Compound Identification
SMILES
CC1=C2CCC3(CCN(CC3)C3=NN=C(C=C3)C(=O)NCC(O)C3=CN=CC=C3)OC2=CC=C1
InChIKey
InChIKey=JRWYOUUHSXSYPM-UHFFFAOYSA-N
Formula
C26H29N5O3
Mass
459.55
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
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Class
Benzopyrans
- Subclass 1-benzopyrans
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Class
Benzopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Benzopyrans
Subclass
1-benzopyrans
Intermediate Tree Nodes
Not available
Direct Parent
1-benzopyrans
Alternative Parents
2-heteroaryl carboxamides Dialkylarylamines Alkyl aryl ethers Aminopyridazines Pyridines and derivatives Piperidines Imidolactams Benzenoids Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Aromatic alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-benzopyran - 2-heteroaryl carboxamide - Dialkylarylamine - Alkyl aryl ether - Aminopyridazine - Piperidine - Pyridazine - Imidolactam - Benzenoid - Pyridine - Heteroaromatic compound - Amino acid or derivatives - Carboxamide group - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Ether - Oxacycle - Azacycle - Organonitrogen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organic oxygen compound - Aromatic alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.
External Descriptors
Not available