cas: 206361-99-1 — see every product listed under this CAS number, including other names
Darunavir (CAS 206361-99-1) is a chemical reagent available from Chemat. Available pack sizes: on request, 50mg, 10mg, 25mg, 5mg, 10mM (in 1ml dmso), 0,025g, 0,05g. Offered by: Chemat Brand, Dr. Ehrenstorfer, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULD371 |
| cas | 206361-99-1 |
| 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 | |
| Dr. Ehrenstorfer | 50mg | price on request | |
| GLPBio | 10mg | 611.08 Pln | |
| GLPBio | 25mg | 709.37 Pln | |
| GLPBio | 5mg | 545.55 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 573.64 Pln | |
| GLPBio | 50mg | 873.19 Pln | |
| Biosynth | 0,025g | price on request | |
| Biosynth | 0,05g | price on request | |
| Thermo Scientific (Acros) | 100MG | 1559.06 Pln | |
| Biosynth | 0,1g | price on request | |
| Biosynth | 0,5g | price on request | |
| Biosynth | 0,25g | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Darunavir is an N,N-disubstituted benzenesulfonamide bearing an unsubstituted amino group at the 4-position, used for the treatment of HIV infection. A second-generation HIV protease inhibitor, darunavir was designed to form robust interactions with the protease enzyme from many strains of HIV, including those from treatment-experienced patients with multiple resistance mutations to other protease inhibitors. It has a role as a HIV protease inhibitor and an antiviral drug. It is a carbamate ester, a sulfonamide and a furofuran.
Source: ChEBI
| Molecular formula | C27H37N3O7S |
|---|---|
| Molecular weight | 547.7 g/mol |
| IUPAC name | [(3aS,4R,6aR)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl] N-[(2S,3R)-4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl]carbamate |
| InChIKey | CJBJHOAVZSMMDJ-HEXNFIEUSA-N |
| SMILES | CC(C)CN(C[C@H]([C@H](CC1=CC=CC=C1)NC(=O)O[C@H]2CO[C@@H]3[C@H]2CCO3)O)S(=O)(=O)C4=CC=C(C=C4)N |
Computed by PubChem (NCBI)