包装 | 价格(元) |
500 μg | 电议 |
1mg | 电议 |
Canonical SMILES | CC(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](N4C=CC(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](N8C=CC(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%12C=CC(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%16C=CC(NC%16=O)=O)O%15)O%14)O[C@H](CO)[C@@H](O)[C@@H]%13O)=O |
分子式 | C39H66N4O16(for TunR116:0) |
分子量 | 847 |
溶解度 | DMF: 20 mg/ml,DMSO: 20 mg/ml,DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml |
储存条件 | Store at -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | TunR1 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. TunR1 (5 µg/ml) is cytotoxic to MDA-MB-231 breast cancer cells and non-cancerous CHO cells. Unlike tunicamycin, TunR1 does not inhibit glycosylation in a protein N-glycosylation assay. 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) |