Leishmanicidal Evaluation of Tetrahydroprotoberberine and Spirocyclic Erythrina-Alkaloids

被引:34
作者
Callejon, Daniel R. [1 ,2 ]
Riul, Thalita B. [3 ]
Feitosa, Luis G. P. [1 ,2 ]
Guaratini, Thais [1 ]
Silva, Denise B. [1 ]
Adhikari, Achyut [1 ,4 ]
Shrestha, Ram L. [5 ]
Marques, Lucas M. M. [1 ]
Baruffi, Marcelo D. [3 ]
Lopes, Joao L. C. [1 ]
Lopes, Norberto P. [1 ]
机构
[1] Univ Sao Paulo, FCFRP, NPPNS, BR-14040903 Ribeirao Preto, SP, Brazil
[2] Lychnoflora Pesquisa & Desenvolvimento Prod Nat L, BR-14030090 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, FCFRP, Dept Anal Clin, BR-14040903 Ribeirao Preto, SP, Brazil
[4] Univ Karachi, ICCBS, HEJ Res Inst Chem, Karachi 75270, Pakistan
[5] Tribhuvan Univ, Kathmandu, Nepal
基金
巴西圣保罗研究基金会;
关键词
Leishmania amazonensis; spirocyclic erythrina-alkaloids; tetrahydroprotoberberine-type alkaloids; Corydalis govaniana; Erythrina verna; PROTOZOAN NEGLECTED DISEASES; IONIZATION MASS-SPECTROMETRY; SECONDARY METABOLITES; FLOWERS; LEADS; ANTICONVULSANT; ERYTHRALINE; LYSISTEMON; PLANTS; DRUGS;
D O I
10.3390/molecules19055692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leishmaniasis is one of the World's most problematic diseases in developing countries. Traditional medicines to treat leishmaniasis have serious side effects, as well as significant parasite resistance problems. In this work, two alkaloids 1 and 2 were obtained from Corydalis govaniana Wall and seven alkaloids 3-9, were obtained from Erythrina verna. The structures of the compounds were confirmed by mass spectrometry and 1D- and 2D-NMR spectroscopy. The leishmanicidal activity of compounds 1-9 against Leishmania amazonensis was tested on promastigote forms and cytotoxicity against J774 (macrophage cell line) was assessed in vitro. Compound 1 showed potent activity (IC50 = 0.18 mu g/mL), compared with the standard amphotericin B (IC50 = 0.20 mu g/mL). The spirocyclic erythrina-alkaloids showed lower leishmanicidal activity than dibenzoquinolizine type alkaloids.
引用
收藏
页码:5692 / 5703
页数:12
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