|
CHO
|
IC50 |
1.1 3
Compound: astemizole
|
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
|
[PMID: 23812503]
|
|
CHO
|
IC50 |
1.1 3
Compound: astemizole
|
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
|
[PMID: 23812503]
|
|
HEK293
|
IC50 |
0.9 1
Compound: astemizole
|
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
|
[PMID: 16722631]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
|
[PMID: 36507890]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
|
[PMID: 34413963]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
|
[PMID: 34413963]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
|
[PMID: 36507890]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
Cytotoxicity against CHO cells measured after 48 hrs by MTT assay
|
[PMID: 36507890]
|
|
CHO
|
IC50 |
|
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
Cytotoxicity against CHO cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay
|
[PMID: 34413963]
|
|
HEK293
|
IC50 |
0.008 3
Compound: astemizole
|
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
|
[PMID: 22694270]
|
|
HEK293
|
IC50 |
2.6 1
Compound: astemizole
|
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
|
[PMID: 23403082]
|
|
HEK293
|
IC50 |
0.023 3
Compound: Astemizole
|
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
|
[PMID: 26985309]
|
|
CHO
|
IC50 |
1.1 3
Compound: astemizole
|
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
Inhibition of Cav1.2 current measured using QPatch automatic path clamp system in CHO cells expressing Cav1.2, beta-2 and alpha-2/delta-1 subunits
|
[PMID: 23812503]
|
|
HEK293
|
IC50 |
0.9 1
Compound: astemizole
|
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
|
[PMID: 16722631]
|
|
HEK293
|
IC50 |
5.1 3
Compound: Astemizole
|
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
HEK293
|
IC50 |
14 1
Compound: Astemizole
|
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
|
[PMID: 29370702]
|
|
HEK293
|
IC50 |
0.023 3
Compound: Astemizole
|
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
|
[PMID: 26985309]
|
|
HEK293
|
IC50 |
2.6 1
Compound: astemizole
|
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
|
[PMID: 23403082]
|
|
HEK293
|
IC50 |
2.7 3
Compound: astemizole
|
Displacement of [3H]astemizole from human ERG potassium channel expressed in HEK293 cell membrane
Displacement of [3H]astemizole from human ERG potassium channel expressed in HEK293 cell membrane
|
[PMID: 18588282]
|
|
HEK293
|
IC50 |
2.6 3
Compound: Astemizole
|
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
|
[PMID: 32392053]
|
|
HEK293
|
IC50 |
0.008 3
Compound: astemizole
|
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
|
[PMID: 22694270]
|
|
HEK293
|
IC50 |
2.6 3
Compound: Astemizole
|
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
|
[PMID: 32392053]
|
|
HEK293
|
IC50 |
26.4 3
Compound: astemizole
|
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
|
[PMID: 23241029]
|
|
HEK293
|
IC50 |
0.008 3
Compound: astemizole
|
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
Inhibition of human ERG expressed in HEK293 cells coexpressing Kir2.3 after 30 mins by FluxOR based FLIPR assay
|
[PMID: 22694270]
|
|
HEK293
|
IC50 |
5.1 3
Compound: Astemizole
|
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
HEK293
|
IC50 |
26.4 3
Compound: astemizole
|
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
|
[PMID: 23241029]
|
|
HepG2
|
IC50 |
7.97 3
Compound: Astemizole
|
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
|
[PMID: 30448235]
|
|
HEK293
|
IC50 |
14 1
Compound: Astemizole
|
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
|
[PMID: 29370702]
|
|
HEK293
|
IC50 |
0.023 3
Compound: Astemizole
|
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
Displacement of [3H] dofetilide from human ERG channel expressed in HEK293 cell membranes incubated for 2 hrs by scintillation counting analysis
|
[PMID: 26985309]
|
|
HT-29
|
IC50 |
15.4 3
Compound: Astemizole
|
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
HEK293
|
IC50 |
0.9 1
Compound: astemizole
|
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
Inhibition of hERG potassium channel in HEK293 cells by patch clamp assay
|
[PMID: 16722631]
|
|
HepG2
|
IC50 |
7.97 3
Compound: Astemizole
|
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
|
[PMID: 30448235]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
HepG2
|
IC50 |
|
HARVARD: Cytotoxicity in HepG2 cell line
HARVARD: Cytotoxicity in HepG2 cell line
|
[PMID: 22586124]
|
|
HEK293
|
IC50 |
14 1
Compound: Astemizole
|
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method
|
[PMID: 29370702]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
HEK293
|
IC50 |
2.6 1
Compound: astemizole
|
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
Displacement of [3H]Astemizole from human recombinant ERG expressed in HEK293 cells at after 60 mins
|
[PMID: 23403082]
|
|
HepG2
|
IC50 |
0.114 3
Compound: 92125178
|
HARVARD: Inhibition of liver stage Plasmodium berghei infection in HepG2 cells
HARVARD: Inhibition of liver stage Plasmodium berghei infection in HepG2 cells
