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T6798TretazicarTretazicar,NQO1,DNA Alkylator/Crosslinker,rat,bifunctional,Inhibitor,inhibit,agent,cross-l
CB1954(Tretazicar), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.
价 格：￥电议型 号：T6798产 地：中国大陆
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T16342KL1333NQO1 activator 1
KL1333 enhances energy metabolism and mitochondrial dysfunction in MELAS fibroblasts. Elevated NAD+ levels trigger the activation of SIRT1 and AMPK, and subsequently activates PGC-1α. NQO1 activator 1 is an orally available NAD+ modulator. It reacts with
价 格：￥电议型 号：T16342产 地：中国大陆
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T13799NQO1 substrateNQO1 substrate
NQO1 substrate acts as a NQO1 substrate, has the potential to treat NQO1-overexpresssing drug-resistant NSCLC.
价 格：￥电议型 号：T13799产 地：美洲
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T16342NQO1 activator 1NQO1 activator 1
NQO1 activator 1 enhances energy metabolism and mitochondrial dysfunction in MELAS fibroblasts. Elevated NAD+ levels trigger the activation of SIRT1 and AMPK, and subsequently activates PGC-1α. NQO1 activator 1 is an orally available NAD+ modulator. It re
价 格：￥电议型 号：T16342产 地：美洲
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T16342KL1333；化合物KL1333NQO1 activator 1；NQO1 activator 1
KL1333 (NQO1 activator 1) enhances energy metabolism and mitochondrial dysfunction in MELAS fibroblasts. Elevated NAD+ levels trigger the activation of SIRT1 and AMPK, and subsequently activates PGC-1α. NQO1 activator 1 is an orally available NAD+ modulator. It reacts with NAD(P)H: NQO1 as a substrate, resulting in increases in intracellular NAD+ levels via NADH oxidation.
价 格：￥电议型 号：T16342产 地：中国大陆
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T13799NQO1 substrateNQO1底物NQO-1 substrate|||NQO1 substrate
NQO1 substrate is a highly potent NQO1 substrate with potential antitumor activity for leukemia research.
价 格：￥电议型 号：T13799产 地：中国大陆
