نتایج جستجو برای: strychnos henningsii

تعداد نتایج: 298  

2014
Christiana N. Teijaro Surendrachary Munagala Senzhi Zhao Gopal Sirasani Praveen Kokkonda Ekaterina V. Malofeeva Elizabeth Hopper-Borge Rodrigo B. Andrade

The selective modulation of ATP-binding cassette (ABC) efflux pumps overexpressed in multidrug resistant cancers (MDR) and attendant resensitization to chemotherapeutic agents represent a promising strategy for treating cancer. We have synthesized four novel pentacyclic Strychnos alkaloids alstolucines B (2), F (3), and A (5) and N-demethylalstogucine (4), in addition to known Strychnos alkaloi...

2013
Karl-Heinz Pawelka Joachim Stöckigt

Eleven main alkaloids were identified from cell suspension cultures of Rhazya stricta grown in 4X-medium for 15 days. The alkaloids comprised the five groups Corynanthe, Strychnos, Eburnan, Secodine, and Aspidosperma and can be regarded as being typical Rhazya alkaloids, al­ though the Strychnos alkaloid akuammicine has been isolated for the first time from the genus Rhazya. The most abundant c...

Journal: :The Malaysian journal of pathology 2009
B Sadananda Naik M Chakrapani

Brucine is the predominant alkaloid present in the bark of the tree Strychnos nux vomica and is a weaker alkaloid when compared to strychnine. However, its toxicological property is akin to strychnine. We report a rare case of brucine poisoning complicated by acute renal failure and rhabdomyolysis. A 24-year-old male presented with a history of consumption of a decoction made from the bark of t...

Journal: :Journal of ethnopharmacology 2005
Alex Asase Alfred A Oteng-Yeboah George T Odamtten Monique S J Simmonds

An ethnobotanical study was conducted in the Wechiau Community Hippopotamus Sanctuary area in Ghana, through interviews and quadrate studies, to investigate the range and abundance of species used in the treatment of malaria. Forty-one species belonging to 17 families were encountered during the study. Of the 17 families studied Leguminosae and Anacardiaceae predominated in terms of number of s...

Journal: :Chemistry, an Asian journal 2011
Ce Shi Chih-Wei Chien Iwao Ojima

A library of new 2,2'-bis(diphenylphosphinoyloxy)-1,1'-binaphthyl (binapo)-type chiral diphosphonite ligands was designed and synthesized based on chiral 3,3',5,5',6,6'-hexasubstituted biphenols. These bop ligands have exhibited excellent efficiency in a palladium-catalyzed intermolecular allylic amination reaction, which provides a key intermediate for the total synthesis of Strychnos indole a...

2017
Tabita N. Randrianarivony Aro Vonjy Ramarosandratana Tefy H. Andriamihajarivo Fortunat Rakotoarivony Vololoniaina H. Jeannoda Armand Randrianasolo Rainer W. Bussmann

BACKGROUND This paper reports a study undertaken in three remote communities (Mahaboboka, Amboronabo, Mikoboka), located in Sakaraha, Southwestern Madagascar. Not only villages are far away from sanitary infrastructures and doctors but drugs and consulting fees are unaffordable to villagers. They rely essentially on natural resources for health care as for most of rural areas in Madagascar. Thi...

Journal: :Zeitschrift für analytische Chemie 1886

2016
Dinesh Kumar Patel Kanika Patel B. Duraiswamy S. P. Dhanabal

Phytochemical analysis and standardization of Strychnos nux-vomica extract through HPTLC techniques Dinesh Kumar Patel , Kanika Patel, B. Duraiswamy, S. P. Dhanabal Department of Pharmaceutics, Institute of Technology, Banaras Hindu University, Varanasi-221005, India. J.S.S. College of Pharmacy, Ooty643 001, India. 3 G.L.A Institute of Pharmaceutical Research, Mathura, India Asian Pacific Journ...

Journal: :Journal of pharmaceutical sciences 1978
R Verpoorte A Baerheim Svendsen

Three alkaloids of the stem bark of Strychnos dolichothyrsa Gilg ex Onochie et Hepper (Loganiaceae) were isolated and identified as caracurine V and its mono- and di-N-oxide by comparison with synthesized compounds. 13C-NMR was used to confirm the structure of the N-oxides. The muscle relaxant activity and the toxicity of the N-oxides were less than those of caracurine V.

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