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关于此项目
经验公式(希尔记法):
C14H11N3O3S
化学文摘社编号:
分子量:
301.32
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
250-626-5
MDL number:
Beilstein/REAXYS Number:
1085978
产品名称
诺考达唑, ≥99% (TLC), powder
Quality Level
assay
≥99% (TLC)
form
powder
mp
300 °C (dec.)
solubility
DMSO: soluble 10 mg/mL (may require heating), H2O: insoluble
storage temp.
2-8°C
SMILES string
COC(=O)Nc1nc2cc(ccc2[nH]1)C(=O)c3cccs3
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 key
KYRVNWMVYQXFEU-UHFFFAOYSA-N
Gene Information
human ... TUBB(203068)
General description
诺考达唑已(NZO)是一种实验性苯并咪唑基试剂,靶向蛋白质激酶和微管。它可作为新秋水仙碱结合位点抑制剂(CBSI)探索中的先导化合物。这种共结晶配体可作为癌症相关激酶 ABL、c-KIT、BRAF和MEK的高亲和力配体,并可作为微管聚合的快速可逆抑制剂。
Application
诺考达唑已被用于诱导小鼠黑色素瘤B16-F1细胞中的微管解聚。它也用于处理A549细胞,实现有丝分裂阻滞。
Biochem/physiol Actions
诺考达唑(Nocodazole)是一种抗有丝分裂剂,通过结合β−−微管蛋白,阻止两对链间二硫键之一的形成,进而抑制微管动力学、破坏有丝分裂纺锤体功能和片段化高尔基复合体来解聚微管。诺考达唑将细胞周期阻滞在G2/M期,也阻止T细胞抗原受体的磷酸化并抑制其活性。在一些正常和肿瘤细胞系中,诺考达唑刺激微管蛋白内在GTP酶活性,激活JNK/SAPK信号传导通路和诱导凋亡。诺考达唑增强CRISPR同源重组修复(HDR)效率和加强Cas9介导的编辑频率。
Physical form
颜色从白色到淡黄色和粉红色
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signalword
Warning
hcodes
Hazard Classifications
Muta. 2 - Repr. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
商品
包含β-肌动蛋白、α-微管蛋白和波形蛋白用于细胞骨架结果蛋白活细胞分析的高滴度慢病毒颗粒。
业内研究了CRISPR基因组编辑背景下的HDR调控,发现各种细胞类型中增强CRISPR介导的HDR效率的小分子。
High titer lentiviral particles including beta-actin, alpha-tubulin and vimentin used for live cell analysis of cytoskeleton structure proteins.
Alessandra Pisciottani et al.
Cells, 8(7) (2019-07-10)
Abscission is the final step of cell division, mediating the physical separation of the two daughter cells. A key player in this process is the microtubule-severing enzyme spastin that localizes at the midbody where its activity is crucial to cut
Muralidharan Mani et al.
Biochimica et biophysica acta. Molecular cell research, 1866(9), 1463-1474 (2019-06-15)
The perinuclear stacks of the Golgi apparatus maintained by dynamic microtubules are essential for cell migration. Activation of Akt (protein kinase B, PKB) negatively regulates glycogen synthase kinase 3β (GSK3β)-mediated tau phosphorylation, which enhances tau binding to microtubules and microtubule
Yuanming Cheng et al.
Cell reports, 28(7), 1703-1716 (2019-08-15)
Stem cells balance cellular fates through asymmetric and symmetric divisions in order to self-renew or to generate downstream progenitors. Symmetric commitment divisions in stem cells are required for rapid regeneration during tissue damage and stress. The control of symmetric commitment remains
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| M1404-10MG | 04061834038344 |
| M1404-2MG | 04061834040569 |
| M1404-50MG | 04061834040576 |
