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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| C336103-100mg |
100mg |
现货 ![]() |
| |
| C336103-1g |
1g |
现货 ![]() |
| |
| C336103-5g |
5g |
现货 ![]() |
| |
| C336103-25g |
25g |
期货 ![]() |
| |
| C336103-100g |
100g |
期货 ![]() |
|
| 英文别名 | NCGC00159465-02 | Cephazolin | CEFAZOLIN [HSDB] | Cefazoline (INN-French) | DivK1c_000014 | J01DB04 | KBio2_003114 | SK&F-41558 | AKOS015962265 | Prestwick0_000736 | (6R,7R)-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl}-8-oxo-7-[(1H-tetrazol-1-ylacetyl |
|---|---|
| 规格或纯度 | Moligand™, ≥98% |
| 英文名称 | Cefazolin |
| 储存温度 | 2-8°C储存 |
| 运输条件 | 冰袋运输 |
| 产品介绍 |
Cefazolin (Cephazolin) 是第一代头孢菌素类抗生素,可用于多种细菌感染的研究。Cefazolin 具有抗炎作用,可以减轻术后认知功能障碍 (POCD)。 Cefazolin (Cephazolin) is a first-generation cephalosporin antibiotic and can be used in varieties of bacterial infections research[1]. Cefazolin has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD). |
| 纯度 | ≥98% |
| pKa值 | pKa: 2.6 (Predicted), pKa: 0.45 (Predicted) |
|---|---|
| Ki Data | OAT1: Ki= 180 nM (human); OAT3: Ki= 550 nM (human); SLC22A11: Ki= 1.74 μM (human); Solute carrier family 22 member 6: Ki= 450 μM (rat); Solute carrier family 22 member 8: Ki= 780 μM (rat) |
| IC50 | MG-63: IC₅₀> 0.88 mM (human); HeLa: IC₅₀> 0.88 mM (human) |
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
| PubChem SID | 488183217 |
|---|---|
| EC号 | 247-362-8 |
| 分子类型 | 小分子 |
| IIUPAC Name | (6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[[2-(tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| INCHI | 1S/C14H14N8O4S3/c1-6-17-18-14(29-6)28-4-7-3-27-12-9(11(24)22(12)10(7)13(25)26)16-8(23)2-21-5-15-19-20-21/h5,9,12H,2-4H2,1H3,(H,16,23)(H,25,26)/t9-,12-/m1/s1 |
| InChi Key | MLYYVTUWGNIJIB-BXKDBHETSA-N |
| Smiles | CC1=NN=C(S1)SCC2=C(N3C(C(C3=O)NC(=O)CN4C=NN=N4)SC2)C(=O)O |
| Isomeric SMILES | CC1=NN=C(S1)SCC2=C(N3[C@@H]([C@@H](C3=O)NC(=O)CN4C=NN=N4)SC2)C(=O)O |
| 分子量 | 454.51 |
| Beilstein号 | 4169371 |
| Reaxy-Rn | 634703 |
| Reaxys-RN link address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=634703&ln= |
| 溶解性 | Soluble in DMF, pyridine, aqueous acetone, and aqueous ethanol. Insoluble in water. |
|---|---|
| 密度 | ~2.0 g/cm3(Predicted) |
| 敏感性 | 对湿度敏感 |
| 折光率 | n20D1.96 (Predicted) |
| 熔点 | 197.8-200° C (dec.) |
| 分子量 | 454.500 g/mol |
| XLogP3 | -0.400 |
| 氢键供体数Hydrogen Bond Donor Count | 2 |
| 氢键受体数Hydrogen Bond Acceptor Count | 12 |
| 可旋转键计数Rotatable Bond Count | 7 |
| 精确质量Exact Mass | 454.03 Da |
| 单同位素质量Monoisotopic Mass | 454.03 Da |
| 拓扑极表面积Topological Polar Surface Area | 235.000 Ų |
| 重原子数Heavy Atom Count | 29 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 740.000 |
| 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 | 2 |
| 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 |
|---|---|
| 信号词 | 危险 |
| 危险声明 |
H317: 可能引起皮肤过敏反应 H334: 吸入可能引起过敏或哮喘病症状或呼吸困难 |
