Structure Information
Structure

Compound Identification

SMILES

COC1=C(C)C(=O)C2=C(C(C)=C3[13CH2]C(CCN23)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)C1=O

InChIKey

InChIKey=GTYKFFLDOFDCPV-BRFAVWQFSA-N

Formula

C25H29N6O10P

Mass

605.505

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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 monophosphates

Direct Parent

Purine 2'-deoxyribonucleoside monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Indole or derivatives - Purine - Aryl ketone - Aminopyrimidine - Pyrimidone - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Substituted pyrrole - Alkyl phosphate - Vinylogous amide - Vinylogous ester - Azole - Pyrrole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Ketone - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organic nitrogen compound - Amine - Organic oxygen compound - Primary amine - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

External Descriptors

Not available

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