Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OCCOC1=CC=C(\C=C\C2=CC=C(OCCOP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3O)N3C=NC4=C3NC(=N)N=C4O)N3C=NC4=C3NC(=N)N=C4O)N3C=NC4=C3NC(=N)N=C4O)C=C2)C=C1)N1C=CC(=N)N=C1O)N1C=CC(=N)N=C1O)N1C=CC(=N)N=C1O

InChIKey

InChIKey=BFTKDTXPJINUDK-HBOXFREASA-N

Formula

C75H92N24O40P6

Mass

2155.532

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Oligonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Oligonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

(3'->5')-oligonucleotide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Purine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Stilbene - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - Styrene - Alkyl aryl ether - Hydroxypyrimidine - Dialkyl phosphate - Monocyclic benzene moiety - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Benzenoid - Alkyl phosphate - Imidazole - Heteroaromatic compound - Azole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Ether - Azacycle - Oxacycle - Organic oxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as oligonucleotides. These are organic polymers made up of a sequence of 3 to 12 purine or pyrimidine nucleotide residues linked to one another from the 5' -end to the 3'-end through a phosphate group.

External Descriptors

Not available

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