Antioxidant and radical-scavenging carbazole alkaloids from the oleoresin of curry leaf (Murraya koenigii Spreng.)

2007 ◽  
Vol 100 (2) ◽  
pp. 742-747 ◽  
Author(s):  
L. Jagan Mohan Rao ◽  
K. Ramalakshmi ◽  
B.B. Borse ◽  
B. Raghavan
1997 ◽  
Vol 46 (4) ◽  
pp. 751-755 ◽  
Author(s):  
Manas Chakrabarty ◽  
Amar C. Nath ◽  
Shampa Khasnobis ◽  
Manju Chakrabarty ◽  
Yaeko Konda ◽  
...  

2012 ◽  
Vol 7 (1) ◽  
pp. 1934578X1200700 ◽  
Author(s):  
Naciye Erkan ◽  
Zhou Tao ◽  
H. P. Vasantha Rupasinghe ◽  
Burcu Uysal ◽  
Birsen S. Oksal

Solvent-free microwave extraction (SFME) for the isolation of essential oil from leaves of Murraya koenigii L. (Rutaceae) has been compared with the conventional hydro-distilled oil (HD) in terms of yield, composition, antioxidant activity, and antibacterial activity against Listeria innocua. The yield of essential oil obtained from 30 min of SFME was similar to that of HD for 180 min. By GC-MS analysis, the major compounds of the essential oil extracted by SFME, which were obtained in somewhat lower amounts than in the essential oil obtained by HD, were α-copaene (44.3%), β-gurjunene (25.5%), isocaryophyllene (12.1%), β-caryophyllene (8.7%) and germacrene D (2.9%). The content of oxygenated terpenes, slightly higher for the SFME-essential oil (2.3%) than the HD-essential oil (1.4%), were much lower than that of nonoxygenated terpenes in both oils. DPPH radical scavenging activities of both essential oils were relatively low (10%-24%). Complete inhibition of growth of L. innocua was observed with both SFME and HD essential oils, at 400 and 600 μg/mL (minimum inhibitory concentration), respectively. The SFME-essential oil at 300 μg/mL provided 92% inhibition, indicating its potential as a natural antimicrobial agent.


2020 ◽  
Vol 12 (4) ◽  
pp. 665-672
Author(s):  
M. Chakraborty

The plant Murraya koenigii, commonly known as curry leaf tree is a rich source of carbazole alkaloids. A number of monomeric as well as dimeric carbazoles with C13, C18 and C23 skeleton have been isolated from the plant. In my present work, a new carbazole alkaloid, designated as mumunine, was isolated from the bark of Murraya koenigii (Linn) Spreng, along with a known carbazole alkaloid, viz. mahanimbine. The structure of the new alkaloid 1 was elucidated on the basis of 1D and 2D NMR spectral data analysis. In this paper, the isolation and structure elucidation of the new compound will be discussed in detail.


Phytomedicine ◽  
2006 ◽  
Vol 13 (5) ◽  
pp. 359-365 ◽  
Author(s):  
C. Ito ◽  
M. Itoigawa ◽  
K. Nakao ◽  
T. Murata ◽  
M. Tsuboi ◽  
...  

1992 ◽  
Vol 31 (8) ◽  
pp. 2877-2879 ◽  
Author(s):  
Johannes Reisch ◽  
Olav Goj ◽  
Anura Wickramasinghe ◽  
H.M.T. Bandara Herath ◽  
Gerald Henkel

2018 ◽  
Vol 47 (8) ◽  
pp. 1749-1756 ◽  
Author(s):  
Rou Chian Ng ◽  
Nur Kartinee Kassim ◽  
Yu Yeap Yunie Soon ◽  
Lian Ee Gwendoline Cheng ◽  
Saiful Latifah Yazan ◽  
...  

2008 ◽  
Vol 3 (10) ◽  
pp. 1934578X0800301 ◽  
Author(s):  
Suvra Mandal ◽  
Anupam Nayak ◽  
Samir K. Banerjee ◽  
Julie Banerji ◽  
Avijit Banerji

A new carbazole alkaloid (kurryam) oxygenated at the 4-position, hitherto unknown among carbazole alkaloids, has been isolated from the seeds of an Indian medicinal plant, Murraya koenigii (Rutaceae). The structure has been established as 4-hydroxy-(2′,2′,3)-trimethyl-(6,7)-dimethoxy pyranocarbazole from extensive 2D NMR spectral studies. In addition, two known carbazole alkaloids, (2′,2′,3)-trimethyl 6-methoxy pyranocarbazole and (2′,2′,3)-trimethyl 6-hydroxy pyranocarbazole were isolated from the seeds of the same plant, of which (2′,2′,3)-trimethyl 6-methoxy pyranocarbazole exhibited significant antidiarrhoeal activity, as also did the new compound.


2016 ◽  
Vol 14 (12) ◽  
pp. 3322-3332 ◽  
Author(s):  
Yedukondalu Nalli ◽  
Vidushi Khajuria ◽  
Shilpa Gupta ◽  
Palak Arora ◽  
Syed Riyaz-Ul-Hassan ◽  
...  

Four new and 18 known carbazole alkaloids were isolated from CHCl3 : MeOH crude extracts of the stem and leaves ofMurraya koenigii(Linn.) Spreng, and evaluated for their anti-inflammatory and antimicrobial activity.


ChemInform ◽  
2010 ◽  
Vol 29 (8) ◽  
pp. no-no
Author(s):  
M. CHAKRABARTY ◽  
A. C. NATH ◽  
S. KHASNOBIS ◽  
M. CHAKRABARTY ◽  
Y. KONDA ◽  
...  

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