Description
PF-07321332 (nirmatrelvir) is a protease inhibitor. It is considered a broad-spectrum inhibitor for coronaviruses.
Product Unit Size | Cost | Quantity | Stock |
---|
PF-07321332 (nirmatrelvir) is a protease inhibitor. It is considered a broad-spectrum inhibitor for coronaviruses.
Cas No. | 2628280-40-8 |
---|---|
Purity | ≥99% |
Formula | C23H32F3N5O4 |
Formula Wt. | 499.5 |
Chemical Name | (1R,2S,5S)-N-[(1S)-1-cyano-2-[(3S)-2-oxopyrrolidin-3-yl]ethyl]-3-[(2S)-3,3-dimethyl-2-[(2,2,2-trifluoroacetyl)amino]butanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide |
IUPAC Name | (1R,2S,5S)-N-[(1S)-1-cyano-2-[(3S)-2-oxopyrrolidin-3-yl]ethyl]-3-[(2S)-3,3-dimethyl-2-[(2,2,2-trifluoroacetyl)amino]butanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide |
Synonym | Nirmatrelvir; 7R9A5P7H32; Paxlovid; PF07321332 |
Appearance | White to off white powder |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Zhao Z, Zhu Q, Zhou X, et al. Structural basis for the inhibition of SARS-CoV-2 Mpro D48N mutant by shikonin and PF-07321332. Viruses. 2023 Dec 30;16(1):65. PMID: 38257765.
J A Mótyán, M Mahdi, G. Hoffka, et.al. Potential Resistance of SARS-CoV-2 Main Protease (Mpro) against Protease Inhibitors: Lessons Learned from HIV-1 Protease. Int J Mol Sci. 2022 Mar 23;23(7):3507.
S. Ullrich, K. B. Ekanayake, G. Otting, etl al. Main protease mutants of SARS-CoV-2 variants remain susceptible to nirmatrelvir. Bioorg Med Chem Lett 2022 Apr 15;62:128629. PMID: 35182772.
J. Li, C. Lin, X. Zhou, et al. Structural Basis of the Main Proteases of Coronavirus Bound to Drug Candidate PF-07321332. J Virol. 2022 Apr 7;e0201321. doi: 10.1128/jvi.02013-21.
Carotene pigment found in red and green fruits ...
Hydrazine; L-amino acid decarboxylase inhibitor...
NSAID; PG synthetase inhibitor.
Diterpene found in tobacco plants and cigarette...
Viral M2 proton channel blocker, MAO-A, NET, NM...
Synthetic derivative of selenocyanate.
Nitrogen mustard, DNA alkylator.
Found in plants in Astragalus, Allium, and Bras...
Peptide, used to study cell-surface binding; po...
Prenylflavinoid, derivative of xanthohumol foun...
Carbonic anhydrase inhibitor.
Butyrophenone; α-adrenergic, D2, histamine ant...
Alkaloid found in Stephania.
Natural antibiotic found in Streptomyces parvul...
Taxane synthesis intermediate.
Tyrosine kinase inhibitor.
Peptide, derivative of AT II, involved in vasoc...
BH3 mimetic; Bcl-2, Bxl-xl, Bcl-w inhibitor.
Endogenous peptide hormone fragment, involved i...
Bone deterioration inhibitor, potential CaR ago...