Compound Identification
SMILES
NC1=NC(=O)C2=C(N1)N(C=N2)C1CCC(COP([O-])(=O)OP([O-])(=O)OP([O-])(=O)OC2=CC3=C(C=C2)N=C2C=CC(=O)C=C2O3)O1
InChIKey
InChIKey=VSCMDGJEMORLMD-UHFFFAOYSA-K
Formula
C22H18N6O14P3
Mass
683.337
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 triphosphates
Direct Parent
Purine 2',3'-dideoxyribonucleoside triphosphates
Alternative Parents
Purine 2',3'-dideoxyribonucleosides Phenoxazines 6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Alkyl phosphates Benzenoids N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides Cyclic ketones Azacyclic compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides Organic anions
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine 2',3'-dideoxyribonucleoside triphosphate - Purine 2',3'-dideoxyribonucleoside - Purine nucleoside - Phenoxazine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Benzenoid - Alkyl phosphate - Azole - Heteroaromatic compound - Oxolane - Vinylogous amide - Imidazole - Cyclic ketone - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organic oxide - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic anion - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleoside triphosphates. These are purine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.
External Descriptors
Not available