Compound Identification
SMILES
CC(C)CCCC(C)C1CCC2C3CC=C4CC(CCC4(C)C3CCC12C)OC(=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=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=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=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O
InChIKey
InChIKey=GQTWXSDNGMSQDL-UHFFFAOYSA-N
Formula
C222H291N81O118P20
Mass
6601.694
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 Cholesteryl esters Cholesterols and derivatives Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Purine 2'-deoxyribonucleoside monophosphates Delta-5-steroids Ribonucleoside 3'-phosphates Alpha amino acid esters 6-oxopurines 6-aminopurines Hypoxanthines Phosphoric monoester monoamides Aminopyrimidines and derivatives Dialkyl phosphates Pyrimidones N-substituted imidazoles Imidolactams Hydropyrimidines Oxolanes Vinylogous amides Heteroaromatic compounds Ureas Secondary alcohols Carboxylic acid esters Lactams Azacyclic compounds Monocarboxylic acids and derivatives Oxacyclic compounds Primary amines Carbonyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Polysaccharide phosphate - Polysaccharide - Cholesteryl ester - Cholesterol - Cholestane-skeleton - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Purine 2'-deoxyribonucleoside monophosphate - Steroid ester - Delta-5-steroid - Steroid - Ribonucleoside 3'-phosphate - Alpha-amino acid ester - Hypoxanthine - 6-oxopurine - 6-aminopurine - Alpha-amino acid or derivatives - Imidazopyrimidine - Purine - Phosphoric monoester monoamide - Dialkyl phosphate - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Alkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Phosphoric acid ester - Pyrimidine - Organic phosphoric acid amide - Oxolane - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Carboxylic acid ester - Lactam - Urea - Secondary alcohol - Amino acid or derivatives - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Primary amine - Amine - Alcohol - Organooxygen compound - Organic oxide - Organonitrogen compound - 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