Compound Identification
SMILES
CCCCCCCCCCCCCCCCCCNC1=NC(=O)N(C=C1)C1OC(C(O)C1O)C(C)(OP(O)([O-])=O)C1OC(CC1O)N1C=C(F)C(NCCCCCCCCCCCCCCCCCC)=NC1=O
InChIKey
InChIKey=QTECOUKUXDEETF-UHFFFAOYSA-M
Formula
C54H95FN6O11P
Mass
1054.358
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
Glycosylamines Pyrimidones Aminopyrimidines and derivatives Halopyrimidines Alkyl phosphates Aryl fluorides Imidolactams Hydropyrimidines Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Amines Organic oxides Organofluorides Hydrocarbon derivatives Organic anions
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine 2'-deoxyribonucleoside monophosphate - Glycosyl compound - N-glycosyl compound - Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Heteroaromatic compound - Oxolane - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Alcohol - Organooxygen compound - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organofluoride - Organonitrogen compound - Organic oxygen compound - Organic oxide - Organic anion - Aromatic 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