相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- CAS号:
6138-41-6
- 规格:
1mLx10mM(inDMSO)/50mg/100mg
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥152.0 |
|---|---|---|---|
| 规格: | 50mg | 产品价格: | ¥174.0 |
| 规格: | 100mg | 产品价格: | ¥253.0 |
Product Introduction
Bioactivity
| 名称 | Trigonelline chloride |
| 描述 | Trigonelline chloride (Coffearine Hydrochloride), an alkaloid with potential antidiabetic activity, is present in considerable amounts in coffee. |
| 存储条件 | Keep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 11.74 mg/mL (67.63 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 1.00 mg/mL (5.76 mM), Sonication is recommended. 10% DMSO+90% Saline : 1.17 mg/mL (6.74 mM), Solution. |
| 关键字 | Trigonelline Hydrochloride | Trigonelline chloride | Trigonelline | Inhibitor | inhibit | HSV | Herpes simplex virus | Fungal | Bacterial |
| 相关产品 | Guanidine hydrochloride | Glycerol | Aceglutamide | Malic acid | Sucrose | Neomycin sulfate | Hemin | Dimethyl sulfoxide | Sodium bicarbonate | Gluconate Calcium | Thymidine | D(+)-Raffinose pentahydrate |
| 相关库 | Bioactive Compound Library | Anti-Fungal Compound Library | Bioactive Compounds Library Max | Alkaloid Natural Product Library | Tibetan medicine Compound Library | Anti-Infection Compound Library | FDA-Approved & Pharmacopeia Drug Library | NO PAINS Compound Library | Anti-Viral Compound Library | Tobacco Monomer Library | Ferroptosis Compound Library | Human Metabolite Library |
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验【分享】强烈推荐---各类学习资源的56@邮箱的汇总(共2975条)
.. 2006.01.20 14:12 19857.91Kb hwzgj-phar,hwzgj-phar2,hwzgj-phar3 hjhw9 40 05版药典微生物限度无菌法方法学验证及演.. 2006.01.20 14:12 19857.91Kb hwzgj-phar,hwzgj-phar2,hwzgj-phar3 hjhw9 41 05年北京版高血压对心脏损害和治疗对策 zrqx8939 42 05年北京版高血压对心脏损害和治疗对策_... 2006.01.24 20:15 706.35
7h以上,药物释放按一级反应动力学方式进行。通过控制微囊粒子大小及改变聚乳酸分子量和药物 载体 ,可控制CPFX的释放,以达到延长药物作用的目的。 3 注射剂 CPFX静注剂型有乳酸盐和盐酸盐,国内多家研究单位〔3,4〕研制成功,与进口CPFX作人体药物动力学性质比较,两者主要药动学参数无显著性差异〔5〕。静注CPFX的血清半衰期为5h,若肾功能正常,每12h给药一次不会引起蓄积。与同等剂量口服比较,CPFX静注的Cmax值比口服高,尿中回收率也比口服
半胱氨酸 0.11 41 盐酸吡哆醛 0.025 12 L-盐酸胱氨酸 26.00 42
技术资料暂无技术资料 索取技术资料










