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Volumn 34, Issue 1, 2011, Pages 37-41

Eudesmanolides from Taraxacum mongolicum and their inhibitory effects on the production of nitric oxide

Author keywords

Eudesmanolide; Macrophage; Nitric oxide; Taraxacum mongolicum

Indexed keywords

1 BETA, 3 BETA DIHYDROXY EUDESMAN 6 ALPHA, 12 OLIDE; 1 BETA,3 BETA DIHYDROXY EUDESMAN 11(13) EN 6 ALPHA,12 OLIDE; EUDESMANOLIDE DERIVATIVE; LOLIOLIDE; NITRIC OXIDE; UNCLASSIFIED DRUG;

EID: 79955069239     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-011-0104-5     Document Type: Article
Times cited : (17)

References (25)
  • 1
    • 0033861839 scopus 로고    scopus 로고
    • Taraxacin, A new guaianolide from Taraxacum wallichii
    • DOI 10.1021/np990495+
    • V. U. Ahmad S. Yasmeen Z. Ali M. A. Khan M. I. Choudhary F. Akhtar G. A. Miana M. Zahid 2000 Taraxacin, a new guaianolide from Taraxacum wallichii J. Nat. Prod. 63 1010 1011 10924189 10.1021/np990495+ 1:CAS:528: DC%2BD3cXjs1Ogt74%3D (Pubitemid 30624495)
    • (2000) Journal of Natural Products , vol.63 , Issue.7 , pp. 1010-1011
    • Ahmad, V.U.1
  • 2
    • 0027975453 scopus 로고
    • Nitric oxide: A physiologic messenger molecule
    • 7526779 10.1146/annurev.bi.63.070194.001135 1:CAS:528:DyaK2cXmsFWrsrw%3D
    • D. S. Bredt S. H. Snyder 1994 Nitric oxide: A physiologic messenger molecule Annu. Rev. Biochem. 63 175 195 7526779 10.1146/annurev.bi.63.070194. 001135 1:CAS:528:DyaK2cXmsFWrsrw%3D
    • (1994) Annu. Rev. Biochem. , vol.63 , pp. 175-195
    • Bredt, D.S.1    Snyder, S.H.2
  • 3
    • 0032797262 scopus 로고    scopus 로고
    • Nitric oxide synthases: Targets for therapeutic strategies in neurological diseases
    • P. E. Chabrier C. Demerlé-Pallardy M. Auguet 1999 Nitric oxide synthases: Targets for therapeutic strategies in neurological diseases Cell. Mol. Life Sci. 55 1029 1035 10442086 10.1007/s000180050353 1:CAS:528: DyaK1MXks1Sltr0%3D (Pubitemid 29361069)
    • (1999) Cellular and Molecular Life Sciences , vol.55 , Issue.8-9 , pp. 1029-1035
    • Chabrier, P.-E.1    Demerle-Pallardy, C.2    Auguet, M.3
  • 4
    • 0029560898 scopus 로고
    • Microbial transformations of 6α- and 6β-eudesmanolides by Rhizopus nigricans cultures
    • DOI 10.1021/np50124a004
    • Y. Garcia A. Garcia-Granados A. Martinez A. Parra F. Rivas 1995 Microbial transformations of 6α- and 6β-eudesmanolides by Rhizopus nigricans cultures J. Nat. Prod. 58 1498 1507 10.1021/np50124a004 1:CAS:528: DyaK2MXhtVSntrzF (Pubitemid 26006880)
    • (1995) Journal of Natural Products , vol.58 , Issue.10 , pp. 1498-1507
    • Garcia, Y.1    Garcia-Granados, A.2    Martinez, A.3    Parra, A.4    Rivas, F.5    Arias, J.M.6
  • 5
    • 0020448709 scopus 로고
    • 15N]nitrate in biological fluids
    • DOI 10.1016/0003-2697(82)90118-X
    • 15N] nitrate in biological fluids Anal. Biochem. 126 131 138 7181105 10.1016/0003-2697(82)90118- X 1:CAS:528:DyaL38XlvFGgtLY%3D (Pubitemid 13203451)
    • (1982) Analytical Biochemistry , vol.126 , Issue.1 , pp. 131-138
    • Green, L.C.1    Wagner, D.A.2    Glogowski, J.3
  • 6
