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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 47 In Stock
5MG 80 In Stock
10MG 120 In Stock
25MG 235 In Stock
50MG 357 In Stock
100MG 531 In Stock
500MG 1134 In Stock
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Biological Information

  • Product Name
    LX-4211
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective SGLT2 inhibitor with IC50 of 14 nM for hSGLT2.
  • Description
    A 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.
  • 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 .
  • In Vivo
    ——
  • Synonyms
    Sotagliflozin | LP-802034 | LX4211 | LX 4211
  • Pathway
    GPCR/G Protein
  • Target
    SGLT
  • Recptor
    SGLT1|SGLT2
  • Research Area
    Metabolic Disease
  • Indication
    Diabetes

Chemical Information

  • CAS Number
    1018899-04-1
  • Formula Weight
    424.9382
  • Molecular Formula
    C21H25ClO5S
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    O[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
  • Chemical Name
    β-L-Xylopyranoside, methyl 5-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-1-thio-, (5S)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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