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Volumn 2013, Issue , 2013, Pages

Review on natural coumarin lead compounds for their pharmacological activity

Author keywords

[No Author keywords available]

Indexed keywords

AEGELINOL BENZOATE; AGASYLLIN; AMMORESINOL; ANTHOGENOL; ANTIDIABETIC AGENT; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTIOXIDANT; AURAPTENE; BERGAPTEN; CHARTREUSIN; COUMAMYCIN; COUMARIN; ESCULETIN; FELAMIDIN; FRAXIDIN; FRAXIN; GRANDIVITTIN; MARMELOSIN; MURRAYATIN; NOVOBIOCIN; OSTHOLE; OSTRUTHIN; PENTOSALEN; PHELLODENOL A; PSORALEN; RUTARETIN; UMBELLIFERONE; UNCLASSIFIED DRUG; UNINDEXED DRUG; XANTHYLETIN; ANTICOAGULANT AGENT; ANTIHYPERTENSIVE AGENT; ANTIINFLAMMATORY AGENT; ANTINEOPLASTIC AGENT; ANTIVIRUS AGENT; COUMARIN DERIVATIVE;

EID: 84876513440     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2013/963248     Document Type: Review
Times cited : (673)

References (85)
  • 1
    • 0026643659 scopus 로고
    • A new antitumor antibiotic product, demethylchartreusin. Isolation and biological activities
    • 2-s2.0-0026643659
    • Aoyama Y., Katayama T., Yamamoto M., Tanaka H., Kon K., A new antitumor antibiotic product, demethylchartreusin. Isolation and biological activities. The Journal of Antibiotics 1992 45 6 875 878 2-s2.0-0026643659
    • (1992) The Journal of Antibiotics , vol.45 , Issue.6 , pp. 875-878
    • Aoyama, Y.1    Katayama, T.2    Yamamoto, M.3    Tanaka, H.4    Kon, K.5
  • 2
    • 68949107709 scopus 로고    scopus 로고
    • Evaluation of antioxidant, anti-inflammatory and lipoxygenase inhibitory activities of the prenylated coumarin umbelliprenin
    • 2-s2.0-68949107709
    • Iranshahi M., Askari M., Sahebkar A., Hadjipavlou-Litina D., Evaluation of antioxidant, anti-inflammatory and lipoxygenase inhibitory activities of the prenylated coumarin umbelliprenin. DARU 2009 17 2 99 103 2-s2.0-68949107709
    • (2009) DARU , vol.17 , Issue.2 , pp. 99-103
    • Iranshahi, M.1    Askari, M.2    Sahebkar, A.3    Hadjipavlou-Litina, D.4
  • 4
    • 0000002155 scopus 로고
    • Studies in detoxication. 72. The metabolism of coumarin and of o-coumaric acid
    • 2-s2.0-0000002155
    • Mead J. A., Smith J. N., Williams R. T., Studies in detoxication. 72. The metabolism of coumarin and of o-coumaric acid. The Biochemical Journal 1958 68 1 67 74 2-s2.0-0000002155
    • (1958) The Biochemical Journal , vol.68 , Issue.1 , pp. 67-74
    • Mead, J.A.1    Smith, J.N.2    Williams, R.T.3
  • 5
    • 0032534897 scopus 로고    scopus 로고
    • Anti-HIV coumarins from calophyllum seed oil
    • DOI 10.1016/S0960-894X(98)00628-3, PII S0960894X98006283
    • Spino C., Dodier M., Sotheeswaran S., Anti-HIV coumarins from calophyllum seed oil. Bioorganic and Medicinal Chemistry Letters 1998 8 24 3475 3478 2-s2.0-0032534897 10.1016/S0960-894X(98)00628-3 (Pubitemid 29012561)
    • (1998) Bioorganic and Medicinal Chemistry Letters , vol.8 , Issue.24 , pp. 3475-3478
    • Spino, C.1    Dodier, M.2    Sotheeswaran, S.3
  • 6
    • 77649261454 scopus 로고    scopus 로고
    • The cytotoxic properties of natural coumarins isolated from roots of Ferulago campestris (Apiaceae) and of synthetic ester derivatives of aegelinol
    • 2-s2.0-77649261454
