Compound Identification
SMILES
CCCCCCCCCCCCCCCCOC(=O)CNP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=CN=C2N)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O
InChIKey
InChIKey=MLCNVQIQCWPWIW-UHFFFAOYSA-N
Formula
C213H283N73O126P20
Mass
6501.467
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 Pyrimidine 2'-deoxyribonucleoside monophosphates Ribonucleoside 3'-phosphates Alpha amino acid esters Hypoxanthines 6-aminopurines 6-oxopurines Dialkyl phosphates Aminopyrimidines and derivatives Pyrimidones Phosphoric monoester monoamides Hydropyrimidines Imidolactams N-substituted imidazoles Heteroaromatic compounds Vinylogous amides Oxolanes Lactams Ureas Secondary alcohols Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Primary amines Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Polysaccharide phosphate - Polysaccharide - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Ribonucleoside 3'-phosphate - Alpha-amino acid ester - 6-aminopurine - 6-oxopurine - Alpha-amino acid or derivatives - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Phosphoric monoester monoamide - Dialkyl phosphate - Pyrimidone - N-substituted imidazole - Organic phosphoric acid derivative - Hydropyrimidine - Phosphoric acid ester - Imidolactam - Organic phosphoric acid amide - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Vinylogous amide - Heteroaromatic compound - Oxolane - Amino acid or derivatives - Secondary alcohol - Lactam - Urea - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alcohol - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - 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