5-oxo-15-HETE - Moligand™ , Agonist of OXE receptor, CAS No.142828-12-4, Agonist of OXE receptor

CAS: 142828-12-4 Cat. No.: O607238 PubChem CID: 6438757

GRADE & PURITY Moligand™

Synonyms

BDBM50338299 | (6E,8Z,11Z,13E,15S)-15-Hydroxy-5-oxo-6,8,11,13-eicosatetraenoic acid | GTPL6167 | 15-hydroxy-5-oxo-eicosa-6(E),8(Z),11(Z),13(E)tetraenoic acid | 6,8,11,13-Eicosatetraenoic acid, 15-hydroxy-5-oxo-, (S-(E,E,Z,Z))- | Q27073999 | DTXSID20115873

Storage

Room temperature

Specifications

Sinónimos

BDBM50338299 | (6E, 8Z, 11Z, 13E, 15S)-15-Hydroxy-5-oxo-6, 8, 11, 13-eicosatetraenoic acid | GTPL6167 | 15-hydroxy-5-oxo-eicosa-6(E), 8(Z), 11(Z), 13(E)tetraenoic acid | 6, 8, 11, 13-Eicosatetraenoic acid, 15-hydroxy-5-oxo-, (S-(E, E, Z, Z))- | Q27073999 | DTXSID20115873

Especificaciones y pureza

Moligand™

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

Moligand™

Tipo de acción

AGONIST

Mecanismo de acción

Agonist of OXE receptor

Nombres e identificadores

• Sonrisas canónicas: CCCCC[C@@H](/C=C/C=C\C/C=C\C=C\C(=O)CCCC(=O)O)O
• IUPAC Name: (6E,8Z,11Z,13E,15S)-15-hydroxy-5-oxoicosa-6,8,11,13-tetraenoic acid
• InChIKey: RIUDRKHGFDAKPO-WWWYWCMOSA-N
• INCHI: 1S/C20H30O4/c1-2-3-9-13-18(21)14-10-7-5-4-6-8-11-15-19(22)16-12-17-20(23)24/h5-8,10-11,14-15,18,21H,2-4,9,12-13,16-17H2,1H3,(H,23,24)/b7-5-,8-6-,14-10+,15-11+/t18-/m0/s1
• Isómeros SMILES: CCCCC[C@@H](/C=C/C=C\C/C=C\C=C\C(=O)CCCC(=O)O)O
• PubChem CID: 6438757

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Eicosanoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Eicosanoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydroxyeicosatetraenoic acids
• Alternative Parents: Long-chain fatty acids Hydroxy fatty acids Unsaturated fatty acids Enones Acryloyl compounds Secondary alcohols Ketones Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Aldehydes
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydroxyeicosatetraenoic acid - Long-chain fatty acid - Hydroxy fatty acid - Fatty acid - Unsaturated fatty acid - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Secondary alcohol - Ketone - Carboxylic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Aldehyde - Organooxygen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydroxyeicosatetraenoic acids. These are eicosanoic acids with an attached hydroxyl group and four CC double bonds.
• 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

Objetivos asociados (humanos)

OXER1 Tchem Oxoeicosanoid receptor 1 (2 Activities)

Discover Target: OXER1

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

Mecanismos de acción