Chemical constituents from the stems of Alyxia schlechteri

Phytochemistry Letters

Volumn 11, Issue , 2015, Pages 80-84

  Sribuhom, Thurdpong ^a   Sriphana, Uraiwan ^b   Thongsri, Yordhathai ^c   Yenjai, Chavi ^a  

^a Khon Kaen University   (Thailand)

^b ROI ET RAJABHAT UNIVERSITY   (Thailand)

^c NARESUAN UNIVERSITY   (Thailand)

Author keywords

Alyterinin; Alyterinone; Alyxia schlechteri; Pythium insidiosum

Indexed keywords

3 HYDROXYCOUMARIN; 3' DEMETHYL 9 OXO PINORESINOL; 4 CONIFERALDEHYDE; 5 HYDROXYCOUMARIN; 6 (4 HYDROXY 3 METHOXYPHENYL) 3,7 DIOXABICYCLO[3.3.0]OCTAN 2 ONE; 6,8 DIHYDROXYCOUMARIN; 7 HYDROXY 8 METHOXYCOUMARIN; 8 HYDROXYPINORESINOL; ALYTERINATE A; ALYTERINATE C; ALYTERININ; ALYTERINONE; ANTIFUNGAL AGENT; COUMARIN; COUMARIN DERIVATIVE; FICUSEQUILIGNAN A; GONIOTHALAMIN; KETOPINORESINOL; MEDIORESINOL; PINORESINOL; PLANT EXTRACT; SESQUITERPENE DERIVATIVE; SYRINGALDEHYDE; SYRINGARESINOL; UNCLASSIFIED DRUG; VANILLIN; VANILLIN ALCOHOL;

ALYXIA SCHLECHTERI; ANALYTIC METHOD; ANTIFUNGAL ACTIVITY; APOCYNACEAE; ARTICLE; CHEMICAL COMPOSITION; COLUMN CHROMATOGRAPHY; CONTROLLED STUDY; CRYSTALLIZATION; EXTRACTION; MASS SPECTROMETRY; MEDICINAL PLANT; MOSHER METHOD; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLANT STEM; PYTHIUM INSIDIOSUM;

ALYXIA; PYTHIUM INSIDIOSUM;

EID: 84916629351     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2014.11.016     Document Type: Article

References (18)

1. Abdullah, N., Sahibul-Anwar, H., Ideris, S., Hasuda, T., Hitotsuyanagi, Y., Takeya, K., Diederich, M., Choo, C.Y., 2013. Goniolandrene A and B from Goniothalamus macrophyllus. Fitoterapia 88, 1-6.
2. Appendino, G., Aviello, G., Ballero, M., Borrelli, F., Fattorusso, E., Petrucci, F., Santelia, F.U., Taglialatela-Scafati, O., 2005. Cytotoxic germacrane sesquiterpenes from the aerial parts of Santolina insularis. J. Nat. Prod. 68, 853-857.
3. De Cock, A.W., Mendoza, L., Padhye, A.A., Ajello, L., Kaufman, L., 1987. Pythium insidiosum sp. nov., the etiologic agent of pythiosis. J. Clin. Microbiol. 25, 344-349.
4. Li, H.Z., Song, H.J., Li, H.M., Pan, Y.Y., Li, R.T., 2012. Characterization of phenolic compounds from Rhododendron alutaceum . Arch. Pharm. Res. 35, 1887-1893.
5. Lou, Y., Zhao, F., Wu, Z., Peng, K.F., Wei, X.C., Chen, L.X., Qiu, F., 2009. Germacrane-type sesquiterpenes from Curcuma wenyujin . Helv. Chim. Acta 92, 1665-1672.
6. Mir, Q.Y., Ali, M., Alam, P., 2009. Syzygiresinol lignan derivatives from the stem bark of Syzygium cumini (L.) Skeels. Nat. Prod. Res. 23, 422-430.
7. Mendoza, L., 2005. Pythium insidiosum. In: Merz, W.G., Hay, R.J. (Eds.), Topley and Wilson's Microbiology and Microbial Infections. Medical Mycology. 10th ed. ASM Press, London, UK, pp. 617-630.
8. Nageswara, R.G., Ravi, G., Kumar, G.S., 2012. Isolation and identification of antioxidizing agents from Alyxia reinwardtii. J. Pharm. Sci. Res. 4, 1859-1860.
9. Ohtani, I., Kusumi, T., Kashman, Y., Kakisawa, H., 1991. High-field FT NMR application of Mosher's method, the absolute configurations of marine terpenoids. J. Am. Chem. Soc. 113, 4092-4096.
10. Phatchana, R., Yenjai, C., 2014. Cytotoxic coumarins from Toddalia asiatica. Planta Med. 80, 719-722.
11. Rattanapan, J., Sichaem, J., Tip-pyang, S., 2012. Chemical constituents and antioxidant activity from the stems of Alyxia reinwardtii. Rec. Nat. Prod. 6, 288-291.
12. Sriphana, U., Thongsri, Y., Ardwichai, P., Poopasit, K., Prariyachatigul, C., Simasathiansophon, S., Yenjai, C., 2013. New lignan esters from Alyxia schlechteri and antifungal activity against Pythium insidiosum. Fitoterapia 91, 39-43.
13. Suthiwong, J., Sriphana, U., Thongsri, Y., Promsuwan, P., Prariyachatigul, C., Yenjai, C., 2014. Coumarinoids from the fruits of Micromelum falcatum. Fitoterapia 94, 134-141.
14. Wangteeraprasert, R., Lipipun, V., Gunaratnam, M., Neidle, S., Gibbons, S., Likhitwitayawuid, K., 2012. Bioactive compounds from Carissa spinarum. Phytother. Res. 26, 1496-1499.
15. Yang, L.J., Chen, W., Luo, Y.P., Li, G.P., Yang, X.D., Li, L., 2009. Lignans and ketonic compounds from Litsea chinpingensis (Lauraceae). Biochem. Syst. Ecol. 37, 696-698.
16. Zhang, M.L., Irwin, D., Li, X.N., Sauriol, F., Shi, X.W., Wang, Y.F., Huo, C.H., Li, L.G., Gu, Y.C., Shi, Q.W., 2012. PPARγ agonist from Chromolaena odorata. J. Nat. Prod. 75, 2076-2081.
17. Zhang, W., Luo, J., Kong, L., 2013. Chemical constituents from Boschniakia himalaica. Biochem. Syst. Ecol. 49, 47-50.
18. Zhou, X.J., Chen, X.L., Li, X.S., Su, J., He, J.B., Wang, Y.H., Li, Y., Cheng, Y.X., 2011. Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production. Bioorg. Med. Chem. Lett. 21, 373-376.