487928
诺考达唑
≥99% (HPLC), solid, microtuble inhibitor, Calbiochem
别名:
诺考达唑, R17934，甲基-[5-（2-噻吩羰基）-1H-苯并咪唑-2-基]-氨基甲酸酯
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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
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
产品名称
诺考达唑, Inhibitor of mitosis.
SMILES string
[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 key
KYRVNWMVYQXFEU-UHFFFAOYSA-N
description
RTECS - DD6521000
assay
≥99% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
color
pale yellow
solubility
DMSO: 5 mg/mL
shipped in
ambient
storage temp.
10-30°C
Quality Level
Biochem/physiol Actions
主要靶标
促进微管蛋白解聚
促进微管蛋白解聚
产物不与ATP竞争。
可逆：否
细胞渗透性：否
Disclaimer
毒性：致癌/致畸（D）
General description
有丝分裂抑制剂。对培养中的哺乳动物细胞具有高度特异性的抗微管活性。促进微管蛋白解聚。也可以50 mM的DMSO溶液（货号487929）提供。
Other Notes
Park, H., et al. 2011.Chem. Med. Chem.in press.
Bunz, F., et al. 1998.Science 282, 1497.
Fleischman, L.F., et al. 1993.Oncogene8, 771.
Pomies, P., and Block, M.R.1992.Biochem.Biophys.Res. Commun.189, 1429.
Rennison, M.E., et al. 1992.J. Cell Sci. 102, 239.
Thyberg, J., and Moskalewski, S. 1992.J. Cell Sci.103, 1167.
Bunz, F., et al. 1998.Science 282, 1497.
Fleischman, L.F., et al. 1993.Oncogene8, 771.
Pomies, P., and Block, M.R.1992.Biochem.Biophys.Res. Commun.189, 1429.
Rennison, M.E., et al. 1992.J. Cell Sci. 102, 239.
Thyberg, J., and Moskalewski, S. 1992.J. Cell Sci.103, 1167.
Preparation Note
复溶后，等分并冷冻长期保存（-20°C），或冷藏（4°C）短期保存。贮备液在4°C下可稳定长达1周，在-20°C下可稳定长达1年。
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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
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Chemical biology & drug design, 88(6), 783-794 (2016-11-05)
Aurora B is a serine/threonine kinase that has a central role in the regulation of mitosis. The observation of Aurora B overexpression in cancer makes it a promising target to develop antitumoral inhibitors. We describe a new potential inhibitor that
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