Rac GTPase (IC50 = 50 μM)

体外活性：NSC23766 以剂量依赖性方式有效抑制 Rac 特异性 GEF Trio 或 Tiam1 的 Rac1 结合和激活，而不干扰密切相关的 Cdc42 或 RhoA 各自 GEF 的结合或激活，也不干扰 Rac1 与 BcrGAP 或效应器的相互作用PAK1。 NSC 23766 积极调节细胞骨架上的 Rac GTPase 功能和许多细胞功能，包括细胞周期、细胞生长、粘附、迁移和基因转录。 NSC 23766 (50 μM) 有效阻断血清或血小板衍生生长因子诱导的 Rac1 激活和板状伪足形成，而不影响 NIH 3T3 细胞中内源性 Cdc42 或 RhoA 的活性。 NSC 23766 减少 Trio 或 Tiam1，但不减少 Vav、Lbc、Intersectin 或组成型活性 Rac1 突变体刺激的 NIH 3T3 细胞生长，并抑制 Trio、Tiam1 或 Ras 诱导的细胞转化。 NSC23766 剂量依赖性地抑制 PC-3 细胞增殖和贴壁依赖性生长。 25 μM NSC23766 可抑制 PC-3 细胞通过 Matrigel 的侵袭 85%。 [1] 50 μM NSC 23766 抑制凝血酶诱导的人血小板中 Rac1 和 Rac2 的激活以及血小板聚集。 NSC23766 可阻止 swAPP-HEK293 细胞中 Aβ40 和 Aβ42 的产生，而不影响 Notch 和 sAPPα。 NSC23766 可阻止细胞中的 γ-分泌酶活性，但不能作为直接的 γ-分泌酶抑制剂。 NSC23766 剂量依赖性地降低分泌型和细胞内 Aβ40 的水平，IC50 为 48.94 μM。 50 μM NSC 23766 可抑制 Aβ42 的释放 57.97%。 NSC23766 调节内皮一氧化氮合酶表达和内皮功能。 100 μM NSC23766 在牛主动脉 EC 中抑制 eNOS 启动子活性 60%，在 bEND.3 细胞中抑制 30% 至 35%。 NSC23766 抑制 Rac1 会破坏 eNOS mRNA 的稳定性，并将其半衰期缩短至 17 小时。 NSC23766 剂量依赖性地减弱 ACh 诱导的野生型小鼠主动脉环松弛。 NSC23766 抑制细胞生长并诱导细胞凋亡。 NSC23766 以剂量依赖性方式降低 MDA-MB-468 和 MDA-MB-231 细胞活力，IC50 约为 10 μM，与雌激素受体 (ER)、孕激素受体 (PR)、Her2、和p53突变。 NSC23766对MCF12A正常乳腺上皮细胞的存活影响很小。暴露于 NSC 23766 24 小时后，MDA-MB-231 细胞的 G1 期细胞数量从 41% 增加至 65%，同时 S 期和 G2-M 期细胞数量减少。 100 μM NSC23766 诱导凋亡 MDA-MB-468 增加六倍。 NSC23766 对乳腺癌细胞细胞周期停滞或凋亡的抑制作用是通过下调细胞周期蛋白 D1、生存素和 X 连锁蛋白凋亡抑制剂介导的。激酶测定：细胞在 10 cm 培养皿中以对数期生长，并在 0.5% 血清培养基中饥饿或以其他方式指示 24 小时，然后在含有 20 mM Tris HCl (pH 7.6)、100 mM NaCl、10 的缓冲液中裂解。 mM MgCl2、1% Nonidet P-40、10% 甘油和 1× 蛋白酶抑制剂混合物。澄清裂解物，标准化蛋白质浓度，并通过效应域下拉测定法测量裂解物中 GTP 结合的 Rac1。对于 His6-PAK1 PBD Pull-down 测定，细胞裂解物与从大肠杆菌中纯化的 Ni2+-琼脂糖固定的 His6-PAK1 PBD 结构域（每个约 1 μg）一起孵育 30 分钟。 Ni2+-琼脂糖共沉淀物在洗涤缓冲液中洗涤两次，并使用抗 Rac1 单克隆抗体进行免疫印迹分析。细胞测定：将细胞（1.5 × 104/mL 人乳腺癌细胞 MDA-MB-468）接种到含有 200 μL 培养基的 96 孔组织培养板的每个孔中。铺板 24 小时后，用 200 μL 含有所示浓度 NSC23766 的新鲜培养基更换培养基。处理结束时，每孔加入20μL MTS溶液，37℃孵育2小时。在 96 孔板读数器上读取 490 nm 处的吸光度。

