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重要文件

SML1665

Sigma-Aldrich

Nocodazole

≥98% (HPLC), DMSO solution, microtubule inhibitor

同義詞:

R 17934, 甲基 N-[6-(噻吩-2-羰基)-1H-苯并咪唑-2-基] 氨基甲酸酯, 诺考达唑

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About This Item

經驗公式(希爾表示法):
C14H11N3O3S
CAS號碼:
分子量::
301.32
分類程式碼代碼:
12352200
NACRES:
NA.77

產品名稱

诺考达唑制备液, 5 mg/mL, DMSO solution

生物源

synthetic

品質等級

形狀

DMSO solution

濃度

5 mg/mL

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[s]1c(ccc1)C(=O)c2cc3nc([nH]c3cc2)NC(=O)OC

InChI

1S/C14H11N3O3S/c1-20-14(19)17-13-15-9-5-4-8(7-10(9)16-13)12(18)11-3-2-6-21-11/h2-7H,1H3,(H2,15,16,17,19)

InChI 密鑰

KYRVNWMVYQXFEU-UHFFFAOYSA-N

生化/生理作用

诺考达唑是一种抗癌药物,已被证明会干扰间期和有丝分裂细胞中微管的结构和功能。
诺考达唑是一种抗癌药物,已被证明会干扰间期和有丝分裂细胞中微管的结构和功能。恶性细胞可能比非恶性细胞对诺考达唑的抗微管效应更敏感。体外培养的哺乳动物细胞 可用 0.04-10μg/mL 剂量进行细胞同步化实验。诺考达唑处理导致的细胞在有丝分裂中长时间停滞通常导致细胞凋亡死亡。由于不溶性,无法使用较高浓度。操作的高特异性可解释为什么对骨髓细胞毒性低和无神经毒性。诺考达唑被认为可直接与微管蛋白结合,引起构象变化,导致一些巯基和可能的酪氨酸残基暴露增加。诺考达唑与阿糖胞苷在 L1210 白血病细胞上表现出明显的协同作用。

準備報告

诺考达唑在冷冻溶液中形成沉淀,因此解冻后应进行超声处理,使溶液均匀。建议解冻后超声 1-3 分钟,以除去可能因冷冻而出现的沉淀。
对于细胞培养工作,用培养基稀释诺考达唑现成溶液 (5 mg/mL DMSO),稀释溶液在生物学中至少可稳定 7 天。体外培养的哺乳动物细胞 可用 0.04-10μg/mL 剂量。

儲存和穩定性

本品在-20C 下可稳定保存 2 年。

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

188.6 °F - closed cup

閃點(°C)

87 °C - closed cup


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Endothelial cells selectively release cargo stored in Weibel-Palade bodies (WPBs) to regulate vascular function, but the underlying mechanisms are poorly understood. Here we show that histamine evokes the release of the proinflammatory ligand, P-selectin, while diverting WPBs carrying non-inflammatory cargo
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The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(26), 4997-5007 (2020-05-24)
Stretch-growth has been defined as a process that extends axons via the application of mechanical forces. In the present article, we used a protocol based on magnetic nanoparticles (NPs) for labeling the entire axon tract of hippocampal neurons, and an

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