GLP-1 receptor agonist 2 - ≥98% , CAS No.2230197-64-3

CAS: 2230197-64-3 Cat. No.: G648746 Peso molecular: 580.05 PubChem CID: 134611104

GRADE & PURITY ≥98%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

GLP-1 receptor agonist 2 is a Glukagon-like peptide-1 receptor (GLP-1R) agonist.

Form:Solid

IC50& Target:GLP-1R

Specifications

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

GLP-1 receptor agonist 2 is a Glukagon-like peptide-1 receptor (GLP-1R) agonist.

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

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

Tipo de acción

AGONIST

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: CC1CN(CCN1CC2=NC3=C(N2CC4CCO4)C=C(C=C3)C(=O)O)C5=NC(=CC=C5)OCC6=C(C=C(C=C6)Cl)F
• IUPAC Name: 2-[[(2S)-4-[6-[(4-chloro-2-fluorophenyl)methoxy]pyridin-2-yl]-2-methylpiperazin-1-yl]methyl]-3-[[(2S)-oxetan-2-yl]methyl]benzimidazole-5-carboxylic acid
• InChIKey: IGXAOFNNKAUXCJ-CVDCTZTESA-N
• INCHI: 1S/C30H31ClFN5O4/c1-19-15-36(27-3-2-4-29(34-27)41-18-21-5-7-22(31)14-24(21)32)11-10-35(19)17-28-33-25-8-6-20(30(38)39)13-26(25)37(28)16-23-9-12-40-23/h2-8,13-14,19,23H,9-12,15-18H2,1H3,(H,38,39)/t19-,23-/m0/s1
• PubChem CID: 134611104
• Peso molecular: 580.05

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Diazinanes
      • Subclass Piperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinylpiperazines
• Alternative Parents: N-arylpiperazines Benzimidazoles Polyhalopyridines Dialkylarylamines N-alkylpiperazines Methylpyridines Hydroxypyridines Heterocyclic fatty acids Halogenated fatty acids Fluorobenzenes Chlorobenzenes Aralkylamines Aminopyridines and derivatives Alkyl aryl ethers 2-halopyridines N-substituted imidazoles Imidolactams Heteroaromatic compounds Trialkylamines Oxetanes Amino acids Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Azacyclic compounds Organopnictogen compounds Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: N-arylpiperazine - Pyridinylpiperazine - Benzimidazole - Polyhalopyridine - Dialkylarylamine - Tertiary aliphatic/aromatic amine - 2-halopyridine - Methylpyridine - Hydroxypyridine - Aralkylamine - N-alkylpiperazine - Heterocyclic fatty acid - Halogenated fatty acid - Halobenzene - Fluorobenzene - Chlorobenzene - Aminopyridine - Alkyl aryl ether - Fatty acyl - Fatty acid - Imidolactam - Benzenoid - Pyridine - N-substituted imidazole - Monocyclic benzene moiety - Heteroaromatic compound - Azole - Amino acid - Tertiary aliphatic amine - Tertiary amine - Oxetane - Amino acid or derivatives - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organochloride - Organohalogen compound - Amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyridinylpiperazines. These are compounds containing a pyridinylpiperazine skeleton, which consists of a pyridine linked (not fused) to a piperazine by a bond by a single bond that is not part of a ring.
• 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

• Solubilidad: DMSO : ≥ 125 mg/mL (215.50 mM)