CC1=C2N=C(O1)[C@H](CO[Si](C1=CC=CC=C1)(C1=CC=CC=C1)C(C)(C)C)NC(=O)C1=COC(=N1)C1=COC(=N1)C1=COC(=N1)[C@H](CO)NC(=O)C1=COC(=N1)C1=C(C)OC2=N1

InChIKey=AXXYPASLXXHVQX-HVNZXBJASA-N

C42H38N8O10Si

842.897

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

2-heteroaryl carboxamides Alkylarylsilanes Benzene and substituted derivatives Oxazoles Heteroaromatic compounds Silyl ethers Secondary carboxylic acid amides Lactams Oxacyclic compounds Azacyclic compounds Organoheterosilanes Organic metalloid salts Organonitrogen compounds Hydrocarbon derivatives Primary alcohols Organopnictogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Macrolactam - 2-heteroaryl carboxamide - Alkylarylsilane - Monocyclic benzene moiety - Benzenoid - Azole - Oxazole - Heteroaromatic compound - Carboxamide group - Lactam - Secondary carboxylic acid amide - Silyl ether - Oxacycle - Carboxylic acid derivative - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organoheterosilane - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organic oxygen compound - Alcohol - Primary alcohol - Organic nitrogen compound - Organopnictogen compound - Organosilicon compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Not available