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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| E129449-10mg |
10mg |
现货 ![]() |
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| E129449-50mg |
50mg |
现货 ![]() |
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| E129449-250mg |
250mg |
现货 ![]() |
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| E129449-1g |
1g |
现货 ![]() |
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| E129449-5g |
5g |
现货 ![]() |
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| 别名 | 9-叔丁基甘氨酰氨基米诺环素,替加环素 |
|---|---|
| 英文别名 | AM20090708 | GAR-936,Tigecycline | TIGECYCLINE [EMA EPAR] | AKOS015895663 | DTXSID2048581 | 9-t-butylglycylamido-minocycline | DTXCID8028507 | (4S,4aS,5aR,12aS)-9-(2-(tert-butylamino)acetamido)-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12 |
| 规格或纯度 | Moligand™, ≥96% |
| 英文名称 | Tigecycline |
| 生化机理 | 替加环素具有抑菌作用,是一种蛋白质合成抑制剂,能与细菌的 30S 核糖体亚基结合,从而在原核生物翻译过程中阻止氨基酰-tRNA 进入核糖体的 A 位点。对革兰氏阴性菌和革兰氏阳性菌具有活性。在体内具有活性。对具有多重耐药性的病原体有效。 |
| 储存温度 | -20°C储存 |
| 运输条件 | 超低温冰袋运输 |
| 作用类型 | 抑制剂 |
| 作用机制 | 细菌 70S 核糖体抑制剂 |
| 备注 | 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
| 产品介绍 |
Tigecycline is a broad spectrum glycylcycline antibiotic. Tigecycline is bacteriostatic. It inhibits protein synthesis throμgh the binding of the 30S ribosomal subunit of bacteria. This blocks entry of Aminoacyl-tRNA into the A site of the ribosome during translation. Tigecycline is active against resistant strains of gram-positive and gram-negative bacteria, avoiding the two most common mechanisms of resistance to the tetracycline antimicrobials: tetracycline efflux pump proteins and ribosomal protection proteins.Tigecycline 是一种广谱的甘氨酰环素抗生素,对 E. coli (MG1655 菌株) 的平均抑制浓度 (MIC) 约为 125 ng/ mL。对 Acinetobacter baumannii (A. baumannii) 的 MIC50 和 MIC90 分别为 1 和 2 mg/L。 Tigecycline is a broad spectrum glycylcycline antibiotic. Tigecycline is bacteriostatic. It inhibits protein synthesis through the binding of the 30S ribosomal subunit of bacteria. This blocks entry of Aminoacyl-tRNA into the A site of the ribosome during translation. Tigecycline is active against resistant strains of gram-positive and gram-negative bacteria, avoiding the two most common mechanisms of resistance to the tetracycline antimicrobials: tetracycline efflux pump proteins and ribosomal protection proteins. |
| 纯度 | ≥96% |
| ALogP | 1.1 |
|---|
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
| 分子类型 | 小分子 |
|---|---|
| IIUPAC Name | (4S,4aS,5aR,12aR)-9-[[2-(tert-butylamino)acetyl]amino]-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4H-tetracene-2-carboxamide |
| INCHI | 1S/C29H39N5O8/c1-28(2,3)31-11-17(35)32-15-10-16(33(4)5)13-8-12-9-14-21(34(6)7)24(38)20(27(30)41)26(40)29(14,42)25(39)18(12)23(37)19(13)22(15)36/h10,12,14,21,31,36-37,40,42H,8-9,11H2,1-7H3,(H2,30,41)(H,32,35)/t12-,14-,21-,29-/m0/s1 |
| InChi Key | SOVUOXKZCCAWOJ-HJYUBDRYSA-N |
| Smiles | CC(C)(C)NCC(=O)NC1=CC(=C2CC3CC4C(C(=O)C(=C(C4(C(=O)C3=C(C2=C1O)O)O)O)C(=O)N)N(C)C)N(C)C |
| Isomeric SMILES | CC(C)(C)NCC(=O)NC1=CC(=C2C[C@H]3C[C@H]4[C@@H](C(=O)C(=C([C@]4(C(=O)C3=C(C2=C1O)O)O)O)C(=O)N)N(C)C)N(C)C |
| 分子量 | 585.65 |
| Reaxy-Rn | 35955618 |
| Reaxys-RN link address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=35955618&ln= |
| 溶解性 | DMSO 100 mg/mL Water 100 mg/mL Ethanol <1 mg/mL |
|---|---|
| 敏感性 | 对热敏感 |
| 比旋光度 | -199° (C=0.15,CH3OH) |
| 熔点 | 185 °C(dec.) |
| 分子量 | 585.600 g/mol |
| XLogP3 | 1.100 |
| 氢键供体数Hydrogen Bond Donor Count | 7 |
| 氢键受体数Hydrogen Bond Acceptor Count | 11 |
| 可旋转键计数Rotatable Bond Count | 7 |
| 精确质量Exact Mass | 585.28 Da |
| 单同位素质量Monoisotopic Mass | 585.28 Da |
