Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3CCP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H](COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3COP(O)(=O)O[C@H]3C[C@@H](O[C@@H]3CO)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=C(N)NC4=O)N3C=C(C)C(N)=NC3=O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)CN3C=NC4=C3N=C3N=C(N)N=C(N)C3=C4)N3C=CC(N)=NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=CN=C4N)N3C=C(C)C(=O)NC3=O)N3C=CC(N)=NC3=O)N3C=C(C)C(=O)NC3=O)N3C=CC(N)=NC3=O)O2)C(=O)NC1=O
InChIKey
InChIKey=GMVCHNXWIQKYJQ-DRKBCLBVSA-N
Formula
C188H237N75O108P18
Mass
5832.909
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 Hypoxanthines Pyrido[2,3-d]pyrimidines Imidazopyridines Pyrimidones Dialkyl phosphates Aminopyrimidines and derivatives Pyridines and derivatives Phosphonic acid esters Hydropyrimidines N-substituted imidazoles Imidolactams Vinylogous amides Oxolanes Heteroaromatic compounds Organic phosphonic acids Ureas Secondary alcohols Lactams Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Primary amines Organophosphorus compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(3'->5')-oligonucleotide - Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Pyrido[2,3-d]pyrimidine - 6-aminopurine - Hypoxanthine - Pyridopyrimidine - 6-oxopurine - Imidazopyridine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - N-substituted imidazole - Alkyl phosphate - Pyrimidine - Pyridine - Imidolactam - Organic phosphoric acid derivative - Hydropyrimidine - Phosphoric acid ester - Phosphonic acid ester - Organophosphonic acid - Organophosphonic acid derivative - Vinylogous amide - Heteroaromatic compound - Imidazole - Oxolane - Azole - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organophosphorus compound - Primary alcohol - Organic nitrogen compound - Amine - Primary amine - 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