1) Angelica benzene Phthalocyanine
当归苯酞
2) Tang-Kuei Phthalide capsule
当归苯酞软胶囊
1.
Objectvie: To evaluate the curative effect and safety and inquire the mechanism of the traditional Chinese herb medicine "Tang-Kuei Phthalide capsule" on primary dysmenorrhea(qi stagnation and blood stasis、cold-damp stagnation),to explore the possible mechanism and provide scientific basis for the clinical application of it.
目的 对当归苯酞软胶囊进行随机、双盲、平行对照临床试验研究,初步评价当归苯酞软胶囊治疗原发性痛经(气滞血瘀、寒湿凝滞证)的临床疗效,观察其安全性。
3) ligustilide
东当归酞内酯
4) cinnamenyl angelic acid
苯乙烯基当归酸
5) phthalide
苯酞
1.
The selective hydrogenation of phthalic anhydride to phthalide in liquid phase was studied with nickel catalysts supported on SiO2, TiO2, γ-Al2O3, TiO2-SiO2, and TiO2-Al2O3 carriers prepared by the incipient wetness impregnation method, using nickel nitrate as the nickel precursor.
分别以SiO2,TiO2,γ-Al2O3,TiO2-SiO2和TiO2-Al2O3为载体,以硝酸镍为镍源,采用等体积浸渍法制备了一系列镍基催化剂,并将其用于苯酐选择性加氢合成苯酞反应。
2.
4-(2-Carboxybenzyloxy)phenylacetic acid (Ⅲ)was synthesized from 4-Hydroxyphenyl acetic acid(Ⅱ)and phthalide in the presence of the catalyst sodium methoxide.
采用对羟基苯乙酸(Ⅱ)和苯酞为原料,在甲醇钠的催化下,以n(Ⅱ)∶n(苯酞)∶n(甲醇钠)=1。
3.
Substituted phthalide derivatives possess a wide range of physiological activities.
3位取代的苯酞类化合物具有广泛的生理活性 ,通过一个新的简便合成路线高收率的得到了 3位取代苯酞衍生物。
6) Radix Angelicae Sinensis
当归
1.
Study on the determination and extraction of ligustilide in Radix Angelicae sinensis and Rhizoma chuanxiong;
当归、川芎中藁本内酯含量测定及醇提工艺研究
2.
Determination of Sucrose in Radix Angelicae Sinensis by HPLC-ELSD;
HPLC-ELSD测定当归中蔗糖的含量
3.
Effects of essential oil from Radix Angelicae Sinensis in mice with sepsis;
当归精油对脓毒症小鼠的治疗作用
补充资料：东当归酞内酯
分子式：
CAS号：
性质：又称东当归酞内酯。微黄色带香味的油状物。沸点168～169℃(800Pa)。折射率nD251.5649。来源于伞形科植物东当归(Ligusticum dcutilobum Sieb.et Zucc.)，川芎(L.walli chii Franch.)中性油，当归[Angelica sinensis(Oliv.)Diels]的根等。动物实验显示具有明显的平喘作用及中枢神经系统抑制作用。
CAS号：
性质：又称东当归酞内酯。微黄色带香味的油状物。沸点168～169℃(800Pa)。折射率nD251.5649。来源于伞形科植物东当归(Ligusticum dcutilobum Sieb.et Zucc.)，川芎(L.walli chii Franch.)中性油，当归[Angelica sinensis(Oliv.)Diels]的根等。动物实验显示具有明显的平喘作用及中枢神经系统抑制作用。
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