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Animal studies
Last updated: 2021 Aug 23
Total hit(s): 5
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Original Article
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Cathepsin L
(CTSL)
levels increased in SARS-CoV-2 infected mice's liver.Cathepsin L
inhibitor,
Amantadine reduced the levels of
CTSL.
CTSL levels increased in the lungs of infected mice, on inhibitor treatment, no statistically significant result was observed.
✍
33774649
(
Signal Transduct Target Ther
)
PMID
33774649
Date of Publishing
: 2021 Mar 27
Title
Cathepsin L plays a key role in SARS-CoV-2 infection in humans and humanized mice and is a promising target for new drug development
Author(s) name
Zhao MM, Yang WL et al.
Journal
Signal Transduct Target Ther
Impact factor
- n/a -
Citation count
: 73
Date of Entry
2021 Aug 23
×
NLM format
Zhao MM, Yang WL, Yang FY, Zhang L, Huang WJ, Hou W, Fan CF, Jin RH, Feng YM, Wang YC, Yang JK. Cathepsin L plays a key role in SARS-CoV-2 infection in humans and humanized mice and is a promising target for new drug development. Signal Transduct Target Ther. 2021 Mar 27;6(1):134. PMID:33774649
Cathepsin L
(CTSL)
levels increased in SARS-CoV-2 infected mice's liver.Cathepsin L
inhibitor,
E64d reduced the levels of
CTSL.
CTSL levels increased in the lungs of mice infected with the pseudovirus, on inhibitor treatment no statistically significant result was observed.
✍
33774649
(
Signal Transduct Target Ther
)
PMID
33774649
Date of Publishing
: 2021 Mar 27
Title
Cathepsin L plays a key role in SARS-CoV-2 infection in humans and humanized mice and is a promising target for new drug development
Author(s) name
Zhao MM, Yang WL et al.
Journal
Signal Transduct Target Ther
Impact factor
- n/a -
Citation count
: 73
Date of Entry
2021 Aug 23
×
NLM format
Zhao MM, Yang WL, Yang FY, Zhang L, Huang WJ, Hou W, Fan CF, Jin RH, Feng YM, Wang YC, Yang JK. Cathepsin L plays a key role in SARS-CoV-2 infection in humans and humanized mice and is a promising target for new drug development. Signal Transduct Target Ther. 2021 Mar 27;6(1):134. PMID:33774649
Efficacy of
remdesivir
in a rhesus macaque infected with SARS-CoV-2 shows reduced
pulmonary
infiltrates and virus titres..
This study shows that remdesivir treatment should be considered as early as clinically possible to prevent progression to pneumonia in COVID-19 patients.
✍
32516797
(
Nature
)
PMID
32516797
Date of Publishing
: 2020 Sep
Title
Clinical benefit of remdesivir in rhesus macaques infected with SARS-CoV-2
Author(s) name
Williamson BN, Feldmann F et al.
Journal
Nature
Impact factor
24.36
Citation count
: 325
×
NLM format
Williamson BN, Feldmann F, Schwarz B, Meade-White K, Porter DP, Schulz J, van Doremalen N, Leighton I, Yinda CK, Pérez-Pérez L, Okumura A, Lovaglio J, Hanley PW, Saturday G, Bosio CM, Anzick S, Barbian K, Cihlar T, Martens C, Scott DP, Munster VJ, de Wit E. Clinical benefit of remdesivir in rhesus macaques infected with SARS-CoV-2. Nature. 2020 Sep;585(7824):273-276. PMID:32516797
Compound 13a has IC50 of 2.39 ± 0.63 µ
;M
against SARS-CoV-2 main protease.
13a was cleared at a rapid rate from plasma, at 24 hours it was found at 135 ng/g tissue in the lung and at 52.7 ng/ml in bronchio-alveolar lavage fluid (BALF), showing it was distributed into the tissues, thus very useful anti-coronavirus drug.
✍
32198291
(
Science
)
PMID
32198291
Date of Publishing
: 2020 Apr 24
Title
Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved -ketoamide inhibitors
Author(s) name
Zhang L, Lin D et al.
Journal
Science
Impact factor
20.57
Citation count
: 1159
×
NLM format
Zhang L, Lin D, Sun X, Curth U, Drosten C, Sauerhering L, Becker S, Rox K, Hilgenfeld R. Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved -ketoamide inhibitors. Science. 2020 Apr 24;368(6489):409-412. PMID:32198291
Compound 13b inhibits the purified recombinant SARS-CoV-2 Mpro with IC50 = 0.67 ± 0.18 μ
;M.
In human Calu-3 cells infected with SARS-CoV-2 it has an EC50 of 4 to 5 μ
;M.
After 24 hours, 13b was found at 33 ng/g in lung tissue. Inhalation was tolerated well and mice did not show any adverse effects, which suggests that direct administration of the compound to the lungs would be possible.
✍
32198291
(
Science
)
PMID
32198291
Date of Publishing
: 2020 Apr 24
Title
Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved -ketoamide inhibitors
Author(s) name
Zhang L, Lin D et al.
Journal
Science
Impact factor
20.57
Citation count
: 1159
×
NLM format
Zhang L, Lin D, Sun X, Curth U, Drosten C, Sauerhering L, Becker S, Rox K, Hilgenfeld R. Crystal structure of SARS-CoV-2 main protease provides a basis for design of improved -ketoamide inhibitors. Science. 2020 Apr 24;368(6489):409-412. PMID:32198291