Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)C1OC(CO[P+](=O)OC2C(CO[P+](=O)OC3C(CO[P+](=O)OC4C(CO[P+](=O)OC5C(CO[P+](=O)OC6C(CO[P+](=O)OC7C(CO[P+](=O)OC8C(CO[P+](=O)OC9C(CO[P+](=O)OC%10C(CO)OC(N%11C=CC(N)=NC%11=O)C%10(F)F)OC(N%10C=CC(N)=NC%10=O)C9(F)F)OC(N9C=CC(N)=NC9=O)C8(F)F)OC(N8C=CC(N)=NC8=O)C7(F)F)OC(N7C=CC(N)=NC7=O)C6(F)F)OC(N6C=CC(N)=NC6=O)C5(F)F)OC(N5C=CC(N)=NC5=O)C4(F)F)OC(N4C=CC(N)=NC4=O)C3(F)F)OC(N3C=CC(N)=NC3=O)C2(F)F)C(O)C1(F)F

InChIKey

InChIKey=YGWQAZCOAPWRBC-UHFFFAOYSA-W

Formula

C90H92F20N30O49P9

Mass

3036.614

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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 heteromonocyclic compounds

Substituents

Purine ribonucleoside phosphonate - Pyrimidine 2'-deoxyribonucleoside - Pyrimidine nucleoside - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Pyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Secondary alcohol - Fluorohydrin - Halohydrin - Organoheterocyclic compound - Oxacycle - Azacycle - Alkyl halide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alcohol - Organic oxide - Alkyl fluoride - Organic nitrogen compound - Amine - Organic cation - Aromatic heteromonocyclic 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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