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Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O[P+](=O)OCCCCCCO)[C@@H](CO[P+](=O)O[C@H]3C[C@@H](O[C@@H]3CO[P+](=O)O[C@H]3C[C@@H](O[C@@H]3CO[P+](=O)O[C@H]3C[C@@H](O[C@@H]3CO[P+](=O)OCCCCCCO)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3NC(N)=NC4=O)O2)C(=O)NC1=O

InChIKey

InChIKey=HEOFXRUYPFBWOU-HCMXSAOCSA-Q

Formula

C51H71N15O25P5

Mass

1449.075

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Deoxyribo- and ribonucleoside phosphonates

Subclass

Purine ribonucleoside phosphonates

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside phosphonates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside phosphonate - 6-aminopurine - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Hydropyrimidine - Pyrimidine - Imidolactam - Oxolane - Azole - Vinylogous amide - Imidazole - Heteroaromatic compound - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside phosphonates. These are n-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.

External Descriptors

Not available

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