Ipragliflozin L-Proline - 10mM in DMSO , Sodium/glucose cotransporter 2 inhibitor, CAS No.951382-34-6, Sodium/glucose cotransporter 2 inhibitor

CAS: 951382-34-6 Cat. No.: I427062 Fórmula: C₂₆H₃₀FNO₇S Peso molecular: 519.58 PubChem CID: 57339444

CALIDAD & PUREZA 10mM in DMSO

Synonyms

IPRAGLIFLOZIN L-PROLINE [WHO-DD] | (2S,3R,4R,5S,6R)-2-(3-(Benzo[b]thiophen-2-ylmethyl)-4-fluorophenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (S)-Pyrrolidine-2-carboxylic acid | Suglat (TN) | AMY16735 | Ipragliflozin L-proline (JAN) | L-proline

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

Information

Ipragliflozin L-Proline is an orally active and selective inhibitor ofSGLT2with IC50 of 7.38 nM, 6.73 nM and 5.64 nM for human SGLT2, rat SGLT2 and mouse SGLT2, respectively.

Targets

mouse SGLT2 (Cell-free assay); rat SGLT2 (Cell-free assay); human SGLT2 (Cell-free assay) 5.64 nM; 6.73 nM; 7.38 nM

Especificaciones

Sinónimos

IPRAGLIFLOZIN L-PROLINE [WHO-DD] | (2S,3R,4R,5S,6R)-2-(3-(Benzo[b]thiophen-2-ylmethyl)-4-fluorophenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (S)-Pyrrolidine-2-carboxylic acid | Suglat (TN) | AMY16735 | Ipragliflozin L-proline (JAN) | L-proline

Especificaciones y pureza

10mM in DMSO

Mecanismos bioquímicos y fisiológicos

Ipragliflozin L-Proline is an orally active and selective inhibitor of SGLT2 with IC50 of 7.38 nM, 6.73 nM and 5.64 nM for human SGLT2, rat SGLT2 and mouse SGLT2, respectively.

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Tipo de acción

INHIBITOR

Mecanismo de acción

Sodium/glucose cotransporter 2 inhibitor

Nombres e identificadores

Pubchem Sid

528769927

Sonrisas canónicas

C1CC(NC1)C(=O)O.C1=CC=C2C(=C1)C=C(S2)CC3=C(C=CC(=C3)C4C(C(C(C(O4)CO)O)O)O)F

IUPAC Name

(2S,3R,4R,5S,6R)-2-[3-(1-benzothiophen-2-ylmethyl)-4-fluorophenyl]-6-(hydroxymethyl)oxane-3,4,5-triol;(2S)-pyrrolidine-2-carboxylic acid

InChIKey

TUVGWWULBZIUBS-FVYIYGEMSA-N

INCHI

1S/C21H21FO5S.C5H9NO2/c22-15-6-5-12(21-20(26)19(25)18(24)16(10-23)27-21)7-13(15)9-14-8-11-3-1-2-4-17(11)28-14;7-5(8)4-2-1-3-6-4/h1-8,16,18-21,23-26H,9-10H2;4,6H,1-3H2,(H,7,8)/t16-,18-,19+,20-,21+;4-/m10/s1

Isómeros SMILES

C1C[C@H](NC1)C(=O)O.C1=CC=C2C(=C1)C=C(S2)CC3=C(C=CC(=C3)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)F

PubChem CID

57339444

Peso molecular

519.58

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Phenolic glycosides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Phenolic glycosides
• Alternative Parents: Proline and derivatives Hexoses C-glycosyl compounds L-alpha-amino acids 1-benzothiophenes Pyrrolidine carboxylic acids 2,3,5-trisubstituted thiophenes Fluorobenzenes Oxanes Aryl fluorides Heteroaromatic compounds 1,2-diols Amino acids Secondary alcohols Monocarboxylic acids and derivatives Dialkylamines Dialkyl ethers Carboxylic acids Azacyclic compounds Oxacyclic compounds Organic oxides Carbonyl compounds Organofluorides Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Not available
• Substituents: Phenolic glycoside - Proline or derivatives - Hexose monosaccharide - C-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - 1-benzothiophene - Benzothiophene - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - 2,3,5-trisubstituted thiophene - Fluorobenzene - Halobenzene - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Oxane - Thiophene - Heteroaromatic compound - Pyrrolidine - Secondary alcohol - Amino acid - 1,2-diol - Amino acid or derivatives - Monocarboxylic acid or derivatives - Oxacycle - Secondary amine - Carboxylic acid derivative - Ether - Secondary aliphatic amine - Dialkyl ether - Azacycle - Organoheterocyclic compound - Carboxylic acid - Polyol - Organic nitrogen compound - Carbonyl group - Organohalogen compound - Organofluoride - Organonitrogen compound - Primary alcohol - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Peso molecular: 519.600 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 5
• Exact Mass: 519.173 Da
• Monoisotopic Mass: 519.173 Da
• Topological Polar Surface Area: 168.000 Ų
• Heavy Atom Count: 36
• Formal Charge: 0
• Complexity: 628.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 6
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3