Structure Information
Structure

Compound Identification

SMILES

[H]\C1=C([H])\[C@@]2([H])[C@]([H])(O)C(C)=C(C)[C@@]3([H])[C@]([H])(C)N=C(O)[C@@]23C(=O)C[C@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]2(C)O[C@]2([H])[C@@]([H])(C)C1

InChIKey

InChIKey=LTGOLMNNBPAJGR-GOOCXTAHSA-N

Formula

C27H34N6O4

Mass

506.607

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Imidazopyrimidines

Subclass

Purines and purine derivatives

Intermediate Tree Nodes

Not available

Direct Parent

6-aminopurines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

6-aminopurine - Isoindole or derivatives - Aminopyrimidine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Cyclic carboximidic acid - Pyrroline - Ketone - Secondary alcohol - Dialkyl ether - Oxirane - Ether - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Organopnictogen compound - Carbonyl group - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. 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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