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Merck
CN
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文件

557303

Sigma-Aldrich

利福平

≥97% (HPLC), powder (or crystals), RNA polymerase inhibitor, Calbiochem®

别名:

利福平

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About This Item

经验公式(希尔记法):
C43H58N4O12
CAS号:
分子量:
822.94
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

product name

利福平, Antibiotic that specifically inhibits DNA-dependent RNA polymerase in bacteria by forming an inactive complex.

质量水平

检测方案

~97-102% (by Assay)

形式

powder (or crystals)

制造商/商品名称

Calbiochem®

储存条件

OK to freeze

颜色

red-brown

运输

ambient

储存温度

−20°C

InChI

1S/C43H58N4O12/c1-21-12-11-13-22(2)42(55)45-33-28(20-44-47-17-15-46(9)16-18-47)37(52)30-31(38(33)53)36(51)26(6)40-32(30)41(54)43(8,59-40)57-19-14-29(56-10)23(3)39(58-27(7)48)25(5)35(50)24(4)34(21)49/h11-14,19-21,23-25,29,34-35,39,49-53H,15-18H2,1-10H3,(H,45,55)/b12-11+,19-14+,22-13-,44-20+/t21-,23+,24+,25+,29-,34-,35+,39+,43-/m0/s1

InChI key

JQXXHWHPUNPDRT-WLSIYKJHSA-N

一般描述

通过与RNA聚合酶形成非活性复合物,特异性抑制DNA依赖性细菌RNA聚合酶的抗生素。不影响哺乳动物RNA聚合酶。通过阻止初始转录复合物进入伸长模式来抑制转录。
通过形成非活性复合物,在细菌中特异性抑制DNA依赖性RNA聚合酶的抗生素。不影响哺乳动物RNA聚合酶。通过阻止初始转录复合物进入伸长模式来抑制转录。

生化/生理作用

细菌中的主要靶标
DNA依赖性RNA聚合酶

警告

毒性:有害&致癌/致畸性(E)

重悬

复溶后,等分并冷冻保存(-20°C)。DMSO贮备溶液可在-20°C最长稳定2个月。

其他说明

Jin, D.J. and Turnbough, Jr., C.L.1994.J. Mol.Biol. 236, 72.
Levin, M.E. and Hatfull, G.F.1993.Mol.Microbiol.8, 277.
Wehrli, W., et al. 1968.Proc.Natl.Acad.Sci. USA61, 667.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Morten Kals et al.
Journal of the Royal Society, Interface, 21(212), 20230730-20230730 (2024-03-27)
We describe a phenotypic antibiotic susceptibility testing (AST) method that can provide an eightfold speed-up in turnaround time compared with the current clinical standard by leveraging advances in microscopy and single-cell imaging. A newly developed growth plate containing 96 agarose
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Journal of biomedical research, 37(6), 431-447 (2023-11-22)
cis-Diamminedichloroplatinum (CDDP) is widely used for the treatment of various solid cancers. Here we reported that CDDP increased the expression and enzymatic activities of carboxylesterase 1 (CES1) and carboxylesterase 2 (CES2), along with the upregulation of pregnane X receptor (PXR)
Lama Shamseddine et al.
iScience, 26(9), 107563-107563 (2023-09-04)
In a scenario where the discovery of new molecules to fight antibiotic resistance is a public health concern, ribosomally synthesized and post-translationally modified peptides constitute a promising alternative. In this context, the Gram-positive human gut symbiont Ruminococcus gnavus E1 produces

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