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.
Items 1 to 10 of 12 total
展示:
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | ¥632.00 ¥2933.00 ¥11056.00 | 163 | |
蛋白酶体抑制剂。通过抑制蛋白酶体,MG-132 可导致泛素化蛋白质的积累,间接影响 QPCTL 的泛素化功能。 | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | ¥1489.00 ¥12004.00 | 115 | |
蛋白酶体抑制剂。硼替佐米可以干扰泛素-蛋白酶体途径,这可能会间接影响 QPCTL 的蛋白质修饰作用。 | ||||||
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | ¥3159.00 | 1 | |
抑制NEDD8激活酶(NAE)。通过破坏cullin蛋白的NEDD8修饰,可以改变泛素连接酶的活性,从而影响QPCTL介导的泛素化过程。 | ||||||
Ubiquitin E1 Inhibitor, PYR-41 | 418805-02-4 | sc-358737 | 25 mg | ¥4062.00 | 4 | |
泛素激活酶(E1)抑制剂。PYR-41可以阻止泛素化级联的初始步骤,这可能会间接影响QPCTL的功能。 | ||||||
MLN7243 | 1450833-55-2 | sc-507338 | 5 mg | ¥3836.00 | ||
泛素激活酶(E1)抑制剂。与PYR-41类似,TAK-243也能抑制泛素化的第一步,从而间接影响QPCTL的功能。 | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | ¥1230.00 ¥3949.00 | 8 | |
靶标是泛素连接酶复合物的一个组成部分 cereblon。通过调节泛素连接酶的活性,它可能间接影响 QPCTL 介导的泛素化过程。 | ||||||
Lenalidomide | 191732-72-6 | sc-218656 sc-218656A sc-218656B | 10 mg 100 mg 1 g | ¥553.00 ¥4140.00 ¥22902.00 | 18 | |
沙利度胺的类似物。它还能靶向 cereblon 并影响泛素连接酶的活性,从而可能影响 QPCTL 的功能。 | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | ¥632.00 ¥2392.00 ¥8619.00 | 24 | |
MDM2抑制剂。MDM2是一种E3泛素连接酶,作用于p53。通过抑制MDM2,Nutlin-3可以破坏p53的泛素化,从而间接影响更广泛的泛素化过程和QPCTL功能。 | ||||||
PR 619 | 2645-32-1 | sc-476324 sc-476324A sc-476324B | 1 mg 5 mg 25 mg | ¥846.00 ¥2076.00 ¥4772.00 | 1 | |
广谱去泛素化酶(DUB)抑制剂。通过抑制 DUB,PR-619 可导致泛素底物的积累,从而可能影响 QPCTL 的功能。 | ||||||
NSC697923 | 343351-67-7 | sc-391107 sc-391107A | 1 mg 5 mg | ¥169.00 ¥575.00 | 3 | |
Ubc13-Uev1A 抑制剂,破坏 Lys63 连接的多泛素链的形成。这会影响某些泛素化过程,有可能影响 QPCTL 的功能。 |