Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@@H]2OP(O)(=O)O[C@H]12)N1C=NC2=C1N=C(Cl)N=C2NC1(CO)CCCC1

InChIKey

InChIKey=MGNYKSKPLMGRPG-IDTAVKCVSA-N

Formula

C16H21ClN5O7P

Mass

461.8

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Cyclic purine nucleotides

Intermediate Tree Nodes

Not available

Direct Parent

2',3'-cyclic purine nucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',3'-cyclic purine ribonucleotide - Ribonucleoside 3'-phosphate - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - 2-halopyrimidine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Halopyrimidine - Aryl chloride - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Monosaccharide - Aryl halide - Pyrimidine - Heteroaromatic compound - Azole - 1,3_dioxaphospholane - Imidazole - Oxolane - Secondary amine - Organoheterocyclic compound - Azacycle - Oxacycle - Organohalogen compound - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',3'-cyclic purine nucleotides. These are purine nucleotides in which the oxygen atoms linked to the C2 and C3 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.

External Descriptors

Not available

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