Compound Identification
SMILES
CCN1C[C@H](C)N2C3C(C(O)=C2C1=O)C(=O)N1CC2=C(OCCCCN4CCN(C3=N1)S4(=O)=O)C=C(F)C=C2
InChIKey
InChIKey=AMMINHBKPQIZNQ-VMEOHVCESA-N
Formula
C25H31FN6O6S
Mass
562.62
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
Alpha amino acids and derivatives Pyridazinones Alkyl aryl ethers N-alkylpiperazines Imidolactams Aryl fluorides Benzenoids Vinylogous acids Thiadiazolidines Tertiary carboxylic acid amides Pyrrolines Organic sulfuric acids and derivatives Trialkylamines Amidrazones Lactams Oxacyclic compounds Amidines Azacyclic compounds Enamines Hydrocarbon derivatives Organofluorides Organic oxides Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid or derivatives - Alkyl aryl ether - Pyridazinone - N-alkylpiperazine - Aryl fluoride - Pyridazine - Piperazine - Aryl halide - Benzenoid - 1,4-diazinane - Imidolactam - Thiadiazolidine - Pyrroline - Vinylogous acid - Organic sulfuric acid or derivatives - Tertiary carboxylic acid amide - Carboxylic acid amidrazone - Amino acid or derivatives - Carboxamide group - Lactam - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Amidine - Ether - Enamine - Oxacycle - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen 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