Compound Identification
SMILES
COC1=C(C)C(=O)C2=C(C(C)=C3[13CH2]C(CCN23)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)C1=O
InChIKey
InChIKey=GTYKFFLDOFDCPV-BRFAVWQFSA-N
Formula
C25H29N6O10P
Mass
605.505
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 monophosphates
Direct Parent
Purine 2'-deoxyribonucleoside monophosphates
Alternative Parents
6-oxopurines Hypoxanthines Indoles and derivatives Aryl ketones Aminopyrimidines and derivatives Dialkyl phosphates Pyrimidones Substituted pyrroles N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Vinylogous esters Secondary alcohols Azacyclic compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine 2'-deoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Indole or derivatives - Purine - Aryl ketone - Aminopyrimidine - Pyrimidone - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Substituted pyrrole - Alkyl phosphate - Vinylogous amide - Vinylogous ester - Azole - Pyrrole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Ketone - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organic nitrogen compound - Amine - Organic oxygen compound - Primary amine - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
External Descriptors
Not available