NSC23766 诱导造血干细胞/祖细胞的动员。将 NSC23766 (2.5 mg/kg) 腹膜内给予“动员能力差的 C57Bl/6 小鼠品系”，导致注射后 6 小时循环造血干细胞祖细胞增加两倍。 NSC23766 可减轻脂多糖诱导的小鼠急性肺损伤。 NSC23766以1或3mg/kg治疗不仅减少炎症细胞浸润和MPO活性，而且抑制促炎介质、肿瘤坏死因子-α和白介素-1β的mRNA表达。 NSC23766 还可以减少 LPS 挑战的肺部中伊文思蓝和白蛋白的积累。

使用蛋白酶和磷酸酶抑制剂将来自腰椎增大的新鲜脊髓组织均质化，然后使用缓冲液将其裂解。将珠子与 PAK-PBD 珠子在 4°C 下在旋转器上孵育 1 小时，然后在 4°C 下以 12,000×g 离心 5 分钟，然后在 4°C 下以 5000×g 离心 3 分钟，从而沉淀珠子。在此期间，收集上清液。第二次煮沸时间为两分钟，将所得沉淀重新悬浮在 LaemmLi 缓冲液中。对珠子样品进行蛋白质印迹分析。通过使用蛋白质印迹分析，还可以找到每个样品中的总 Rac1。

在 96 孔组织培养板中，每孔添加 200 μL 培养基，然后以 1.5 × 10⁴/mL 的细胞生长量进行接种。铺板 24 小时后，将 200 μL 含有指定浓度 NSC23766 的新培养基添加到培养基中。处理期结束时，将 20 微升 MTS 溶液添加到每个孔中，并在 37°C 下孵育两小时。我们使用 96 孔板读数器测量 490 nm 处的吸光度。

At seven weeks of age, Balb/c control and NOD mice are split into four groups (n=8/group). At eight weeks of age, two experimental groups—Balb/c and NOD mice—receive NSC23766 (2.5 mg/kg/day, i.p./daily), while the other two groups—control Balb/c and NOD mice—receive an equivalent volume of saline. For 34 weeks, blood glucose and body weight are measured weekly.

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Two groups of experimental animals (Balb/c and NOD mice) received NSC23766, while the two control groups received equal volume of saline. Body weights and blood glucose were measured every week for 34 weeks. Rac1 activation in pancreatic islets was measured by GLISA activation assay. Rac1 and CHOP expression was determined by Western Blotting.[1]

[1]. NSC23766, a Known Inhibitor of Tiam1-Rac1 Signaling Module, Prevents the Onset of Type 1 Diabetes in the NOD Mouse Model. Cell Physiol Biochem. 2016;39(2):760-7.

[2]. Inhibition of Rac1 GTPase activity affects porcine oocyte maturation and early embryo development. Sci Rep. 2016 Oct 3;6:34415.

[3]. Rac1 modulates the formation of primordial follicles by facilitating STAT3-directed Jagged1, GDF9 and BMP15 transcription in mice. Sci Rep. 2016 Apr 6;6:23972.

[4]. Involvement of Rac1 signalling pathway in the development and maintenance of acute inflammatory pain induced by bee venom injection. Br J Pharmacol. 2016 Mar;173(5):937-50.

NSC 23766 trihydrochloride is a hydrochloride resulting from the formal reaction of NSC 23766 with 3 mol eq. of hydrogen chloride. An inhibitor of the signalling G-protein known as RAC1 (Ras-related C3 botulinum toxin substrate 1). It has a role as an EC 3.6.5.2 (small monomeric GTPase) inhibitor, an antiviral agent, an apoptosis inducer and a muscarinic antagonist. It contains a NSC 23766.

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Background/aims: Type 1 diabetes (T1D) is characterized by absolute insulin deficiency due to destruction of pancreatic β-cells by cytokines (e.g., interleukin-1β; IL-1β) released by invading immune cells. The mechanisms by which these cytokines induce β-cell dysfunction remain poorly understood. Recent evidence suggests that excessive generation of reactive oxygen species (ROS) by the phagocyte-like NADPH oxidase2 (Nox2), along with significantly low levels of antioxidants in β-cells, drive them toward oxidative damage. Rac1, a small G-protein, is one of the members of Nox2 holoenzyme. We recently reported that NSC23766, a known inhibitor of Rac1, significantly attenuated cytokine-induced Nox2 activation and ROS generation in pancreatic islet β-cells in vitro. Herein, we determined the effects of NSC23766 (2.5 mg/kg/day, i.p/daily) on the development of diabetes in the NOD mouse, a model for T1D. Methods: Two groups of experimental animals (Balb/c and NOD mice) received NSC23766, while the two control groups received equal volume of saline. Body weights and blood glucose were measured every week for 34 weeks. Rac1 activation in pancreatic islets was measured by GLISA activation assay. Rac1 and CHOP expression was determined by Western Blotting. Results: Our findings indicate that administration of NSC23766 significantly prevented the development of spontaneous diabetes in the NOD mice. Furthermore, NSC23766 markedly suppressed Rac1 expression and activity and the endoplasmic reticulum stress (CHOP expression) in NOD islets. Conclusions: Our findings provide the first evidence implicating the role of Tiam1-Rac1-Nox2 signaling pathway in the onset of spontaneous diabetes in the NOD mouse model.[1]

