Structure Information
Structure

Compound Identification

SMILES

CCN1N=NC(=N1)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=C(NCCN1CCOCC1)N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=CCYUSUQOSHABQD-OVDFTCDZSA-N

Formula

C32H39N11O4

Mass

641.737

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Benzenoid - Morpholine - N-substituted imidazole - Oxazinane - Imidolactam - Monocyclic benzene moiety - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Tetrazole - Oxolane - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - 1,2-diol - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Alcohol - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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