메뉴 건너뛰기




Volumn 140, Issue 1, 2012, Pages 141-144

Anti-mycobacterial diynes from the Canadian medicinal plant Aralia nudicaulis

Author keywords

Antimycobacterial; Aralia nudicaulis; Falcarinol; Mycobacterium tuberculosis; Panaxydol; Polyacetylenes

Indexed keywords

ANTIMYCOBACTERIAL AGENT; METHANOL; PANAXYDOL; PANAXYNOL; PLANT EXTRACT; POLYACETYLENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84862807864     PISSN: 03788741     EISSN: 18727573     Source Type: Journal    
DOI: 10.1016/j.jep.2011.12.048     Document Type: Article
Times cited : (19)

References (44)
  • 1
    • 0000424282 scopus 로고
    • Floral sex-ratios and life-history in Aralia nudicaulis (Araliaceae)
    • S.C.H. Barrett, and K. Helenurm Floral sex-ratios and life-history in Aralia nudicaulis (Araliaceae) Evolution 35 1981 752 762
    • (1981) Evolution , vol.35 , pp. 752-762
    • Barrett, S.C.H.1    Helenurm, K.2
  • 2
    • 0028349798 scopus 로고
    • Stereochemistry of enynols - A caveat on the exciton chirality method
    • DOI 10.1016/S0040-4039(00)79947-3
    • M.W. Bernart, Y.F. Hallock, J.H. Cardellina, and I.I.M.R. Boyd Stereochemistry of enynols - a caveat on the exciton chirality method Tetrahedron Letters 35 1994 993 994 (Pubitemid 24084844)
    • (1994) Tetrahedron Letters , vol.35 , Issue.7 , pp. 993-994
    • Bernart, M.W.1    Hallock, Y.F.2    Cardellina II, J.H.3    Boyd, M.R.4
  • 3
    • 25144480300 scopus 로고    scopus 로고
    • Effect of Aralia cachemirica Decne root extracts on blood glucose level in normal and glucose loaded rats
    • Z.A. Bhat, S.H. Ansari, H.M. Mukhtar, T. Naved, J.I. Siddiqui, and N.A. Khan Effect of Aralia cachemirica Decne root extracts on blood glucose level in normal and glucose loaded rats Pharmazie 60 2005 712 713 (Pubitemid 41345468)
    • (2005) Pharmazie , vol.60 , Issue.9 , pp. 712-713
    • Bhat, Z.A.1    Ansari, S.H.2    Mukhtar, H.M.3    Naved, T.4    Siddiqui, J.I.5    Khan, N.A.6
  • 4
    • 84979420363 scopus 로고
    • Polyacetylenverbindungen. 118. Uber neue polyine mit C17-kette
    • F. Bohlmann, U. Niedball, and K.M. Rode Polyacetylenverbindungen. 118. Uber neue polyine mit C17-kette Chemische Berichte 99 1966 3552 3554
    • (1966) Chemische Berichte , vol.99 , pp. 3552-3554
    • Bohlmann, F.1    Niedball, U.2    Rode, K.M.3
  • 5
    • 77950340103 scopus 로고    scopus 로고
    • Inhibitory effects of diterpene acids from root of Aralia cordata on IgE-mediated asthma in guinea pigs
    • J.H. Cho, J.Y. Lee, S.S. Sim, W.K. Whang, and C.J. Kim Inhibitory effects of diterpene acids from root of Aralia cordata on IgE-mediated asthma in guinea pigs Pulmonary Pharmacology and Therapeutics 23 2010 190 199
    • (2010) Pulmonary Pharmacology and Therapeutics , vol.23 , pp. 190-199
    • Cho, J.H.1    Lee, J.Y.2    Sim, S.S.3    Whang, W.K.4    Kim, C.J.5
  • 6
    • 79955006811 scopus 로고    scopus 로고
    • Aliphatic C (17)-polyacetylenes of the falcarinol type as potential health promoting compounds in food plants of the Apiaceae family
    • L.P. Christensen Aliphatic C (17)-polyacetylenes of the falcarinol type as potential health promoting compounds in food plants of the Apiaceae family Recent Patents on Food, Nutrition and Agriculture 3 2011 64 77
    • (2011) Recent Patents on Food, Nutrition and Agriculture , vol.3 , pp. 64-77
    • Christensen, L.P.1
  • 8
    • 0030903133 scopus 로고    scopus 로고
    • Microplate Alamar blue assay versus BACTEC 460 system for high- throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium
    • L.A. Collins, and S.G. Franzblau Microplate Alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium Antimicrobial Agents and Chemotherapy 41 1997 1004 1009 (Pubitemid 27194176)
