Antibacterial activity and QSAR of homoisoflavanones isolated from six Hyacinthaceae species

被引:22
|
作者
Du Toit, K.
Elgorashi, E. E.
Malan, S. F.
Mulholland, D. A.
Drewes, S. E.
Van Staden, J.
机构
[1] Univ KwaZulu Natal, Sch Pharm & Pharmacol, ZA-4000 Durban, South Africa
[2] Univ KwaZulu Natal, Sch Chem, ZA-4041 Durban, South Africa
[3] Univ KwaZulu Natal, Res Ctr Plant Growth & Dev, Sch Biol & Conservat Sci, ZA-3201 Scottsville, South Africa
[4] NW Univ, Dept Pharmaceut Chem, ZA-2520 Potchefstroom, South Africa
[5] Univ Surrey, Sch Biomed & Mol Sci, Guildford GU2 5XH, Surrey, England
[6] Univ KwaZulu Natal Pietermaritzburg, Sch Chem & Phys Sci, ZA-3201 Scottsville, South Africa
基金
新加坡国家研究基金会;
关键词
antibacterial activity; homoisoflavanones; Hyacinthaceae; physicochemical descriptors; quantitative structure-activity relationships;
D O I
10.1016/j.sajb.2007.01.002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Antibacterial activity, as detected in the bioautographic and microplate assays against Staphylococcus aureus, was shown for thirteen homoisoflavanones isolated from six Hyacinthaceae species. Four of these homoisoflavanones were isolated from Eucomis comosa, one from Eucomis schijffii, one from Albuca fastigiata, one from Drimia delagoensis, five from Drimiopsis maculata and one from Drimiopsis burkei. Extracts from most of these plants are employed as traditional medicines in South Africa. Biological screening was followed by a computer-based quantitative structure-activity relationship (QSAR) study. Stepwise multiple linear regression analysis of the data yielded a statistically significant two-component model (R-2=0.81, p<0.003), depicting logP and electron potential at O-1 as effective descriptors of antimicrobial activity against S. aureus. The derived model provides valuable parameter guidelines for those properties influencing the antibacterial activity of these homoisoflavanones. (c) 2007 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 241
页数:6
相关论文
共 50 条
  • [1] Norlignans and homoisoflavanones from two south African Drimiopsis species (Hyacinthaceae: Hyacinthoideae)
    Koorbanally, Chantal
    Mulholland, Dulcie A.
    Crouch, Neil R.
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2006, 34 (07) : 588 - 592
  • [2] Anti-inflammatory activity and QSAR studies of compounds isolated from Hyacinthaceae species and Tachiadenus longiflorus Griseb. (Gentianaceae)
    du Toit, K
    Elgorashi, EE
    Malan, SF
    Drewes, SE
    van Staden, J
    Crouch, NR
    Mulholland, DA
    BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (07) : 2561 - 2568
  • [3] Scillascillin-type homoisoflavanones from Drimiopsis maculata (Hyacinthaceae)
    Koorbanally, C
    Crouch, NR
    Mulholland, DA
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2001, 29 (05) : 539 - 541
  • [4] Homoisoflavanones from Pseudoprospero firmifolium of the monotypic tribe Pseudoprospereae (Hyacinthaceae: Hyacinthoideae)
    Koorbanally, Chantal
    Sewjee, Sarisha
    Mulholland, Dulcie A.
    Crouch, Neil R.
    Dold, Anthony
    PHYTOCHEMISTRY, 2007, 68 (22-24) : 2753 - 2756
  • [5] ANTIFUNGAL AND ANTIBACTERIAL ACTIVITY OF ENDOPHYTIC PENICILLIUM SPECIES ISOLATED FROM SALVADORA SPECIES
    Korejo, Farzana
    Ali, Syed Abid
    Shafique, Hafiza Asma
    Sultana, Viqar
    Ara, Jehan
    Ehteshamul-Haque, Syed
    PAKISTAN JOURNAL OF BOTANY, 2014, 46 (06) : 2313 - 2318
  • [6] Composition and antibacterial activity of the essential oil of six Stachys species from Serbia
    Grujic-Jovanovic, S
    Skaltsa, HD
    Marin, P
    Sokovic, M
    FLAVOUR AND FRAGRANCE JOURNAL, 2004, 19 (02) : 139 - 144
  • [7] Antibacterial activity and QSAR of chalcones against biofilm-producing bacteria isolated from marine waters
    Sivakumar, P. M.
    Prabhawathi, V.
    Doble, M.
    SAR AND QSAR IN ENVIRONMENTAL RESEARCH, 2010, 21 (3-4) : 247 - 263
  • [8] 3-Benzyl-4-chromanones (homoisoflavanones) from bulbs of the ethnomedicinal geophyte Ledebouria revoluta (Hyacinthaceae)
    Moodley, N.
    Crouch, N. R.
    Mulholland, D. A.
    Slade, D.
    Ferreira, D.
    SOUTH AFRICAN JOURNAL OF BOTANY, 2006, 72 (04) : 517 - 520
  • [9] 10 HOMOISOFLAVANONES FROM 2 MUSCARI SPECIES
    ADINOLFI, M
    CORSARO, MM
    LANZETTA, R
    LAONIGRO, G
    MANGONI, L
    PARRILLI, M
    PHYTOCHEMISTRY, 1987, 26 (01) : 285 - 290
  • [10] COX-2 inhibitory activity of homoisoflavanones and xanthones from the bulbs of the Southern African Ledebouria socialis and Ledebouria ovatifolia (Hyacinthaceae: Hyacinthoideae)
    Waller, Catherine P.
    Thumser, Alfred E.
    Langat, Moses K.
    Crouch, Neil R.
    Mulholland, Dulcie A.
    PHYTOCHEMISTRY, 2013, 95 : 284 - 290