1) Pretiadil
普硫地尔
2) mepramidil
美普地尔
3) tipropidil
替普地尔
4) Bepridil
苄普地尔
1.
AIM To study the effects of bepridil on the rapidly activating component ( I Kr ), the slowly activating component ( I Ks ) of the delayed rectifier potassium current and the inward rectifier potassium current ( I K1 ) in hypertrophied guinea pig ventricular myocytes.
目的 研究苄普地尔 (bepridil)对肥厚心肌细胞延迟整流钾电流 (IK)中快激活成份 (IKr)和慢激活成份(IKs)及内向整流钾电流 (IK1 )的作用。
5) Carprazidil
卡普地尔
6) diltiazem
地尔硫
1.
Compound 2 was then treated with thionyl chloride to give (4S,5R)-4-(4-methoxyphenyl)-5-ethoxycarbonyl-1,3-dioxathiolane 2-oxide in 85% yield, the latter compound is a key chiral intermediate for preparation of diltiazem .
以1,4-双(9-O-奎宁基)-2,3-二氮杂萘为手性配体,经锇催化的不对称二羟化反应将反式-对甲氧基肉桂酸乙酯转化为(2R,3S)-2,3-二羟基-3-(4-甲氧基苯基)丙酸乙酯(2),收率87%,ee值大于99%;2与氯化亚砜反应得到地尔硫的手性中间体(4S,5R)-4-(4-甲氧基苯基)-5-乙氧羰基-1,3-二氧杂-2-氧代硫杂环戊烷,收率85%。
2.
Objective To establish reversed phase HPLC method for simultaneous determination of the concentration of carbamazepine(CBZ)and diltiazem(DZ) in serum,using diazepam as internal standard.
目的建立反相高效液相色谱(HPLC)法,以安定为内标,同时测定血清中卡马西平(CBZ)和地尔硫(DZ)的浓度。
3.
The delayed-release tablets were prepared by film-coating technology using diltiazem hydrochloride asmodel drug, insoluble ethylcellulose as retarding material and Eudragit L100 and S100 as porous agents.
以盐酸地尔硫为模型药物,不溶性乙基纤维素为阻滞材料,Eudragit L100及S100为致孔剂,采用薄膜包衣法制得延迟释放片。
补充资料：美普地尔
分子式：
CAS号：
性质：又名双苯克冠胺，心痛平。熔点145～147℃。有显著扩张冠脉作用，增加冠脉血流量，有轻度抑制心肌收缩力及降压作用。用于缓解心绞痛。制剂为片剂。
CAS号：
性质：又名双苯克冠胺，心痛平。熔点145～147℃。有显著扩张冠脉作用，增加冠脉血流量，有轻度抑制心肌收缩力及降压作用。用于缓解心绞痛。制剂为片剂。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条