    • 0028902552 scopus 로고
    • Nitric oxide synthases: Properties and catalytic mechanism
    • 7539994 10.1146/annurev.ph.57.030195.003423 1:CAS:528:DyaK2MXksVeqsbs%3D
    • O. W. Griffith D. J. Stuehr 1995 Nitric oxide synthases: Properties and catalytic mechanism Annu. Rev. Physiol. 57 707 736 7539994 10.1146/annurev.ph. 57.030195.003423 1:CAS:528:DyaK2MXksVeqsbs%3D
    • (1995) Annu. Rev. Physiol. , vol.57 , pp. 707-736
    • Griffith, O.W.1    Stuehr, D.J.2
  • 7
    • 0028922422 scopus 로고
    • Nitric oxide: Pathophysiological mechanisms
    • 7539995 10.1146/annurev.ph.57.030195.003513 1:CAS:528:DyaK2MXksVeqsbg%3D
    • S. S. Gross M. S. Wolin 1995 Nitric oxide: Pathophysiological mechanisms Annu. Rev. Physiol. 57 737 769 7539995 10.1146/annurev.ph.57.030195.003513 1:CAS:528:DyaK2MXksVeqsbg%3D
    • (1995) Annu. Rev. Physiol. , vol.57 , pp. 737-769
    • Gross, S.S.1    Wolin, M.S.2
  • 8
    • 0032948112 scopus 로고    scopus 로고
    • Inhibition of nitric oxide synthase as a potential therapeutic target
    • DOI 10.1146/annurev.pharmtox.39.1.191
    • A. J. Hobbs A. Higgs S. Moncada 1999 Inhibition of nitric oxide synthase as a potential therapeutic target Annu. Rev. Pharmacol. Toxicol. 39 191 220 10331082 10.1146/annurev.pharmtox.39.1.191 1:CAS:528:DyaK1MXjtVejt7k%3D (Pubitemid 29222557)
    • (1999) Annual Review of Pharmacology and Toxicology , vol.39 , pp. 191-220
    • Hobbs, A.J.1    Higgs, A.2    Moncada, S.3
  • 9
    • 16644362216 scopus 로고    scopus 로고
    • Luteolin and luteolin-7-O-glucoside from dandelion flower suppress iNOS and COX-2 in RAW264.7 cells
    • DOI 10.1023/B:MCBI.0000044364.73144.fe
    • C. Hu D. D. Kitts 2004 Luteolin and luteolin-7-O-glucoside from dandelion flower suppress iNOS and COX-2 in RAW264.7 cells Mol. Cell. Biochem. 265 107 113 15543940 10.1023/B:MCBI.0000044364.73144.fe 1:CAS:528:DC%2BD2cXotlWlsb8%3D (Pubitemid 41461870)
    • (2004) Molecular and Cellular Biochemistry , vol.265 , Issue.1-2 , pp. 107-113
    • Hu, C.1    Kitts, D.D.2
  • 10
    • 77953623305 scopus 로고    scopus 로고
    • Naphthoquinones from Catalpa ovata and their inhibitory effects on the production of nitrix oxide
    • 20361302 10.1007/s12272-010-0306-2 1:CAS:528:DC%2BC3cXktFCitbk%3D
    • B. M. Park S. S. Hong C. Lee M. S. Lee S. J. Kang Y. S. Shin J. K. Jung J. T. Hong Y. Kim M. K. Lee B. Y. Hwang 2010 Naphthoquinones from Catalpa ovata and their inhibitory effects on the production of nitrix oxide Arch. Pharm. Res. 33 381 385 20361302 10.1007/s12272-010-0306-2 1:CAS:528:DC%2BC3cXktFCitbk%3D
    • (2010) Arch. Pharm. Res. , vol.33 , pp. 381-385
    • Park, B.M.1    Hong, S.S.2    Lee, C.3    Lee, M.S.4    Kang, S.J.5    Shin, Y.S.6    Jung, J.K.7    Hong, J.T.8    Kim, Y.9    Lee, M.K.10    Hwang, B.Y.11
  • 11
    • 0036209846 scopus 로고    scopus 로고
    • A new inhibitor of nitric oxide production in microglia cells from Streptomyces sp. 91614
    • 12003002 1:CAS:528:DC%2BD38XitVeit7Y%3D
    • W. G. Kim N. K. Song I. D. Yoo G. Trienomycin 2002 a new inhibitor of nitric oxide production in microglia cells from Streptomyces sp. 91614 J. Antibiot. 55 204 207 12003002 1:CAS:528:DC%2BD38XitVeit7Y%3D
