Compound Identification
SMILES
CC1=CN(CC(C)(COP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)N2C=NC3=C2N=C(N)NC3=O)COP(O)(=O)O[C@H]2C[C@@H](O[C@@H]2COP(O)(=O)O[C@@H]2[C@@H](COP(O)(=O)O[C@@H]3[C@@H](COP(O)(=O)O[C@H]4C[C@@H](O[C@@H]4COP(O)(=O)O[C@@H]4[C@@H](COP(O)(=O)O[C@H]5C[C@@H](O[C@@H]5COP(O)(=O)O[C@@H]5[C@@H](COP(O)(=O)O[C@@H]6[C@@H](COP(O)(=O)O[C@H]7C[C@@H](O[C@@H]7COP(O)(=O)O[C@H]7C[C@@H](O[C@@H]7COP(O)(=O)O[C@@H]7[C@@H](COP(O)(=O)O[C@@H]8[C@@H](CO)O[C@H]([C@@H]8O)N8C=NC9=C8N=C(N)NC9=O)O[C@H]([C@@H]7O)N7C=NC8=C7N=C(N)NC8=O)N7C=C(C)C(=O)NC7=O)N7C=C(C)C(=O)NC7=O)O[C@H]([C@@H]6O)N6C=NC7=C6N=C(N)NC7=O)O[C@H]([C@@H]5O)N5C=NC6=C5N=C(N)NC6=O)N5C=C(C)C(=O)NC5=O)O[C@H]([C@@H]4O)N4C=NC5=C4N=C(N)NC5=O)N4C=C(C)C(=O)NC4=O)O[C@H]([C@@H]3O)N3C=NC4=C3N=C(N)NC4=O)O[C@H]([C@@H]2O)N2C=NC3=C2N=C(N)NC3=O)N2C=C(C)C(=O)NC2=O)C(=O)NC1=O
InChIKey
InChIKey=VJBSCXJVUUEMAN-RUDRXZIHSA-N
Formula
C150H189N57O102P14
Mass
4856.092
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 ribonucleoside 3',5'-bisphosphates Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Purine ribonucleoside monophosphates Ribonucleoside 3'-phosphates Pentose phosphates Glycosylamines 6-oxopurines Hypoxanthines Aminopyrimidines and derivatives Dialkyl phosphates Pyrimidones Hydropyrimidines N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Ureas 1,2-diols Secondary alcohols Lactams Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(3'->5')-oligonucleotide - Polysaccharide phosphate - Polysaccharide - Purine ribonucleoside bisphosphate - Purine ribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Purine ribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Pentose-5-phosphate - Pentose phosphate - N-glycosyl compound - Glycosyl compound - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Dialkyl phosphate - Pyrimidone - Aminopyrimidine - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Pyrimidine - Vinylogous amide - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Urea - 1,2-diol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organic oxygen compound - Primary alcohol - Primary amine - 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