InAADR

Drug Information

Drug Name: Asparaginase (9015-68-3)
PubChem ID: 124081179
SMILES: C/C/1=C/2[C@@]([C@@H](C([N-]2)/C=C3/C([C@@H](/C(=C(/C4[C@]([C@H]([C@@H]([N-]4)[C@]5([C@@]([C@@H](C1[N-]5)CCC(=O)N)(C)CC(=O)N)C)CC(=O)N)(C)CCC(=O)NC[C@@H](C)O)C)/[N-]3)CCC(=O)N)(C)C)CCC(=O)N)(C)CC(=O)N.[Co]
InchiKey: CPIBXUNAEPETCR-DEFJPDJUSA-N
Therapeutic Category: Antineoplastic Agents

Computed Drug Properties

Molecular Weight (dalton): 993.13
LogP: 3.4215
Ring Count: 0
Hydrogen Bond Acceptor Count: 8
Hydrogen Bond Donor Count: 8
Total Polar Surface Area: 364.27

This panel provides information on interacting drugs and their ADRs along with references

Interacting drug Toxicity Interaction Type Mechanism Reference

This panel provides drug-protein interaction and their ADRs along with references

Toxicity Interacting Protein Mechanism Reference
Bleeding Histidine-rich glycoprotein (P04196) L-Asparaginase therapy reduced plasma levels of plasminogen and histidine-rich glycoprotein ( HRG ) and influenced the equilibrium between HRG , plasminogen and HRG -plasminogen complex,which leads to the bleeding tendency [ ADR Type 1 ] The influence of L-asparaginase therapy on the fibrinolytic system
Deficiency Of Coagulation Factors Alpha-2-antiplasmin (P08697) Bleeding tendency described during L-asparaginase therapy can be ascribed not only to a temporary deficiency of coagulation factors but also to temporary alpha 2-antiplasmin deficiency [ ADR Type 3 ] The influence of L-asparaginase therapy on the fibrinolytic system
Deficiency Of Coagulation Factors Coagulation factor (P00742) Bleeding tendency described during L-asparaginase therapy can be ascribed not only to a temporary deficiency of coagulation factors but also to temporary alpha 2-antiplasmin deficiency. [ ADR Type 3 ] The influence of L-asparaginase therapy on the fibrinolytic system

This panel provides drug-food interactions and their ADRs along with references

Food Toxicity Reference

This panel provides information on metabolites and their ADRs along with references

Metabolite Toxicity Place of Metabolism Mechanism Reference

InAADR: Drug-Protein-ADRs database