|
[PMID: 22586124]
|
|
HEK293
|
IC50 |
2.6 3
Compound: Astemizole
|
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
Inhibition of human ERG expressed in HEK293 cells measured after 30 mins by FluxOR dye based FLIPR TETRA assay
|
[PMID: 32392053]
|
|
LLC-PK1
|
IC50 |
1.7 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
HT-29
|
IC50 |
15.4 3
Compound: Astemizole
|
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
HEK293
|
IC50 |
2.7 3
Compound: astemizole
|
Displacement of [3H]astemizole from human ERG potassium channel expressed in HEK293 cell membrane
Displacement of [3H]astemizole from human ERG potassium channel expressed in HEK293 cell membrane
|
[PMID: 18588282]
|
|
Huh-7
|
CC50 |
20.89 3
Compound: GNF-Pf-2461
|
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
|
[PMID: 18579783]
|
|
RBL-2H3
|
IC50 |
0.0533 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
|
[PMID: 31703894]
|
|
HEK293
|
IC50 |
26.4 3
Compound: astemizole
|
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
Inhibition of human MATE1-mediated ASP+ uptake expressed in HEK293 cells after 1.5 mins by fluorescence assay
|
[PMID: 23241029]
|
|
RBL-2H3
|
IC50 |
0.0819 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
|
[PMID: 31703894]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
RBL-2H3
|
IC50 |
0.156 3
Compound: Astemizole
|
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
|
[PMID: 31703894]
|
|
HEK293
|
IC50 |
5.1 3
Compound: Astemizole
|
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
Cytotoxicity against human ERG transfected HEK293 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
LLC-PK1
|
IC50 |
1.7 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
Vero C1008
|
EC50 |
1.1 3
Compound: Astemizole
|
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
|
[PMID: 32511357]
|
|
RBL-2H3
|
IC50 |
0.156 3
Compound: Astemizole
|
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
|
[PMID: 31703894]
|
|
RBL-2H3
|
IC50 |
0.0819 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
|
[PMID: 31703894]
|
|
RBL-2H3
|
IC50 |
0.0533 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
|
[PMID: 31703894]
|
|
Vero C1008
|
EC50 |
1.1 3
Compound: Astemizole
|
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
|
10.1101/2020.04.16.044016
|
|
HT-29
|
IC50 |
15.4 3
Compound: Astemizole
|
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
Cytotoxicity against human HT-29 cells after 24 hrs by MTT assay
|
[PMID: 26985309]
|
|
HepG2
|
IC50 |
0.114 3
Compound: 92125178
|
HARVARD: Inhibition of liver stage Plasmodium berghei infection in HepG2 cells
HARVARD: Inhibition of liver stage Plasmodium berghei infection in HepG2 cells
|
[PMID: 22586124]
|
|
HepG2
|
IC50 |
|
HARVARD: Cytotoxicity in HepG2 cell line
HARVARD: Cytotoxicity in HepG2 cell line
|
[PMID: 22586124]
|
|
HepG2
|
IC50 |
7.97 3
Compound: Astemizole
|
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
Cytotoxicity against human HepG2 cells after 24 hrs by MTT assay
|
[PMID: 30448235]
|
|
Huh-7
|
CC50 |
20.89 3
Compound: GNF-Pf-2461
|
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
|
[PMID: 18579783]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in MDR1-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in MDR1-expressing LLC-PK1 cells
|
[PMID: 12699389]
|
|
LLC-PK1
|
IC50 |
1.3 3
Compound: Astemizole
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1a-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1a-expressing LLC-PK1 cells
|
[PMID: 12699389]
|
|
LLC-PK1
|
IC50 |
1.7 3
Compound: Astemizole
|
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389]
|
|
LLC-PK1
|
IC50 |
1.7 3
Compound: Astemizole
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1b-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1b-expressing LLC-PK1 cells
|
[PMID: 12699389]
|
|
RBL-2H3
|
IC50 |
0.0533 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced mast cell degranulation preincubated with compound for 30 mins and then treated with C48/80 for 1 hr by neutral red dye based method
|
[PMID: 31703894]
|
|
RBL-2H3
|
IC50 |
0.0819 3
Compound: Astemizole
|
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
Antiallergic activity in rat RBL2H3 cells assessed as inhibition of C48/80-induced histamine release preincubated with compound for 30 mins followed by C48/80 stimulation for 1 hr
|
[PMID: 31703894]
|
|
RBL-2H3
|
IC50 |
0.156 3
Compound: Astemizole
|
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
Antiallergic activity in IgE/Ag-stimulated rat RBL2H3 cells assessed as inhibition of HSA-induced beta-hexosaminidase release preincubated with compound for 30 mins and then stimulated with HSA for 15 mins followed by incubation with P-nitrophenyl-N-acety
|
[PMID: 31703894]
|
|
Vero C1008
|
EC50 |
1.1 3
Compound: Astemizole
|
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
Determination of antiviral efficacy in high-content imaging assay in Vero E6 cells infected with SARS-CoV-2 (USA-WA1/2020 isolate) at MOI 0.75 after 24 hrs
|
10.1101/2020.04.16.044016
|