Constituents of Leonotis leonurus flowering tops

Phytochemistry Letters

Volumn 2, Issue 3, 2009, Pages 103-105

  Agnihotri, Vijai K ^a,c   ElSohly, Hala N ^a   Smillie, Troy J ^a   Khan, Ikhlas A ^a,b   Walker, Larry A ^a  

^a UNIVERSITY OF MISSISSIPPI   (United States)

^b UNIVERSITY OF MISSISSIPPI   (United States)

^c Pharmacopoeial Laboratory for Indian Medicine   (India)

Author keywords

1,2,3 Trihydroxy 3,7,11,15 tetramethylhexadecan 1 yl palmitate; Biological activities; Lamiaceae; Leonotis leonurus

Indexed keywords

1,2,3 TRIHYDROXY 3,7,11,15 TETRAMETHYLHEXADECAN 1 YL PALMITATE; ACTEOSIDE; ARTEMISININ; CHLOROQUINE; DITERPENE; DRUG METABOLITE; GENIPOSIDIC ACID; LUTEOLIN 7 GLUCOSIDE; PALMITIC ACID DERIVATIVE; PLANT MEDICINAL PRODUCT; SUCCINIC ACID; UNCLASSIFIED DRUG; URACIL;

ANTIMALARIAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG CYTOTOXICITY; FLOWERING; HUMAN; HUMAN CELL; IC 50; LEONOTIS LEONURUS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; SHRUB; SPECTROSCOPY; STRUCTURE ANALYSIS; VERO CELL;

LAMIACEAE; LEONOTIS LEONURUS;

EID: 67651172823     PISSN: 18743900     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytol.2009.02.001     Document Type: Article

References (22)

1. Bienvenu E., Amabeoku G.J., Eagles P.K., Scott G., and Springfield E.P. Anticonvulsant activity of aqueous extract of Leonotis leonurus. Phytomedicine 9 (2002) 217-223
2. Inouye H., Takeda Y., Uobe K., Yamauchi K., Yabuuchi N., and Kuwano S. Purgative activities of iridoid glucosides. Planta Medica 25 (1974) 285-288
3. Jain M., Khan S.I., Tekwani B.L., Jacob M.R., Singh S., Singh P.P., and Jain R. Synthesis, antimalarial, antileishmanial, and antimicrobial activities of some 8-quinolinamine analogues. Bioorganic & Medicinal Chemistry 13 (2005) 4458-4466
4. Kim S., Son Y., Chun J., Kim S., Chung G., Hwang K., and Lee J. Antioxidant property of an active component purified from the leaves of paraquat-tolerant Rehmannia glutinosa. Redox Report 10 (2005) 311-318
5. Kirmizibekmez H., Calis I., Perozzo R., Brun R., Doenmez A.A., Linden A., Rueedi P., and Tasdemir D. Inhibiting activities of the secondary metabolites of Phlomis brunneogaleata against parasitic Protozoa and plasmodial enoyl-ACP reductase, a crucial enzyme in fatty acid biosynthesis. Planta Medica 70 (2004) 711-717
6. Kunvari M., Paska C., Laszio M., Orfi L., Kovesdi I., Eros D., et al. Biological activity and structure of antitumor compounds from Plantago media L. Acta Pharmaceutica Hungarica 69 (1999) 232-239
7. Li Y., Sato T., Metori K., Koike K., Che Q.-M., and Takahashi S. The promoting effects of geniposidic acid and aucubin in Eucommia ulmoides oliver leaves on collagen synthesis. Biological & Pharmaceutical Bulletin 21 (1998) 1306-1310
8. Markham K.R., Ternai B., Stanley R., Geiger H., and Mabry T.J. Carbon-13 NMR studies of flavonoids-III: naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron 34 (1978) 1389-1397
9. Milkowska L.K., Borkowski B., and Rozanski M. Selected polyphenolic compounds Part III. Biological properties of iridoids. Herba Polonica 45 (1999) 232-241
10. Mustafa G., Anis E., Ahmed S., Anis I., Ahmed H., Malik A., Shahzad-ul-Hassan S., and Choudhary M.I. Lupene-type triterpenes from Periploca aphylla. Journal of Natural Products 63 (2000) 881-883
11. NCCLS. Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard M27-A2 (Vol. 22, No. 15) (2002), National Committee on Clinical Laboratory Standards, Villanova, PA
12. Nishibe S. Bioactive phenolic compounds in traditional medicines. Pure and Applied Chemistry 66 (1994) 2263-2266
13. Nishimura H., Sasaki H., Inagaki N., Masao C., Chen Z., and Mitsuhashi H. Nine phenethyl alcohol glycosides from Stachys sieboldii. Phytochemistry 30 (1991) 965-969
14. Numata A., Pettit G.R., Nabae M., Yamamoto K., Yamamoto E., Matsumura E., and Kawano T. Assignment of quaternary carbons in aromatic compounds by long-range heteronuclear shift correlated 2D-NMR spectroscopy and its application to acteoside. Agricultural and Biological Chemistry 51 (1987) 1199-1201
15. Ojewole J.A.O. Antinociceptive, antiinflammatory and antidiabetic effects of Leonotis leonurus (L) R. BR. [Lamiaceae] leaf aqueous extract in mice and rats. Methods and Findings in Experimental and Clinical Pharmacology 27 (2005) 257-264
16. Pan N., and Hori H. The interaction of acteoside with mitochondrial lipid peroxidation as an ischemia/reperfusion injury model. Advances in Experimental Medicine and Biology 361 (1994) 319-325
17. Park S.-W., Chung S.-K., and Park J.-C. Active oxygen scavenging activity of luteolin 7-O-β-d-glucoside isolated from Humulus japonicus. Han'guk Sikp'um Yongyang Kwahak Hoechi 29 (2000) 106-110
18. Richard E.S., Albert H., and Christian R. Plants of the Gods (2001), Healing Arts Press p. 46
19. Speight W.J. South Africa's medicinal herbs. Pharmaceutical Journal 126 (1931) 478-479
20. Tadahiro T., Yuji N., and Noriyasu H. Studies on the constituents of Leonotis nepetaefolia. Chemical & Pharmaceutical Bulletin 47 (1999) 284-286
21. Wu S.D., Jiang X.Y., Chen Q.Y., and Chen X.Q. Comparison of techniques for the extraction of the hypotensive drugs geniposidic acid and geniposide from Eucommia ulmoides. Journal of the Iranian Chemical Society 4 (2007) 205-214
22. Yim D.S., Yoo S.J., and Lee S.Y. Biological activities of verbascoside from Pedicularis resupinata var. oppositifolia. Saengyak Hakhoechi 28 (1997) 252-256