Verteporfin
A benzoporphyrin derivative.
General information
Verteporfin is a benzoporphyrin derivative used as a photosensitizer in the photodynamic therapy of wet-form macular degeneration (DrugBank).
Verteporfin on PubChem
Verteporfin on Wikipedia
Synonyms
Verteporphin
Marketed as
VISUDINE
CC1=C(C2=CC3=NC(=CC4=C(C(=C(N4)C=C5[C@@]6([C@@H](C(=CC=C6C(=N5)C=C1N2)C(=O)OC)C(=O)OC)C)C)CCC(=O)OC)C(=C3C)CCC(=O)O)C=C
Supporting references
Link | Tested on | Impact factor | Notes | Publication date |
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Protoporphyrin IX and verteporfin potently inhibit SARS-CoV-2 infection in vitro and in a mouse model expressing human ACE2
Biophysical assay Animal model In vitro |
In vitro biophysical assay; in vitro binding assay; Vero E6 cells; HEK293T cells; BALB/c mice; SARS-CoV-2 (S protein) pseudovirus; SARS-CoV-2 strain nCoV-SH01 (GenBank: MT121215.1) | 9.51 | Eliminates SARS-CoV-2 infection-induced cytopathic effect and N protein expression in Vero E6 cells at 0.31 μM. The compound was estimated to have EC50 of 0.03 μM and selectivity index of 368.93 (1.35 μM and 224.61 for remdesivir, respectively). Pre-treatment of cells by 1.25 μM solution completely prevented SARS-CoV-2 infection and treatment after infection resulted in 95.4% decrease in viral RNA replication. The drug binds human ACE2 in vitro. It reduces viral loads, pulmonary tissue damage and outer signs of infection in hACE2-expressing mice. |
Dec/09/2020 |
Repurposing FDA-approved drugs for SARS-CoV-2 through an ELISA-based screening for the inhibition of RBD/ACE2 interaction
Small molecule In vitro |
in vitro binding assay; HEK 293T cells; Vero E6 cells; Calu-3 cells | 10.16 | Disrupted ACE2-RBD (of SARS-CoV-2 spike protein) interaction and inhibited RBD binding to ACE2 on cell surface in vitro in dose-dependent manners. Inhibited pseudotyped- and live virus entry into cells. |
Nov/18/2020 |
AI-suggested references
Link | Publication date |
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Modeling the binding of protoporphyrin IX, verteporfin, and chlorin e6 to SARS-CoV-2 proteins.
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May/14/2021 |