Protein glycation inhibitory activities of Lawsonia inermis and its active principles

References

• YK Hye, and K Kyong. (2003). Protein glycation and antioxidative activity of some plant extracts in vitro. J Agric Food Chem 51:1586–1591.
   PubMedGoogle Scholar
• D Amelio, and FS Botanicals. A phytocosmetic desk reference. Boca Raton: CRC Press; (1999). p 126–135.
   Google Scholar
• HC Ong, and J Norzalina. (1997). 70:10–14. Malay Herbal Medicine in Gemencheh, Negri, Sembilan, Malaysia. Fitoterapia
   Google Scholar
• RWJ Keay. Trees in Nigeria. Oxford: Clarendon Press; (1989). p 50.
   Google Scholar
• DJ Mabberley. The plant book. London: Cambridge University Press; (1990) 318.
   Google Scholar
• HH EI-Kamali, and SA Khalid. (1996). 68:301–366. The Most Common Herbal Remedies in Central Sudan. Fitoterapia
   Google Scholar
• BH Ali, AK Bashir, and MO Tanira. (1995). Anti-inflammatory, antipyretic, and analgesic effects of Lawsonia inermis L. (henna) in rats. Pharmacology 51 (6):356–363.
   PubMedGoogle Scholar
• BR Mikhaeil, FA Badria, GT Maatooq, and MM Amer. (2004). Antioxidant and immunomodulatory constituents of henna leaves. Z Naturforsch [C] 59 (7–8):468–476.
   PubMedGoogle Scholar
• Bep-Oliver-Bever. Medicinal plants in tropical west Africa. London: Cambridge University Press; (1986). p 53.
   Google Scholar
• JM Dalziel. The useful plants of west tropical Africa. London: Crown Agents; (1937). p 40–41.
   Google Scholar
• HM Burkill. (1995). The Useful Plants of West Tropical Africa. Families J-L, Royal Botanic Gardens 3:562–564.
   Google Scholar
• A KI-Merzabani, AA EI-Hazer, MA Attia, AK Al Duweini, and AM Ghazal. (1976). Screening system for Egyptian plants with potential anti-tumor activity. Planta Med 36:150–155.
   Google Scholar
• A Zargari. Medicinal plants. Vol.2 Tehran University Publication; (1991). p 353–358.
   Google Scholar
• UN Dhur. Chopra's indigenous drugs of India, 2nd ed. Calcutta: Dhur UN and sons Pvt. Ltd; New Delhi, (1958). p 48–55.
   Google Scholar
• WC Evans. Trease and evans pharmacognosy. 4th ed. London: WB Saunders Co. Ltd.. (1996). p248.
   Google Scholar
• PK Warrier, VP Nambiar, and C Ramankutty. editors. Indian medicinal plants, compoundium of 500 species. Chennai: Orient Longmann Pvt. Ltd.. (1995). p 303–306.
   Google Scholar
• JA Duke. Handbook of medicinal herbs. Haemolytic activity and nephrotoxiCIT000y of 2-hydroxy-1,4-naphthoquinone in rats. Boca Raton: CRC Press; (1985). p 274.
   Google Scholar
• DK Bhardway, R Murari, TR Seshadri, and R Singh. (1976). Lacoumarin from Lawsonia inermis. Phytochemistry 15:1789–1792.
   Web of Science ®Google Scholar
• DK Bhardway, TR Seshadri, and R Singh. (1977). Xanthones from Lawsonia inermis. Phytochemistry 16:1616–1617.
   Web of Science ®Google Scholar
• DK Bhardway, RK Jain, BC Jain, and CK Mehta. (1978). 1-Hydroxy-3,7-dimethoxy-6-acetoxyxanthone, A new xanthone from Lawsonia inermis. Phytochemistry 17:1440–1441.
   Web of Science ®Google Scholar
• RH Stanley, and AF Gilbert. Hair dyes and hair- dyeing chemistry and technique. London: Great Britain Whitefriars press Ltd; (1939). p 72–77.
   Google Scholar
• G Sarita, A Mohammed, AM Sarwar, N Masatake, and S Tatsuko. (1994). Isolation and characterization of a dihydroxysterol from Lawsonia inermis. Nat Prod Lett 4:195–201.
   Google Scholar
• G Handa, A Kapil, S Sharma, and J Singh. (1977). Lawnermis acid: A new anticomplementary triterpenoid from Lawsonia inermis seeds. Indian J Chem VB (36B):252–256.
   Google Scholar
• KC Wong, and YE Teng. (1995). Volatile components of Lawsonia inermis L Flowers. J Essent oil Res 7:425–428.
