(1)硝苯吡啶(Nifedipine)、维拉帕米(Verapamil)及硫氮卓酮(Dilthiazem):由于钙通道阻滞剂抑制钙的内流,使平滑肌收缩性下降,能降低肠易激综合征患者餐后结肠锋电位活动,有...
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Verapamil Hydrochloride 盐酸维拉帕米 ; 维拉帕米盐酸盐 ; 维拉帕米 ; 异博定
Verapamil HCl 盐酸维拉帕米 ; 盐酸异博定
Verapamil Hydrochloride Tablets 盐酸维拉帕米片
verapamil SR 缓释剂 ; 维拉帕米缓释剂
Verapamil Hydrochloride Injection 盐酸维拉帕米注射液
Verapamil Related Compound A 维拉帕米杂质A
Verapamil Related Compound B 维拉帕米杂质B ; 盐酸维拉帕米杂质B
Verapamil Hydrochloride Sustained-release Tablets 盐酸维拉帕米缓释片 ; 维拉帕米缓释片
Asarum-Verapamil 细辛与维拉帕米
The inhibitors, cyclosporine A and verapamil,significantly enhanced the uptake amount of 9-nitrocamptothecin (. P<0.05) .
P-糖蛋白抑制剂维拉帕米能显著增加各段小肠对9-NC的吸收(P<0.05),在小肠下端更加明显。
参考来源 - 9ALL the five drugs, retinoic acid, tamoxifen, indometacin,verapamil and octreotide, enhanced the inhibition ability of antitumordrugs to both primary cells and PANG-i cell lines.
乃)维甲酸,三苯氧胺,异搏定可以增加阿霉素在PANC习细胞内积聚。
参考来源 - 胰腺癌化疗药敏及增敏的实验研究The results showed that PI-PLC activities were decreased in the tumor cells after treated with verapamil. These changes occurred simultaneously with those changes indexes of calcium homeostasis.
结果表明经异搏定处理后的A_2细胞PI-PLC活性显著降低,并与钙恒稳的指标基本呈现相应的平行变化趋势。
参考来源 - 异搏定对小鼠肝癌腹水瘤细胞系PIMDR results showed that compounds 7 and 10 exhibited moderate reversal activities,and were slightly less potent than those of verapamil against K562 cell line. It is believed that compounds 7 and 10 have MDR activity.
结果和结论:化合物的结构均由核磁共振氢谱,质谱,红外和元素分析确证,活性实验结果显示,化合物7,10逆转活性略低于维拉帕米,但是仍具有一定的多药耐药逆转活性。
参考来源 - 1·2,447,543篇论文数据,部分数据来源于NoteExpress
N a calcium-channel blocker used in the treatment of angina pectoris, hypertension, and some types of irregular heart rhythm 戊酸丙胺; 一种治疗心脏疾病的药物 [医学]
Results: The total clinical effective rate of verapamil was 94%.
结果:维拉帕米治疗室上性心动过速总有效率94%。
The protective effect of verapamil was most prominent by 6 hours.
异搏停对急性心肌梗塞起保护作用,以6小时内最为明显。
We topically applied verapamil cream on the ears of guinea pigs to observe its effect.
将维拉·帕米霜外涂于豚鼠耳部,观察其对豚鼠表皮的影响。
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