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Technology Process of Luseogliflozin

Luseogliflozin

Base Information
  • Chemical Name:Luseogliflozin
  • CAS No.:898537-18-3
  • Molecular Formula:C23H30O6S
  • Molecular Weight:434.55
  • Hs Code.:
  • UNII:C596HWF74Z
  • ChEMBL ID:CHEMBL1093423
  • DSSTox Substance ID:DTXSID10237921
  • Metabolomics Workbench ID:153243
  • NCI Thesaurus Code:C174652
  • Nikkaji Number:J3.054.663F
  • Pharos Ligand ID:W1VYUY24VD11
  • Wikidata:Q27275212
  • Wikipedia:Luseogliflozin
  • Mol file:898537-18-3.mol
Luseogliflozin

Synonyms:1,5-anhydro-1-(5-(4-ethoxybenzyl)-2-methoxy-4-methylphenyl)-1-thioglucitol;Lusefi;luseogliflozin;TS 071;TS-071;TS071 cpd

Suppliers and Price of Luseogliflozin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Luseogliflozin
  • 10mg
  • $ 15490.00
  • Crysdot
  • Luseogliflozin 95+%
  • 25mg
  • $ 872.00
  • Crysdot
  • Luseogliflozin 95+%
  • 100mg
  • $ 2183.00
  • American Custom Chemicals Corporation
  • (1S)-1,5-DIDEOXY-1,5-EPITHIO-1-C-[5-[(4-ETHOXYPHENYL)METHYL]-2-METHOXY-4-METHYLPHENYL]-D-GLUCITOL 95.00%
  • 10G
  • $ 1712.87
Total 23 raw suppliers
Chemical Property of Luseogliflozin
Chemical Property:
  • Melting Point:155.0-157.0℃ 
  • Boiling Point:624.5±55.0 °C(Predicted) 
  • PKA:13.25±0.70(Predicted) 
  • PSA：124.68000 
  • Density:1.278±0.06 g/cm3(Predicted) 
  • LogP:2.22460 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:7
  • Exact Mass:434.17630985
  • Heavy Atom Count:30
  • Complexity:514
Purity/Quality:

97% *data from raw suppliers

Luseogliflozin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1=CC=C(C=C1)CC2=CC(=C(C=C2C)OC)C3C(C(C(C(S3)CO)O)O)O
  • Isomeric SMILES:CCOC1=CC=C(C=C1)CC2=CC(=C(C=C2C)OC)[C@H]3[C@@H]([C@H]([C@@H]([C@H](S3)CO)O)O)O
  • Recent ClinicalTrials:The Clinical Study to Assess the Effect of the Amount of Carbohydrate Intake and Meals Differing in Glycemic Index (GI) in Patients Treated With a Sodium-dependent Glucose Cotransporter 2 (SGLT2) Inhibitor
  • Recent NIPH Clinical Trials:Effects of SGLT2 inhibitor on gut microbiota in the patients with type 2 diabetes
  • Uses Luseogliflozin is used n biological studies as a potent and selective renal sodium-glucose cotransporter 2 (SGLT2) inhibitor with anti-hyperglycemic activity.
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