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](O2)[C@H](CC=C)OP(=O)(OCCC#N)O[C@H]2C[C@@H](O[C@@H]2[C@@H](O)CC=C)N2C=C(C)C(=O)NC2=O)C(=O)NC1=O

InChIKey

InChIKey=PKHPBGNXZYCLAV-OLJIJHBASA-N

Formula

C45H56N5O12PSi

Mass

918.025

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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 heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Trialkyl phosphate - Alkylarylsilane - Pyrimidone - Hydropyrimidine - Pyrimidine - Organic phosphoric acid derivative - Benzenoid - Monocyclic benzene moiety - Alkyl phosphate - Phosphoric acid ester - Heteroaromatic compound - Oxolane - Vinylogous amide - Silyl ether - Secondary alcohol - Urea - Lactam - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Nitrile - Organoheterosilane - Carbonitrile - Alcohol - Organosilicon compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic metalloid moeity - Organic oxide - Cyanide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic 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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