Compound Identification
SMILES
COC1=CC=C(C=C1)C(O[C@H]1[C@@H]2O[C@@H]3[C@@H](O[C@H]1[C@]3(OP(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)OC[C@H]1O[C@H](C[C@@H]1OP(O)(=O)OC[C@H]1O[C@H](C[C@@H]1O)N1C=CC(N)=NC1=O)N1C=NC3=C1N=C(N)NC3=O)N1C=C(C)C(=O)NC1=O)N1C=NC3=C1N=CN=C3N)[C@@H]2OP(O)(=O)O[C@H]1C[C@@H](O[C@@H]1COP(O)(=O)O[C@H]1C[C@@H](O[C@@H]1COP(O)(=O)O[C@H]1C[C@@H](O[C@@H]1COP(O)(=O)O[C@H]1C[C@@H](O[C@@H]1CO)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=C(C)C(=O)NC1=O)(C1=CC=CC=C1)C1=CC=C(OC)C=C1
InChIKey
InChIKey=VGWBSCWGDUVKFU-FHVYQNRJSA-N
Formula
C111H130N32O57P8
Mass
3072.218
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass Oligonucleotides
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Class
Nucleoside and nucleotide analogues
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Superclass
Nucleosides, nucleotides, and analogues
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
Purine deoxyribonucleoside 3',5'-bisphosphates Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Pyrimidine 2'-deoxyribonucleoside monophosphates Triphenyl compounds Ribonucleoside 3'-phosphates Glycosylamines 6-aminopurines 6-oxopurines Hypoxanthines Benzylethers Anisoles Furofurans Methoxybenzenes Phenoxy compounds Alkyl aryl ethers Aminopyrimidines and derivatives 1,4-dioxepanes Dialkyl phosphates Pyrimidones Imidolactams N-substituted imidazoles Hydropyrimidines Oxanes Oxolanes Heteroaromatic compounds Vinylogous amides Ureas Lactams Secondary alcohols Azacyclic compounds Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Primary amines Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(3'->5')-oligonucleotide - Purine deoxyribonucleoside bisphosphate - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Triphenyl compound - Ribonucleoside 3'-phosphate - N-glycosyl compound - Glycosyl compound - 6-oxopurine - 6-aminopurine - Hypoxanthine - Benzylether - Imidazopyrimidine - Purine - Methoxybenzene - Furofuran - Phenol ether - Phenoxy compound - Anisole - Pyrimidone - Dialkyl phosphate - Dioxepane - Aminopyrimidine - Alkyl aryl ether - 1,4-dioxepane - Monocyclic benzene moiety - Imidolactam - Benzenoid - Hydropyrimidine - Alkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Secondary alcohol - Oxacycle - Azacycle - Dialkyl ether - Organoheterocyclic compound - Ether - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Primary amine - Primary alcohol - Hydrocarbon derivative - Organic oxygen 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