoxybenzyl)-2-methoxy-4-methylphenyl)-6-(hydroxymethyl)tetrahydro-2H-thiopyran-3,4,5-triol
InChIKey: WHSOLWOTCHFFBK-ZQGJOIPISA-N
SMILES: OC[C@@H](S1)[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1C2=C(OC)C=C(C)C(CC3=CC=C(OCC)C=C3)=C2
Biological Activity: Luseogliflozin (TS 071) is a potent, selective, orally active sodium-dependent glucose cotransporter (SGLT) 2 inhibitor, with an IC50 of 2.26 nM, about 1765-fold selectivity over SGLT1 (IC50, 3990 nM). Luseogliflozin has the protential for researching type 2 diabetes[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Luseogliflozin | 99.33% | Luseogliflozin (TS 071) is a potent, selective, orally active sodium-dependent glucose cotransporter (SGLT) 2 inhibitor, with an IC50 of 2.26 nM, about 1765-fold selectivity over SGLT1 (IC50, 3990 nM). Luseogliflozin has the protential for researching type 2 diabetes. | ||||||||||||||||||||
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Luseogliflozin (Standard) | ≥98% | Luseogliflozin (Standard) is the analytical standard of Luseogliflozin (HY-10449). This product is intended for research and analytical applications. Luseogliflozin (TS 071) is a potent, selective, orally active sodium-dependent glucose cotransporter (SGLT) 2 inhibitor, with an IC50 of 2.26 nM, about 1765-fold selectivity over SGLT1 (IC50, 3990 nM). Luseogliflozin has the protential for researching type 2 diabetes. | ||||||||||||||||||||
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Similarity Score 0.99
HY-10449ALuseogliflozin hydrate -
Similarity Score 0.58
HY-10450Dapagliflozin -
Similarity Score 0.58
HY-137145galacto-Dapagliflozin -
Similarity Score 0.56
HY-I1122R(2S,3R,4R,5S,6R)-2-(3-(4-Ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (Standard) -
Similarity Score 0.56
HY-116223Tianagliflozin -
Similarity Score 0.56
HY-180201SGLT2-IN-4 -
Similarity Score 0.55
HY-15516RSotagliflozin (Standard) -
Similarity Score 0.55
HY-10450ARDapagliflozin ((2S)-1,2-propanediol, hydrate) (Standard) -
Similarity Score 0.54
HY-I1119Dapagliflozin impurity 111 -
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References
- [1]. Anthony Markham,et al. Luseogliflozin: first global approval. Drugs. 2014 Jun;74(8):945-50. [Content Brief]
- [2]. Jun Shirakawa,et al. Luseogliflozin increases beta cell proliferation through humoral factors that activate an insulin receptor- and IGF-1 receptor-independent pathway. Diabetologia. 2020 Mar;63(3):577-587. [Content Brief]
