Compound Identification
SMILES
COC1=NC2=C(C=CN=C2C=C1)[C@@H](O)CN1CCC(CC1)NCC1=CC2=C(SCC(=O)N2)C=C1F
InChIKey
InChIKey=YWRKWLVHPFBAJS-NRFANRHFSA-N
Formula
C25H28FN5O3S
Mass
497.59
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Diazanaphthalenes
- Subclass Naphthyridines
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Class
Diazanaphthalenes
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Naphthyridines
Intermediate Tree Nodes
Not available
Direct Parent
Naphthyridines
Alternative Parents
Benzothiazines Alkyl aryl ethers Alkylarylthioethers Aminopiperidines Aralkylamines Pyridines and derivatives Benzenoids Aryl fluorides 1,4-thiazines Heteroaromatic compounds Secondary carboxylic acid amides Lactams Secondary alcohols Amino acids and derivatives Trialkylamines 1,2-aminoalcohols Dialkylamines Azacyclic compounds Carbonyl compounds Organofluorides Organic oxides Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Benzothiazine - Aryl thioether - Alkyl aryl ether - Aralkylamine - Alkylarylthioether - 4-aminopiperidine - Para-thiazine - Aryl halide - Benzenoid - Aryl fluoride - Piperidine - Pyridine - Heteroaromatic compound - Lactam - 1,2-aminoalcohol - Carboxamide group - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Secondary aliphatic amine - Thioether - Ether - Carboxylic acid derivative - Secondary amine - Azacycle - Organic nitrogen compound - Organohalogen compound - Carbonyl group - Organofluoride - Organonitrogen compound - Organooxygen compound - Aromatic alcohol - Hydrocarbon derivative - Amine - Organic oxide - Alcohol - Organic oxygen 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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