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      KCI등재 SCIE SCOPUS

      In Vitro Na^+/K^+-ATPase Inhibitory Activity and Antimicrobial Activity of Sesquiterpenes Isolated from Thujopsis dolabrata

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      https://www.riss.kr/link?id=A104667537

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      다국어 초록 (Multilingual Abstract)

      A series of sesquiterpenes and hinokitiol-related compounds (1-15) was isolated from the essential oil of Thujopsis dolabrata Sieb. et Zucc. var. hondai Makino, and their structures were determined by combined spectroscopic analyses. The inhibitory effects of these compounds on microbial cell growth and Na^+/K^+-ATPase were evaluated in vitro. It was found that (-)-elema-1,3,11(13)-trien-12-ol (5), α,β,γ-costol (8), and chamigrenol (11) inhibit the activities of Na^+/K^+-ATPase, with IC_50 values of 11.2 ± 0.11, 12.2 ± 0.09, and 15.9 ± 0.54 μg/mL, respectively. Thujopsene (1), cedrol (9), γ-cuparenol (10), and chamigrenol (11) showed potent antibacterial activity, with MIC values in the range of 25-50 μg/mL, and β-thujaplicin (12) exhibited a broad spectrum of antibacterial and antifungal activity. These results indicate that these isolated compounds are promising candidates for the development of potent Na^+/K^+ ATPase inhibitors and antimicrobial agents.
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      A series of sesquiterpenes and hinokitiol-related compounds (1-15) was isolated from the essential oil of Thujopsis dolabrata Sieb. et Zucc. var. hondai Makino, and their structures were determined by combined spectroscopic analyses. The inhibitory ef...

      A series of sesquiterpenes and hinokitiol-related compounds (1-15) was isolated from the essential oil of Thujopsis dolabrata Sieb. et Zucc. var. hondai Makino, and their structures were determined by combined spectroscopic analyses. The inhibitory effects of these compounds on microbial cell growth and Na^+/K^+-ATPase were evaluated in vitro. It was found that (-)-elema-1,3,11(13)-trien-12-ol (5), α,β,γ-costol (8), and chamigrenol (11) inhibit the activities of Na^+/K^+-ATPase, with IC_50 values of 11.2 ± 0.11, 12.2 ± 0.09, and 15.9 ± 0.54 μg/mL, respectively. Thujopsene (1), cedrol (9), γ-cuparenol (10), and chamigrenol (11) showed potent antibacterial activity, with MIC values in the range of 25-50 μg/mL, and β-thujaplicin (12) exhibited a broad spectrum of antibacterial and antifungal activity. These results indicate that these isolated compounds are promising candidates for the development of potent Na^+/K^+ ATPase inhibitors and antimicrobial agents.

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      참고문헌 (Reference)

      1 Akiyama, H., "Topical use of hinokitiol ointment in atopic dermatitis patients with special reference to colony count of Staphylococcus aureus on the surfaces of atopic dermatitis" 42 : 1202-1211, 1994

      2 Enzell, C., "The chemistry of the natural order cupressales 47. The structures and absolute configurations of widdrol and widdrol-aepoxide" 16 : 1552-1568, 1962

      3 Huang, B. S., "The central role of the brain in salt-sensitive hypertension" 21 : 295-304, 2006

      4 Yamaji, K., "The antifungal compound totarol of Thujopsisdolabrata var. hondai seeds selects for fungi on seedling root surfaces" 33 : 2254-2265, 2007

      5 Fang, J. M., "Terpenes from heartwood of Juniperuschinensis" 41 : 1361-1365, 1996

      6 Oh, K. B., "Synthesis and antimicrobial activities of halogenated bis(hydroxyphenyl) methanes" 19 : 945-948, 2009

      7 Maurer, B., "Sesquiterpenoids from costus root oil (Saussurealappa Clarke)" 60 : 2177-2190, 1977

      8 Jaitovich, A., "Salt, Na+/K+ ATPase and hypertension" 86 : 73-78, 2010

      9 Sjöström, M., "SIK1 is part of a cell sodium-sensing network that regulates active sodium transport through a calcium-dependent process" 104 : 16922-16927, 2007

      10 Sakagami, Y., "Phytogrowth-Inhibitory activities of beta-dolabrin and gamma-thujaplicin, hinokitiolrelated compounds and constituents of Thujopsisdola-brata Sieb. et Zucc. varhondai Makino" 23 : 645-648, 2000

      1 Akiyama, H., "Topical use of hinokitiol ointment in atopic dermatitis patients with special reference to colony count of Staphylococcus aureus on the surfaces of atopic dermatitis" 42 : 1202-1211, 1994

      2 Enzell, C., "The chemistry of the natural order cupressales 47. The structures and absolute configurations of widdrol and widdrol-aepoxide" 16 : 1552-1568, 1962

