Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=C(C2=C1N=CN=C2NC1=CC=C(F)C=C1)C1=CC=CC=C1

InChIKey

InChIKey=ZKBPMAPXKNCAKX-SVOGPNEYSA-N

Formula

C32H39FN4O4Si

Mass

590.771

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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 - 3-phenylpyrrole - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - Aniline or substituted anilines - Aminopyrimidine - Ketal - Halobenzene - Fluorobenzene - Pyrimidine - Substituted pyrrole - Aryl fluoride - Benzenoid - Imidolactam - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Meta-dioxolane - Oxolane - Pyrrole - Trialkylheterosilane - Heteroaromatic compound - Silyl ether - Acetal - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic metalloid moeity - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organosilicon 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

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