| 拓扑极表面积Topological Polar Surface Area | 206.000 Ų |
| 重原子数Heavy Atom Count | 42 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 1240.000 |
| 同位素原子数Isotope Atom Count | 0 |
| 定义的原子立体中心计数Defined Atom Stereocenter Count | 4 |
| 未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
| 定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
| 未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
| 所有立体化学键的总数The total count of all stereochemical bonds | 0 |
| 共价键合单元计数Covalently-Bonded Unit Count | 1 |
| 象形图 | GHS07, GHS08, GHS09 |
|---|---|
| 信号词 | 危险 |
| 危险声明 |
H319: 引起严重眼睛刺激 H360: 可能损害生育力或未出生的孩子 H411: 对水生生物有毒并具有长期持续影响 |
| 预防措施声明 |
P273: 避免释放到环境中。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P391: 收集溢出物 P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。 P405: 密闭存放 P501: 将内容物/容器处理到。。。 P203: 使用前,获取、阅读并遵守所有安全说明。 P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。 P318: 如果暴露或担心,请就医。 P337+P317: 如果眼睛刺激持续:寻求医疗帮助。 |
| Merck Index | 9432 |
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
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| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 | |
| 分析证书 | E129449 |
¥639.90
| 1. Bhavnani SM, Rubino CM, Ambrose PG, Babinchak TJ, Korth-Bradley JM, Drusano GL. (2010) Impact of different factors on the probability of clinical response in tigecycline-treated patients with intra-abdominal infections.. Antimicrob Agents Chemother, 54 (3): (1207-12). [PMID:20038623] |
| 2. Hajdu S, Holinka J, Reichmann S, Hirschl AM, Graninger W, Presterl E. (2010) Increased temperature enhances the antimicrobial effects of daptomycin, vancomycin, tigecycline, fosfomycin, and cefamandole on staphylococcal biofilms.. Antimicrob Agents Chemother, 54 (10): (4078-84). [PMID:20679509] |
| 3. Cercenado E, Marín M, Sánchez-Martínez M, Cuevas O, Martínez-Alarcón J, Bouza E. (2007) In vitro activities of tigecycline and eight other antimicrobials against different Nocardia species identified by molecular methods.. Antimicrob Agents Chemother, 51 (3): (1102-4). [PMID:17194827] |
| 4. Lingling Rong, Ligui Wu, Tiao Zhang, Cui Hu, Haihui Tang, Hongcheng Pan, Xiaoming Zou. (2024) Significant Differences in the Effects of Nitrogen Doping on Pristine Biochar and Graphene-like Biochar for the Adsorption of Tetracycline. MOLECULES, 29 (1): (173). [PMID:38202756] [10.3390/molecules29010173] |
| 5. Shunlan Li, Dongdong Chen, Ziqing Liu, Shipin Tao, Tianyi Zhang, Yiwen Chen, Lingzhi Bao, Jie Ma, Yuee Huang, Shengmin Xu, Lijun Wu, Shaopeng Chen. (2023) Directed evolution of TetR for constructing sensitive and broad-spectrum tetracycline antibiotics whole-cell biosensor. JOURNAL OF HAZARDOUS MATERIALS, 460 (132311). [PMID:37633019] [10.1016/j.jhazmat.2023.132311] |
| 6. Xinyi Liao, Chen Chen, Zhijie Liang, Zhiwei Zhao, Fuyi Cui. (2023) Selective adsorption of antibiotics on manganese oxide-loaded biochar and mechanism based on quantitative structure–property relationship model. BIORESOURCE TECHNOLOGY, 367 (128262). [PMID:36343776] [10.1016/j.biortech.2022.128262] |
| 7. Wang Xiaojuan, Xu Xiaoling, Zhang Shaojun, Chen Na, Sun Yunfeng, Ma Kuifen, Hong Dongsheng, Li Lu, Du Yongzhong, Lu Xiaoyang, Jiang Saiping. (2022) TPGS-based and S-thanatin functionalized nanorods for overcoming drug resistance in Klebsiella pneumonia. Nature Communications, 13 (1): (1-17). [PMID:35768446] [10.1038/s41467-022-31500-3] |
| 8. Guiqiu Li, Ying Wei, Yan Guo, Hui Gong, Jie Lian, Guangjian Xu, Bing Bai, Zhijian Yu, Qiwen Deng. (2022) Omadacycline Efficacy against Streptococcus Agalactiae Isolated in China: Correlation between Resistance and Virulence Gene and Biofilm Formation. Computational Intelligence and Neuroscience, 2022 (7636983). [PMID:35510054] [10.1155/2022/7636983] |
