UPSI Digital Repository (UDRep)

Terpenes and phenolic compounds of Murraya Koenigii

LIMITED Article 1323 Views
Scan QR Code to share or view item link:

Digital Assets & Download Files
Only metadata is available for this item (LIMITED status).
General Information Cached
Title
Terpenes and phenolic compounds of Murraya Koenigii
Type
Article
Main Author
Siow-Ping, Tan
Additional Authors
  • Abdul Manaf Ali
  • Mohd Azlan Nafiah
  • Ulil Amna
  • Shuhaibah Akma Ramli
  • Kartini Ahmad
Subject
R Medicine (General)
ISSN
0009-3130
Language Code
eng
Bibliographic Details
Place of Production
N/A
Year of publication
2017

Abstract

Murraya koenigii (L.) Spreng, an evergreen plant, is mostly distributed in tropical and subtropical regions [1]. It belongs to the Murraya genus of the Rutaceae family, which is widely grown in home gardens in Malaysia for its aromatic leaves and as one of the important ingredients in Indian cuisine. Previous phytochemical studies on M. koenigii revealed the presence of carbazole alkaloids [2–7] and coumarins [8]. Herein, we present data on the isolation and identification of three triterpenes and two phenolic compounds from the hexane crude extracts of the bark and leaves of M. koenigii collected from Pahang, Malaysia. The hexane crude extract of the bark (30.0 g) was chromatographed over silica gel 60F254 (70–230 mesh) and extensively subjected to silica gel 60F254 (230–400 mesh) column chromatography and preparative TLC on silica gel GF254, leading to the isolation of compounds 1–3, and 5. Meanwhile, compounds 1, 4, and 6 were isolated from the leaves hexane extract (20.0 g) of M. koenigii.

References

1. L. Wei, Y. Z. Wang, Z. Y. Li, Plant Biol., 14 (1), 190 (2012) 2. S. Nakamura, S. Nakashima, Y. Oda, N. Yokota, K. Fujimoto, T. Matsumoto, T. Ohta, K. Ogawa, S. Maeda, S. Nishida, H. Matsuda, M. Yoshikawa, Bioorg. Med. Chem., 21 (5), 1043 (2013) 3. C. Ito, Y. Thoyama, M. Omura, I. Kajiura, H. Furukawa, Chem. Pharm. Bull., 41 (12), 2096 (1993) 4. Q. Ma, J. Tian, J. Yang, A. Wang, T. Ji, Y. Wang, Y. Su, Fitoterapia, 87, 1 (2013) 5. K. Ahmad, S. P. Tan, M. A. Sukari, A. M. Ali, M. A. Nafiah, Am. J. Plant Sci., 5 (19), 2869 (2014) 6. S. P. Tan, M. A. Ali, M. A. Nafiah, K. Awang, K. Ahmad, Tetrahedron, 71, 3946 (2015) 7. C. Tantapakul, W. Phakhodee, S. Laphookhioe, T. Ritthiwigrom, S. Cheenpracha, Chem. Nat. Compd., 50 (1), 186 (2014) 8. C. A. Adebajo, J. Reisch, Fitoterapia, 71, 334 (2000) 9. D. Borchman, M. C. Yappert, S. E. Milliner, R. J. Smith, R. Bhola, Lipids, 48 (12), 1269 (2013) 10. S. Ivanova, V. Tonchev, N. Yokoi, M. C. Yappert, D., G. As. Georgiev, Int. J. Mol. Sci., 16, 21813 (2015) 11. V. S. P.Chaturvedula, I. Prakasu, Int. Curr. Pharm. J., 1 (9), 239 (2012) 12. A. Barla, H. Birman, S. Kultur, S. Oksuz, Turkey J. Chem., 30, 325 (2006) 13. C. S. Chanotiya, S. S. Sammal, C. S. Mathela, Indian J. Chem., 44B, 1922 (2005) 14. M. S. M. Rawat, V. Shukla, S. Negi, G. Pant, Indian J. Chem.,45B, 2566 (2006) 15. M. Matsuo, S. Urano, Tetrahedron, 32, 229 (1976)


Installed and configured by Bahagian Automasi, Perpustakaan Tuanku Bainun, Universiti Pendidikan Sultan Idris
If you have enquiries, kindly contact us at pustakasys@upsi.edu.my or 016-3630263. Office hours only.