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 — 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.

brandChemat
catalog numberCh12FNPR-25mg
cas1809249-37-3
size25mg
availability 100g
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Available pack sizes

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

properties

purity99%
delivery time3 weeks
Structural formula: {0} (CAS {1})

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

Identity
Molecular formulaC27H35N6O8P
Molecular weight602.6 g/mol
IUPAC name2-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
InChIKeyRWWYLEGWBNMMLJ-YSOARWBDSA-N
SMILESCCC(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)

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