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Pobeguinine: a monoterpene indole alkaloid and other bioactive constituents from the stem bark of Nauclea pobeguinii

机译:二苯基喹啉:来自Nauclea Pobeguinii的茎树皮的单萜吲哚生物碱和其他生物活性成分

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摘要

Phytochemical investigation of dichloromethane neutral phase of stem bark of Nauclea pobeguinii led to the isolation of a new monoterpene indole alkaloid, pobeguinine 1 along with 14 known compounds including (?)-naucleofficine D (2a), (+)-naucleofficine D (2b), naucleidinal (3), quafrinoic acid (4), betulinic acid (5), ursolic acid (6), quinovic acid (7), quinovic acid 3-O-α-L-rhamnopyranoside (8a), quinovic acid 3-O-β-D-fucopyranoside (8b), β-sitosterol (9), β-sitosterol 3-O-β-D-glucopyranoside (10), benzoic acid (11), lacceroic acid (12) and n-heptacosane (13). The structure of compound 1 was unambiguously assigned on the basis of single-crystal X-ray diffraction technique. The Hirshfeld surface analysis was further carried out to quantitatively analyze the role of various types of hydrogen bonding in crystal stability. These structures were elucidated using spectroscopic methods. The isolates were evaluated for their radical scavenging properties as well as inhibitory activities against urease and tyrosinase enzymes with IC50 values ranging from 13.4 to 58.9, 46.0 to 86.7 and 39.4 to 87.1 μg/mL, respectively. Compound 6 exhibited maximum radical scavenging activity with IC50 13.4 μg/mL, while compound 4 exhibited maximum tyrosinase with IC50 39.4 μg/mL. All the isolates showed moderate urease inhibition.
机译:Nauclea Pobeguinii茎树皮二氯甲烷中性阶段的植物化学研究LED将新的单萜吲哚生物碱,二苯基1与14种已知化合物分离,包括(α) - Nucleofficine D(2a),(+) - Nucleofficine d(2b) ,亚核素(3),QuafrinoIc acid(4),桦酸(5),熊酸(6),喹甲酸(7),喹甲酸3-O-α-L- rhamyanide(8A),喹啉酸3-O. -β-D-粘合剂(8b),β-谷甾醇(9),β-谷甾醇3-O-β-d-吡喃葡萄糖苷(10),苯甲酸(11),脱脂酸(12)和n-庚膜(13 )。基于单晶X射线衍射技术明确地分配化合物1的结构。进一步开展了HIRSHFELD表面分析,以定量分析各种类型氢键在晶体稳定性中的作用。使用光谱方法阐明这些结构。评估分离物的自由基清除性质以及抑制尿素和酪氨酸酶的抑制活性,IC 50值分别为13.4-58.9,46.0-86.7和39.4至87.1μg/ ml。化合物6与IC5013.4μg/ mL表示最大的自由基清除活性,而化合物4表现出具有IC5039.4μg/ mL的最大酪氨酸酶。所有分离物显示出中等的脲酶抑制。

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    Department of Chemistry Faculty of Science The University of Bamenda P.O. Box 39 Bambili Cameroon Phone: (+237) 677 95 56 30;

    Department of Organic Chemistry Faculty of Science University of Yaoundé I P.O. Box 812 Yaoundé Cameroon;

    Department of Chemistry Faculty of Science Scientific and Technical University of Masuku Box 943 Franceville Gabon;

    Department of Chemistry Higher Teacher Training College University of Maroua P.O. Box 55 Maroua Cameroon;

    H.E.J. Research Institute of Chemistry International Center for Chemical and Biological Sciences University of Karachi Karachi 75270 Pakistan;

    Department of Chemistry Karakoram International University 15100-Gilgit Gilgit-Baltistan Pakistan;

    Pharmaceutical Research Centre of Pakistan Council of Scientific and Industrial Research Laboratories Complex Karachi 75280 Pakistan;

    Department of Chemistry Higher Teacher Training College University of Yaoundé I P.O. Box 47 Yaoundé Cameroon Phone: (+237) 675 097 561;

    H.E.J. Research Institute of Chemistry International Center for Chemical and Biological Sciences University of Karachi Karachi 75270 Pakistan;

    Department of Organic Chemistry Faculty of Science University of Yaoundé I P.O. Box 812 Yaoundé Cameroon;

    Department of Organic Chemistry Faculty of Science University of Yaoundé I P.O. Box 812 Yaoundé Cameroon;

    H.E.J. Research Institute of Chemistry International Center for Chemical and Biological Sciences University of Karachi Karachi 75270 Pakistan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物科学;
  • 关键词

    monoterpene indole alkaloid; Nauclea pobeguinii; radical scavenging activities; single-crystal X-ray; tyrosinase inhibition; urease inhibition;

    机译:单萜吲哚生物碱;Nauclea pobeguinii;自由基清除活动;单晶X射线;酪氨酸酶抑制;脲酶抑制;

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