Compound Identification
SMILES
CNC1=NC(Cl)=NC2=C1N=CN2[C@H]1C[C@@H](OP(O)(O)=O)[C@@H](COP(O)(O)=O)O1
InChIKey
InChIKey=AWSMOXWWSLFSCL-FSDSQADBSA-N
Formula
C11H16ClN5O9P2
Mass
459.67
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleotides
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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 6-alkylaminopurines Secondary alkylarylamines 2-halopyrimidines Aminopyrimidines and derivatives Monoalkyl phosphates Aryl chlorides N-substituted imidazoles Imidolactams Oxolanes Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Organic oxides Organochlorides Organooxygen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine deoxyribonucleoside 3',5'-bisphosphate - Ribonucleoside 3'-phosphate - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - 2-halopyrimidine - Secondary aliphatic/aromatic amine - Halopyrimidine - Organic phosphoric acid derivative - Aryl chloride - Aryl halide - Imidolactam - Alkyl phosphate - N-substituted imidazole - Pyrimidine - Phosphoric acid ester - Imidazole - Oxolane - Azole - Heteroaromatic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organic oxygen compound - Amine - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organohalogen compound - Organonitrogen compound - Organochloride - 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