Melagatran

Modify Date: 2026-07-15 18:40:01

Melagatran Structure
Melagatran structure
Common Name Melagatran
CAS Number 159776-70-2 Molecular Weight 429.51300
Density 1.41g/cm3 Boiling Point N/A
Molecular Formula C22H31N5O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Melagatran


Melagatran is a direct and oral active inhibitor of thrombin, without interacting with any other enzymes in the coagulation cascade or fibrinolytic enzymes aside from thrombin. Melagatran does not require endogenous co-factors for its antithrombin effect and may help to alleviate some of the damaging effects of endotoxemia[1]. Melagatran has the potential to provide a rational approach in the prevention of arterial occlusion[2].

 Names

Name melagatran
Synonym More Synonyms

 Melagatran Biological Activity

Description Melagatran is a direct and oral active inhibitor of thrombin, without interacting with any other enzymes in the coagulation cascade or fibrinolytic enzymes aside from thrombin. Melagatran does not require endogenous co-factors for its antithrombin effect and may help to alleviate some of the damaging effects of endotoxemia[1]. Melagatran has the potential to provide a rational approach in the prevention of arterial occlusion[2].
Related Catalog
Target

Thrombin[1]

References

[1]. Eriksson M, et al. Effects of melagatran, a novel direct thrombin inhibitor, during experimental septic shock. Expert Opin Investig Drugs. 2000 May;9(5):1129-37.

[2]. Mehta JL, et al. Melagatran, an oral active-site inhibitor of thrombin, prevents or delays formation of electrically induced occlusive thrombus in the canine coronary artery. J Cardiovasc Pharmacol. 1998 Mar;31(3):345-51.

 Chemical & Physical Properties

Density 1.41g/cm3
Molecular Formula C22H31N5O4
Molecular Weight 429.51300
Exact Mass 429.23800
PSA 148.61000
LogP 2.33060
Index of Refraction 1.67
InChIKey DKWNMCUOEDMMIN-PKOBYXMFSA-N
SMILES N=C(N)c1ccc(CNC(=O)C2CCN2C(=O)C(NCC(=O)O)C2CCCCC2)cc1

 MelagatranBioassay

View more

Name: Anticoagulant activity in Sprague-Dawley rat deep vein thrombosis model assessed as r...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421920
Name: Plasma protein binding in rat at 1 ug/ml by ultra-filtration method
Source: ChEMBL
Target: Plasma
External Id: CHEMBL2421918
Name: Plasma protein binding in human at 1 ug/ml by ultra-filtration method
Source: ChEMBL
Target: Plasma
External Id: CHEMBL2421917
Name: Anticoagulant activity in rat assessed as time to first arrest of bleeding at 2 x ED5...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421908
Name: Anticoagulant activity in rat assessed as blood loss at ED50 measured as hemoglobin l...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421907
Name: Apparent permeability across human Caco2 cells measured every 30 mins for 2 hrs
Source: ChEMBL
Target: N/A
External Id: CHEMBL4229781
Name: Anticoagulant activity in rat assessed as blood loss at ED80 measured as hemoglobin l...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421906
Name: Human coagulation factor II, thrombin (S1: Chymotrypsin)
Source: IUPHAR-DB
Target: coagulation factor II, thrombin (S1: Chymotrypsin) [Homo sapiens]
External Id: 2362_Human
Name: Anticoagulant activity in rat assessed as time to first arrest of bleeding at ED50 me...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421910
Name: Anticoagulant activity in rat assessed as time to first arrest of bleeding at ED80 me...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2421909
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 Synonyms

2-[[(1R)-2-[(2S)-2-[(4-carbamimidoylphenyl)methylcarbamoyl]azetidin-1-yl]-1-cyclohexyl-2-oxoethyl]amino]acetic acid
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