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氨基苄基化曼尼希碱的驱虫性能研究。

Studies on the anthelmintic property of aminobenzylated mannich bases.

作者信息

Chaluvaraju Kc, Bhat Ki

机构信息

Department of Pharmaceutical Chemistry, Government College of Pharmacy, Bangalore, India.

出版信息

J Young Pharm. 2011 Jul;3(3):243-5. doi: 10.4103/0975-1483.83775.

DOI:10.4103/0975-1483.83775
PMID:21897666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3159280/
Abstract

Studies were conducted on the anthelmintic property of about 15(e-h, 1e-1h, 2d-2f and 3e-3h) synthesized aminobenzylated Mannich bases bearing N-methyl piperazine using Indian earthworms Pheritima Posthuma against piperazine citrate as standard reference. Three concentrations of each compound (0.1, 0.2, 0.3% w/v) were studied, which involved the determination of paralysis and death time of the worms. The compound 1g exhibited the most significant anthelmintic activity among all the compounds screened against the worms as compared to standard drug.

摘要

使用印度蚯蚓正蚓(Pheritima Posthuma),以枸橼酸哌嗪作为标准对照,对约15种(e-h、1e-1h、2d-2f和3e-3h)合成的带有N-甲基哌嗪的氨基苄基化曼尼希碱的驱虫特性进行了研究。研究了每种化合物的三种浓度(0.1、0.2、0.3% w/v),其中包括测定蚯蚓的麻痹和死亡时间。与标准药物相比,在筛选的所有化合物中,化合物1g对蚯蚓表现出最显著的驱虫活性。

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本文引用的文献

1
Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum.苯甲醛酚醛曼尼希碱及(硫)缩氨基脲衍生物对疟原虫半胱氨酸蛋白酶恶性疟原虫蛋白酶-2和耐氯喹恶性疟原虫株的合成与生物学评价
Bioorg Med Chem. 2007 Jan 1;15(1):273-82. doi: 10.1016/j.bmc.2006.09.055. Epub 2006 Sep 29.
2
In vitro study of some medicinally important Mannich bases derived from antitubercular agent.源自抗结核药物的一些具有重要药用价值的曼尼希碱的体外研究。
Bioorg Med Chem. 2004 Feb 1;12(3):571-6. doi: 10.1016/j.bmc.2003.11.001.
3
Synthesis characterization and anticancer activity studies on some Mannich bases derived from 1,2,4-triazoles.
一些源自1,2,4-三唑的曼尼希碱的合成、表征及抗癌活性研究
Eur J Med Chem. 2003 Jul-Aug;38(7-8):759-67. doi: 10.1016/s0223-5234(03)00128-4.
4
Pharmaceutical quality of anthelmintics sold in Kenya.肯尼亚销售的驱虫药的药品质量。
Vet Rec. 1998 Apr 11;142(15):396-8. doi: 10.1136/vr.142.15.396.