CC[C@H](C(=O)NC\C=C\C=C(\C)[C@H](OC)[C@@H](C)[C@H](O)[C@@H](O)\C=C\C=C\C=C\C=C(/C)\C(\O)=C1\C(=O)C=CN(C)C1=O)[C@]1(O)C[C@H](O)C(C)(C)[C@@H](O1)\C=C\C=C/C

InChIKey=JKQJDRQAQBSLDH-JXQRJNBJSA-N

C44H62N2O10

778.984

Organic compounds

Organoheterocyclic compounds

Pyridines and derivatives

Hydropyridines

Not available

Tetrahydropyridines

Oxanes N-acyl amines Vinylogous amides Vinylogous acids Tertiary carboxylic acid amides Secondary carboxylic acid amides Secondary alcohols Cyclic ketones Hemiacetals Lactams Azacyclic compounds Polyols Dialkyl ethers Enols Oxacyclic compounds Hydrocarbon derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides

Aliphatic heteromonocyclic compounds

Tetrahydropyridine - Fatty amide - N-acyl-amine - Oxane - Fatty acyl - Vinylogous amide - Vinylogous acid - Tertiary carboxylic acid amide - Hemiacetal - Ketone - Carboxamide group - Cyclic ketone - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Enol - Ether - Oxacycle - Azacycle - Polyol - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Aliphatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as tetrahydropyridines. These are derivatives of pyridine in which two double bonds in the pyridine moiety are reduced by adding four hydrogen atoms.

Not available