Structure Information
Structure

Compound Identification

SMILES

CCN(CC)C1=NC(C)=C2N=C(SCC(=O)NCCCN)N(CCNC3=NC(N)=NC4=C3NC=N4)C2=N1

InChIKey

InChIKey=NNVYGOUXMXWRPW-UHFFFAOYSA-N

Formula

C22H33N13OS

Mass

527.66

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Imidazopyrimidines

Subclass

Purines and purine derivatives

Intermediate Tree Nodes

6-aminopurines

Direct Parent

6-alkylaminopurines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

6-alkylaminopurine - Aryl thioether - Dialkylarylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Alkylarylthioether - N-substituted imidazole - Pyrimidine - Imidolactam - Heteroaromatic compound - Azole - Imidazole - Carboxamide group - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary amine - Thioether - Secondary amine - Azacycle - Carboxylic acid derivative - Sulfenyl compound - Organic oxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organooxygen compound - Organosulfur compound - Primary amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.

External Descriptors

Not available

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