    • (2002) J. Antibiot. , vol.55 , pp. 204-207
    • Kim, W.G.1    Song, N.K.2    Yoo, I.D.3    Trienomycin, G.4
  • 12
    • 0036165656 scopus 로고    scopus 로고
    • New loliolide derivatives from the brown alga Undaria pinnatifida
    • DOI 10.1021/np0103057
    • J. Kimura N. Maki 2002 New loliolide derivatives from the brown alga Undaria pinnatifida J. Nat. Prod. 65 57 58 11809066 10.1021/np0103057 1:CAS:528:DC%2BD3MXovF2qsL8%3D (Pubitemid 34118814)
    • (2002) Journal of Natural Products , vol.65 , Issue.1 , pp. 57-58
    • Kimura, J.1    Maki, N.2
  • 13
    • 0034213372 scopus 로고    scopus 로고
    • Further sesquiterpenoids and phenolics from Taraxacum officinale
    • DOI 10.1016/S0367-326X(99)00158-6, PII S0367326X99001586
    • W. Kisiel B. Barszcz 2000 Further sesquiterpenoids and phenolics from Taraxacum officinale Fitoterapia 71 269 273 10844166 10.1016/S0367-326X(99) 00158-6 1:CAS:528:DC%2BD3cXltlyhtbc%3D (Pubitemid 30323677)
    • (2000) Fitoterapia , vol.71 , Issue.3 , pp. 269-273
    • Kisiel, W.1    Barszcz, B.2
  • 14
    • 26944503560 scopus 로고    scopus 로고
    • Sesquiterpenoids and phenolics from Taraxacum hondoense
    • DOI 10.1016/j.fitote.2005.04.016, PII S0367326X05001085
    • W. Kisiel K. Michalska 2005 Sesquiterpenoids and phenolics from Taraxacum hondoense Fitoterapia 76 520 524 15972248 10.1016/j.fitote.2005.04.016 1:CAS:528:DC%2BD2MXpslyis7s%3D (Pubitemid 41749739)
    • (2005) Fitoterapia , vol.76 , Issue.6 , pp. 520-524
    • Kisiel, W.1    Michalska, K.2
  • 15
    • 24944468612 scopus 로고    scopus 로고
    • Chemical constituents from roots of Taraxacum formosanum
    • DOI 10.1248/cpb.53.853
    • Y. L. Leu Y. L. Wang S. C. Huang L. S. Shi 2005 Chemical constituents from roots of Taraxacum formosanum Chem. Pharm. Bull. 53 853 855 15997153 10.1248/cpb.53.853 1:CAS:528:DC%2BD2MXpsFaiurw%3D (Pubitemid 41327640)
    • (2005) Chemical and Pharmaceutical Bulletin , vol.53 , Issue.7 , pp. 853-855
    • Leu, Y.-L.1    Wang, Y.-L.2    Huang, S.-C.3    Shi, L.-S.4
  • 16
    • 0028026868 scopus 로고
    • Nitric oxide synthase: Aspects concerning structure and catalysis
    • DOI 10.1016/0092-8674(94)90268-2
    • M. A. Marletta 1994 Nitric oxide synthase: Aspects concerning structure and catalysis Cell 78 927 930 7522970 10.1016/0092-8674(94)90268-2 1:STN:280:DyaK2M%2FgslOlsQ%3D%3D (Pubitemid 24292321)
    • (1994) Cell , vol.78 , Issue.6 , pp. 927-930
    • Marietta, M.A.1
  • 17
    • 0037303060 scopus 로고    scopus 로고
    • Sesquiterpene lactones from Taraxacum obovatum
    • DOI 10.1055/s-2003-37702
    • K. Michalska W. Kisiel 2003 Sesquiterpene lactones from Taraxacum obovatum Planta Med. 69 181 183 12624831 10.1055/s-2003-37702 1:CAS:528:DC%2BD3sXisVCgs7g%3D (Pubitemid 36384509)
    • (2003) Planta Medica , vol.69 , Issue.2 , pp. 181-183
    • Michalska, K.1    Kisiel, W.2
  • 18
    • 0028092958 scopus 로고
    • Nitric oxide synthases: Roles, tolls, and controls
    • DOI 10.1016/0092-8674(94)90266-6
