CCOC(=O)C1=C(CSC2=NC3=C(CC(CC3)C(C)(C)C)C=C2C#N)N(C)C(=O)NC1C1=CC=C(OC)C=C1

InChIKey=HTJJQHLBHVZXAK-UHFFFAOYSA-N

C30H36N4O4S

548.7

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Hydroquinolines

Not available

Hydroquinolines

Hydropyrimidine carboxylic acids and derivatives Anisoles Methoxybenzenes Phenoxy compounds Alkyl aryl ethers Alkylarylthioethers Pyrimidones Pyridines and derivatives Vinylogous amides Heteroaromatic compounds Enoate esters Ureas Nitriles Monocarboxylic acids and derivatives Azacyclic compounds Sulfenyl compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Tetrahydroquinoline - Hydropyrimidine carboxylic acid derivative - Phenoxy compound - Aryl thioether - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Pyrimidone - Alkylarylthioether - Monocyclic benzene moiety - Hydropyrimidine - 1,2,3,4-tetrahydropyrimidine - Pyridine - Pyrimidine - Benzenoid - Vinylogous amide - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Urea - Carboxylic acid ester - Thioether - Azacycle - Carboxylic acid derivative - Sulfenyl compound - Ether - Monocarboxylic acid or derivatives - Carbonitrile - Nitrile - Organic oxygen compound - Cyanide - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.

Not available