S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
S119-8 is a broad spectrum inhibitor of influenza A and B viruses, showing activity against multiple influenza B viruses and an oseltamivir-resistant influenza A virus, but does not inhibit a non-influenza virus, vesicular stomatitis nirus (VSV)In
SG3199 is a cytotoxic DNA minor groove interstrand crosslinking pyrrolobenzodiazepine (PBD) dimer. SG3199 is the released warhead component of the ADC payload Tesirine (SG3249)In VitroSG3199 is potently cytotoxic against a panel of human solid
SG3199 is a cytotoxic DNA minor groove interstrand crosslinking pyrrolobenzodiazepine (PBD) dimer. SG3199 is the released warhead component of the ADC payload Tesirine (SG3249)In VitroSG3199 is potently cytotoxic against a panel of human solid
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis , and has antitumor activity in vitroIn Vitroζ-Stat (0.1-20 µM) shows only 13% inhibition
S2116, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2116 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 induces apoptosis in
S2116, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2116 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 induces apoptosis in
S2116, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2116 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 induces apoptosis in
S2116, a N-alkylated tranylcypromine (TCP) derivative, is a potent lysine-specific demethylase 1 (LSD1) inhibitor. S2116 increases H3K9 methylation and reciprocal H3K27 deacetylation at super-enhancer regions. S2116 induces apoptosis in