Lincomycin hydrochloride (Synonyms: 盐酸林可霉素; U10149A)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Lincomycin hydrochloride  (Synonyms: 盐酸林可霉素; U10149A)

Lincomycin (U10149A)盐酸盐是由林可链霉菌产生的抗生素。

Lincomycin hydrochloride                                          (Synonyms: 盐酸林可霉素; U10149A)

Lincomycin hydrochloride Chemical Structure

CAS No. : 859-18-7

规格 价格 是否有货
100 mg ¥340 询问价格 & 货期

* Please select Quantity before adding items.

Lincomycin hydrochloride 的其他形式现货产品:

Lincomycin hydrochloride monohydrate

Lincomycin hydrochloride 相关产品

同靶点产品:

同靶点蛋白产品:

生物活性

Lincomycin Hydrochloride(U10149A) is an antibiotic produced by Streptomyces lincolnensis var. lincolnensis. Target: Antibacterial Lincomycin hydrochloride is a systemic antibiotic, which is active against most common gram positive bacteria. It has proved to be excellent for infectious diseases like acne, anthrax, pneumonia, and also for the treatment of furunculosis, carbuncles, impetigo, burns and wounds, carrying to gram positive bacteria. Lincomycin hydrochloride inhibits cell growth and microbial protein synthesis, by interacting strongly and specifically with the 50S ribosomal subunit, at mutually related sites [1-3].

Clinical Trial

分子量

443.00

Formula

C18H35ClN2O6S

CAS 号

859-18-7

中文名称

盐酸林可霉素

结构分类
  • Antibiotics
  • Disease Research
  • Antibacterial
  • Antibiotics
  • Other Antibiotics
  • Antibiotics
  • Plant agriculture research
  • Antibiotics
  • Mammalian Cell Culture
初始来源
  • 微生物

Streptomyces lincolnensis

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
Data Sheet (527 KB) 产品使用指南 (1538 KB)

参考文献
  • [1]. Griaznova, N.S., et al., [Effect of lincomycin and other protein synthesis inhibitors on the metabolism of Actinomyces roseolus, a producer of lincomycin]. Antibiotiki, 1980. 25(4): p. 250-6.  [Content Brief]

    [2]. Hummel, H., W. Piepersberg, and A. Bock, Analysis of lincomycin resistance mutations in Escherichia coli. Mol Gen Genet, 1979. 169(3): p. 345-7.  [Content Brief]

    [3]. Champney, W.S. and C.L. Tober, Specific inhibition of 50S ribosomal subunit formation in Staphylococcus aureus cells by 16-membered macrolide, lincosamide, and streptogramin B antibiotics. Curr Microbiol, 2000. 41(2): p. 126-35.  [Content Brief]

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务