Compound Identification
SMILES
COC1CC(O)C(OC)C2=C1C(=O)C1=C(O2)C2=C3C(CC4=CC5=C(C(=O)N(N\C(C)=C(\C)O)C(C)=C5)C(=O)C4=C3C1=O)OCO2
InChIKey
InChIKey=WGPBBJROUQQTBF-SEYXRHQNSA-N
Formula
C32H30N2O11
Mass
618.595
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Naphthopyrans
- Subclass Naphthopyranones
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Class
Naphthopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Naphthopyrans
Subclass
Naphthopyranones
Intermediate Tree Nodes
Not available
Direct Parent
Naphthopyranones
Alternative Parents
Isoquinolones and derivatives Naphthalenes Aryl ketones Pyridinones Pyranones and derivatives Methylpyridines Vinylogous amides Heteroaromatic compounds Secondary alcohols Lactams Acetals Oxacyclic compounds Azacyclic compounds Dialkyl ethers Aldehydes Organopnictogen compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthopyranone - Isoquinolone - Naphthalene - Aryl ketone - Pyranone - Methylpyridine - Pyridinone - Pyran - Pyridine - Heteroaromatic compound - Vinylogous amide - Ketone - Lactam - Secondary alcohol - Acetal - Ether - Dialkyl ether - Oxacycle - Azacycle - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Aldehyde - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthopyranones. These are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.
External Descriptors
Not available