Compound Identification
SMILES
CC(C)CCCC(C)[C@H]1CC[C@H]2C3CC=C4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)OP(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(CC1OP(O)(=O)OCC1OC(CC1OP(O)(=O)OCC1OC(CC1O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=CN=C2N)N1C=CC(N)=NC1=O)N1C=C(C)C(=O)NC1=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=CN=C2N)N1C=C(C)C(=O)NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=CC(N)=NC1=O)N1C=NC2=C1N=C(N)NC2=O)N1C=NC2=C1N=C(N)NC2=O)N1C=C(C)C(=O)NC1=O
InChIKey
InChIKey=QYCQTGCSZHSERP-OIZVNQQKSA-N
Formula
C238H314N80O134P22
Mass
7120.979
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 Cholesterols and derivatives Pyrimidine deoxyribonucleoside 3',5'-bisphosphates Pyrimidine 2'-deoxyribonucleoside monophosphates Delta-5-steroids Ribonucleoside 3'-phosphates 6-aminopurines 6-oxopurines Hypoxanthines Aminopyrimidines and derivatives Pyrimidones Dialkyl phosphates N-substituted imidazoles Imidolactams Hydropyrimidines Heteroaromatic compounds Vinylogous amides Oxolanes Lactams Ureas Secondary alcohols Azacyclic compounds Oxacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Polysaccharide phosphate - Polysaccharide - Cholesterol - Cholestane-skeleton - Purine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside 3',5'-bisphosphate - Pyrimidine deoxyribonucleoside bisphosphate - Pyrimidine 2'-deoxyribonucleoside monophosphate - Delta-5-steroid - Steroid - Ribonucleoside 3'-phosphate - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Pyrimidone - Alkyl phosphate - Imidolactam - Pyrimidine - Hydropyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Vinylogous amide - Azole - Oxolane - Heteroaromatic compound - Imidazole - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Organooxygen compound - Organonitrogen 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