Compound Identification
SMILES
CC1(O)C(OCC2=C(Cl)C=C(Cl)C=C2)C(COCC2=C(Cl)C=C(Cl)C=C2)OC1N1C=C(C#C[Si](C)(C)C)C2=C1N=CN=C2Cl
InChIKey
InChIKey=DJQNWJKTLGSMEI-UHFFFAOYSA-N
Formula
C31H30Cl5N3O4Si
Mass
713.93
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrrolopyrimidine nucleosides and nucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrrolopyrimidine nucleosides and nucleotides
Alternative Parents
Glycosylamines Benzylethers Pyrrolo[2,3-d]pyrimidines Dichlorobenzenes Halopyrimidines Aryl chlorides Substituted pyrroles Monosaccharides Heteroaromatic compounds Oxolanes Tertiary alcohols Trialkylsilanes Organic metalloid salts Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organochlorides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - N-glycosyl compound - Glycosyl compound - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - Benzylether - 1,3-dichlorobenzene - Halobenzene - Halopyrimidine - Chlorobenzene - Substituted pyrrole - Aryl halide - Aryl chloride - Benzenoid - Monosaccharide - Pyrimidine - Monocyclic benzene moiety - Heteroaromatic compound - Oxolane - Tertiary alcohol - Pyrrole - Trialkylsilane - Oxacycle - Dialkyl ether - Azacycle - Ether - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Organosilicon compound - Alkylsilane - Organohalogen compound - Organic metalloid moeity - Organochloride - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyrrolopyrimidine nucleosides and nucleotides. These are nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.
External Descriptors
Not available