cas: 503612-47-3 — see every product listed under this CAS number, including other names
Apixaban (CAS 503612-47-3) is a chemical reagent available from Chemat. Available pack sizes: on request, 100mg, 10mg, 200mg, 10mM (in 1ml dmso), 50mg, 1g, 2g. Offered by: Chemat Brand, Mikromol, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULA10201 |
| cas | 503612-47-3 |
| 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 | |
| Chemat Brand | on request | price on request | |
| Mikromol | 100mg | price on request | |
| GLPBio | 10mg | 877.87 Pln | |
| GLPBio | 200mg | 2080.76 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 1046.37 Pln | |
| GLPBio | 50mg | 1172.74 Pln | |
| Biosynth | 1g | price on request | |
| Biosynth | 2g | price on request | |
| Thermo Scientific (Acros) | 100MG | 346.56 Pln | |
| Thermo Scientific (Acros) | 500MG | 966.62 Pln | |
| Biosynth | 5g | price on request | |
| Biosynth | 10g | price on request | |
| Biosynth | 25g | price on request | |
| Sigma-Aldrich | 200MG | 5366.00 Pln | |
| HPC Standards | 1x10mg | 1200.11 Pln |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Apixaban is a pyrazolopyridine that is 7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxamide substituted at position 1 by a 4-methoxyphenyl group and at position 6 by a 4-(2-oxopiperidin-1-yl)phenyl group. It is used for the prevention and treatment of thromboembolic diseases. It has a role as an anticoagulant and an EC 3.4.21.6 (coagulation factor Xa) inhibitor. It is a lactam, an aromatic ether, a pyrazolopyridine and a member of piperidones.
Source: ChEBI
| Molecular formula | C25H25N5O4 |
|---|---|
| Molecular weight | 459.5 g/mol |
| IUPAC name | 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-yl)phenyl]-4,5-dihydropyrazolo[5,4-c]pyridine-3-carboxamide |
| InChIKey | QNZCBYKSOIHPEH-UHFFFAOYSA-N |
| SMILES | COC1=CC=C(C=C1)N2C3=C(CCN(C3=O)C4=CC=C(C=C4)N5CCCCC5=O)C(=N2)C(=O)N |
Computed by PubChem (NCBI)