cas: 376348-65-1 — see every product listed under this CAS number, including other names
Maraviroc (CAS 376348-65-1) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 25mg, 5mg, 10mM (in 1ml dmso), 0,25g, 0,1g, 0,5g. Offered by: Chemat Brand, Mikromol, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULM581 |
| cas | 376348-65-1 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
Ask us about this product — we're happy to help.
| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Mikromol | 250mg | price on request | |
| GLPBio | 25mg | 1107.21 Pln | |
| GLPBio | 5mg | 583.00 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 657.89 Pln | |
| Biosynth | 0,25g | price on request | |
| Biosynth | 0,1g | price on request | |
| Biosynth | 0,5g | price on request | |
| Biosynth | 5g | price on request | |
| Biosynth | 10g | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Maraviroc is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of 4,4-difluorocyclohexanecarboxylic acid and the primary amino group of (1S)-3-[(3-exo)-3-(3-isopropyl-5-methyl-4H-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropylamine. An antiretroviral drug, it prevents the interaction of HIV-1 gp120 and chemokine receptor 5 (CCR5) necessary for CCR5-tropic HIV-1 to enter cells. It has a role as an antiviral drug, a HIV fusion inhibitor and a chemokine receptor 5 antagonist. It is a monocarboxylic acid amide, a member of triazoles, an organofluorine compound and an azabicycloalkane.
Source: ChEBI
| Molecular formula | C29H41F2N5O |
|---|---|
| Molecular weight | 513.7 g/mol |
| IUPAC name | 4,4-difluoro-N-[(1S)-3-[(1S,5R)-3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]cyclohexane-1-carboxamide |
| InChIKey | GSNHKUDZZFZSJB-HLMSNRGBSA-N |
| SMILES | CC1=NN=C(N1C2C[C@H]3CC[C@@H](C2)N3CC[C@@H](C4=CC=CC=C4)NC(=O)C5CCC(CC5)(F)F)C(C)C |
Computed by PubChem (NCBI)