Details
Stereochemistry | EPIMERIC |
Molecular Formula | C23H36N6O5S.H2O |
Molecular Weight | 526.649 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.C[C@@H]1CCN([C@H](C1)C(O)=O)C(=O)[C@H](CCCNC(N)=N)NS(=O)(=O)C2=C3NCC(C)CC3=CC=C2
InChI
InChIKey=AIEZTKLTLCMZIA-CZSXTPSTSA-N
InChI=1S/C23H36N6O5S.H2O/c1-14-8-10-29(18(12-14)22(31)32)21(30)17(6-4-9-26-23(24)25)28-35(33,34)19-7-3-5-16-11-15(2)13-27-20(16)19;/h3,5,7,14-15,17-18,27-28H,4,6,8-13H2,1-2H3,(H,31,32)(H4,24,25,26);1H2/t14-,15?,17+,18-;/m1./s1
Molecular Formula | H2O |
Molecular Weight | 18.0153 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C23H36N6O5S |
Molecular Weight | 508.634 |
Charge | 0 |
Count |
|
Stereochemistry | EPIMERIC |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Argatroban is a synthetic direct thrombin inhibitor derived from L-arginine. Argatroban is a direct thrombin inhibitor that reversibly binds to the thrombin active site. Argatroban does not require the co-factor antithrombin III for antithrombotic activity. Argatroban exerts its anticoagulant effects by inhibiting thrombin-catalyzed or -induced reactions, including fibrin formation; activation of coagulation factors V, VIII, and XIII; protein C; and platelet aggregation. Argatroban is highly selective for thrombin with an inhibitory constant (Ki) of 0.04 µM. At therapeutic concentrations, Argatroban has little or no effect on related serine proteases (trypsin, factor Xa, plasmin, and kallikrein). Argatroban is capable of inhibiting the action of both free and clot-associated thrombin. Argatroban is indicated as an anticoagulant for prophylaxis or treatment of thrombosis in patients with heparin-induced thrombocytopenia.
Argatroban is indicated as an anticoagulant in patients with or at risk for heparin-induced thrombocytopenia undergoing percutaneous coronary intervention (PCI).
Originator
Sources: http://adisinsight.springer.com/drugs/800004018
Curator's Comment: Argatroban was approved and launched during the 1990s in Japan for the initial indications of arterial thrombosis and acute ischaemic stroke.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL204 |
0.04 µM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | ARGATROBAN Approved UseArgatroban is a direct thrombin inhibitor indicated:
• For prophylaxis or treatment of thrombosis in adult patients with
heparin-induced thrombocytopenia (HIT) (1.1)
• As an anticoagulant in adults patients with or at risk for HIT undergoing
percutaneous coronary intervention (PCI) (1.2) Launch Date2000 |
|||
Primary | ARGATROBAN Approved UseArgatroban is a direct thrombin inhibitor indicated:
• For prophylaxis or treatment of thrombosis in adult patients with
heparin-induced thrombocytopenia (HIT) (1.1)
• As an anticoagulant in adults patients with or at risk for HIT undergoing
percutaneous coronary intervention (PCI) (1.2) Launch Date2000 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
538.6 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10730687 |
2.5 μg/kg/min other, intravenous dose: 2.5 μg/kg/min route of administration: Intravenous experiment type: OTHER co-administered: |
ARGATROBAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
1727.7 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10730687 |
2.5 μg/kg/min other, intravenous dose: 2.5 μg/kg/min route of administration: Intravenous experiment type: OTHER co-administered: |
ARGATROBAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
60.6 min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10730687 |
2.5 μg/kg/min other, intravenous dose: 2.5 μg/kg/min route of administration: Intravenous experiment type: OTHER co-administered: |
ARGATROBAN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
46% |
ARGATROBAN serum | Homo sapiens population: UNKNOWN age: UNKNOWN sex: UNKNOWN food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
125 mg single, intravenous Overdose Dose: 125 mg Route: intravenous Route: single Dose: 125 mg Sources: |
unhealthy, 74 years n = 1 Health Status: unhealthy Condition: Crohn’s disease, ileorectal fistula Age Group: 74 years Sex: M Population Size: 1 Sources: |
|
125 mg single, intravenous Highest studied dose Dose: 125 mg Route: intravenous Route: single Dose: 125 mg Sources: Page: 6.1 |
unhealthy, adult n = 568 Health Status: unhealthy Condition: thrombosis Age Group: adult Sex: unknown Population Size: 568 Sources: Page: 6.1 |
Other AEs: Haemorrhage... Other AEs: Haemorrhage (57.3%) Sources: Page: 6.1 |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Haemorrhage | 57.3% | 125 mg single, intravenous Highest studied dose Dose: 125 mg Route: intravenous Route: single Dose: 125 mg Sources: Page: 6.1 |
unhealthy, adult n = 568 Health Status: unhealthy Condition: thrombosis Age Group: adult Sex: unknown Population Size: 568 Sources: Page: 6.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
---|---|---|
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
no | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
yes | |||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
yes | no (co-administration study) Comment: In 10 healthy subjects, orally administered erythromycin (a potent inhibitor of CYP3A4/5) at 500 mg four times daily for 7 days had no effect on the pharmacokinetics of argatroban at a dose of 1 mcg/kg/min for 5 hours. These data suggest oxidative metabolism by CYP3A4/5 is not an important elimination pathway in-vivo for argatroban. Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
||
Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
