UPSI Digital Repository (UDRep)
Start | FAQ | About

QR Code Link :

Type :article
Subject :Q Science (General)
Main Author :Mohd Nor Siti Mariam, Osman Fatin Nurul Atiqah, Ahmad Kartini, Nafiah Mohd Azlan,
Title :Synthesis of n-alkylated and n-acylated derivatives of girinimbine
Year of Publication :2017

Full Text :
Girinimbine, a carbazole alkaloid has drawn an attention due to its wide range of pharmacological effects such as antiplatelet, antibacterial and anticancer activities. Five new derivatives of girinimbine were successfully semi-synthesized via modification on N-terminal of naturally isolated girinimbine. N-Benzylgirinimbine, N-butylgirinimbine and N-isopentylgirinimbine were obtained from alkylation reaction,whereas, N-butyrylgirinimbine and N- methylbutyrylgirinimbine were obtained from acylation reaction.The structures of synthesized girinimbine derivatives were confirmed by spectroscopic techniques.

References

1.D.P.Chakraborty,B.K.Barman and P.K.Bose, Sci. Cult., 30, 445 (1964). 2.B.S.Joshi, V.N.Kamat and D.H.Gawad,Tetrahedron, 26, 1475 (1970); https://doi.org/10.1016/S0040-4020(01)92976-X. 3.B.S.Joshi,V.N.Kamat, D.H.Gawad and T.R.Govindachari, Phytochemistry, 11, 2065 (1972); https://doi.org/10.1016/S0031-9422(00)90173-0. 4.H.Furukawa,T.Wu,T. Ohta and C.Kuoh,Chem. Pharm. Bull., 33, 4132 (1985); https://doi.org/10.1248/cpb.33.4132. 5.A.S.Shah, A.S.Wakade and A.R. Juvekar, Indian J. Exp. Biol., 46, 505 (2008). 6.S.Mohan, S.I.Abdelwahab, S.C.Cheah, M.A.Sukari, S.Syam, N. Shamsuddin and M.R. Mustafa, Evid. Based Compl. Altern. Med., Article ID 689865 (2013); https://doi.org/10.1155/2013/689865. 7.K.Feng-Nien, L.Yi-San, W.Tian-Shung and T.Che-Ming, Biochem. Pharmacol., 48, 353 (1994); https://doi.org/10.1016/0006-2952(94)90107-4. 8.Y.Y. Kok, L.Y.Mooi, K.Ahmad, M.A.Sukari, N.Mat, M. Rahmani and A.M. Ali, Molecules, 17, 4651 (2012); https://doi.org/10.3390/molecules17044651. 9.S.L. Wang, B.Cai, C.B.Cui, S.Y.Yan and C.F.Wu, Chin. Tradit. Herbal Drugs, 38, 1677 (2007). 10.M.A.Sukari, H.M.Noor, N.A.Bakar, I.S.Ismail, M.Rahmani and A.B.Abdul, Asian J. Chem., 25, 7719 (2013); https://doi.org/10.14233/ajchem.2013.14579. 11.L.J.M.Rao, K.Ramalakshmi, B.B.Borse and B.Raghavan, Food Chem., 100, 742 (2007); https://doi.org/10.1016/j.foodchem.2005.10.033. 12.Y.Hieda, M.Anraku, T.Choshi, H.Tomida, H.Fujioka, N. Hatae, O.Hori, J.Hirose and S.Hibino, Bioorg. Med. Chem. Lett., 24, 3530 (2014); https://doi.org/10.1016/j.bmcl.2014.05.050. 13 M.B.Gawande, S.S.Deshpande, J.R.Satam and R.V. Jayaram, Catal Commun., 8, 576 (2007); https://doi.org/10.1016/j.catcom.2006.08.011. 14.J.Muzart, Tetrahedron, 65, 8313 (2009); https://doi.org/10.1016/j.tet.2009.06.091. 15. D.A. White, Synth. Commun., 7, 559 (1977); https://doi.org/10.1080/00397917709409277. 16.K.Arnold, B.Davies, R.L.Giles, C.Grosjean, G.E. Smith and A. Whiting, Adv. Synth. Catal., 348, 813 (2006); https://doi.org/10.1002/adsc.200606018.


This material may be protected under Copyright Act which governs the making of photocopies or reproductions of copyrighted materials.
You may use the digitized material for private study, scholarship, or research.

Back to previous page

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.