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      KCI등재 SCIE SCOPUS

      Artocarpus nigrifolius: Cytotoxic and Antibacterial Constituents

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      https://www.riss.kr/link?id=A104738766

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      다국어 초록 (Multilingual Abstract)

      Six known compounds including α-amyrin 3-acetate (1), β-sitosterol (2), betulinic acid (3), friedelan-3-one (4),artochamin B (5), and 2-C-methyl-D-erythritol 4-O-α-D-glucopyranoside (6) were isolated from the stem barks and leaves of Artocarpus nigrifolius (Moraceae) for the first time. Their structures were identified by spectroscopic methods as well as comparison with literatures. Cytotoxicity and antibacterial activity of 1-6 were evaluated. Results showed that artochamin B (5)possessed the highest cytotoxicity towards MCF7, Lu, HepG2,and KB cell lines with IC50 values of 4.59, 20.00, 3.60, and 1.18μg/mL, respectively. It also inhibited the growth of Gram-positive bacteria (Bacillus subtilis, Staphylococcus aureus), whereas inactive on the growth of both Gram-negative bacteria and yeast.
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      Six known compounds including α-amyrin 3-acetate (1), β-sitosterol (2), betulinic acid (3), friedelan-3-one (4),artochamin B (5), and 2-C-methyl-D-erythritol 4-O-α-D-glucopyranoside (6) were isolated from the stem barks and leaves of Artocarpus nig...

      Six known compounds including α-amyrin 3-acetate (1), β-sitosterol (2), betulinic acid (3), friedelan-3-one (4),artochamin B (5), and 2-C-methyl-D-erythritol 4-O-α-D-glucopyranoside (6) were isolated from the stem barks and leaves of Artocarpus nigrifolius (Moraceae) for the first time. Their structures were identified by spectroscopic methods as well as comparison with literatures. Cytotoxicity and antibacterial activity of 1-6 were evaluated. Results showed that artochamin B (5)possessed the highest cytotoxicity towards MCF7, Lu, HepG2,and KB cell lines with IC50 values of 4.59, 20.00, 3.60, and 1.18μg/mL, respectively. It also inhibited the growth of Gram-positive bacteria (Bacillus subtilis, Staphylococcus aureus), whereas inactive on the growth of both Gram-negative bacteria and yeast.

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      참고문헌 (Reference)

      1 Syah YM, "Two new cytotoxic isoprenylated avones, artoindonesianin U and V from heartwood of Artocapus chempeden" 75 : 134-140, 2004

      2 Feleke S, "Triterpene compounds from the latex of Ficus sur I" 19 : 307-310, 2005

      3 Chang YC, "The constituents of Lindera glauca" 47 : 373-380, 2000

      4 Suhartati T, "The bioactivity test of artonin E from the bark of Artocarpus rigida Blume" 23 : 330-337, 2008

      5 Hakim EH, "Prenylated favonoids and related compounds of the Indonesian Artocarpus(Moraceae)" 60 : 161-184, 2006

      6 Wang YH, "New isoprenylated flavones, Artochamins A-E, and cytotoxic principles from Artocarpus chama" 67 : 757-761, 2004

      7 Ngoc DDT, "Inhibition by Artocarpus tonkinensis of the development of collageninduced arthritis in rats" 61 : 234-241, 2005

      8 Goncalves JLS, "In vitro anti-rotavirus activity of some medicinal plants used in Brazil against diarrhea" 99 : 403-407, 2005

      9 Junichi K, "Glycosides of 2-C-methyl-D-erythritol from the fruits of anise, coriander and cumin" 62 : 115-120, 2003

      10 Igoli OJ, "Friedelanone and other triterpenoids from Hymenocardia acida" 3 : 156-158, 2008

      1 Syah YM, "Two new cytotoxic isoprenylated avones, artoindonesianin U and V from heartwood of Artocapus chempeden" 75 : 134-140, 2004

      2 Feleke S, "Triterpene compounds from the latex of Ficus sur I" 19 : 307-310, 2005

      3 Chang YC, "The constituents of Lindera glauca" 47 : 373-380, 2000

      4 Suhartati T, "The bioactivity test of artonin E from the bark of Artocarpus rigida Blume" 23 : 330-337, 2008

      5 Hakim EH, "Prenylated favonoids and related compounds of the Indonesian Artocarpus(Moraceae)" 60 : 161-184, 2006

      6 Wang YH, "New isoprenylated flavones, Artochamins A-E, and cytotoxic principles from Artocarpus chama" 67 : 757-761, 2004

      7 Ngoc DDT, "Inhibition by Artocarpus tonkinensis of the development of collageninduced arthritis in rats" 61 : 234-241, 2005

      8 Goncalves JLS, "In vitro anti-rotavirus activity of some medicinal plants used in Brazil against diarrhea" 99 : 403-407, 2005

      9 Junichi K, "Glycosides of 2-C-methyl-D-erythritol from the fruits of anise, coriander and cumin" 62 : 115-120, 2003

      10 Igoli OJ, "Friedelanone and other triterpenoids from Hymenocardia acida" 3 : 156-158, 2008

      11 Fontana A, "Evidence for the biosynthesis of squalene via the methylerythritol phosphate pathway in Streptomyces sp. obtained from a marine sediment" 66 : 6202-6206, 2001

      12 Carmichael J, "Evaluation of a tetrazolium-based semiautomated colorimetric assay : assessment of radio-sensitivity" 47 : 943-946, 1987

      13 Fernando MR, "Effect of Artocarpus heterophyllus and Asteracanthus longifolia on glucose tolerance in normal human subjects and in maturity-onset diabetic patients" 31 : 277-282, 1991

      14 Seo EK, "Bioactive prenylated avonoids from the stem bark of Artocarpus kemando" 26 : 124-127, 2003

      15 Namdaung U, "Bioactive constituents of the root bark of Artocarpus rigidus subsp. rigidus" 54 : 1433-1436, 2006

      16 Suhartati T, "Artoindonesianin L, a new prenylated avone with cytotoxicity activity from Artocarpus rotunda" 72 : 912-918, 2001

      17 Jagtap UB, "Artocarpus : A review of its traditional uses, phytochemistry and pharmacology" 129 : 142-166, 2010

      18 Boonphong S, "Antitubercular and antiplasmodial prenylated avones from the roots of Artocarpus altilis" 34 : 339-344, 2007

      19 Weng JR, "Antiplatelet prenylflavonoids from Artocarpus communis" 67 : 824-829, 2006

      20 Lin KW, "Antioxidant prenylflavonoids from Artocarpus communis and Artocarpus elasticus" 115 : 558-562, 2009

      21 Wei BL, "Antiinflammatory flavonoids from Artocarpus heterophyllus and Artocarpus communis" 53 : 3867-3871, 2005

      22 Khan MR, "Antibacterial activity of Artocarpus heterophyllus" 74 : 501-505, 2003

      23 Shashi BM, "13C-NMR spectra of pentacyclic triterpenoids, a compilation and some salient features" 37 : 1517-1575, 1994

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2015-12-30 학술지명변경 한글명 : Journal of the Korean Society for Applied Biological Chemistry -> Applied Biological Chemistry
      외국어명 : Journal of the Korean Society for Applied Biological Chemistry -> Applied Biological Chemistry
      KCI등재
      2010-05-06 학술지명변경 한글명 : 한국응용생명화학회지 -> Journal of the Korean Society for Applied Biological Chemistry KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.81 0.21 0.61
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.49 0.43 0.422 0.06
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