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Mammalian oocyte asymmetric division relies on the eccentric positioning of the spindle, resulting in the polar body formation. Small signaling G protein Rac1 is a member of GTPases, which regulates a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. However, effects of Rac1 on the porcine oocyte maturation and early embryo development are not fully understood. In present study we investigated the role of Rac1 in oocyte maturation and embryo cleavage. We first found that Rac1 localized at the cortex of the porcine oocytes, and disrupting the Rac1 activities by treating with NSC 23766 led to the failure of polar body emission. In addition, a majority of treated oocytes exhibited abnormal spindle morphology, indicating that Rac1 may involve into porcine oocyte spindle formation. This might be due to the regulation of Rac1 on MAPK, since p-MAPK expression decreased after NSC 23766 treatments. Moreover, we found that the position of most meiotic spindles in treated oocytes were away from the cortex, indicating the roles of Rac1 on meiotic spindle positioning. Our results also showed that inhibition of Rac1 activity caused the failure of early embryo development. Therefore, our study showed the critical roles of Rac1 GTPase on porcine oocyte maturation and early embryo cleavage.[2]

C24H35N7.3HCL

530.96

529.225427

1177865-17-6

NSC 23766;733767-34-5

16759159

White to khaki solid powder

1.2±0.1 g/cm3

632.4±65.0 °C at 760 mmHg

336.2±34.3 °C

0.0±1.9 mmHg at 25°C

1.647

3.86

91.99

6

7

10

34

514

0

NC1=CC(C)=NC2=CC=C(NC3=NC(NC(C)CCCN(CC)CC)=NC(C)=C3)C=C12.[H]Cl.[H]Cl.[H]Cl

CPUHORIUXPQCHW-UHFFFAOYSA-N

InChI=1S/C24H35N7.3ClH/c1-6-31(7-2)12-8-9-16(3)27-24-28-18(5)14-23(30-24)29-19-10-11-22-20(15-19)21(25)13-17(4)26-22;;;/h10-11,13-16H,6-9,12H2,1-5H3,(H2,25,26)(H2,27,28,29,30);3*1H

6-N-[2-[5-(diethylamino)pentan-2-ylamino]-6-methylpyrimidin-4-yl]-2-methylquinoline-4,6-diamine;trihydrochloride

2934.99.9001

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

注意： 请将本产品存放在密封且受保护的环境中，避免吸湿/受潮。

Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

配方 1 中的溶解度: ≥ 2.5 mg/mL (4.71 mM) (饱和度未知) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (这些助溶剂从左到右依次添加，逐一添加), 澄清溶液。
例如，若需制备1 mL的工作液，可将100 μL 25.0 mg/mL澄清DMSO储备液加入900 μL 20% SBE-β-CD生理盐水溶液中，混匀。
*20% SBE-β-CD 生理盐水溶液的制备（4°C，1 周）：将 2 g SBE-β-CD 溶解于 10 mL 生理盐水中，得到澄清溶液。

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AO:AO ≥ 2.5 mg/mL (4.71 mM) (饱和度未知) in 10% DMSO + 90% Corn Oil (这些助溶剂从左到右依次添加，逐一添加), 澄清溶液。
例如，若需制备1 mL的工作液，可将 100 μL 25.0 mg/mL 澄清 DMSO 储备液添加到 900 μL 玉米油中并混合均匀。

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配方 2 中的溶解度: 110 mg/mL (207.17 mM) in PBS (这些助溶剂从左到右依次添加，逐一添加), clear solution; 超声助溶。

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请根据您的实验动物和给药方式选择适当的溶解配方/方案：
1、请先配制澄清的储备液(如：用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液，按从左到右的顺序依次添加助溶剂，澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明，并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀/澄清；向上述体系中加入50 μL Tween-80，混合均匀/澄清；然后继续加入450 μL ddH2O (或 saline)定容至 1 mL；
3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出，可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果，工作液请现配现用！
6、如不确定怎么将母液配置成体内动物实验的工作液，请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。