Compound Identification
SMILES
CCSC1=NC2=C(N=CN2C2CC(OP(O)(O)=O)C(COP(O)(O)=O)O2)C(NC)=N1
InChIKey
InChIKey=DZGOMQYNNHDHEU-UHFFFAOYSA-N
Formula
C13H21N5O9P2S
Mass
485.34
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 Alkylarylthioethers Aminopyrimidines and derivatives Monoalkyl phosphates Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organooxygen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine deoxyribonucleoside 3',5'-bisphosphate - Ribonucleoside 3'-phosphate - 6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - Aryl thioether - Aminopyrimidine - Monoalkyl phosphate - Alkylarylthioether - Secondary aliphatic/aromatic amine - Pyrimidine - Phosphoric acid ester - Imidolactam - Organic phosphoric acid derivative - N-substituted imidazole - Alkyl phosphate - Oxolane - Heteroaromatic compound - Imidazole - Azole - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Secondary amine - Organic oxygen compound - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - 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