The chemical class of "Arp3 inhibitors" encompasses a diverse array of compounds that indirectly inhibit the function of Arp3 by targeting various aspects of actin dynamics and related signaling pathways. Arp3, as part of the Arp2/3 complex, plays a pivotal role in actin filament nucleation and branching, which is integral to various cellular processes, including cell motility, vesicle trafficking, and cell shape maintenance. One primary feature of these inhibitors is their action on actin dynamics, either by stabilizing actin filaments, disrupting actin polymerization, or affecting actin monomer availability. For example, compounds like Latrunculin A and Cytochalasin D disrupt actin polymerization, while Phalloidin and Jasplakinolide stabilize actin filaments. These actions indirectly inhibit Arp3 by altering the actin filament landscape, essential for Arp3-mediated actin branching.
Another aspect of these inhibitors is their influence on signaling pathways that regulate actin cytoskeleton remodeling. Inhibitors like Y-27632, ML141, and Rhosin target kinases and GTPases such as ROCK, Cdc42, and RhoA, which are upstream regulators of actin cytoskeleton dynamics. By modulating these pathways, these compounds indirectly affect Arp3 function. Additionally, specific inhibitors like CK-666 target the Arp2/3 complex directly, leading to a more direct inhibition of Arp3 within this complex. In conclusion, the chemical class of "Arp3 inhibitors" includes compounds that target various aspects of actin dynamics and related signaling pathways, indirectly inhibiting Arp3 activity. These inhibitors act through diverse mechanisms, including disrupting actin polymerization, stabilizing actin filaments, and modulating key signaling pathways involved in actin cytoskeleton remodeling. Their indirect mode of action reflects the complexity of cellular mechanisms regulating actin dynamics and underscores the crucial role of Arp3 in these processes.
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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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Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
组蛋白去乙酰化酶的抑制因子,可改变染色质结构,并可能减少基因(包括 ARP 蛋白的编码基因)的转录。 | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 18 | |
一种组蛋白去乙酰化酶抑制剂,可导致组蛋白过度乙酰化,从而通过改变染色质的可及性抑制 ARP 基因的表达。 | ||||||
Histone Lysine Methyltransferase Inhibitor 抑制剂 | 935693-62-2 free base | sc-202651 | 5 mg | $148.00 | 4 | |
抑制 G9a 组蛋白甲基转移酶,可能影响 ARP 基因位点附近组蛋白的甲基化,从而抑制 ARP 的转录物。 | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
DNA 甲基转移酶抑制剂,可阻止 ARP 基因启动子区域的甲基化,从而抑制 ARP 的表达。 | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
结合到 DNA 中并抑制 DNA 甲基转移酶,可能导致低甲基化和 ARP 基因表达的改变。 | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
一种能调节基因表达的多酚,通过其对细胞信号通路的广泛影响,可能会抑制 ARP 基因转录物。 | ||||||
Chaetocin | 28097-03-2 | sc-200893 | 200 µg | $120.00 | 5 | |
组蛋白甲基转移酶 SUV39H1 的特异性抑制因子,可改变 ARP 基因周围的染色质结构,影响其转录物。 | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
抑制乙醛脱氢酶,可干扰多种细胞过程,可能会抑制 ARP 基因的表达。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
组蛋白去乙酰化酶抑制剂,可导致染色质结构发生变化,并可能抑制 ARP 基因的转录。 | ||||||
2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
一种糖酵解抑制因子,可能会造成细胞压力,改变各种基因的转录抑制因子,可能包括 ARPs。 |