Structure Information
Structure

Compound Identification

SMILES

CCOC1=C(OC)C=C2C(=C1)[C@H]1C[C@@H](CC[C@H]1N=C2C1=CN=C(SC)N=C1)OC(=O)CCC(=O)C(=O)O[C@@H]1CC[C@H]2N=C(C3=CN=C(SC)N=C3)C3=CC(OC)=C(OCC)C=C3[C@H]2C1

InChIKey

InChIKey=LSINWERFRJBGAB-LNKSCYCASA-N

Formula

C47H52N6O9S2

Mass

909.09

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Quinolines and derivatives

Subclass

Benzoquinolines

Intermediate Tree Nodes

Not available

Direct Parent

Phenanthridines and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phenanthridine - Dihydroisoquinoline - Aryl thioether - Anisole - Phenol ether - Gamma-keto acid - Alkyl aryl ether - Fatty acid ester - Alkylarylthioether - Keto acid - Alpha-keto acid - Pyrimidine - Benzenoid - Fatty acyl - Dicarboxylic acid or derivatives - Heteroaromatic compound - Carboxylic acid ester - Ketone - Ketimine - Carboxylic acid derivative - Azacycle - Organic 1,3-dipolar compound - Ether - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Imine - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included.

External Descriptors

Not available

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