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C648939-10mgCensavudine (OBP-601: BMS-986001), a nucleoside analog , is a nucleoside reverse transcriptase inhibitor. Censavudine is a potent HIV inhibitor with EC 50 ranges from 30 nM to 81 nM and 450 nM to 890 nM for HIV-2 and HIV-1 , respectivelyIn
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C648939-25mgCensavudine (OBP-601: BMS-986001), a nucleoside analog , is a nucleoside reverse transcriptase inhibitor. Censavudine is a potent HIV inhibitor with EC 50 ranges from 30 nM to 81 nM and 450 nM to 890 nM for HIV-2 and HIV-1 , respectivelyIn
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C648939-5mgCensavudine (OBP-601: BMS-986001), a nucleoside analog , is a nucleoside reverse transcriptase inhibitor. Censavudine is a potent HIV inhibitor with EC 50 ranges from 30 nM to 81 nM and 450 nM to 890 nM for HIV-2 and HIV-1 , respectivelyIn
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C646686-100mgCentanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter , with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.In
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C646686-10mgCentanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter , with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.In
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C646686-50mgCentanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter , with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.In
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C646686-5mgCentanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter , with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.In
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C654699-1mlCentanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter , with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.In
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C651400-10mgCephaeline dihydrochloride is a selective CYP2D6 inhibtor with an IC 50 of 121 μM.In VitroCYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for
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C651400-25mgCephaeline dihydrochloride is a selective CYP2D6 inhibtor with an IC 50 of 121 μM.In VitroCYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for
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C651400-50mgCephaeline dihydrochloride is a selective CYP2D6 inhibtor with an IC 50 of 121 μM.In VitroCYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for
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C651400-5mgCephaeline dihydrochloride is a selective CYP2D6 inhibtor with an IC 50 of 121 μM.In VitroCYP2D6 reveals the highest metabolic activity for the generation of 9-O-demethylEmetine, whereas this enzyme also shows a significant metabolic activity for