    • Rosselli S., Maggio A. M., Faraone N., Spadaro V., Morris-Natschke S. L., Bastow K. F., Lee K. H., Bruno M., The cytotoxic properties of natural coumarins isolated from roots of Ferulago campestris (Apiaceae) and of synthetic ester derivatives of aegelinol. Natural Product Communications 2009 4 12 1701 1706 2-s2.0-77649261454
    • (2009) Natural Product Communications , vol.4 , Issue.12 , pp. 1701-1706
    • Rosselli, S.1    Maggio, A.M.2    Faraone, N.3    Spadaro, V.4    Morris-Natschke, S.L.5    Bastow, K.F.6    Lee, K.H.7    Bruno, M.8
  • 7
    • 0031080931 scopus 로고    scopus 로고
    • Cinnamates and coumarins from the leaves of Murraya paniculata
    • DOI 10.1016/S0031-9422(96)00617-6, PII S0031942296006176
    • Atta-ur-Rahman, Shabbir M., Ziauddin Sultani S., Jabbar A., Choudhary M. I., Cinnamates and coumarins from the leaves of Murraya paniculata. Phytochemistry 1997 44 4 683 685 2-s2.0-0031080931 10.1016/S0031-9422(96)00617-6 (Pubitemid 27073871)
    • (1997) Phytochemistry , vol.44 , Issue.4 , pp. 683-685
    • Atta-ur-Rahman1    Shabbir, M.2    Sultani, S.Z.3    Jabbar, A.4    Choudhary, M.I.5
  • 8
    • 0018736331 scopus 로고
    • Critical review of the toxicology of coumarin with special reference to interspecies differences in metabolism and hepatotoxic response and their significance to man
    • DOI 10.1016/0015-6264(79)90289-X
    • Cohen A. J., Critical review of the toxicology of coumarin with special reference to interspecies differences in metabolism and hepatotoxic response and their significance to man. Food and Cosmetics Toxicology 1979 17 3 277 289 2-s2.0-0018736331 (Pubitemid 10224817)
    • (1979) Food and Cosmetics Toxicology , vol.17 , Issue.3 , pp. 277-289
    • Cohen, A.J.1
  • 10
    • 0035488216 scopus 로고    scopus 로고
    • Constituents of the Essential Oil of the Cinnamomum cassia Stem Bark and the Biological Properties
    • Choi J., Lee K. T., Ka H., Jung W. T., Jung H. J., Park H. J., Constituents of the essential oil of the Cinnamomum cassia stem bark and the biological properties. Archives of Pharmacal Research 2001 24 5 418 423 2-s2.0-0035488216 (Pubitemid 33647260)
    • (2001) Archives of Pharmacal Research , vol.24 , Issue.5 , pp. 418-423
    • Choi, J.1    Lee, K.-T.2    Ka, H.3    Jung, W.-T.4    Jung, H.-J.5    Park, H.-J.6
  • 11
    • 33845445814 scopus 로고    scopus 로고
    • Biosynthesis of coumarins in plants: A major pathway still to be unravelled for cytochrome P450 enzymes
    • DOI 10.1007/s11101-006-9040-2, Exploring cytochromes P450 functions and applications
    • Bourgaud F., Hehn A., Larbat R., Doerper S., Gontier E., Kellner S., Matern U., Biosynthesis of coumarins in plants: a major pathway still to be unravelled for cytochrome P450 enzymes. Phytochemistry Reviews 2006 5 2-3 293 308 2-s2.0-33845445814 10.1007/s11101-006-9040-2 (Pubitemid 44900350)
    • (2006) Phytochemistry Reviews , vol.5 , Issue.2-3 , pp. 293-308
    • Bourgaud, F.1    Hehn, A.2    Larbat, R.3    Doerper, S.4    Gontier, E.5    Kellner, S.6    Matern, U.7
  • 12
    • 2542501959 scopus 로고    scopus 로고
    • Coumarins: Fast Synthesis by Knoevenagel Condensation under Microwave Irradiation
    • Bogdal D., Coumarins: fast synthesis by Knoevenagel condensation under microwave irradiation. Journal of Chemical Research, Synopses 1998 8 468 469 2-s2.0-2542501959 (Pubitemid 128522397)
