Compound Identification
SMILES
CCN1CCCC1CNC(=O)CC1=CC=C(S1)C1=NC2=C(C=C1)C(=O)C(C(=O)NC)=C(N)N2CC
InChIKey
InChIKey=BNJUPHYVIJCYRB-UHFFFAOYSA-N
Formula
C25H32N6O3S
Mass
496.63
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazanaphthalenes
- Subclass Naphthyridines
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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
Pyridinecarboxylic acids and derivatives Aminopyridines and derivatives 2,5-disubstituted thiophenes N-alkylpyrrolidines Vinylogous amides Heteroaromatic compounds Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Pyridine carboxylic acid or derivatives - Aminopyridine - 2,5-disubstituted thiophene - Pyridine - N-alkylpyrrolidine - Pyrrolidine - Thiophene - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Tertiary amine - Secondary carboxylic acid amide - Tertiary aliphatic amine - Carboxamide group - Azacycle - Carboxylic acid derivative - Amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Primary amine - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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