Compound Identification
SMILES
CC1=CN([C@H]2C[C@H](OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3OP(O)(=O)OC[C@H]3O[C@H](C[C@@H]3SC(C3=CC=CC=C3)(C3=CC=CC=C3)C3=CC=CC=C3)N3C=NC4=C3N=CN=C4N)N3C=CC(N)=NC3=O)N3C=CC(N)=NC3=O)N3C=C(C)C(=O)NC3=O)N3C=C(C)C(=O)NC3=O)N3C=CC(N)=NC3=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]3CO)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)O2)C(=O)NC1=O
InChIKey
InChIKey=IPDBBAIYWZEWDW-HNMWKVEQSA-N
Formula
C116H138N35O56P9S
Mass
3229.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Oligonucleotides
-
Class
Nucleoside and nucleotide analogues
-
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 Purine 2',3'-dideoxyribonucleosides 2',3'-dideoxy-3'-thionucleoside monophosphates Ribonucleoside 3'-phosphates 2',3'-dideoxy-3'-thionucleosides 6-aminopurines Aminopyrimidines and derivatives Dialkyl phosphates Pyrimidones Benzene and substituted derivatives N-substituted imidazoles Imidolactams Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Ureas Lactams Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Dialkylthioethers Primary alcohols Organic oxides Hydrocarbon derivatives Primary amines
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 - Purine nucleoside - Purine 2',3'-dideoxyribonucleoside - 2',3'-dideoxy-3'-thionucleoside monophosphate - Ribonucleoside 3'-phosphate - 2',3'-dideoxy-3'-thionucleoside - 6-aminopurine - Purine - Imidazopyrimidine - Dialkyl phosphate - Aminopyrimidine - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyrimidine - Alkyl phosphate - Benzenoid - Heteroaromatic compound - Imidazole - Oxolane - Azole - Vinylogous amide - Urea - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Sulfenyl compound - Thioether - Dialkylthioether - Hydrocarbon derivative - Amine - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organosulfur compound - Primary alcohol - Primary amine - Alcohol - 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