Compound Identification
SMILES
CONC1=NC=NC2=C1N=CN2[C@H]1C[C@H](OP(O)(O)=O)[C@@H](COP(O)(O)=O)O1
InChIKey
InChIKey=CJJFDBWBZJGYIY-XLPZGREQSA-N
Formula
C11H17N5O10P2
Mass
441.23
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleotides
-
Superclass
Nucleosides, nucleotides, and analogues
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
Ribonucleoside 3'-phosphates Purines and purine derivatives Monoalkyl phosphates Pyrimidines and pyrimidine derivatives N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Oxacyclic compounds N-organohydroxylamines Azacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine deoxyribonucleoside 3',5'-bisphosphate - Ribonucleoside 3'-phosphate - Imidazopyrimidine - Purine - Monoalkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - 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