    • (1997) Antimicrobial Agents and Chemotherapy , vol.41 , Issue.5 , pp. 1004-1009
    • Collins, L.A.1    Franzblau, S.G.2
  • 11
    • 0001062267 scopus 로고
    • The diacetylene 11,12-dehydrofalcarinol from Hedera helix
    • F. Gafner, G.W. Reynolds, and E. Rodriguez The diacetylene 11,12-dehydrofalcarinol from Hedera helix Phytochemistry 28 1989 1256 1257
    • (1989) Phytochemistry , vol.28 , pp. 1256-1257
    • Gafner, F.1    Reynolds, G.W.2    Rodriguez, E.3
  • 15
    • 0005550766 scopus 로고    scopus 로고
    • Isolation of a new cerebroside from the root bark of Aralia elata
    • DOI 10.1021/np990018r
    • S.S. Kang, J.S. Kim, Y.N. Xu, and Y.H. Kim Isolation of a new cerebroside from the root bark of Aralia elata Journal of Natural Products 62 1999 1059 1060 (Pubitemid 29357468)
    • (1999) Journal of Natural Products , vol.62 , Issue.7 , pp. 1059-1060
    • Kang, S.S.1    Kim, J.S.2    Xu, Y.N.3    Kim, Y.H.4
  • 16
    • 77954507858 scopus 로고    scopus 로고
    • The analgesic and anti-inflammatory effects of 7-oxosandaracopimaric acid isolated from the roots of Aralia cordata
    • T.D. Kim, J.Y. Lee, B.J. Cho, T.W. Park, and C.J. Kim The analgesic and anti-inflammatory effects of 7-oxosandaracopimaric acid isolated from the roots of Aralia cordata Archives of Pharmacal Research 33 2010 509 514
    • (2010) Archives of Pharmacal Research , vol.33 , pp. 509-514
    • Kim, T.D.1    Lee, J.Y.2    Cho, B.J.3    Park, T.W.4    Kim, C.J.5
  • 17
    • 0020550397 scopus 로고
    • Chemical studies on crude drug precession. I. On the constituents of Ginseng Radix Rubra (1)
    • I. Kitagawa, M. Yoshikawa, M. Yoshihara, T. Hayashi, and T. Taniyama Chemical studies on crude drug precession. 1. On the constituents of Ginseng Radix Rubra Journal of the Pharmaceutical Society of Japan 103 1983 612 622 (Pubitemid 13027064)
    • (1983) Yakugaku Zasshi , vol.103 , Issue.6 , pp. 612-622
    • Kitagawa, I.1    Yoshikawa, M.2    Yoshihara, M.3
  • 18
    • 14644402382 scopus 로고    scopus 로고
    • Inhibitory effects of feeding with carrots or (-)-falcarinol on development of azoxymethane-induced preneoplastic lesions in the rat colon
    • DOI 10.1021/jf048519s
    • M. Kobaek-Larsen, L.P. Christensen, W. Vach, J. Ritskes-Hoitinga, and K. Brandt Inhibitory effects of feeding with carrots or (-)-falcarinol on development of azoxymethane-induced preneoplastic lesions in the rat colon Journal of Agricultural and Food Chemistry 53 2005 1823 1827 (Pubitemid 40322190)
    • (2005) Journal of Agricultural and Food Chemistry , vol.53 , Issue.5 , pp. 1823-1827
    • Kobaek-Larsen, M.1    Christensen, L.P.2    Vach, W.3    Ritskes-Hoitinga, J.4    Brandt, K.5
  • 20
    • 0030835144 scopus 로고    scopus 로고
    • The absolute stereostructures of the polyacetylenic constituents of Ginseng Radix Rubra
    • DOI 10.1016/S0040-4020(97)10026-6, PII S0040402097100266
    • M. Kobayashi, T. Mahmud, T. Umezome, W.W. Wang, N. Murakami, and I. Kitagawa The absolute stereostructures of the polyacetylenic constituents of Ginseng Radix Rubra Tetrahedron 53 1997 15691 15700 (Pubitemid 27472958)
    • (1997) Tetrahedron , vol.53 , Issue.46 , pp. 15691-15700
    • Kobayashi, M.1    Mahmud, T.2    Umezome, T.3    Wang, W.4    Murakami, N.5    Kitagawa, I.6
  • 21
    • 9544257137 scopus 로고
    • Constituents of umbelliferous plants. 12. Absolute configuration of falcarinol, an acetylenic compound from roots of Seseli gummiferum Pall
