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R5777

Sigma-Aldrich

利福平

Biotechnology Performance Certified, suitable for plant cell culture

同義詞:

3-(4-甲基-1-哌嗪基亚胺甲基)利福霉素SV, 利米定, 甲哌利福霉素

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About This Item

經驗公式（希爾表示法）:
C43H58N4O12
CAS號碼:
13292-46-1
分子量：:
822.94
Beilstein:
5723476
EC號碼:
236-312-0
MDL號碼:
MFCD00151389
分類程式碼代碼:
12352200
PubChem物質ID:
24899383

等級

Biotechnology Performance Certified

技術

cell culture | plant: suitable

雜質

endotoxin, tested

抗生素活性譜

Gram-negative bacteria
Gram-positive bacteria
mycobacteria

作用方式

protein synthesis | interferes

儲存溫度

−20°C

SMILES 字串

CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(NC(=O)C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(\C=N\N5CCN(C)CC5)c(O)c4c3C2=O

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 密鑰

JQXXHWHPUNPDRT-WLSIYKJHSA-N

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一般說明

Chemical structure: macrolide

生化／生理作用

作用方式：通过与RNA聚合酶的β-亚基结合抑制RNA合成的起始。
抑制DNA和蛋白质组装成成熟的病毒颗粒。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H302

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 1

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。

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Susanne Schjørring et al.
The Journal of antimicrobial chemotherapy, 62(5), 1086-1093 (2008-08-16)
Klebsiella pneumoniae is a nosocomial pathogen and is considered the most common gram-negative bacterium that exhibits multiple antimicrobial resistances. In this study, the transfer of antimicrobial resistance genes from the clinical multiresistant K. pneumoniae MGH75875 isolate was assessed in vitro
Daniel A Bachovchin et al.
Nature biotechnology, 27(4), 387-394 (2009-03-31)
High-throughput screening to discover small-molecule modulators of enzymes typically relies on highly tailored substrate assays, which are not available for poorly characterized enzymes. Here we report a general, substrate-free method for identifying inhibitors of uncharacterized enzymes. The assay measures changes
Thomas J Long et al.
Drug metabolism and disposition: the biological fate of chemicals, 44(12), 1940-1948 (2016-10-27)
Traditional in vitro human liver cell culture models lose key hepatic functions such as metabolic activity during short-term culture. Advanced three-dimensional (3D) liver coculture platforms offer the potential for extended hepatocyte functionality and allow for the study of more complex
Melissa A Kramer et al.
Molecular pharmacology, 73(6), 1751-1760 (2008-03-04)
There are a considerable number of reports identifying and characterizing genetic variants within the CYP2C9 coding region. Much less is known about polymorphic promoter sequences that also might contribute to interindividual differences in CYP2C9 expression. To address this problem, approximately
Ralph Carvalho et al.
PloS one, 6(2), e16779-e16779 (2011-03-11)
One-third of the world population is infected with Mycobacterium tuberculosis and multi-drug resistant strains are rapidly evolving. The noticeable absence of a whole organism high-throughput screening system for studying the progression of tuberculosis is fast becoming the bottleneck in tuberculosis
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