    • (1998) Journal of Chemical Research - Part S , Issue.8 , pp. 468-469
    • Bogdal, D.1
  • 13
    • 0032767738 scopus 로고    scopus 로고
    • Coumarin metabolism, toxicity and carcinogenicity: Relevance for human risk assessment
    • DOI 10.1016/S0278-6915(99)00010-1, PII S0278691599000101
    • Lake B. G., Coumarin metabolism, toxicity and carcinogenicity: relevance for human risk assessment. Food and Chemical Toxicology 1999 37 4 423 453 2-s2.0-0032767738 10.1016/S0278-6915(99)00010-1 (Pubitemid 29335767)
    • (1999) Food and Chemical Toxicology , vol.37 , Issue.4 , pp. 423-453
    • Lake, B.G.1
  • 14
    • 0025663358 scopus 로고
    • The pharmacology, metabolism, analysis, and applications of coumarin and coumarin-related compounds
    • 2-s2.0-0025663358
    • Egan D., O'Kennedy R., Moran E., Cox D., Prosser E., Thornes R. D., The pharmacology, metabolism, analysis, and applications of coumarin and coumarin-related compounds. Drug Metabolism Reviews 1990 22 5 503 529 2-s2.0-0025663358
    • (1990) Drug Metabolism Reviews , vol.22 , Issue.5 , pp. 503-529
    • Egan, D.1    O'Kennedy, R.2    Moran, E.3    Cox, D.4    Prosser, E.5    Thornes, R.D.6
  • 17
    • 0016728457 scopus 로고
    • A comparison of the effectiveness of some anti inflammatory drugs on thermal oedema
    • 2-s2.0-0016728457
    • Piller N. B., A comparison of the effectiveness of some anti inflammatory drugs on thermal oedema. British Journal of Experimental Pathology 1975 56 6 554 560 2-s2.0-0016728457
    • (1975) British Journal of Experimental Pathology , vol.56 , Issue.6 , pp. 554-560
    • Piller, N.B.1
  • 18
    • 77953537918 scopus 로고    scopus 로고
    • Intestinal anti-inflammatory activity of esculetin and 4-methylesculetin in the trinitrobenzenesulphonic acid model of rat colitis
    • 2-s2.0-77953537918 10.1016/j.cbi.2010.03.045
    • Witaicenis A., Seito L. N., Di Stasi L. C., Intestinal anti-inflammatory activity of esculetin and 4-methylesculetin in the trinitrobenzenesulphonic acid model of rat colitis. Chemico-Biological Interactions 2010 186 2 211 218 2-s2.0-77953537918 10.1016/j.cbi.2010.03.045
    • (2010) Chemico-Biological Interactions , vol.186 , Issue.2 , pp. 211-218
    • Witaicenis, A.1    Seito, L.N.2    Di Stasi, L.C.3
  • 19
    • 0014057744 scopus 로고
    • On the antibiotic effects of natural coumarins. VI. The relation of structure to the antibacterial effects of some natural coumarins and the neutralization of such effects
    • Hodák K., Jakesová V., Dadák V., On the antibiotic effects of natural coumarins. VI. The relation of structure to the antibacterial effects of some natural coumarins and the neutralization of such effects. Cesko-Slovenska Farmacie 1967 16 2 86 91
    • (1967) Cesko-Slovenska Farmacie , vol.16 , Issue.2 , pp. 86-91
    • Hodák, K.1    Jakesová, V.2    Dadák, V.3
  • 20
    • 70449629066 scopus 로고    scopus 로고
    • Efficacy of osthol, a potent coumarin compound, in controlling powdery mildew caused by Sphaerotheca fuliginea
    • 2-s2.0-70449629066 10.1080/10286020903158964
    • Wang C. M., Zhou W., Li C. X., Chen H., Shi Z. Q., Fan Y. J., Efficacy of osthol, a potent coumarin compound, in controlling powdery mildew caused by Sphaerotheca fuliginea. Journal of Asian Natural Products Research 2009 11 9 783 791 2-s2.0-70449629066 10.1080/10286020903158964
