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描述
Merck USA index - 14, 4626
质量水平
方案
≥95% (HPLC)
表单
solid
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
desiccated
protect from light
颜色
white to off-white
溶解性
DMSO: 10 mg/mL
运输
ambient
储存温度
−20°C
SMILES字符串
O1[C@H]2[C@H]([C@@H]([C@]3([C@H]([C@@H](C2)C)C=CC3=O)C)O)C(=C)C1=O
InChI
1S/C15H18O4/c1-7-6-10-12(8(2)14(18)19-10)13(17)15(3)9(7)4-5-11(15)16/h4-5,7,9-10,12-13,17H,2,6H2,1,3H3/t7-,9+,10-,12-,13+,15+/m1/s1
InChI key
ZVLOPMNVFLSSAA-XEPQRQSNSA-N
一般描述
A cell-permeable anti-inflammatory sesquiterpene lactone that acts as a specific NF-κB-DNA binding inhibitor by irreversibly alkylating free sulfhydryls of the cysteine residues on the p65 subunit. Exhibits no effect against the DNA-binding activity of the homodimer of p50 subunit, nor does it affect cellular NF-κB activation/nuclear translocation or IκB dissociation/degradation. An excellent research tool for studying NF-κB-mediated biological processes both in cultures in vitro and in animals in vivo.
包装
Packaged under inert gas
警告
Toxicity: Toxic (F)
重悬
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
其他说明
Boulanger, D., et al. 2007. Vet. Microbiol.119, 330.
Auld, C.A., et al. 2006. Biochem. Biophys. Res. Commun.346, 314.
Huang, P.R., et al. 2005. Cancer Lett.227, 169.
Lyss, G., et al. 1998. J. Biol. Chem.273, 33508.
Lyss, G., et al. 1997. Biol. Chem.378, 951.
Auld, C.A., et al. 2006. Biochem. Biophys. Res. Commun.346, 314.
Huang, P.R., et al. 2005. Cancer Lett.227, 169.
Lyss, G., et al. 1998. J. Biol. Chem.273, 33508.
Lyss, G., et al. 1997. Biol. Chem.378, 951.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
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