Benzoic acid, 4-(((2,3-dihydro-6-((2-methylpropyl)(2-thiazolylsulfonyl)amino)-1H-inden-5-yl)oxy)methyl)-3-methyl- , Prostanoid EP1 receptor antagonist, CAS No.459842-29-6, Prostanoid EP1 receptor antagonist

CAS: 459842-29-6 Cat. No.: B671153 Peso molecular: 500.6 PubChem CID: 23106477

Synonyms

ONO-8539 | DB15325 | 3-methyl-4-((6-(2-methylpropyl(1,3-thiazol-2-ylsulfonyl)amino)-2,3-dihydro-1-(H)-inden-5-yl)oxymethyl)benzoic acid | US9181187, Compound A | 94W010PZ1Z | SCHEMBL214853 | Benzoic acid, 4-(((2,3-dihydro-6-((2-methylpropyl)(2-thiazolylsu

Storage

Room temperature

Specifications

Sinónimos

ONO-8539 | DB15325 | 3-methyl-4-((6-(2-methylpropyl(1, 3-thiazol-2-ylsulfonyl)amino)-2, 3-dihydro-1-(H)-inden-5-yl)oxymethyl)benzoic acid | US9181187, Compound A | 94W010PZ1Z | SCHEMBL214853 | Benzoic acid, 4-(((2, 3-dihydro-6-((2-methylpropyl)(2-thiazolylsu

Condiciones de almacenamiento de almacenamiento

Room temperature

Tipo de acción

ANTAGONIST

Mecanismo de acción

Prostanoid EP1 receptor antagonist

Propiedades del producto

• ALogP: 5.5

Nombres e identificadores

• Sonrisas canónicas: CC1=C(C=CC(=C1)C(=O)O)COC2=C(C=C3CCCC3=C2)N(CC(C)C)S(=O)(=O)C4=NC=CS4
• IUPAC Name: 3-methyl-4-[[6-[2-methylpropyl(1,3-thiazol-2-ylsulfonyl)amino]-2,3-dihydro-1H-inden-5-yl]oxymethyl]benzoic acid
• InChIKey: ALLLQQUASFFEKP-UHFFFAOYSA-N
• INCHI: 1S/C25H28N2O5S2/c1-16(2)14-27(34(30,31)25-26-9-10-33-25)22-12-18-5-4-6-19(18)13-23(22)32-15-21-8-7-20(24(28)29)11-17(21)3/h7-13,16H,4-6,14-15H2,1-3H3,(H,28,29)
• Isómeros SMILES: CC1=C(C=CC(=C1)C(=O)O)COC2=C(C=C3CCCC3=C2)N(CC(C)C)S(=O)(=O)C4=NC=CS4
• PubChem CID: 23106477
• Peso molecular: 500.6

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Sulfanilides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Sulfanilides
• Intermediate Tree Nodes: Not available
• Direct Parent: Sulfanilides
• Alternative Parents: Indanes Benzoic acids Benzoyl derivatives Toluenes Alkyl aryl ethers Organosulfonamides Thiazoles Heteroaromatic compounds Aminosulfonyl compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Sulfanilide - Indane - Benzoic acid - Benzoic acid or derivatives - Benzoyl - Toluene - Alkyl aryl ether - Organosulfonic acid amide - Heteroaromatic compound - Aminosulfonyl compound - Thiazole - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azole - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.
• 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

Mecanismos de acción