Compound Identification
SMILES
COC1=CC=C(C=C1)N(C(C)=O)C1=NC2=C(N=C(N)NC2=O)N1[C@H]1C[C@H](OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=CC(N)=NC2=O)N2C=NC3=C2N=CN=C3N)N2C=C(C)C(=O)NC2=O)N2C=CC(N)=NC2=O)N2C=C(C)C(=O)NC2=O)N2C=C(C)C(=O)NC2=O)N2C=NC3=C2N=CN=C3N)N2C=NC3=C2N=CN=C3N)[C@@H](COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2CO)N2C=NC3=C2N=C(N)NC3=O)N2C=C(C)C(=O)NC2=O)N2C=NC3=C2N=CN=C3N)O1
InChIKey
InChIKey=QFMYRUFSVHJKDQ-AIMWMXENSA-N
Formula
C127H158N45O72P11
Mass
3807.615
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
Polysaccharide phosphates Purine deoxyribonucleoside 3',5'-bisphosphates Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Pyrimidine 2'-deoxyribonucleoside monophosphates Ribonucleoside 3'-phosphates 6-aminopurines 6-oxopurines Acetanilides Hypoxanthines Methoxyanilines Anisoles Methoxybenzenes Phenoxy compounds Alkyl aryl ethers Pyrimidones Aminopyrimidines and derivatives Dialkyl phosphates N-substituted imidazoles Imidolactams Hydropyrimidines Oxolanes Acetamides Tertiary carboxylic acid amides Vinylogous amides Heteroaromatic compounds Ureas Amino acids and derivatives Lactams Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(3'->5')-oligonucleotide - Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - Hypoxanthine - 6-oxopurine - Acetanilide - Imidazopyrimidine - Purine - Methoxyaniline - Anilide - Phenol ether - Anisole - Methoxybenzene - Phenoxy compound - Alkyl aryl ether - Dialkyl phosphate - Aminopyrimidine - Pyrimidone - Organic phosphoric acid derivative - Pyrimidine - N-substituted imidazole - Hydropyrimidine - Imidolactam - Alkyl phosphate - Phosphoric acid ester - Monocyclic benzene moiety - Benzenoid - Acetamide - Vinylogous amide - Tertiary carboxylic acid amide - Imidazole - Oxolane - Azole - Heteroaromatic compound - Carboxamide group - Secondary alcohol - Lactam - Urea - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Primary alcohol - Primary amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organic oxide - Amine - Organonitrogen 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