    • (2009) Journal of Asian Natural Products Research , vol.11 , Issue.9 , pp. 783-791
    • Wang, C.M.1    Zhou, W.2    Li, C.X.3    Chen, H.4    Shi, Z.Q.5    Fan, Y.J.6
  • 21
    • 18244363825 scopus 로고
    • Chemistry and biochemistry of antibiotics
    • 2-s2.0-18244363825
    • Chain E. B., Chemistry and biochemistry of antibiotics. Annual Review of Biochemistry 1958 27 3 167 222 2-s2.0-18244363825
    • (1958) Annual Review of Biochemistry , vol.27 , Issue.3 , pp. 167-222
    • Chain, E.B.1
  • 23
    • 0141953878 scopus 로고    scopus 로고
    • Chartreusin, elsamicin A and related anti-cancer antibiotics
    • DOI 10.2174/1568011033482215
    • Portugal J., Chartreusin, elsamicin A and related anti-cancer antibiotics. Current Medicinal Chemistry. Anti-Cancer Agents 2003 3 6 411 420 2-s2.0-0141953878 10.2174/1568011033482215 (Pubitemid 37236411)
    • (2003) Current Medicinal Chemistry - Anti-Cancer Agents , vol.3 , Issue.6 , pp. 411-420
    • Portugal, J.1
  • 25
    • 77954694508 scopus 로고    scopus 로고
    • A novel dimeric coumarin analog and antimycobacterial constituents from Fatoua pilosa
    • 2-s2.0-77954694508 10.1002/cbdv.200900326
    • Chiang C. C., Cheng M. J., Peng C. F., Huang H. Y., Chen I. S., A novel dimeric coumarin analog and antimycobacterial constituents from Fatoua pilosa. Chemistry and Biodiversity 2010 7 7 1728 1736 2-s2.0-77954694508 10.1002/cbdv.200900326
    • (2010) Chemistry and Biodiversity , vol.7 , Issue.7 , pp. 1728-1736
    • Chiang, C.C.1    Cheng, M.J.2    Peng, C.F.3    Huang, H.Y.4    Chen, I.S.5
  • 26
    • 34250388042 scopus 로고
    • Fraxidin and isofraxidin from Artemisia scotina
    • 2-s2.0-34250388042 10.1007/BF00567042
    • Yusupov M. I., Sidyakin G. P., Fraxidin and isofraxidin from Artemisia scotina. Chemistry of Natural Compounds 1975 11 1 94 2-s2.0-34250388042 10.1007/BF00567042
    • (1975) Chemistry of Natural Compounds , vol.11 , Issue.1 , pp. 94
    • Yusupov, M.I.1    Sidyakin, G.P.2
  • 27
    • 77957595091 scopus 로고    scopus 로고
    • Inhibitory effects of coumarins from the stem barks of Fraxinus rhynchophylla on adipocyte differentiation in 3T3-L1 cells
    • 2-s2.0-77957595091 10.1248/bpb.33.1610
    • Shin E., Choi K. M., Yoo H. S., Lee C. K., Hwang B. Y., Lee M. K., Inhibitory effects of coumarins from the stem barks of Fraxinus rhynchophylla on adipocyte differentiation in 3T3-L1 cells. Biological and Pharmaceutical Bulletin 2010 33 9 1610 1614 2-s2.0-77957595091 10.1248/bpb.33.1610
    • (2010) Biological and Pharmaceutical Bulletin , vol.33 , Issue.9 , pp. 1610-1614
    • Shin, E.1    Choi, K.M.2    Yoo, H.S.3    Lee, C.K.4    Hwang, B.Y.5    Lee, M.K.6
  • 28
    • 0011365572 scopus 로고
    • Murrayatin, a coumarin from Murraya exotica
    • 2-s2.0-0011365572
    • Barik B. R., Dey A. K., Chatterjee A., Murrayatin, a coumarin from Murraya exotica. Phytochemistry 1983 22 10 2273 2275 2-s2.0-0011365572
    • (1983) Phytochemistry , vol.22 , Issue.10 , pp. 2273-2275
    • Barik, B.R.1    Dey, A.K.2    Chatterjee, A.3
  • 30
    • 0033960956 scopus 로고    scopus 로고
    • Single-dose methoxsalen effects on human cytochrome P-450 2A6 activity