yes | no (co-administration study) Comment: In 10 healthy subjects, orally administered erythromycin (a potent inhibitor of CYP3A4/5) at 500 mg four times daily for 7 days had no effect on the pharmacokinetics of argatroban at a dose of 1 mcg/kg/min for 5 hours. These data suggest oxidative metabolism by CYP3A4/5 is not an important elimination pathway in-vivo for argatroban. Sources: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/20-883_Acova_biopharmr_P1.pdf#page=34 Page: 34.0 |
PubMed
Title | Date | PubMed |
---|---|---|
Anticoagulation with Novastan (argatroban) in patients with heparin-induced thrombocytopenia and heparin-induced thrombocytopenia and thrombosis syndrome. | 1997 |
|
Inhibition of collagen-induced platelet aggregation by argatroban in patients with acute cerebral infarction. | 1997 Oct 15 |
|
The first report of successful carotid stent implant using argatroban anticoagulation in a patient with heparin-induced thrombocytopenia and thrombosis syndrome: a case report. | 1998 Jan |
|
Severe argatroban-induced coagulopathy in a patient with a history of heparin-induced thrombocytopenia. | 2004 Dec |
|
Heparin-induced thrombocytopenia in patients administered heparin solely for hemodialysis. | 2006 |
|
Argatroban tPA stroke study: study design and results in the first treated cohort. | 2006 Aug |
|
Heparin-induced thrombocytopenia: treatment options and special considerations. | 2007 Apr |
|
Risk factors for major bleeding in patients with heparin-induced thrombocytopenia treated with argatroban: a retrospective study. | 2008 Dec |
|
Bivalirudin. | 2008 May |
|
Reducing harm associated with anticoagulation: practical considerations of argatroban therapy in heparin-induced thrombocytopenia. | 2009 |
|
Extremely low doses of lepirudin in a patient with heparin-induced thrombocytopenia, high bleeding risk and renal insufficiency. | 2009 Aug |
|
A report of outcomes after orthotopic liver transplant with allografts from heparin antibody-positive donors. | 2009 Mar |
|
Argatroban dosage requirements and outcomes in intensive care versus non-intensive care patients. | 2009 Sep |
|
Heparin induced thrombocytopenia and re-thrombosis associated with warfarin and fondaparinux in a child. | 2009 Sep |
|
Prolonged elevation of plasma argatroban in a cardiac transplant patient with a suspected history of heparin-induced thrombocytopenia with thrombosis. | 2010 Apr |
|
Identification of old drugs as potential inhibitors of HIV-1 integrase - human LEDGF/p75 interaction via molecular docking. | 2012 Dec |
|
Therapeutic administration of the direct thrombin inhibitor argatroban reduces hepatic inflammation in mice with established fatty liver disease. | 2012 Oct |
|
Use of argatroban and catheter-directed thrombolysis with alteplase in an oncology patient with heparin-induced thrombocytopenia with thrombosis. | 2014 May 1 |
Patents
Sample Use Guides
Initial Dosage: Before administering Argatroban, discontinue heparin therapy and obtain a baseline aPTT. The recommended initial
dose of Argatroban for adult patients without hepatic impairment is 2 mcg/kg/min, administered as a continuous infusion
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25193406
In the presence of 10 nM thrombomodulin (TM) argatroban (1 uM) prolonged clot lysis time and enhanced thrombin generation.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:25:09 GMT 2023
by
admin
on
Sat Dec 16 08:25:09 GMT 2023
|
Record UNII |
IY90U61Z3S
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NDF-RT |
N0000175980
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
NCI_THESAURUS |
C263
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
NDF-RT |
N0000009963
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
NDF-RT |
N0000175518
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
WHO-VATC |
QB01AE03
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
WHO-ATC |
B01AE03
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
||
|
LOINC |
68981-0
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID5057888
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
Argatroban
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
II-67
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
6385
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
141396-28-3
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
IY90U61Z3S
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
SUB48842
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
100000132863
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
ARGATROBAN
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
IY90U61Z3S
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
C031942
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
C28833
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
DB00278
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
15202
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | RxNorm | ||
|
92721
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
1042408
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
CHEMBL1166
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
SUB05559MIG
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | |||
|
m2039
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY | Merck Index | ||
|
239
Created by
admin on Sat Dec 16 08:25:09 GMT 2023 , Edited by admin on Sat Dec 16 08:25:09 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE | |||
|
ANHYDROUS->SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |