Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)[C@@H]1CO[C@H](COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(O)=O)N2C=NC3=C2N=CN=C3N)[C@H]1O

InChIKey

InChIKey=LPGFNCONVZCCCG-PMTXTEDRSA-N

Formula

C19H26N8O12P2

Mass

620.409

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine deoxyribonucleotides

Intermediate Tree Nodes

Purine deoxyribonucleoside bisphosphates

Direct Parent

Purine deoxyribonucleoside 3',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine deoxyribonucleoside 3',5'-bisphosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - Purine - Imidazopyrimidine - Pyrimidone - Aminopyrimidine - Monoalkyl phosphate - Dialkyl phosphate - Hydropyrimidine - Imidolactam - Alkyl phosphate - Pyrimidine - Primary aromatic amine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Organic oxygen compound - Organic oxide - Alcohol - Organopnictogen compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Primary amine - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 3',5'-bisphosphates. These are purine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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