   Google Scholar
• VJ Reichling, M Harkenthal, H Brandt, and C Bayerl. (1999). Temporare HennaTaottoos. Deut Apoth Ztg 33:35–41.
   Google Scholar
• K Bhuvaneswari, S Gnana Poongothai, A Kuruvilla, and B Appala Raju. (2002). Inhibitory concentrations of lawsonia innermis dry powder for urinary pathogens. Indian Journal of Pharmacology 34:260–263.
   Google Scholar
• D Kirkland, and D Marzin. (2003). An assessment of the genotoxiCIT000y of 2-hydroxy-1, 4-naphthoquinone, the natural dye ingredient of Henn. Mutat Res 537 (2):183–199.
   PubMedGoogle Scholar
• DK Pandy, H Cahandra, AR Sexena, and SN Dixit. (1982). Indian Drugs 19:459.
   Google Scholar
• Y Yan, HW Guo, WP Jian, KE Yang, SL Tong, CG Fang, Q Li, and X Chang. (2004). Catalytic Conversion of 2-naphthol to 2-hydroxy-1,4-naphthoquinone under mild conditions. Chinese Journal of Chemistry 22:487–491.
   Google Scholar
• R Morris, J Nagarkatti, J Heaton, and C Lane. Aldrich catalog handbook of fine chemical 1996–1997. Aldrich Chemical Co., Inc.; (1996). p 829.
   Google Scholar
• YX Zhao, and XY Sun. Spectrum analysis and structure identifying of organic compounds (Chinese). ed. I Chinese Science and Technology University Press; (June 1992) p 315–325.
   Google Scholar
• CJ Pouchert. The Aldrich library of infrared spectra. ed. III. Aldrich Chemical Company, Inc, (1981) p 897A.
   Google Scholar
• RM Silverstein, GC Bassler, and TC Morrill. Spectrometric identification of organic compounds. ed. 3 John Wiley; (1977) p 65.
   Google Scholar
• N Takako, Y Takako, T Katsutoshi, S Seui, and RJ Lekh. (2002). J Agric Food Chem 50:2418–2422.
   PubMedGoogle Scholar
• Y Fumio, A Toshiaki, Y Yoshihiro, and N Hiroyuki. (2000). Antioxidative and anti- glycation activity of Garcinol from Garcinia indica fruit rind. J Agric Food Chem 48:180–185.
   PubMedGoogle Scholar
• M Nobuyasu, A Tadashi, S Chihiro, K Hiroyuki, O Mitsuharu, H Junichi, and U Makoto. (2002). Screening system for the Maillard reaction inhibitors from natural product extracts. J Health Sci 48 (6):520–526.
   Google Scholar
• Atta-ur-Rahman, N Sultana, S Jahan, and MI Choudhary. (2005). Studies on the constituents of Commiphora mukul. Z Naturforsch 60b:1202–1206.
   Google Scholar
• Atta-ur-Rahman, N Sultana, S Jahan, and MI Choudhary. (1998). Phytochemical studies on Skimmia laureola. Nat Prod Lett 12 (3):223.
   Google Scholar
• K Fatima, and N Sultana. (2003). Studies on bioassay directed antifungal activity of medicinal plants of Skimmia laureola, Calotropis procera and P. pterocarpum. J Chem Soc Pak 25:328.
   Web of Science ®Google Scholar
• Atta-ur-Rahman, N Sultana, MI Choudhary, PM Shah, and MR Khan. (1998). Isolation and structural studies on the chemical constituents of Skimmia laureola. J Nat Prod 61 (6):713.
   PubMed Web of Science ®Google Scholar
• Atta-ur-Rahman. Nuclear magnetic resonance spectroscopy, basic principles. New York: Springer-Verlag; (1986) 227.
   Google Scholar
• Atta-ur-Rahman. One-and two-dimentional NMR spectroscopy. Amsterdam: Elsevier Science Publishers; (1989) p 406.
   Google Scholar
• N Sultana, Atta-ur-Rahman, and A Khalid. (2006). New natural cholinesterase inhibiting and calcium channel blocking quinoline alkaloids. J Enz Inhib Med Chem 21 (6):703.
   PubMed Web of Science ®Google Scholar
• N Sultana, Atta-ur-Rahman, A Khalid. A new fatty ester and a new triterpene from Skimmia laureola Nat Prod Res 2008., (in press).
   Google Scholar
• N Sultana, Atta-ur-Rahman, and TH Khan. (2005). Tyrosinase inhibitor fatty ester and a quinoline alkaloid from Skimmia laureola. Z Naturforsch B 60:1186.
   Google Scholar
• Atta-ur-Rahman, and N Sultana. (1997). Phytochemical studies on Adhatoda vasica. Nat Prod Lett 10:249.
   Web of Science ®Google Scholar