| 9. Rouying Cai, Chenfang Miao, Liang Zhang, Yi Zhou, Yuebin Liu, Chen Zheng, Wendi Han, Zhengjun Huang, Xin Zhou, Shaohuang Weng. (2022) Determination and the pharmacokinetic study of tigecycline by fluorescence strategy with F, N codoping carbon dots as probe. SENSORS AND ACTUATORS B-CHEMICAL, 361 (131721). [10.1016/j.snb.2022.131721] |
| 10. Jin-xin Zheng, Zhi-wei Lin, Xiang Sun, Wei-hong Lin, Zhong Chen, Yang Wu, Guo-bin Qi, Qi-wen Deng, Di Qu, Zhi-jian Yu. (2018) Overexpression of OqxAB and MacAB efflux pumps contributes to eravacycline resistance and heteroresistance in clinical isolates of Klebsiella pneumoniae. Emerging Microbes & Infections, 7 (1): (1-11). [PMID:30068997] [10.1038/s41426-018-0141-y] |
| 11. Xiaodan Zheng, Menglin Wang, Shiqi Zhang, Zhima Yangcuo, Lifang He, Lingfang Xie, Yurou Ye, Guifen Xu, Zhonghui Chen, Qihong Cai. (2024) Development of a new synchronous fluorescence spectrometry combined with Al3+ sensitized for simultaneous and rapid determination of trace flumequine, ciprofloxacin and doxycycline hydrochloride residues in wastewater. WATER RESEARCH, 260 (121941). [PMID:38908313] [10.1016/j.watres.2024.121941] |
| 12. Lei Xu, Yaling Wang, Sangyu Hu, Yuzhu Pei, Chenliang Qian, Wenjie Xue, Gao Zhang, Song Wu, Xinxin Si, Xuming Deng, Jie Xia, Jianfeng Wang. (2025) Discovery of Metabolic Reprogramming 2-Quinolones as Effective Antimicrobials for MRSA-Infected Wound Therapy. JOURNAL OF MEDICINAL CHEMISTRY, [PMID:39869779] [10.1021/acs.jmedchem.4c02185] |
| 13. Ruoyi Li, Muchen Lu, Jiaqi Yu, Jian Zhang, Jia Li, Xinyan Wang. (2025) Efficient electrocatalytic degradation of tigecycline by copper foam-supported Pd-ZnS dual nanoparticle structures: A study of H* reduction and mechanism of action. PROCESS SAFETY AND ENVIRONMENTAL PROTECTION, 197 (107019). [10.1016/j.psep.2025.107019] |
| 14. Haina Bai, Jian Zhang, Shipeng Li, Muchen Lu, Jia Li, Ruoyi Li. (2025) Electrocatalytic study on the degradation of tigecycline wastewater using a three-dimensional porous agarose@MXene hydrogel carbon cloth electrode with high conductivity. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 285 (138231). [PMID:39626821] [10.1016/j.ijbiomac.2024.138231] |
| 15. Yuwei Zheng, Jiaying Chi, Jiayu Ou, Ling Jiang, Liqing Wang, Rui Luo, Yilang Yan, Zejun Xu, Tingting Peng, Jianfeng Cai, Chuanbin Wu, Peng Teng, Guilan Quan, Chao Lu. (2024) Imidazole-Rich, Four-Armed Host-Defense Peptidomimetics as Promising Narrow-Spectrum Antibacterial Agents and Adjuvants against Pseudomonas Aeruginosa Infections. Advanced Healthcare Materials, (2400664). [PMID:39039988] [10.1002/adhm.202400664] |
| 16. Lili Zheng, Yangyuan Cao, Shaohua Chen. (2024) Molecular imprinting sensors based on laser-induced graphene for tigecycline sensing. International Journal of Electrochemical Science, 19 (100710). [10.1016/j.ijoes.2024.100710] |
| 17. Xiangrong Li, Jingjing Zhao, Xianfei Liu, Zhizhi Song, Wanqing Xu, Zheng Li. (2025) Probing the interaction mechanism of tigecycline with γ-globulin and hemoglobin in the absence and presence of amikacin. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 291 (139109). [PMID:39722387] [10.1016/j.ijbiomac.2024.139109] |
| 18. Xinxin Jiang, Jingfei Long, Yanzhen Song, Xiaoyu Qi, Ping Li, Kuiquan Pan, Chenyang Yan, Hongzhou Xu, Haixia Liu. (2024) The effect of triclosan on intergeneric horizontal transmission of plasmid-mediated tigecycline resistance gene tet(X4) from Citrobacter freundii isolated from grass carp gut. ENVIRONMENTAL POLLUTION, 346 (123658). [PMID:38432343] [10.1016/j.envpol.2024.123658] |