Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(COCCOP(O)(=O)O[C@H]1[C@@H](O[C@H](COP(O)(=O)O[C@H]3[C@@H](O[C@H](CO)[C@@H]3N=[N+]=[N-])N3C=NC4=C3N=CN=C4N)[C@@H]1N=[N+]=[N-])N1C=NC3=C1N=CN=C3N)C=N2

InChIKey

InChIKey=YVTVOXBOXXFXLX-UREOUGFISA-N

Formula

C28H33N21O13P2

Mass

933.654

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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 2',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine deoxyribonucleoside 2',5'-bisphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Imidolactam - Alkyl phosphate - Pyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Azo compound - Azo imide - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic zwitterion - Alcohol - Organic oxygen compound - Organic nitrogen compound - Amine - Primary amine - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organic salt - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 2',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 3.

External Descriptors

Not available

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