cas: 1809249-37-3 — see every product listed under this CAS number, including other names
2-ethylbutyl (2S)-2-[[[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxyoxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate, 99%, 99% (CAS 1809249-37-3) is a chemical reagent available from Chemat. Available pack sizes: 25mg, 5mg, 100mg, 250mg, 500mg, 1g, 5g, 10g. Offered by: Chemat.
| brand | Chemat |
|---|---|
| catalog number | Ch12FNPR-25mg |
| cas | 1809249-37-3 |
| size | 25mg |
| availability | 100g |
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| brand | size | price | |
|---|---|---|---|
| Chemat | 25mg | 83.60 Pln | |
| Chemat | 5mg | 78.80 Pln | |
| Chemat | 100mg | 98.00 Pln | |
| Chemat | 250mg | 107.60 Pln | |
| Chemat | 500mg | 136.40 Pln | |
| Chemat | 1g | 184.40 Pln | |
| Chemat | 5g | 491.60 Pln | |
| Chemat | 10g | 909.20 Pln | |
| Chemat | 25g | 1888.40 Pln |
| purity | 99% |
|---|---|
| delivery time | 3 weeks |
Remdesivir is a carboxylic ester resulting from the formal condensation of the carboxy group of N-[(S)-{[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxytetrahydrofuran-2-yl]methoxy}(phenoxy)phosphoryl]-L-alanine with the hydroxy group of 2-ethylbutan-1-ol. A broad-spectrum antiviral prodrug with potent in vitro antiviral activity against a diverse panel of RNA viruses such as Ebola virus, MERS-CoV and SARS-CoV. It is currently in Phase III clinical trials for the treatment of Covid-19 in adults. It has a role as an anticoronaviral agent, an antiviral drug and a prodrug. It is a nitrile, a phosphoramidate ester, a carboxylic ester, an aromatic amine, a C-nucleoside and a pyrrolotriazine. It is functionally related to a GS-441524.
Source: ChEBI
| Molecular formula | C27H35N6O8P |
|---|---|
| Molecular weight | 602.6 g/mol |
| IUPAC name | 2-ethylbutyl (2S)-2-[[[(2R,3S,4R,5R)-5-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxyoxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate |
| InChIKey | RWWYLEGWBNMMLJ-YSOARWBDSA-N |
| SMILES | CCC(CC)COC(=O)[C@H](C)N[P@](=O)(OC[C@@H]1[C@H]([C@H]([C@](O1)(C#N)C2=CC=C3N2N=CN=C3N)O)O)OC4=CC=CC=C4 |
Computed by PubChem (NCBI)