Compound Identification
SMILES
COC1=CN=C2C=CC(=O)N(CCN3CC[C@H](NCC4=CC(Cl)=C(CO)N=C4)[C@H](O)C3)C2=C1
InChIKey
InChIKey=SMPUDTYJUOWOTB-SIKLNZKXSA-N
Formula
C23H28ClN5O4
Mass
473.96
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazanaphthalenes
- Subclass Naphthyridines
-
Class
Diazanaphthalenes
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Naphthyridines
Intermediate Tree Nodes
Not available
Direct Parent
Naphthyridines
Alternative Parents
Pyridinones Alkyl aryl ethers Aminopiperidines Aralkylamines Aryl chlorides Heteroaromatic compounds Trialkylamines Secondary alcohols 1,2-aminoalcohols Lactams Dialkylamines Azacyclic compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides Organochlorides Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Alkyl aryl ether - 4-aminopiperidine - Aralkylamine - Pyridinone - Aryl chloride - Aryl halide - Pyridine - Piperidine - Heteroaromatic compound - 1,2-aminoalcohol - Lactam - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Azacycle - Secondary aliphatic amine - Ether - Secondary amine - Organohalogen compound - Amine - Aromatic alcohol - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
External Descriptors
Not available