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211914-51-1

211914-51-1 Structure

211914-51-1 Structure
IdentificationBack Directory
[Name]

Dabigatran
[CAS]

211914-51-1
[Synonyms]

BIB-953
CS-1864
BIBR 953
BIBR 953ZW
Dabigatran
Dabiga group
Dabigatran API
Dabigatran base
Dabigatran (Acid)
Dabigatran(BIB-953
BIBR 953(Dabigatran)
Dabigatran USP/EP/BP
Dabigatran (BIBR 953)
Dabigatran Impurity U
Dabigatran etexilate-1
Dabigatran Impurity b
BIBR953;BIBR 953;BIBR-953
Dabigatran Ester Impurity B
Dabigatran Etexilate Mesilate
BIBR 953 (Dabigatran, Pradaxa)
Dabigatran etexilate impurity189
Dabigatran etexilate impurity1513
BIBR 953;BIBR 953ZW;BIBR953;BIB-953
N- (2-{ (4-carbaMiMidoylphenyl)aMino Methyl}-1-Met
3-[[2-[[(4-carbaMiMidoylphenyl)aMino]Methyl]-1-Met
N-[(2-{[(4-carbamimidoylphenyl)amino]methyl}-1-methyl-1H-ben...
3-[[2-[[(4-carbaMiMidoylphenyl)aMino]Methyl]-1-Methyl-benzoiMidazole-5-carbonyl]-pyridin-2-yl-aMino]
3-[[2-[(4-carbamimidoylanilino)methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic
3-[[2-[(4-carbamimidoylanilino)methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic acid
N-[(2-{[(4-carbaMiMidoylphenyl)aMino]Methyl}-1-Methyl-1HbenziMidazol- 5-yl)carbonyl]-N-pyridin-2-yl-beta-alanine
β-Alanine,N-[[2-[[[4-(aMinoiMinoMethyl)phenyl]aMino]Methyl]-1-Methyl-1H-benziMidazol-5-yl]carbonyl]-N-2-pyridinyl-
3-[[2-[[(4-carbamimidoylphenyl)amino]methyl]-1-methyl-benzoimidazole-5-carbonyl]-pyridin-2-yl-amino]propanoic acid
b-Alanine,N-[[2-[[[4-(aminoiminomethyl)phenyl]amino]methyl]-1-methyl-1H-benzimidazol-5-yl]carbonyl]-N-2-pyridinyl-
N-[[2-[[[4-(Aminoiminomethyl)phenyl]amino]methyl]-1-methyl-1H-benzimidazol-5-yl]carbonyl]-N-2-pyridinyl-beta-alanine
3-(2-((4-carbamimidoylphenylamino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoic acid
N-[[2-[[[4-(AMinoiMinoMethyl)phenyl]aMino]Methyl]-1-Methyl-1H-benzo[d]iMidazol-5-yl]carbonyl]-N-pyridin-2-yl-beta-alanine
Dabigatran3-(2-((4-carbamimidoylphenylamino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoic acid
3-[[2-[(4-carbamimidoylanilino)methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic acid Dabigatran (BIBR 953)
ethyl 3-(2-(((4-(N'-((hexan-2-yloxy)carbonyl)carbamimidoyl)phenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate
DabigatranQ: What is Dabigatran Q: What is the CAS Number of Dabigatran Q: What is the storage condition of Dabigatran Q: What are the applications of Dabigatran
[Molecular Formula]

C25H25N7O3
[MDL Number]

MFCD09837830
[MOL File]

211914-51-1.mol
[Molecular Weight]

471.51
Chemical PropertiesBack Directory
[Melting point ]

268-272°C
[Boiling point ]

797.1±70.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[storage temp. ]

Refrigerator, Under Inert Atmosphere
[solubility ]

Aqueous Acid
[form ]

Solid
[pka]

4.17±0.10(Predicted)
[color ]

White to Brown
Safety DataBack Directory
[Hazardous Substances Data]

211914-51-1(Hazardous Substances Data)
Hazard InformationBack Directory
[Chemical Properties]

Tan Solid
[Uses]

BIBR 953 (Dabigatran, Pradaxa) is potent nonpeptide thrombin inhibitor with an IC50 of 9.3 nM
[Uses]

Nonpeptide, direct thrombin inhibitor. Antithrombotic.
[Definition]

ChEBI: An aromatic amide obtained by formal condensation of the carboxy group of 2-{[(4-carbamimidoylphenyl)amino]methyl}-1-methyl-1H-benzimidazole-5-carboxylic acid with the secondary amoino group of N-pyridin-2-yl-b ta-alanine. The active metabolite of the prodrug dabigatran etexilate, it acts as an anticoagulant which is used for the prevention of stroke and systemic embolism.
[Biological Activity]

bibr 953 is a potent, reversible, and direct inhibitor of thrombin with ic50 value of 9.3nm [1].bibr 953 shows a favorable selectivity profile and strong activity in vitro with a ki value of 4.5nm. it also exhibits the best activity profile in vivo following administration to rats. bibr 953 is designed to be converted into an orally active prodrug bibr 1048 due to its highly polar, zwitterionic nature and poor oral absorption. bibr 953 inhibits thrombin in a competitive fashion. this inhibition is rapid and reversible. bibr 953 inhibits both clot-bound and free thrombin. bibr 953 is demonstrated to have an anticoagulant efficacy both in vitro and ex vivo. since thrombin can affect cell behavior and response in various tissue types via par signaling, bibr 953 is found to be beneficial in many diseases including inflammation, infection, fibrosis and cancer.
[target]

thrombin
[References]

[1] hauel nh, nar h, priepke h, ries u, stassen jm, wienen w. structure-based design of novel potent nonpeptide thrombin inhibitors. j med chem. 2002 apr 25;45(9):1757-66.
[2] van ryn j, goss a, hauel n, wienen w, priepke h, nar h, clemens a. the discovery of dabigatran etexilate. front pharmacol. 2013 feb 12;4:12.
Spectrum DetailBack Directory
[Spectrum Detail]

Dabigatran(211914-51-1)1HNMR
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