    • Kharasch E. D., Hankins D. C., Taraday J. K., Single-dose methoxsalen effects on human cytochrome P-450 2A6 activity. Drug Metabolism and Disposition 2000 28 1 28 33 2-s2.0-0033960956 (Pubitemid 30027508)
    • (2000) Drug Metabolism and Disposition , vol.28 , Issue.1 , pp. 28-33
    • Kharasch, E.D.1    Hankins, D.C.2    Taraday, J.K.3
  • 31
    • 84856216145 scopus 로고    scopus 로고
    • Alkaloid and coumarins from the green fruits of Aegle marmelos
    • 10.1016/j.phytochem.2011.11.018
    • Chakthong S., Weaaryee P., Puangphet P., Alkaloid and coumarins from the green fruits of Aegle marmelos. Phytochemistry 2012 75 108 113 10.1016/j.phytochem.2011.11.018
    • (2012) Phytochemistry , vol.75 , pp. 108-113
    • Chakthong, S.1    Weaaryee, P.2    Puangphet, P.3
  • 32
    • 63449137987 scopus 로고    scopus 로고
    • Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (apiaceae)
    • 2-s2.0-63449137987 10.3390/molecules14030939
    • Basile A., Sorbo S., Spadaro V., Bruno M., Maggio A., Faraone N., Rosselli S., Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (apiaceae). Molecules 2009 14 3 939 952 2-s2.0-63449137987 10.3390/molecules14030939
    • (2009) Molecules , vol.14 , Issue.3 , pp. 939-952
    • Basile, A.1    Sorbo, S.2    Spadaro, V.3    Bruno, M.4    Maggio, A.5    Faraone, N.6    Rosselli, S.7
  • 35
    • 0031716318 scopus 로고    scopus 로고
    • Pharmaceutical properties of related calanolide compounds with activity against human immunodeficiency virus
    • DOI 10.1021/js980122d
    • Newman R. A., Chen W., Madden T. L., Pharmaceutical properties of related calanolide compounds with activity against human immunodeficiency virus. Journal of Pharmaceutical Sciences 1998 87 9 1077 1080 2-s2.0-0031716318 10.1021/js980122d (Pubitemid 28452106)
    • (1998) Journal of Pharmaceutical Sciences , vol.87 , Issue.9 , pp. 1077-1080
    • Newman, R.A.1    Chen, W.2    Madden, T.L.3
  • 37
    • 0345209275 scopus 로고
    • Isolation and structure of mammea A/BA, A/AB and A/BB: A group of 4-aryl-coumarin extractives of Mammea americana L
    • 2-s2.0-0345209275
    • Crombie L., Games D. E., McCormick A., Isolation and structure of mammea A/BA, A/AB and A/BB: a group of 4-aryl-coumarin extractives of Mammea americana L. Tetrahedron Letters 1966 7 2 145 149 2-s2.0-0345209275
    • (1966) Tetrahedron Letters , vol.7 , Issue.2 , pp. 145-149
    • Crombie, L.1    Games, D.E.2    McCormick, A.3
  • 38
    • 37049076378 scopus 로고
    • Thin-layer chromatographic method for the determination of the principal polar aromatic flavour compounds of the cinnamons of commerce
    • 2-s2.0-37049076378 10.1039/AN9941900113
    • Poole S. K., Poole C. F., Thin-layer chromatographic method for the determination of the principal polar aromatic flavour compounds of the cinnamons of commerce. The Analyst 1994 119 1 113 120 2-s2.0-37049076378 10.1039/AN9941900113
    • (1994) The Analyst , vol.119 , Issue.1 , pp. 113-120
    • Poole, S.K.1    Poole, C.F.2
  • 39
    • 84863130953 scopus 로고    scopus 로고
    • Inducible nitric oxide synthase and cyclooxygenase-2 participate in anti-inflammatory activity of imperatorin from Glehnia littoralis
    • 10.1021/jf204297e
    • Huang G. J., Deng J. S., Liao J. C., Inducible nitric oxide synthase and cyclooxygenase-2 participate in anti-inflammatory activity of imperatorin from Glehnia littoralis. Journal of Agricultural and Food Chemistry 2012 60 7 1673 1681 10.1021/jf204297e