    • P.K. Larsen, B.E. Nielsen, and J. Lemmich Constituents of umbelliferous plants. 12. Absolute configuration of falcarinol, an acetylenic compound from roots of Seseli gummiferum Pall Acta Chemica Scandinavica 23 1969 2552 2554
    • (1969) Acta Chemica Scandinavica , vol.23 , pp. 2552-2554
    • Larsen, P.K.1    Nielsen, B.E.2    Lemmich, J.3
  • 22
    • 33746926693 scopus 로고    scopus 로고
    • Cytotoxic and COX-2 inhibitory constituents from the aerial parts of Aralia cordata
    • I.S. Lee, W.Y. Jin, X.F. Zhang, T.M. Hung, K.S. Song, Y.H. Seong, and K. Bae Cytotoxic and COX-2 inhibitory constituents from the aerial parts of Aralia cordata Archives of Pharmacal Research 29 2006 548 555 (Pubitemid 44199354)
    • (2006) Archives of Pharmacal Research , vol.29 , Issue.7 , pp. 548-555
    • Ik, S.L.1    Jin, W.2    Zhang, X.3    Tran, M.H.4    Kyung, S.S.5    Yeon, H.S.6    Bae, K.7
  • 23
    • 68149161143 scopus 로고    scopus 로고
    • Isolation and tandem mass fragmentations of an anti-inflammatory compound from Aralia elata
    • J.H. Lee, Y.W. Ha, C.S. Jeong, Y.S. Kim, and Y. Park Isolation and tandem mass fragmentations of an anti-inflammatory compound from Aralia elata Archives of Pharmacal Research 32 2009 831 840
    • (2009) Archives of Pharmacal Research , vol.32 , pp. 831-840
    • Lee, J.H.1    Ha, Y.W.2    Jeong, C.S.3    Kim, Y.S.4    Park, Y.5
  • 31
    • 0006873940 scopus 로고
    • Cytotoxic polyacetylenes from Aralia cordata
    • S.Y. Park, and J. Kim Cytotoxic polyacetylenes from Aralia cordata Yakhak Hoeji 39 1995 681 688
    • (1995) Yakhak Hoeji , vol.39 , pp. 681-688
    • Park, S.Y.1    Kim, J.2
  • 32
    • 0000664012 scopus 로고
    • Panaxydol, a new polyacetylenic epoxide from Panax ginseng roots
    • J. Poplawski, J.T. Wrobel, and T. Glinka Panaxydol, a new polyacetylenic epoxide from Panax ginseng roots Phytochemistry 19 1980 1539 1541
    • (1980) Phytochemistry , vol.19 , pp. 1539-1541
    • Poplawski, J.1    Wrobel, J.T.2    Glinka, T.3
  • 33
    • 44149126192 scopus 로고    scopus 로고
    • Antimycobacterial polyacetylenes from Levisticum officinale
    • DOI 10.1002/ptr.2408
    • A. Schinkovitz, M. Stavri, S. Gibbons, and F. Bucar Antimycobacterial polyacetylenes from Levisticum officinale Phytotherapy Research 22 2008 681 684 (Pubitemid 351716559)
    • (2008) Phytotherapy Research , vol.22 , Issue.5 , pp. 681-684
    • Schinkovitz, A.1    Stavri, M.2    Gibbons, S.3    Bucar, F.4
  • 35
    • 36849079326 scopus 로고    scopus 로고
    • Cytotoxic and DNA topoisomerases i and II inhibitory constituents from the roots of Aralia cordata
    • C.S. Seo, G. Li, C.H. Kim, C.S. Lee, Y. Jahng, H.W. Chang, and J.K. Son Cytotoxic and DNA topoisomerases I and II inhibitory constituents from the roots of Aralia cordata Archives of Pharmacal Research 30 2007 1404 1409
    • (2007) Archives of Pharmacal Research , vol.30 , pp. 1404-1409
    • Seo, C.S.1    Li, G.2    Kim, C.H.3    Lee, C.S.4    Jahng, Y.5    Chang, H.W.6    Son, J.K.7
  • 36
    • 77951296363 scopus 로고
    • Studies on the components of Panax ginseng Meyer. 3. on the ethereal extract of Ginseng Radix Alba. The structure of anew acetylene derivative Panaxynol
    • M. Takahashi, and M. Yoshikura Studies on the components of Panax ginseng Meyer. 3. On the ethereal extract of Ginseng Radix Alba. The structure of anew acetylene derivative Panaxynol Journal of the Pharmaceutical Society of Japan 84 1964 757 759
    • (1964) Journal of the Pharmaceutical Society of Japan , vol.84 , pp. 757-759
    • Takahashi, M.1    Yoshikura, M.2
  • 37
    • 0013966459 scopus 로고
    • Studies on the components of Panax ginseng Meyer. 5. on the structure of a new acetylene derivative panaxynol. Synthesis of 1,9-(cis)-heptadeeadiene-4,6- diyn-3-ol
