Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=C(COC2=C(OCC3=CC=C(C=C3)[N+]([O-])=O)\C(OC2=O)=C\CN2C=NC3=C2N=CN=C3Cl)C=C1

InChIKey

InChIKey=UDKAVQZAAGEEIO-OCKHKDLRSA-N

Formula

C25H17ClN6O8

Mass

564.9

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Imidazopyrimidines

Subclass

Purines and purine derivatives

Intermediate Tree Nodes

Not available

Direct Parent

Purines and purine derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Nitrobenzene - Purine - Nitroaromatic compound - Halopyrimidine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - 2-furanone - N-substituted imidazole - Pyrimidine - Benzenoid - Azole - Dihydrofuran - Enol ester - Imidazole - Heteroaromatic compound - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous ester - Organic nitro compound - C-nitro compound - Carboxylic acid ester - Lactone - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Organic salt - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purines and purine derivatives. These are aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring.

External Descriptors

Not available

Previous Back Next