Structure Information
Structure

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

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

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

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

Previous Back Next