Chemical constituents, antimicrobial and cytotoxic activities of Hypericum riparium (Guttiferae)

Records of Natural Products

Volumn 7, Issue 1, 2013, Pages 65-68

  Tala, Michel F ^a,b   Tchakam, Patricia D ^a   Wabo, Hippolyte K ^a   Talontsi, Ferdinand M ^b   Tane, Pierre ^a   Kuiate, Jules R ^a   Tapondjou, Léon A ^a   Laatsch, Hartmut ^b  

^a UNIVERSITY OF DSCHANG   (Cameroon)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Antibacterial; Antifungal; Cytotoxic; Hypericum riparium

Indexed keywords

1 HYDROXY 6,7 DIMETHOXYXANTHONE; 1,6 DIHYDROXY 7 METHOXYXANTHONE; 5 HYDROXY 1,3 DIMETHOXYXANTHONE; 5 HYDROXY 3 METHOXYXANTHONE; ACETIC ACID ETHYL ESTER; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; BETULIC ACID; BIJAPONICAXANTHONE; CADENSIN D; DACTINOMYCIN; DAUCOSTEROL; HYPERCALIN C; PLANT MEDICINAL PRODUCT; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTEMIA SALINA; ARTICLE; BIOASSAY; CHEMOTAXONOMY; CLAVISPORA LUSITANIAE; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG DETERMINATION; DRUG EFFECT; DRUG ISOLATION; DRUG POTENCY; DRUG SCREENING; DRUG STRUCTURE; HYPERICUM; HYPERICUM CALYCINUM; HYPERICUM LANCEOLATUM; HYPERICUM PERFORATUM; HYPERICUM RIPARIUM; HYPERICUM SUBALATUM; LD 50; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PLANT ROOT; PLASMODIUM FALCIPARUM;

ARTEMIA; ARTEMIA SALINA; CLUSIACEAE; HYPERICUM;

EID: 84870333527     PISSN: None     EISSN: 13076167     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. A. Pinarosa (2005). A survey on the Hypericum genus: secondary metabolites and bioactivity, Stud. Nat. Prod. Chem. 30, 603-634.
2. B. Williams, J. Hoch, T. E. Glass, R. Evans, J. S. Miller, J. H. Wisse and D. G. I. Kingston (2003). A novel cytotoxic guttiferone analogue from Garcinia macrophylla from the Suriname Rainforest, Planta. Med. 64, 864-866.
3. N. Tanaka and Y. Takaishi (2006). Xanthones from Hypericum chinense, Phytochemistry. 67, 2146-2151.
4. F. Ferrari, G. Pasqua, B. Monacelli, P. Cimino and B. Botta (2005). Xanthones from calli of Hypericum Perforatum subsp. Perforatum, Nat. Prod. Res. 19, 171-176.
5. M. T. Chen (1988). Xanthonolignoids from Hypericum subalatum, Heterocycles 27, 2589-2594.
6. H. K. Wabo, T. K. Kowa, A. H. N. Lonfouo, A. T. Tchinda, P. Tane, H. Kikuchi, M. Frédérich and Y. Oshima (2012). Phenolic compounds and terpenoids from Hypericum lanceolatum, Rec. Nat. Prod. 6, 94-100.
7. D. Zofou, T. K. Kowa, H. K. Wabo, M. N. Ngemenya, P. Tane and V. P. K. Titanji (2011). Hypericum lanceolatum (Hypericaceae) as a potential source of new anti-malarial agents: a bioassay-guided fractionation of the stem bark, Malar. J. 10, 167, 1-7.
8. R. M. Ngoumfo, J.-B. Jouda, F. T. Mouafo, J. Komguem, C. D. Mbazoa, T. C. Shiao, M. I. Choudhary, H. Laatsch, J. Legault, A. Pichette and R. Roy (2010). In vitro cytotoxic activity of isolated acridones alkaloids from Zanthoxylum leprieurii Guill. et Perr, Bioorg. Med. Chem. 18, 3601-3605.
9. J. D. Tamokou, M. F. Tala, H. K. Wabo, J. R. Kuiate and P. Tane (2009). Antimicrobial activities of methanol extract and compounds from stem bark of Vismia albescens, J. Ethnopharmacol. 124, 571-575.
10. P. Fu, W. D. Zhang, T. Z. Li, R. H. Liu, H. L. Li, W. Zhang and H. S. Chen (2005). A new bisxanthone from Hypericum japonicum Thunb. Ex Murray, Chin. Chem. Lett. 16, 771-773.
11. L. A. Decosterd, H. Stoeckli-Evans, J.-C. Chapuis, B. Sordat and K. Hostettmann. (1989). New cell growth-inhibitory cyclohexadienone derivatives from Hypericum calycinum L., Helv.Chim. Acta. 72, 1833-1845.
12. D. B. Orrea, G. L. F. e Silva, O. R. Gottlieb and S. J. Goncalves (1970). Chemistry of Brazilian Guttiferae. XVIII. Quinone and xanthone constituents of Kielmeyera rupestris, Phytochemistry. 9, 447-451.
13. F.-F. Hong, Y. Chen and G.-Z. Yang (2008). Chemical constituents from the bark of Garcinia xanthochymus and their 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activities, Helv. Chim. Acta. 91, 1695-1703.
14. H. Tosa, M. Iiunuma, K.-I. Murakami, T. Ito, T. Tanaka, V. Chelladurai and S. Riswan (1997). Three xanthones from Poeciloneuron pauciflorum and Mammea acuminata, Phytochemistry. 45, 133-136.