1278 Results for: "MEDCHEMEXPRESS"

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6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine DON) is a glutamine antagonist that irreversibly inhibits the catabolic effe ct of glutamine. 6-Diazo-5-oxo-L-nor-Leucine shows good anticancer activity (especially in pancreatic cancer) and red 1 * 50 mg

Supplier: MEDCHEMEXPRESS

6-Diazo-5-oxo-L-nor-Leucine (L-6-Diazo-5-oxonorleucine DON) is a glutamine antagonist that irreversibly inhibits the catabolic effe ct of glutamine. 6-Diazo-5-oxo-L-nor-Leucine shows good anticancer activity (especially in pancreatic cancer) and red 1 * 50 mg

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Proteinase K (Protease K) is a nonspecific serine protease that is useful for general digestion of proteins. Proteinase K is active in the presence of SDS or urea and over a wide range of pH (4-12), salt concentrations, and temperatures. Proteinase K 1 * 25 mg

Supplier: MEDCHEMEXPRESS

Proteinase K (Protease K) is a nonspecific serine protease that is useful for general digestion of proteins. Proteinase K is active in the presence of SDS or urea and over a wide range of pH (4-12), salt concentrations, and temperatures. Proteinase K 1 * 25 mg

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Palbociclib (PD 0332991) isethionate is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respect ively. Palbociclib isethionate has potent anti-proliferative activity and induces cell cycle arrest in cancer cells, 1 * 100 mg

Supplier: MEDCHEMEXPRESS

Palbociclib (PD 0332991) isethionate is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respect ively. Palbociclib isethionate has potent anti-proliferative activity and induces cell cycle arrest in cancer cells, 1 * 100 mg

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U0126 is a potent, non-ATP competitive and selective MEK1 and MEK2 inhibitor, with IC50s of 72 nM and 58 nM, respectively. U0126 is an autophagy and mitophagy inhibitor[1][2][3][4]. 1 * 25 mg

Supplier: MEDCHEMEXPRESS

U0126 is a potent, non-ATP competitive and selective MEK1 and MEK2 inhibitor, with IC50s of 72 nM and 58 nM, respectively. U0126 is an autophagy and mitophagy inhibitor[1][2][3][4]. 1 * 25 mg

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Etanercept, a dimeric fusion protein that binds TNF, acts as a TNF inhibitor. Etanercept competitively inhibits the binding of both TNF-α and TNF-β to cell surface TNF receptors, rendering TNF biologically inactive. Etanercept shows efficacy against 1 * 10 mg

Supplier: MEDCHEMEXPRESS

Etanercept, a dimeric fusion protein that binds TNF, acts as a TNF inhibitor. Etanercept competitively inhibits the binding of both TNF-α and TNF-β to cell surface TNF receptors, rendering TNF biologically inactive. Etanercept shows efficacy against 1 * 10 mg

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Asunaprevir (BMS-650032) is a potent and orally bioavailable hepatitis C virus (HCV) NS3 protease inhibitor, with IC50 of 0.2 nM-3.5 nM[1]. Asunaprevir inhibits SARS-CoV-2 3CLpro activity[5]. 1 * 5 mg

Supplier: MEDCHEMEXPRESS

Asunaprevir (BMS-650032) is a potent and orally bioavailable hepatitis C virus (HCV) NS3 protease inhibitor, with IC50 of 0.2 nM-3.5 nM[1]. Asunaprevir inhibits SARS-CoV-2 3CLpro activity[5]. 1 * 5 mg

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4-Hydroperoxy cyclophosphamide is the active metabolite form of the precursor Cyclophosphamide. 4-Hydroperoxy cyclophosphamide cross -links DNA to induce T cell apoptosis independent of caspase receptor activation, and can activate the mitochondrial 1 * 10 mg

Supplier: MEDCHEMEXPRESS

4-Hydroperoxy cyclophosphamide is the active metabolite form of the precursor Cyclophosphamide. 4-Hydroperoxy cyclophosphamide cross -links DNA to induce T cell apoptosis independent of caspase receptor activation, and can activate the mitochondrial 1 * 10 mg