Compound Identification
SMILES
CC1(O)C(O)N([C@H]2C[C@H](O)[C@@H](COP(O)(O)=O)O2)C(=O)NC1=O
InChIKey
InChIKey=QWAYKDYQHLTLIL-SKAWGCAZSA-N
Formula
C10H17N2O10P
Mass
356.224
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 monophosphates
Direct Parent
Pyrimidine 2'-deoxyribonucleoside monophosphates
Alternative Parents
Pentose phosphates Barbituric acid derivatives Monoalkyl phosphates Diazinanes Tetrahydrofurans Tertiary alcohols Dicarboximides Secondary alcohols Organic carbonic acids and derivatives Oxacyclic compounds Azacyclic compounds Alkanolamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Pyrimidine 2'-deoxyribonucleoside monophosphate - Pentose phosphate - Barbiturate - Monoalkyl phosphate - Pyrimidone - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - Monosaccharide - 1,3-diazinane - Tetrahydrofuran - Tertiary alcohol - Dicarboximide - Secondary alcohol - Carbonic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Alcohol - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside monophosphates. These are pyrimidine nucleotides with a monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
External Descriptors
Not available