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Bicyclomycin Benzoate
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Bicyclomycin Benzoate图片
CAS NO:37134-40-0
包装与价格:
包装价格(元)
5mg电议
25mg电议

产品介绍

化学性质

Physical AppearanceA white solid
StorageStore at -20°C
M.Wt406.4
Cas No.37134-40-0
FormulaC19H22N2O8
SynonymsFR2054
SolubilitySoluble in DMSO
Chemical Name3'-benzoate bicyclomycin
Canonical SMILESO=C1[C@@](O)(NC2=O)C(CCO[C@]2([C@@H](O)[C@@](C)(O)COC(C3=CC=CC=C3)=O)N1)=C
运输条件蓝冰运输或根据您的需求运输。
一般建议为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

Bicyclomycin benzoate is a novel antibiotic produced by S. sapporonensi [1]. Bicyclomycin shows an inhibitory effect on Gram-negative bacteria, such as E. coli, Klebsiella, Shigella, Salmonella, Citrobacter, E. cloacae, and the pathogenic group of Neisseria [2]. Bicyclomycin benzoate is inactive against Proteus, P. aeruginosa, and Gram-positive bacteria [1,2].

In vitro: The MIG of bicyclomycin for E.coli NIHJ JC-2 was 25-50 μg/ml. Bicyclomycin (25-50 μg/ml) completely inhibited formation of visible colonies or turbidity of this organism on agar plates, in nutrient broth, and in heart infusion broth [2]. Bicyclomycin inhibited ATPase activity in the presence of poly(dC) and ribo(C)10. The approximate IC50 value for inhibition of transcription termination at Rho-dependent sites was 5 μM. The inhibitory effect of bicyclomycin on Rho-dependent transcripts was accompanied by the appearance of a new set of transcripts. In the presence of poly(dC), bicyclomycin reversibly inhibited the ribo(C)10-stimulated ATPase activity. The extrapolated Ki for bicyclomycin was 2.8 μM without ribo(C)10, which was increased to 26 μM in the presence of ribo(C)10 [3].

In vivo: Bicyclomycin showed therapeutic activity for infections with several strains of E. coli which were resistant to the control antibiotics. The ED50 of bicyclomycin for infection with GP-resistant E.coli 312 was 3.05 (1.47-7.66) mg/mouse [2].

References:
[1] Miyoshi, T. ,Miyairi, N.,Aoki, H., et al. Bicyclomycin, a new antibiotic. I. Taxonomy, isolation and characterization. J.Antibiot.(Tokyo) 25(10), 569-575(1972).
[2] Nishida, M. ,Mine, Y.,Matsubara, T., et al. Bicyclomycin, a new antibiotic. III. In vitro and in vivo antimicrobial activity. J.Antibiot.(Tokyo) 25(10), 582-593(1972).
[3] Magyar A, Zhang X, Kohn H, et al.  The antibiotic bicyclomycin affects the secondary RNA binding site of Escherichia coli transcription termination factor Rho[J]. Journal of Biological Chemistry, 1996, 271(41): 25369-25374.