Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](SCCNC(=O)OC(C)(C)C)[C@@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)O2)C(=O)NC1=O
InChIKey
InChIKey=TYZQSVVFUHLHST-FRRDWIJNSA-J
Formula
C17H26N3O15P3S
Mass
637.38
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleotides
Subclass
Pyrimidine deoxyribonucleotides
Intermediate Tree Nodes
Pyrimidine deoxyribonucleoside triphosphates
Direct Parent
Pyrimidine 2',3'-dideoxyribonucleoside triphosphates
Alternative Parents
2',3'-dideoxy-3'-thionucleoside triphosphates 2',3'-dideoxy-3'-thionucleosides Pyrimidones Alkyl phosphates Hydropyrimidines Vinylogous amides Oxolanes Carbamate esters Heteroaromatic compounds Ureas Lactams Dialkylthioethers Azacyclic compounds Oxacyclic compounds Sulfenyl compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Organonitrogen compounds Organic anions
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine 2',3'-dideoxyribonucleoside triphosphate - 2',3'-dideoxy-3'-thionucleoside triphosphate - 2',3'-dideoxy-3'-thionucleoside - Pyrimidone - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Oxolane - Heteroaromatic compound - Vinylogous amide - Carbamic acid ester - Lactam - Urea - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Thioether - Sulfenyl compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organic anion - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleoside triphosphates. These are pyrimidine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at positions 2 and 3.
External Descriptors
Not available