Compound Identification
SMILES
CC1=CN(C2CC(OP(O)(=O)OCC3OC(CC3OP(C)(=O)OCC3OC(CC3OP(C)(=O)OCC3OC(CC3O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)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)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)OC3CC(OC3COP(C)(=O)OC3CC(OC3COP(C)(=O)OC3CC(OC3CO)N3C=CC(N)=NC3=O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=C(C)C(=O)NC3=O)N3C=C(C)C(=O)NC3=O)N3C=CC(N)=NC3=O)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=CN=C4N)O2)C(=O)NC1=O
InChIKey
InChIKey=RJNNAZAHHQZHOU-UHFFFAOYSA-N
Formula
C211H266N84O115P20
Mass
6438.397
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleotides
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Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleotides
Subclass
Purine deoxyribonucleotides
Intermediate Tree Nodes
Purine deoxyribonucleoside bisphosphates
Direct Parent
Purine deoxyribonucleoside 3',5'-bisphosphates
Alternative Parents
Polysaccharide phosphates Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Ribonucleoside 3'-phosphates Hypoxanthines 6-aminopurines 6-oxopurines Dialkyl phosphates Dialkyl alkylphosphonates Pyrimidones Aminopyrimidines and derivatives Hydropyrimidines Imidolactams N-substituted imidazoles Phosphonic acid esters Heteroaromatic compounds Vinylogous amides Oxolanes Ureas Lactams Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organophosphorus compounds Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Ribonucleoside 3'-phosphate - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Dialkyl alkylphosphonate - Aminopyrimidine - Phosphonic acid diester - Dialkyl phosphate - Pyrimidone - Phosphonic acid ester - Alkyl phosphate - Pyrimidine - Imidolactam - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Hydropyrimidine - Azole - Heteroaromatic compound - Imidazole - Organophosphonic acid derivative - Oxolane - Vinylogous amide - Secondary alcohol - Urea - Lactam - Oxacycle - Organoheterocyclic compound - Azacycle - Primary alcohol - Amine - Organonitrogen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organooxygen compound - Organophosphorus compound - Primary amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine deoxyribonucleoside 3',5'-bisphosphates. These are purine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at position 2.
External Descriptors
Not available