Clinical stage molecule PT150 is a modulator of glucocorticoid and androgen receptors with antiviral activity against SARS-CoV-2.
Alveolar Epithelial Cells
/ drug effects
Angiotensin-Converting Enzyme 2
/ metabolism
Antiviral Agents
/ pharmacology
Cell Line
Disease Progression
Down-Regulation
Glucocorticoids
/ antagonists & inhibitors
Humans
Hydrocortisone
/ antagonists & inhibitors
Immunologic Factors
/ pharmacology
Middle East Respiratory Syndrome Coronavirus
/ drug effects
Receptors, Androgen
/ metabolism
Receptors, Glucocorticoid
/ agonists
SARS-CoV-2
/ drug effects
Serine Endopeptidases
/ metabolism
COVID-19 Drug Treatment
Androgen receptor
COVID-19
Glucocorticoid antagonist
SARS-CoV-2
Therapeutic
Journal
Cell cycle (Georgetown, Tex.)
ISSN: 1551-4005
Titre abrégé: Cell Cycle
Pays: United States
ID NLM: 101137841
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
pubmed:
12
12
2020
medline:
23
1
2021
entrez:
11
12
2020
Statut:
ppublish
Résumé
PT150 is a clinical-stage molecule, taken orally, with a strong safety profile having completed Phase 1 and Phase 2 clinical trials for its original use as an antidepressant. It has an active IND for COVID-19. Antiviral activities have been found for PT150 and other members of its class in a variety of virus families; thus, it was now tested against SARS-CoV-2 in human bronchial epithelial lining cells and showed effective 90% inhibitory antiviral concentration (EC90) of 5.55 µM. PT150 is a member of an extended platform of novel glucocorticoid receptor (GR) and androgen receptor (AR) modulating molecules. In vivo, their predominant net effect is one of systemic glucocorticoid antagonism, but they also show direct downregulation of AR and minor GR agonism at the cellular level. We hypothesize that anti-SARS-CoV-2 activity depends in part on this AR downregulation through diminished TMPRSS2 expression and modulation of ACE2 activity. Given that hypercortisolemia is now suggested to be a significant co-factor for COVID-19 progression, we also postulate an additive role for its potent immunomodulatory effects through systemic antagonism of cortisol.
Identifiants
pubmed: 33305659
doi: 10.1080/15384101.2020.1859752
pmc: PMC7738205
doi:
Substances chimiques
Antiviral Agents
0
Glucocorticoids
0
Immunologic Factors
0
Receptors, Androgen
0
Receptors, Glucocorticoid
0
ACE2 protein, human
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Serine Endopeptidases
EC 3.4.21.-
TMPRSS2 protein, human
EC 3.4.21.-
Hydrocortisone
WI4X0X7BPJ
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
3632-3638Références
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