      3 Huang, B. S., "The central role of the brain in salt-sensitive hypertension" 21 : 295-304, 2006

      4 Yamaji, K., "The antifungal compound totarol of Thujopsisdolabrata var. hondai seeds selects for fungi on seedling root surfaces" 33 : 2254-2265, 2007

      5 Fang, J. M., "Terpenes from heartwood of Juniperuschinensis" 41 : 1361-1365, 1996

      6 Oh, K. B., "Synthesis and antimicrobial activities of halogenated bis(hydroxyphenyl) methanes" 19 : 945-948, 2009

      7 Maurer, B., "Sesquiterpenoids from costus root oil (Saussurealappa Clarke)" 60 : 2177-2190, 1977

      8 Jaitovich, A., "Salt, Na+/K+ ATPase and hypertension" 86 : 73-78, 2010

      9 Sjöström, M., "SIK1 is part of a cell sodium-sensing network that regulates active sodium transport through a calcium-dependent process" 104 : 16922-16927, 2007

      10 Sakagami, Y., "Phytogrowth-Inhibitory activities of beta-dolabrin and gamma-thujaplicin, hinokitiolrelated compounds and constituents of Thujopsisdola-brata Sieb. et Zucc. varhondai Makino" 23 : 645-648, 2000

      11 Nozoe, T., "On the acidic constituents of the essential oil of Thujopsisdolabrata. Occurence of α-thujaplicin" 27 : 15-17, 1951

      12 Ohta, Y., "New sesquiterpenoids from Schisandrachinensis" 20 : 2483-2485, 1968

      13 Ito, S., "New constituents of Thujopsisdolabrata" 42 : 3777-3781, 1965

      14 Sakai, I., "Japan. KokaiTokkyoKoho"

      15 L'Oreal Cosmetic, K. K., "Japan. KokaiTokkyoKoho"

      16 Noshita, T., "Isolation of (-)-4'-demethyl traxillagenin from ThujopsisdolabrataSieb. etZucc. var. hondai Makino" 63 : 105-106, 2009

      17 Ahn, Y. J., "Insecticidal and acaricidal activity of carvacrol and β-thujaplicine derived from Thujopsisdolabratavar. hondai sawdust" 24 : 81-90, 1998

      18 Baba, T., "Inhibitory effect of betathujaplicin on ultraviolet B-induced apoptosis in mouse keratinocytes" 110 : 24-28, 1998

      19 Nam, K. W., "Essential oil of Thujopsisdolabratasuppresses atopic dermatitis-like skin lesions in NC/Nga mice" 19 : 102-108, 2011

      20 Lee, S. G., "Effectiveness of carvacrol derived from Thujopsisdolabrata var. hondai sawdust against Thecodiplosisjaponensis (Diptera: Cecidomyiidae)" 49 : 119-124, 1997

      21 Lee, K. H., "Discovery and development of natural productderived chemotherapeutic agents based on a medicinal chemistry approach" 73 : 500-516, 2010

      22 Inamori, Y., "Cytotoxic effect of hinokitiol and tropolone on the growth of mammalian cells and on blastogenesis of mouse splenic T cells" 16 : 521-523, 1993

      23 Takahashi, K., "Chemotaxonomy on the leaf constituents of Thujopsis dolabrata Sieb. et Zucc.-Analysis of neutral extracts (diterpene hydrocarbon)" 29 : 839-848, 2001

      24 Borchardt, R. T., "Catechol O-methyltransferase. 1. Kinetics of tropolone inhibition" 16 : 377-382, 1973

      25 Morita, Y., "Biological activity of beta-dolabrin, gamma-thujaplicin, and 4-acetyltropolone, hinokitiolrelated compounds" 27 : 1666-1669, 2004

      26 Morita, Y., "Biological activity of tropolone" 26 : 1487-1490, 2003

      27 SON, DONG-JU, "Antiplatelet Activity of Thujopsis dolabrata var. hondai-Derived Component Against Platelet Aggregation" 한국미생물·생명공학회 15 (15): 425-427, 2005

      28 Inamori, Y., "Antimicrobial activity and metalloprotease inhibition of hinokitiolrelated compounds, the constituents of Thujopsisdolabrata S. and Z. hondai MAK" 22 : 990-993, 1999

      29 Ahn, Y. J., "Antignawing factor of crude oil derived from ThujopsisdolabrataS. et Z. var. hondai sawdust against mice" 21 : 263-271, 1995

      30 Johansson, M., "Activity and protein expression of Na+/ K+ ATPase are reduced in microvillous syncytiotrophoblast plasma membranes isolated from pregnancies complicated by intrauterine growth restriction" 88 : 2831-2837, 2003

      31 Dholwani, K. K., "A review on plant-derived natural products and their analogs with anti-tumor activity" 40 : 49-58, 2008

      32 Joseph-Nathan, P., "13C NMR Study of Cedrol, 6-isocedrol, and α-cedrene" 47 : 924-933, 1984

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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
      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
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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