    • C. Nathan Q. W. Xie 1994 Nitric oxide synthases: Roles, tolls, and controls Cell 78 915 918 7522969 10.1016/0092-8674(94)90266-6 1:CAS:528:DyaK2cXmsV2jsLg%3D (Pubitemid 24292319)
    • (1994) Cell , vol.78 , Issue.6 , pp. 915-918
    • Nathan, C.1    Xie, Q.-W.2
  • 19
    • 0036242431 scopus 로고    scopus 로고
    • Progress in the development of selective nitric oxide synthase (NOS) inhibitors
    • DOI 10.2174/1381612023396375
    • L. Salerno V. Sorrenti C. Di Giacomo G. Romeo M. A. Siracusa 2002 Progress in the development of selective nitric oxide synthase inhibitors Curr. Pharm. Des. 8 177 200 11812267 10.2174/1381612023396375 1:CAS:528: DC%2BD38XhvFKmurg%3D (Pubitemid 34449889)
    • (2002) Current Pharmaceutical Design , vol.8 , Issue.3 , pp. 177-200
    • Salerno, L.1    Sorrenti, V.2    Di Giacomo, C.3    Romeo, G.4    Siracusa, M.A.5
  • 21
    • 66749109535 scopus 로고    scopus 로고
    • A high-speed counter-current chromatography-HPLCDAD method for preparative isolation and purification of two polymethoxylated flavones from Taraxacum mongolicum
    • 19476701 1:CAS:528:DC%2BD1MXmtFemuro%3D
    • S. Shi H. Zhou Y. Zhang Y. Zhao K. Huang S. Liu 2009 A high-speed counter-current chromatography-HPLCDAD method for preparative isolation and purification of two polymethoxylated flavones from Taraxacum mongolicum J. Chromatogr. Sci. 47 349 353 19476701 1:CAS:528:DC%2BD1MXmtFemuro%3D
    • (2009) J. Chromatogr. Sci. , vol.47 , pp. 349-353
    • Shi, S.1    Zhou, H.2    Zhang, Y.3    Zhao, Y.4    Huang, K.5    Liu, S.6
  • 23
    • 53149109780 scopus 로고    scopus 로고
    • A newly found cadmium accumulator-Taraxacum mongolicum
    • 18378396 10.1016/j.jhazmat.2008.02.052 1:CAS:528:DC%2BD1cXht1arurfI
    • S. Wei Q. Zhou S. Mathews 2008 A newly found cadmium accumulator- Taraxacum mongolicum J. Hazard. Mater. 159 544 547 18378396 10.1016/j.jhazmat. 2008.02.052 1:CAS:528:DC%2BD1cXht1arurfI
    • (2008) J. Hazard. Mater. , vol.159 , pp. 544-547
    • Wei, S.1    Zhou, Q.2    Mathews, S.3
  • 24
    • 0033008456 scopus 로고    scopus 로고
    • Effects of Taraxacum mongolicum on the bioavailability and disposition of ciprofloxacin in rats
    • DOI 10.1021/js980367q
    • M. Zhu P. Y. Wong R. C. Li 1999 Effects of Taraxacum mongolicum on the bioavailability and disposition of ciprofloxacin in rats J. Pharm. Sci. 88 632 634 10350500 10.1021/js980367q 1:CAS:528:DyaK1MXislansbw%3D (Pubitemid 29260787)
    • (1999) Journal of Pharmaceutical Sciences , vol.88 , Issue.6 , pp. 632-634
    • Zhu, M.1    Wong, P.Y.2    Li, R.C.3
  • 25
    • 0344224267 scopus 로고    scopus 로고
    • Eudesmanolides and inositol derivatives from Taraxacum linearisquameum
    • DOI 10.1016/S0031-9422(99)00163-6, PII S0031942299001636
    • C. Zidorn E. P. Ellmerer-Müller H. Stuppner 1999 Eudesmanolides and inositol derivatives from Taraxacum linearis-quameum Phytochemistry 51 991 994 10.1016/S0031-9422(99)00163-6 1:CAS:528:DyaK1MXltFait7s%3D (Pubitemid 29350045)
    • (1999) Phytochemistry , vol.51 , Issue.8 , pp. 991-994
    • Zidorn, C.1    Ellmerer-Muller, E.P.2    Stuppner, H.3


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