| 预防措施声明 |
P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾 P272: 被污染的工作服不允许离开工作场所 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P284: 如果通风不良,请佩戴呼吸防护装置。 P321: 特殊处理(请参阅此标签上的...)。 P302+P352: 如皮肤沾染:用水充分清洗。 P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。 P333+P313: 如发生皮肤刺激或皮疹:求医/就诊。 P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。 P501: 将内容物/容器处理到。。。 P342+P316: 如果出现呼吸道症状:立即寻求急救。 |
| RTECS | XI0389900 |
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 | |
| 分析证书 | C336103 |
¥411.92
| 1. Nudelman A, Karoly H, Braun F, Böhme EH, Erickson RC. (1978) Semisynthetic cephalosporins. Synthesis and structure-activity relationships of 7-(1-pyrryl)- and 7-(1-indolyl)acetamidocephalosporin derivatives.. J Med Chem, 21 (9): (962-4). [PMID:722761] |
| 2. Yexuan Mao, Yichao Fan, Ran Yang, Youyi Wang, Qingyue Li, Meng Dang, Xianqing Huang, Lianjun Song, Pingan Zhang, Miao Song, Liang Liu, Linli Wang, Shun Yu, Qiuyan Zhao, Xiya Zhang. (2023) A highly sensitive electrochemical sensor derived from peptide amphiphilic inspired self-assembled, ordered gold nanoparticles for determination of 22 β-lactams. ELECTROCHIMICA ACTA, 461 (142669). [10.1016/j.electacta.2023.142669] |
| 3. Lishan Zhang, Zujie Yao, Huamei Tang, Qingli Song, Huanhuan Song, Jindong Yao, Zhen Li, Xiaofang Xie, Yuexu Lin, Xiangmin Lin. (2022) The Lysine Acetylation Modification in the Porin Aha1 of Aeromonas hydrophila Regulates the Uptake of Multidrug Antibiotics. MOLECULAR & CELLULAR PROTEOMICS, 21 (9): [PMID:35605723] [10.1016/j.mcpro.2022.100248] |
| 4. Shuangmin Wu, Wei Shen, Yushuang Chen, Yongli Zhu, Ren Hou, Menghong Dai, Dapeng Peng. (2022) Rapid Determination of Cephalexin in Animal-Derived Food by an Indirect Competitive Enzyme-Linked Immunosorbent Assay. ANALYTICAL LETTERS, 55 (17): (2803-2816). [10.1080/00032719.2022.2072857] |
| 5. Zhenbin Chen, Haohan Cai, Feng Huang, Zongping Wang, Yiqun Chen, Zizheng Liu, Pengchao Xie. (2024) Degradation of β-lactam antibiotics by Fe(III)/HSO3− system and their quantitative structure-activity relationship. ENVIRONMENTAL RESEARCH, 259 (119577). [PMID:38986801] [10.1016/j.envres.2024.119577] |
| 6. Yaowei Zhu, Ruijie Tang, Jun Zhao, Changlong Jiang, Lingfei Li, Bianhua Liu. (2025) Design and application of metal-organic framework based chemo-fluorescent sensor for selective sensing of the full spectrum of tetracyclines in complex samples. CHEMICAL ENGINEERING JOURNAL, 507 (160281). [10.1016/j.cej.2025.160281] |
| 7. Aftab Khan, Samreen Sadiq, Iltaf Khan, Muhammad Humayun, Guo Jiyuan, Muhammad Usman, Abbas Khan, Shoaib Khan, Amal Faleh Alanazi, Mohamed Bououdina. (2024) Preparation of visible-light active MOFs-Perovskites (ZIF-67/LaFeO3) nanocatalysts for exceptional CO2 conversion, organic pollutants and antibiotics degradation. Heliyon, 10 [PMID:38486780] [10.1016/j.heliyon.2024.e27378] |