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TunR2
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。
TunR2图片
包装与价格：
包装价格(元)
500 μg询价
1mg询价

An antibiotic and derivative of tunicamycin
Canonical SMILESCC(N[C@H]1[C@@H](O[C@H]2[C@H](NC(CCCCCCCCCCC(C)C)=O)[C@@H](O)[C@@H](O)[C@@H](C[C@@H](O)[C@@H]3[C@@H](O)[C@@H](O)[C@H](N4CCC(NC4=O)=O)O3)O2)O[C@H](CO)[C@@H](O)[C@@H]1O)=O.CC(N[C@H]5[C@@H](O[C@H]6[C@H](NC(CCCCCCCCCCCC(C)C)=O)[C@@H](O)[C@@H](O)[C@@H](C[C@@H](O)[C@@H]7[C@@H](O)[C@@H](O)[C@H](N8CCC(NC8=O)=O)O7)O6)O[C@H](CO)[C@@H](O)[C@@H]5O)=O.CC(N[C@H]9[C@@H](O[C@H]%10[C@H](NC(CCCCCCCCCCCCC(C)C)=O)[C@@H](O)[C@@H](O)[C@@H](C[C@@H](O)[C@@H]%11[C@@H](O)[C@@H](O)[C@H](N%12CCC(NC%12=O)=O)O%11)O%10)O[C@H](CO)[C@@H](O)[C@@H]9O)=O.CC(N[C@H]%13[C@@H](O[C@H]%14[C@H](NC(CCCCCCCCCCCCCC(C)C)=O)[C@@H](O)[C@@H](O)[C@@H](C[C@@H](O)[C@@H]%15[C@@H](O)[C@@H](O)[C@H](N%16CCC(NC%16=O)=O)O%15)O%14)O[C@H](CO)[C@@H](O)[C@@H]%13O)=O
分子式C39H68N4O16(for TunR216:0)
分子量0
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

TunR2 is an antibiotic and derivative of tunicamycin .1It is active againstB. subtilis(MIC = 0.3 µg/ml) and increases the efficacy of the β-lactam antibiotics oxacillin , methicillin , and penicillin G againstB. subtiliswhen used at a concentration of 0.4 μg/ml. Unlike tunicamycin, TunR2 is non-toxic toS. cerevisiae(MIC = >10 μg/ml) and does not inhibit glycosylation in a protein N-glycosylation assay. TunR2 also has reduced antiproliferative activity against MDA-MB-231 and CHO cells compared with tunicamycin.

1.Price, N.P., Hartman, T.M., Li, J., et al.Modified tunicamycins with reduced eukaryotic toxicity that enhance the antibacterial activity of β-lactamsJ. Antibiot. (Tokyo)70(11)1070-1077(2017)

 
 
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