Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](O[Si](C3=CC=CC=C3)(C3=CC=CC=C3)C(C)(C)C)[C@@H](CO[P@]3(=O)OC[C@]4(CO)O[C@H](C[C@@H]4O3)N3C=C(C)C(=O)NC3=O)O2)C(=O)NC1=O

InChIKey

InChIKey=JWNSDBFMQRRPCE-PYFIMOQBSA-N

Formula

C37H45N4O12PSi

Mass

796.842

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside monophosphate - Glycerophospholipid - Pyrimidone - Alkylarylsilane - Monocyclic benzene moiety - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Benzenoid - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Silyl ether - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Alcohol - Organic metalloid moeity - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organosilicon compound - Aromatic heteropolycyclic 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

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