Structure Information
Structure

Compound Identification

SMILES

CCN1N=NN=C1[C@H]1O[C@H]([C@@H]2OP(O)(=O)O[C@H]12)N1C=NC2=C1N=C(NC)N=C2NC(CO)CC1=CC=C(OC)C=C1

InChIKey

InChIKey=KTMMFPFKXNGHRI-IZCMTSBYSA-N

Formula

C23H29N10O7P

Mass

588.522

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Ribonucleoside 3'-phosphates

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Ribonucleoside 3'-phosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Ribonucleoside 3'-phosphate - 6-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Purine - Imidazopyrimidine - Phenoxy compound - Phenol ether - Methoxybenzene - Anisole - Alkyl aryl ether - Secondary aliphatic/aromatic amine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Benzenoid - Organic phosphoric acid derivative - Monocyclic benzene moiety - Pyrimidine - Heteroaromatic compound - Azole - 1,3_dioxaphospholane - Imidazole - Tetrazole - Oxolane - Organoheterocyclic compound - Azacycle - Ether - Oxacycle - Secondary amine - Amine - Organic oxygen compound - Alcohol - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as ribonucleoside 3'-phosphates. These are ribonucleosides that contain a phosphate group attached to the C-3 carbon of the ribose or deoxyribose moiety. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

Previous Back Next