    • M. Takahashi, and M.A.S.A. Yoshikura Studies on the components of Panax ginseng Meyer. 5. On the structure of a new acetylene derivative panaxynol. Synthesis of 1,9-(cis)-heptadeeadiene-4,6-diyn-3-ol Journal of the Pharmaceutical Society of Japan 86 1966 1053 1056
    • (1966) Journal of the Pharmaceutical Society of Japan , vol.86 , pp. 1053-1056
    • Takahashi, M.1    Yoshikura, M.A.S.A.2
  • 38
    • 0013971564 scopus 로고
    • Studies on the components of Panax ginseng Meyer. 4. on the structure of a new acetylene derivative Panaxynol. Synthesis of 1,7,9-heptadecatrien-4-yn-3- ol
    • M. Takahashi, and M.A.S.A. Yoshikura Studies on the components of Panax ginseng Meyer. 4. On the structure of a new acetylene derivative Panaxynol. Synthesis of 1,7,9-heptadecatrien-4-yn-3-ol Journal of the Pharmaceutical Society of Japan 86 1966 1051 1053
    • (1966) Journal of the Pharmaceutical Society of Japan , vol.86 , pp. 1051-1053
    • Takahashi, M.1    Yoshikura, M.A.S.A.2
  • 39
    • 33645090927 scopus 로고    scopus 로고
    • Anti-hepatoma activity and mechanism of ursolic acid and its derivatives isolated from Aralia decaisneana
    • Z. Tian, G. Lin, R.X. Zheng, F. Huang, M.S. Yang, and P.G. Xiao Anti-hepatoma activity and mechanism of ursolic acid and its derivatives isolated from Aralia decaisneana World Journal of Gastroenterology 12 2006 874 879
    • (2006) World Journal of Gastroenterology , vol.12 , pp. 874-879
    • Tian, Z.1    Lin, G.2    Zheng, R.X.3    Huang, F.4    Yang, M.S.5    Xiao, P.G.6
  • 40
    • 0041878896 scopus 로고    scopus 로고
    • Aralin, a new cytotoxic protein from Aralia elata, inducing apoptosis in human cancer cells
    • DOI 10.1016/S0304-3835(03)00348-3
    • M. Tomatsu, M. Ohnishi-Kameyama, and N. Shibamoto Aralin, a new cytotoxic protein from Aralia elata, inducing apoptosis in human cancer cells Cancer Letters 199 2003 19 25 (Pubitemid 37088134)
    • (2003) Cancer Letters , vol.199 , Issue.1 , pp. 19-25
    • Tomatsu, M.1    Ohnishi-Kameyama, M.2    Shibamoto, N.3
  • 41
    • 33745614896 scopus 로고    scopus 로고
    • Anticancer effect of extracts from a North American medicinal plant - wild sarsaparilla
    • J. Wang, Q.Z. Li, G. Ivanochko, and Y.G. Huang Anticancer effect of extracts from a North American medicinal plant wild sarsaparilla Anticancer Research 26 2006 2157 2164 (Pubitemid 43989484)
    • (2006) Anticancer Research , vol.26 , Issue.3 A , pp. 2157-2164
    • Wang, J.1    Li, Q.2    Ivanochko, G.3    Huang, Y.4
  • 43
    • 84871551600 scopus 로고    scopus 로고
    • Systematics and biogeography of Aralia L. (Araliaceae): Revision of Aralia Sects. Aralia, Humiles, Nanae, and Sciadodendron
    • J. Wen Systematics and biogeography of Aralia L. (Araliaceae): revision of Aralia Sects. Aralia, Humiles, Nanae, and Sciadodendron Contributions from the United States National Herbarium 57 2011 2
    • (2011) Contributions from the United States National Herbarium , vol.57 , pp. 2
    • Wen, J.1
  • 44
    • 0032783094 scopus 로고    scopus 로고
    • A cytotoxic triterpene saponin from the root bark of Aralia dasyphylla
    • DOI 10.1021/np9805185
    • K. Xiao, Y.H. Yi, Z.Z. Wang, H.F. Tang, Y.Q. Li, and H.W. Lin A cytotoxic triterpene saponin from the root bark of Aralia dasyphylla Journal of Natural Products 62 1999 1030 1032 (Pubitemid 29357459)
    • (1999) Journal of Natural Products , vol.62 , Issue.7 , pp. 1030-1032
    • Xiao, K.1    Yi, Y.-H.2    Wang, Z.-Z.3    Tang, H.-F.4    Li, Y.-Q.5    Lin, H.-W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.