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F649416-50mgFIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC 50 of 2.1 μM. FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-5 has anticancer activitiesIn VitroFIDAS-5
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F649416-5mgFIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC 50 of 2.1 μM. FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-5 has anticancer activitiesIn VitroFIDAS-5
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F647152-10mgFilapixant is a purinoreceptor antagonist extracted from patent WO2016091776A1, example 348. Filapixant is the active reference substance of EliapixantForm:SolidIC50&: Target:purinoreceptor.
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F647152-1mgFilapixant is a purinoreceptor antagonist extracted from patent WO2016091776A1, example 348. Filapixant is the active reference substance of EliapixantForm:SolidIC50&: Target:purinoreceptor.
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F647152-5mgFilapixant is a purinoreceptor antagonist extracted from patent WO2016091776A1, example 348. Filapixant is the active reference substance of EliapixantForm:SolidIC50&: Target:purinoreceptor.
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F654889-1mlFilapixant is a purinoreceptor antagonist extracted from patent WO2016091776A1, example 348. Filapixant is the active reference substance of EliapixantIC50&: Target:purinoreceptor.
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F647698-1mgFilibuvir is an orally active, selective non-nucleoside inhibitor of the HCV nonstructural 5B protein (NS5B) RNA-dependent RNA polymerase (RdRp). Filibuvir binds noncovalently in the thumb II allosteric pocket of NS5B. Filibuvir inhibits genotype 1a
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F647698-5mgFilibuvir is an orally active, selective non-nucleoside inhibitor of the HCV nonstructural 5B protein (NS5B) RNA-dependent RNA polymerase (RdRp). Filibuvir binds noncovalently in the thumb II allosteric pocket of NS5B. Filibuvir inhibits genotype 1a
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F156753-1gFinasteride is an orally active testosterone 5-alpha-reductase inhibitor (Ki= 10 nM).An antiandrogen that inhibits 5α-Reductase 2.
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F156753-250mgFinasteride is an orally active testosterone 5-alpha-reductase inhibitor (Ki= 10 nM).An antiandrogen that inhibits 5α-Reductase 2.
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F156753-5gFinasteride is an orally active testosterone 5-alpha-reductase inhibitor (Ki= 10 nM).An antiandrogen that inhibits 5α-Reductase 2.
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F126599-100mgFingolimod (FTY720) is a S1P antagonist with IC50 of 0.033 nM.A cell-permeable aminopropanediol immunosuppressive agent that displays lymphocyte sequestration properties.