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Tenatoprazole is a prodrug of the proton pump inhibitor (PPI) class, which inhibits proton transport with IC50 of 3.2 μM.
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Teniposide, a derivative of podophyllotoxin, can interact with DNA topoisomerase II and is used in cancer medicine.
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Teniposide, a derivative of podophyllotoxin, can interact with DNA topoisomerase II and is used in cancer medicine.
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CSNpharm
Teniposide, a derivative of podophyllotoxin, can interact with DNA topoisomerase II and is used in cancer medicine.
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CSNpharm
Teniposide, a derivative of podophyllotoxin, can interact with DNA topoisomerase II and is used in cancer medicine.
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CSNpharm
Teniposide, a derivative of podophyllotoxin, can interact with DNA topoisomerase II and is used in cancer medicine.
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Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV.
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Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV.
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CSNpharm
Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV.
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CSNpharm
Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV.
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Tenofovir dsoproxil acts as an anti-HIV agent and a reverse transcriptase inhibitor that is used to prevent HIV/AIDS and chronic hepatitis B.
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CSNpharm
Tenofovir dsoproxil acts as an anti-HIV agent and a reverse transcriptase inhibitor that is used to prevent HIV/AIDS and chronic hepatitis B.
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CSNpharm
Tenofovir dsoproxil acts as an anti-HIV agent and a reverse transcriptase inhibitor that is used to prevent HIV/AIDS and chronic hepatitis B.
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CSNpharm
Tenofovir dsoproxil acts as an anti-HIV agent and a reverse transcriptase inhibitor that is used to prevent HIV/AIDS and chronic hepatitis B.
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Tenofovir is a nucleotide analogue reverse transcriptase inhibitors (NRTIs) which reduces the viral cytopathic effect of HIV-1 (IIIB), HIV-2(ROD) with EC50 of 1.15 μg/ml and 1.12 μg/ml.
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CSNpharm
Tenofovir is a nucleotide analogue reverse transcriptase inhibitors (NRTIs) which reduces the viral cytopathic effect of HIV-1 (IIIB), HIV-2(ROD) with EC50 of 1.15 μg/ml and 1.12 μg/ml.
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CSNpharm
Tenofovir is a nucleotide analogue reverse transcriptase inhibitors (NRTIs) which reduces the viral cytopathic effect of HIV-1 (IIIB), HIV-2(ROD) with EC50 of 1.15 μg/ml and 1.12 μg/ml.
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Tenosal is a new compound obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid and displays anti-inflammatory, analgesic and antipyretic properties.
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Tenosal is a new compound obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid and displays anti-inflammatory, analgesic and antipyretic properties.
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CSNpharm
Tenosal is a new compound obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid and displays anti-inflammatory, analgesic and antipyretic properties.
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Tephrosin, a natural product isolated and purified from the herbs of Derris robusta, may be valuable for augmenting the therapeutic efficacy of 2-Deoxy-D-glucose(DG), has potent antitumor activity by inducing autophagy pathway, internalization and degradation of inactivated EGFR and ErbB2, and exerts antitumor effects by inducing internalization and degradation of inactivated EGFR and ErbB2 in human […]
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Tephrosin, a natural product isolated and purified from the herbs of Derris robusta, may be valuable for augmenting the therapeutic efficacy of 2-Deoxy-D-glucose(DG), has potent antitumor activity by inducing autophagy pathway, internalization and degradation of inactivated EGFR and ErbB2, and exerts antitumor effects by inducing internalization and degradation of inactivated EGFR and ErbB2 in human […]
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Teprenone is used as an anti-ulcer drug, a cardioprotective agent, a hepatoprotective agent, a nephroprotective agent, a neuroprotective agent and a Hsp70 inducer.
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Terazosin HCl is a selective antagonist for alpha-adrenergic receptor, used for treatment for hypertension and prostate enlargement (BPH) through lowering the blood pressure with elimination half-life of 12 hours.
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Terazosin HCl is a selective antagonist for alpha-adrenergic receptor, used for treatment for hypertension and prostate enlargement (BPH) through lowering the blood pressure with elimination half-life of 12 hours.
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Terazosin HCl is an α-adrenergic (AL-fa ad-ren-ER-jik) blocker used in the therapy of hypertension and benign prostatic hypertrophy with climination half-life of 12 hours.
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Terazosin HCl is an α-adrenergic (AL-fa ad-ren-ER-jik) blocker used in the therapy of hypertension and benign prostatic hypertrophy with climination half-life of 12 hours.
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Terbinafine is a naphthalene-derived allylamine antifungal, working by inhibiting squalene monooxygenase thereby blocking the biosynthesis of ergosterol, which is an essential component of fungal cell membranes.
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Terbinafine is a naphthalene-derived allylamine antifungal, working by inhibiting squalene monooxygenase thereby blocking the biosynthesis of ergosterol, which is an essential component of fungal cell membranes.
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Terbinafine HCl is a naphthalene-derived allylamine antifungal, working by inhibiting squalene monooxygenase thereby blocking the biosynthesis of ergosterol, which is an essential component of fungal cell membranes.
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Terbinafine HCl is a naphthalene-derived allylamine antifungal, working by inhibiting squalene monooxygenase thereby blocking the biosynthesis of ergosterol, which is an essential component of fungal cell membranes.
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Terbufibrol highly reduces serum total cholesterol (TC) levels in the normal and hypercholesterolemic male rat by blocking the hepatic cholesterol synthesis in a step between acetate and HMG-CoA.
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Terbufibrol highly reduces serum total cholesterol (TC) levels in the normal and hypercholesterolemic male rat by blocking the hepatic cholesterol synthesis in a step between acetate and HMG-CoA.
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Terbufibrol highly reduces serum total cholesterol (TC) levels in the normal and hypercholesterolemic male rat by blocking the hepatic cholesterol synthesis in a step between acetate and HMG-CoA.
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Terbufibrol highly reduces serum total cholesterol (TC) levels in the normal and hypercholesterolemic male rat by blocking the hepatic cholesterol synthesis in a step between acetate and HMG-CoA.
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Terconazole is used to treat vaginal yeast infection, working by disrupting the biosynthesis of fats in a yeast cell.
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Terconazole is used to treat vaginal yeast infection, working by disrupting the biosynthesis of fats in a yeast cell.
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Terconazole is used to treat vaginal yeast infection, working by disrupting the biosynthesis of fats in a yeast cell.
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Terephthalic acid, a raw material for polyethylene terephthalate (PET) production, is one of the most important chemicals in petrochemical industry.
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