Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3O)N3C=NC4=C3NC(N)=NC4=O)N3C=NC4=C3NC(N)=NC4=O)[C@@H](COCC3=CC(OCC4=CC=CC=C4)=C(OCC4=CC=CC=C4)C=C3)O2)C(=O)NC1=O

InChIKey

InChIKey=RTLLVDHQUUOHMI-OLSFUZPDSA-N

Formula

C51H56N12O19P2

Mass

1203.022

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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 - Purine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - 6-oxopurine - Hypoxanthine - Benzylether - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Benzenoid - Pyrimidine - Alkyl phosphate - Oxolane - Azole - Vinylogous amide - Imidazole - Heteroaromatic compound - Urea - Secondary alcohol - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Dialkyl ether - Ether - Organic oxide - Alcohol - Hydrocarbon derivative - Primary amine - Organic oxygen compound - Amine - Organonitrogen compound - Organic nitrogen 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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