cas: 211914-51-1 — see every product listed under this CAS number, including other names
Dabigatran (CAS 211914-51-1) is a chemical reagent available from Chemat. Available pack sizes: on request, 10mg, 1mg, 5mg, 25mg, 500mg, 250mg, 1000mg. Offered by: Chemat Brand, TRC, Mikromol, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULD591 |
| cas | 211914-51-1 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| TRC | 10mg | price on request | |
| TRC | 1mg | price on request | |
| TRC | 5mg | price on request | |
| Mikromol | 25mg | price on request | |
| Biosynth | 500mg | price on request | |
| Biosynth | 250mg | price on request | |
| Biosynth | 1000mg | price on request | |
| Biosynth | 2000mg | price on request | |
| Biosynth | 5000mg | price on request | |
| HPC Standards | 1x10mg | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Dabigatran is 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-beta-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. It has a role as an anticoagulant, an EC 3.4.21.5 (thrombin) inhibitor and an EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor. It is a member of benzimidazoles, a beta-alanine derivative, a member of pyridines, a carboxamidine and an aromatic amide.
Source: ChEBI
| Molecular formula | C25H25N7O3 |
|---|---|
| Molecular weight | 471.5 g/mol |
| IUPAC name | 3-[[2-[(4-carbamimidoylanilino)methyl]-1-methylbenzimidazole-5-carbonyl]-pyridin-2-ylamino]propanoic acid |
| InChIKey | YBSJFWOBGCMAKL-UHFFFAOYSA-N |
| SMILES | CN1C2=C(C=C(C=C2)C(=O)N(CCC(=O)O)C3=CC=CC=N3)N=C1CNC4=CC=C(C=C4)C(=N)N |
Computed by PubChem (NCBI)