Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(=O)OC3=CC=CC=C3)O2)C(=O)NC1=O
InChIKey
InChIKey=ZLHPERFFKWXVJK-BFHYXJOUSA-N
Formula
C16H21N2O14P3
Mass
558.265
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleotides
Subclass
Pyrimidine deoxyribonucleotides
Intermediate Tree Nodes
Pyrimidine deoxyribonucleoside triphosphates
Direct Parent
Pyrimidine 2'-deoxyribonucleoside triphosphates
Alternative Parents
Phenoxy compounds Pyrimidones Monoalkyl phosphates Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Secondary alcohols Lactams Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine 2'-deoxyribonucleoside triphosphate - Phenoxy compound - Pyrimidone - Monoalkyl phosphate - Pyrimidine - Monocyclic benzene moiety - Alkyl phosphate - Hydropyrimidine - Benzenoid - Phosphoric acid ester - Organic phosphoric acid derivative - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - Urea - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside triphosphates. These are pyrimidine nucleotides with a triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
External Descriptors
Not available