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[ CAS No. 7304-32-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 7304-32-7
Chemical Structure| 7304-32-7
Structure of 7304-32-7 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Khatua, Kaustav ; Alugubelli, Yugendar R. ; Yang, Kai S. , et al. DOI:

Abstract: Main protease (MPro) of SARS-CoV-2, the viral pathogen of COVID-19, is a crucial nonstructural protein that plays a vital role in the replication and pathogenesis of the virus. Its protease function relies on three active site pockets to recognize P1, P2, and P4 amino acid residues in a substrate and a catalytic cysteine residue for catalysis. By converting the P1 Cα atom in an MPro substrate to nitrogen, we showed that a large variety of azapeptide inhibitors with covalent warheads targeting the MPro catalytic cysteine could be easily synthesized. Through the characterization of these inhibitors, we identified several highly potent MPro inhibitors. Specifically, one inhibitor, MPI89 that contained an aza-2,2-dichloroacetyl warhead, displayed a 10 nM EC50 value in inhibiting SARS-CoV-2 from infecting ACE2+ A549 cells and a selectivity index of 875. The crystallog. analyses of MPro bound with 6 inhibitors, including MPI89, revealed that inhibitors used their covalent warheads to covalently engage the catalytic cysteine and the aza-amide carbonyl oxygen to bind to the oxyanion hole. MPI89 represents one of the most potent MPro inhibitors developed so far, suggesting that further exploration of the azapeptide platform and the aza-2,2-dichloroacetyl warhead is needed for the development of potent inhibitors for the SARS-CoV-2 MPro as therapeutics for COVID-19.

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Product Details of [ 7304-32-7 ]

CAS No. :7304-32-7 MDL No. :MFCD00134238
Formula : C7H4FNO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :ICXSHFWYCHJILC-UHFFFAOYSA-N
M.W : 185.11 Pubchem ID :280997
Synonyms :

Calculated chemistry of [ 7304-32-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.18
TPSA : 83.12 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.36 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.73
Log Po/w (XLOGP3) : 1.5
Log Po/w (WLOGP) : 1.85
Log Po/w (MLOGP) : 0.94
Log Po/w (SILICOS-IT) : -0.48
Consensus Log Po/w : 0.91

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.14
Solubility : 1.33 mg/ml ; 0.00721 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.26 mg/ml ; 0.0014 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.43
Solubility : 6.85 mg/ml ; 0.037 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.74

Safety of [ 7304-32-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 7304-32-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 7304-32-7 ]
  • Downstream synthetic route of [ 7304-32-7 ]

[ 7304-32-7 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 7304-32-7 ]
  • [ 84832-00-8 ]
Reference: [1] Chemical and Pharmaceutical Bulletin, 1982, vol. 30, # 10, p. 3530 - 3543
  • 2
  • [ 7304-32-7 ]
  • [ 870281-82-6 ]
Reference: [1] RSC Advances, 2018, vol. 8, # 28, p. 15863 - 15869
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