Compound Identification
SMILES
CC1=CN(C2CC(O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(O)=O)N3C=NC4=C3N=CN=C4N)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=C(N)NC4=O)N3C=CC(N)=NC3=O)N3C=CC(N)=NC3=O)N3C=CC(N)=NC3=O)O2)C(=O)NC1=O.CC1=CN(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)N3C=NC4=C3N=C(N)NC4=O)N3C=CC(N)=NC3=O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(O)=O)N3C=CC(N)=NC3=O)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=C(N)NC4=O)O2)C(=O)NC1=O
InChIKey
InChIKey=NOJMZJCBWMMMRN-UHFFFAOYSA-N
Formula
C154H200N56O99P16
Mass
4915.167
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 Purine 2'-deoxyribonucleoside monophosphates Pyrimidine 2'-deoxyribonucleoside monophosphates Ribonucleoside 3'-phosphates Hypoxanthines 6-aminopurines 6-oxopurines Dialkyl phosphates Aminopyrimidines and derivatives Pyrimidones Monoalkyl phosphates Hydropyrimidines Imidolactams N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Lactams Secondary alcohols Ureas Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Primary amines
Molecular Framework
Not available
Substituents
(3'->5')-oligonucleotide - Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Purine deoxyribonucleoside bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Purine 2'-deoxyribonucleoside monophosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Monoalkyl phosphate - Pyrimidone - Alkyl phosphate - Imidolactam - Pyrimidine - Hydropyrimidine - Phosphoric acid ester - N-substituted imidazole - Organic phosphoric acid derivative - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Organic oxide - Primary amine - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - 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