Compound Identification
SMILES
COC1=CC=C(C=C1)C(S[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]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]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=NC2=C1N=CN=C2N)N1C=NC2=C1N=CN=C2N)N1C=NC2=C1N=CN=C2N)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)(C1=CC=CC=C1)C1=CC=C(OC)C=C1
InChIKey
InChIKey=YBVUTAPOXJZHRV-AZYWWWDTSA-N
Formula
C117H142N33O59P9S
Mass
3265.42
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 Triphenyl compounds 2',3'-dideoxy-3'-thionucleoside monophosphates Ribonucleoside 3'-phosphates 2',3'-dideoxy-3'-thionucleosides 6-aminopurines Anisoles Methoxybenzenes Phenoxy compounds Alkyl aryl ethers Aminopyrimidines and derivatives Pyrimidones Dialkyl phosphates N-substituted imidazoles Imidolactams Hydropyrimidines Heteroaromatic compounds Vinylogous amides Oxolanes Lactams Ureas Dialkylthioethers Azacyclic compounds Sulfenyl compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides 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 - Triphenyl compound - 2',3'-dideoxy-3'-thionucleoside monophosphate - Ribonucleoside 3'-phosphate - 2',3'-dideoxy-3'-thionucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Methoxybenzene - Phenoxy compound - Anisole - Phenol ether - Aminopyrimidine - Dialkyl phosphate - Alkyl aryl ether - Pyrimidone - Phosphoric acid ester - Monocyclic benzene moiety - Hydropyrimidine - Imidolactam - Pyrimidine - Alkyl phosphate - Benzenoid - N-substituted imidazole - Organic phosphoric acid derivative - Imidazole - Oxolane - Vinylogous amide - Azole - Heteroaromatic compound - Lactam - Urea - Oxacycle - Azacycle - Ether - Thioether - Organoheterocyclic compound - Dialkylthioether - Sulfenyl compound - Primary alcohol - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Primary amine - 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