cas: 361442-04-8 — see every product listed under this CAS number, including other names
Saxagliptin (CAS 361442-04-8) is a chemical reagent available from Chemat. Available pack sizes: on request, 100mg, 10mg, 25mg, 5mg, 10mM (in 1ml dmso), 50mg, 0,05g. Offered by: Chemat Brand, Mikromol, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULS321 |
| cas | 361442-04-8 |
| 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 | |
| Mikromol | 100mg | price on request | |
| GLPBio | 10mg | 620.44 Pln | |
| GLPBio | 100mg | 1182.10 Pln | |
| GLPBio | 25mg | 756.18 Pln | |
| GLPBio | 5mg | 564.28 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 578.32 Pln | |
| GLPBio | 50mg | 929.36 Pln | |
| Biosynth | 0,05g | price on request | |
| Biosynth | 0,025g | price on request | |
| Thermo Scientific (Acros) | 1g | 1835.23 Pln | |
| Thermo Scientific (Acros) | 250MG | 556.81 Pln | |
| Biosynth | 0,1g | price on request | |
| Biosynth | 0,25g | price on request | |
| Biosynth | 0,5g | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Saxagliptin is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2S)-amino(3-hydroxyadamantan-1-yl)acetic acid with the amino group of (1S,3S,5S)-2-azabicyclo[3.1.0]hexane-3-carbonitrile. Used in its monohydrate form for the treatment of Type II diabetes. It has a role as a hypoglycemic agent and an EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor. It is a nitrile, a tertiary alcohol, a monocarboxylic acid amide, an azabicycloalkane and a member of adamantanes.
Source: ChEBI
| Molecular formula | C18H25N3O2 |
|---|---|
| Molecular weight | 315.4 g/mol |
| IUPAC name | (1S,3S,5S)-2-[(2S)-2-amino-2-(3-hydroxy-1-adamantyl)acetyl]-2-azabicyclo[3.1.0]hexane-3-carbonitrile |
| InChIKey | QGJUIPDUBHWZPV-SGTAVMJGSA-N |
| SMILES | C1[C@@H]2C[C@@H]2N([C@@H]1C#N)C(=O)[C@H](C34CC5CC(C3)CC(C5)(C4)O)N |
Computed by PubChem (NCBI)