Ertugliflozin L-pyroglutamic acid - ≥99% , CAS No.1210344-83-4

CAS: 1210344-83-4 Cat. No.: E413099 Formule: C₂₇H₃₂ClNO₁₀ Poids moléculaire: 566 Numéro CE: 863-196-4 PubChem CID: 57339449

GRADE & PURITY ≥99%

Synonyms

ERTUGLIFLOZIN PIDOLATE COMPONENT OF SEGLUROMET | D80789 | (S)-5-oxopyrrolidine-2-carboxylic acid compound with (1S,2S,3S,4R,5S)-5-(4-chloro-3-(4-ethoxybenzyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol (1:1) | PF-4971729 | AKOS0376

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Information

Ertugliflozin (MK-8835, PF-04971729) L-pyroglutamic acid is a potent, selective and orally active inhibitor of thesodium-dependent glucose cotransporter 2 (SGLT2)with IC50 of 0.877 nM for h-SGLT2. Ertugliflozin has the potential for the treatment of type 2 diabetes mellitus.

Targets

h-SGLT2 (Cell-free assay) 0.877 nM

Specifications

Synonymes

ERTUGLIFLOZIN PIDOLATE COMPONENT OF SEGLUROMET | D80789 | (S)-5-oxopyrrolidine-2-carboxylic acid compound with (1S,2S,3S,4R,5S)-5-(4-chloro-3-(4-ethoxybenzyl)phenyl)-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol (1:1) | PF-4971729 | AKOS0376

Spécifications et pureté

≥99%

Mécanismes biochimiques et physiologiques

Ertugliflozin (MK-8835, PF-04971729) L-pyroglutamic acid is a potent, selective and orally active inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2) with IC50 of 0.877 nM for h-SGLT2. Ertugliflozin has the potential for the treatment of typ

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥99%

Propriétés du produit

• ALogP: 1.349
• Nombre de HBD: 5
• Liaison rotative: 7

Noms et identifiants

• Pubchem Sid: 504771552
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771552
• Sourires canoniques: CCOC1=CC=C(C=C1)CC2=C(C=CC(=C2)C34C(C(C(C(O3)(CO4)CO)O)O)O)Cl.C1CC(=O)NC1C(=O)O
• IUPAC Name: (1S,2S,3S,4R,5S)-5-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol;(2S)-5-oxopyrrolidine-2-carboxylic acid
• InChIKey: YHIUPZFKHZTLSH-LXYIGGQGSA-N
• INCHI: 1S/C22H25ClO7.C5H7NO3/c1-2-28-16-6-3-13(4-7-16)9-14-10-15(5-8-17(14)23)22-20(27)18(25)19(26)21(11-24,30-22)12-29-22;7-4-2-1-3(6-4)5(8)9/h3-8,10,18-20,24-27H,2,9,11-12H2,1H3;3H,1-2H2,(H,6,7)(H,8,9)/t18-,19-,20+,21-,22-;3-/m00/s1
• Isomères SMILES: CCOC1=CC=C(C=C1)CC2=C(C=CC(=C2)[C@@]34[C@@H]([C@H]([C@@H]([C@@](O3)(CO4)CO)O)O)O)Cl.C1CC(=O)N[C@@H]1C(=O)O
• PubChem CID: 57339449
• Poids moléculaire: 566

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Diphenylmethanes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Diphenylmethanes
• Intermediate Tree Nodes: Not available
• Direct Parent: Diphenylmethanes
• Alternative Parents: Proline and derivatives Pyrrolidine carboxylic acids Phenoxy compounds Phenol ethers Oxoprolines Chlorobenzenes Ketals Oxepanes Alkyl aryl ethers Pyrrolidine-2-ones Monosaccharides Aryl chlorides Oxanes 1,3-dioxolanes Secondary carboxylic acid amides Lactams Secondary alcohols Polyols Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Oxacyclic compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Organochlorides Organonitrogen compounds Organopnictogen compounds Primary alcohols
• Molecular Framework: Not available
• Substituents: Proline or derivatives - Diphenylmethane - Alpha-amino acid or derivatives - Phenol ether - Phenoxy compound - Oxoproline - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Alkyl aryl ether - Ketal - Oxepane - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - 2-pyrrolidone - Pyrrolidone - Oxane - Monosaccharide - Meta-dioxolane - Pyrrolidine - Carboxamide group - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Polyol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Ether - Organoheterocyclic compound - Acetal - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Primary alcohol - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
• 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

Propriétés chimiques et physiques

• Solubilité: Solubility (25°C) In vitro DMSO: 100 mg/mL (176.67 mM); Ethanol: 100 mg/mL (176.67 mM); Water: 10 mg/mL (17.66 mM)
• DMSO (mg/mL) Solubilité maximale: 100
• DMSO (mM) Solubilité maximale: 176.678445229682
• Eau (mg/mL) Solubilité maximale: 10
• Eau (mM) Solubilité maximale: 17.6678445229682
• Poids moléculaire: 566.000 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 565.171 Da
• Monoisotopic Mass: 565.171 Da
• Topological Polar Surface Area: 175.000 Ų
• Heavy Atom Count: 39
• Formal Charge: 0
• Complexity: 740.000
• 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