Compound Identification
SMILES
CCC(O)(CC)C(=O)N[C@H]1CC2=CC3=C(OC4NC5=C6C=CC=C5C34C3=C(N=C(O3)[C@@H](NC1=O)C(C)C)C1=NC=C(O1)C1=CNC3=C(OP(O)(O)=O)C=CC6=C13)C=C2
InChIKey
InChIKey=HCSIGLASGYFOSQ-TYKOKSJISA-N
Formula
C41H39N6O10P
Mass
806.769
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Macrolactams
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Macrolactams
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Macrolactams
Alternative Parents
N-acyl-alpha amino acids and derivatives Aryl phosphomonoesters Coumarans Indolines Indoles Secondary alkylarylamines Benzenoids N-acyl amines Tertiary alcohols Pyrroles Oxazoles Heteroaromatic compounds Secondary carboxylic acid amides Lactams Oxacyclic compounds Azacyclic compounds Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Aryl phosphate - Aryl phosphomonoester - Indole - Coumaran - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Fatty amide - N-acyl-amine - Fatty acyl - Benzenoid - Organic phosphoric acid derivative - Phosphoric acid ester - Azole - Heteroaromatic compound - Tertiary alcohol - Oxazole - Pyrrole - Secondary carboxylic acid amide - Lactam - Amino acid or derivatives - Carboxamide group - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organonitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Organooxygen compound - Organic nitrogen compound - Amine - Aromatic heteropolycyclic compound
Description
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.
External Descriptors
Not available