COOH - Moligand™ , Agonist of Peroxisome proliferator-activated receptor-γ, CAS No.209808-51-5, Agonist of Peroxisome proliferator-activated receptor-γ

CAS: 209808-51-5 Cat. No.: C609545 PubChem CID: 10025649

GRADE & PURITY Moligand™

Synonyms

L 805645 | 2-(2-(4-phenoxy-2-propylphenoxy)ethyl)indole-5-acetic acid | 1H-Indole-5-acetic acid, 2-(2-(4-Phenoxy-2-propylphenoxy)ethyl)- | GTPL2715 | COOH | Q27076884 | 2-[2-(4-Phenoxy-2-propylphenoxy)ethyl]-1H-indole-5-acetic acid | DTXSID30434399 | LS-1

Storage

Room temperature

Specifications

Synonyms

L 805645 | 2-(2-(4-phenoxy-2-propylphenoxy)ethyl)indole-5-acetic acid | 1H-Indole-5-acetic acid, 2-(2-(4-Phenoxy-2-propylphenoxy)ethyl)- | GTPL2715 | COOH | Q27076884 | 2-[2-(4-Phenoxy-2-propylphenoxy)ethyl]-1H-indole-5-acetic acid | DTXSID30434399 | LS-1

Specifications & Purity

Moligand™

Storage

Room temperature

Grade

Moligand™

Action Type

AGONIST

Mechanism of action

Agonist of Peroxisome proliferator-activated receptor-γ

Names and Identifiers

• Canonical Smiles: CCCC1=C(C=CC(=C1)OC2=CC=CC=C2)OCCC3=CC4=C(N3)C=CC(=C4)CC(=O)O
• IUPAC Name: 2-[2-[2-(4-phenoxy-2-propylphenoxy)ethyl]-1H-indol-5-yl]acetic acid
• InChIKey: DFFOSEJNFZUOSK-UHFFFAOYSA-N
• INCHI: 1S/C27H27NO4/c1-2-6-20-18-24(32-23-7-4-3-5-8-23)10-12-26(20)31-14-13-22-17-21-15-19(16-27(29)30)9-11-25(21)28-22/h3-5,7-12,15,17-18,28H,2,6,13-14,16H2,1H3,(H,29,30)
• Isomeric SMILES: CCCC1=C(C=CC(=C1)OC2=CC=CC=C2)OCCC3=CC4=C(N3)C=CC(=C4)CC(=O)O
• Alternate CAS: 209808-51-5
• PubChem CID: 10025649
• MeSH Entry Terms: 2-(2-(4-phenoxy-2-propylphenoxy)ethyl)indole-5-acetic acid;2-PPPE-IAA;PPEIA cpd

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Diphenylethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Diphenylethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Diphenylethers
• Alternative Parents: Indolyl carboxylic acids and derivatives Diarylethers Indoles Phenylpropanes Phenoxy compounds Phenol ethers Alkyl aryl ethers Substituted pyrroles Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Diphenylether - Indolyl carboxylic acid derivative - Diaryl ether - Indole - Indole or derivatives - Phenylpropane - Phenoxy compound - Phenol ether - Alkyl aryl ether - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Azacycle - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.
• 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

Associated Targets(Human)

PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)

Discover Target: PPARG

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)