QPCTL inhibitors belong to a distinctive chemical class primarily associated with the modulation of the enzyme quinolinate phosphoribosyltransferase-like protein (QPCTL). QPCTL, a member of the phosphoribosyltransferase superfamily, plays a crucial role in the quinolinic acid (QA) biosynthetic pathway. This pathway is essential for the de novo synthesis of nicotinamide adenine dinucleotide (NAD+), a critical coenzyme involved in various cellular processes. The QPCTL enzyme catalyzes the conversion of quinolinic acid to nicotinic acid mononucleotide (NAMN), a pivotal step in NAD+ biosynthesis. Inhibition of QPCTL, therefore, has the potential to modulate NAD+ levels within cells.
QPCTL inhibitors are characterized by their ability to selectively interact with the active site of the QPCTL enzyme, disrupting its catalytic function. These inhibitors typically possess a defined pharmacophore that engages specific residues within the enzyme's binding pocket, thereby hindering the conversion of quinolinic acid to NAMN. Understanding the structural determinants of QPCTL inhibition is crucial for the design and development of potent inhibitors with enhanced selectivity and efficacy. Research in this chemical class aims to elucidate the molecular mechanisms governing the interaction between QPCTL inhibitors and the enzyme, providing valuable insights for future drug discovery efforts targeting NAD+ biosynthesis modulation.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Chloroquine | 54-05-7 | sc-507304 | 250 mg | ¥767.00 | 2 | |
影响内膜/溶酶体酸化,并可能导致抑制蛋白质降解。这种间接效应可能会影响泛素化过程,从而影响 QPCTL 的功能。 | ||||||
FCM Lysing solution (1x) | sc-3621 | 150 ml | ¥459.00 | 8 | ||
溶酶体促进剂,类似于氯喹。通过改变溶酶体功能,NH4Cl 可影响蛋白质降解,并可能影响 QPCTL 的功能。 |