
LX-4211
CAS No. 1018899-04-1
LX-4211( Sotagliflozin | LP-802034 | LX4211 | LX 4211 )
Catalog No. M10090 CAS No. 1018899-04-1
A potent, selective SGLT2 inhibitor with IC50 of 14 nM for hSGLT2.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 47 | In Stock |
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5MG | 80 | In Stock |
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10MG | 120 | In Stock |
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25MG | 235 | In Stock |
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50MG | 357 | In Stock |
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100MG | 531 | In Stock |
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500MG | 1134 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameLX-4211
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, selective SGLT2 inhibitor with IC50 of 14 nM for hSGLT2.
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DescriptionA potent, selective SGLT2 inhibitor with IC50 of 14 nM for hSGLT2; exhibits excellent selectivity over hSGLT1 (IC50=19 uM); inhibits SGLT2 in vitro and urinary glucose reabsorption in vivo.Diabetes Phase 2 Clinical(In Vitro):LX4211 enhanced urinary glucose excretion by inhibiting SGLT2-mediated renal glucose reabsorption; markedly and significantly improved multiple measures of glycemic control, including fasting plasma glucose, oral glucose tolerance, and HbA(1c); and significantly lowered serum triglycerides. LX4211 also mediated trends for lower weight, lower blood pressure, and higher glucagon-like peptide-1 levels. In a follow-up single-dose study in 12 patients with T2DM, LX4211 (300 mg) significantly increased glucagon-like peptide-1 and peptide YY levels relative to pretreatment values, probably by delaying SGLT1-mediated intestinal glucose absorption . LX4211-treated mice and SGLT1-/- mice also had increased GLP-1 AUC values, decreased glucose-dependent insulinotropic polypeptide (GIP) AUC values, and decreased blood glucose excursions during the 6 hours after a challenge with oral glucose alone.
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In VitroLX4211 enhanced urinary glucose excretion by inhibiting SGLT2-mediated renal glucose reabsorption; markedly and significantly improved multiple measures of glycemic control, including fasting plasma glucose, oral glucose tolerance, and HbA(1c); and significantly lowered serum triglycerides. LX4211 also mediated trends for lower weight, lower blood pressure, and higher glucagon-like peptide-1 levels. In a follow-up single-dose study in 12 patients with T2DM, LX4211 (300 mg) significantly increased glucagon-like peptide-1 and peptide YY levels relative to pretreatment values, probably by delaying SGLT1-mediated intestinal glucose absorption . LX4211-treated mice and SGLT1-/- mice also had increased GLP-1 AUC values, decreased glucose-dependent insulinotropic polypeptide (GIP) AUC values, and decreased blood glucose excursions during the 6 hours after a challenge with oral glucose alone .
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In Vivo——
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SynonymsSotagliflozin | LP-802034 | LX4211 | LX 4211
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PathwayGPCR/G Protein
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TargetSGLT
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RecptorSGLT1|SGLT2
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Research AreaMetabolic Disease
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IndicationDiabetes
Chemical Information
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CAS Number1018899-04-1
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Formula Weight424.9382
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Molecular FormulaC21H25ClO5S
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO[C@@H]([C@@H]([C@H]([C@H](C1=CC=C(Cl)C(CC2=CC=C(OCC)C=C2)=C1)O3)O)O)[C@H]3SC
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Chemical Nameβ-L-Xylopyranoside, methyl 5-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-1-thio-, (5S)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Goodwin NC, et al. J Med Chem. 2009 Oct 22;52(20):6201-4.
2. Zambrowicz B, et al. Clin Pharmacol Ther. 2012 Aug;92(2):158-69.
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