    • (2012) Journal of Agricultural and Food Chemistry , vol.60 , Issue.7 , pp. 1673-1681
    • Huang, G.J.1    Deng, J.S.2    Liao, J.C.3
  • 41
    • 0028291809 scopus 로고
    • Inhibitory effects of phenolics on xanthine oxidase
    • 2-s2.0-0028291809
    • Chang W. S., Chang Y. H., Lu F. J., Chiang H. C., Inhibitory effects of phenolics on xanthine oxidase. Anticancer Research 1994 14 2A 501 506 2-s2.0-0028291809
    • (1994) Anticancer Research , vol.14 , Issue.A2 , pp. 501-506
    • Chang, W.S.1    Chang, Y.H.2    Lu, F.J.3    Chiang, H.C.4
  • 42
    • 80755125291 scopus 로고    scopus 로고
    • Inhibition of 5-lipoxygenase and skin inflammation by the aerial parts of Artemisia capillaris and its constituents
    • Kwon O. S., Choi J. S., Islam M. N., Inhibition of 5-lipoxygenase and skin inflammation by the aerial parts of Artemisia capillaris and its constituents. Archives of Pharmacal Research 2011 34 9 1561 1569
    • (2011) Archives of Pharmacal Research , vol.34 , Issue.9 , pp. 1561-1569
    • Kwon, O.S.1    Choi, J.S.2    Islam, M.N.3
  • 43
    • 6944222563 scopus 로고    scopus 로고
    • Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities
    • DOI 10.2174/1381612043382710
    • Fylaktakidou K. C., Hadjipavlou-Litina D. J., Litinas K. E., Nicolaides D. N., Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities. Current Pharmaceutical Design 2004 10 30 3813 3833 2-s2.0-6944222563 10.2174/1381612043382710 (Pubitemid 39409872)
    • (2004) Current Pharmaceutical Design , vol.10 , Issue.30 , pp. 3813-3833
    • Fylaktakidou, K.C.1    Hadjipavlou-Litina, D.J.2    Litinas, K.E.3    Nicolaides, D.N.4
  • 44
    • 0035128503 scopus 로고    scopus 로고
    • Oral anticoagulants: Mechanism of action, clinical effectiveness, and optimal therapeutic range
    • Hirsh J., Dalen J. E., Anderson D. R., Poller L., Bussey H., Ansell J., Deykin D., Oral anticoagulants: mechanism of action, clinical effectiveness, and optimal therapeutic range. Chest 2001 119 1, supplement 8S 21S 2-s2.0-0035128503 (Pubitemid 32154192)
    • (2001) Chest , vol.119 , Issue.SUPPL. 1
    • Hirsh, J.1    Dalen, J.E.2    Anderson, D.R.3    Poller, L.4    Bussey, H.5    Ansell, J.6    Deykin, D.7
  • 45
    • 0016259925 scopus 로고
    • The mode of action of vitamin K. Identification of γ carboxyglutamic acid as a component of prothrombin
    • 2-s2.0-0016259925
    • Nelsestuen G. L., Zytkovicz T. H., Howard J. B., The mode of action of vitamin K. Identification of γ carboxyglutamic acid as a component of prothrombin. The Journal of Biological Chemistry 1974 249 19 6347 6350 2-s2.0-0016259925
    • (1974) The Journal of Biological Chemistry , vol.249 , Issue.19 , pp. 6347-6350
    • Nelsestuen, G.L.1    Zytkovicz, T.H.2    Howard, J.B.3
  • 47
    • 0018136725 scopus 로고
    • Mechanism of coumarin action: significance of vitamin K epoxide reductase inhibition
    • DOI 10.1021/bi00601a003
    • Whitlon D. S., Sadowski J. A., Suttie J. W., Mechanism of coumarin action: significance of vitamin K epoxide reductase inhibition. Biochemistry 1978 17 8 1371 1377 2-s2.0-0018136725 (Pubitemid 8330368)
    • (1978) Biochemistry , vol.17 , Issue.8 , pp. 1371-1377
    • Whitlon, D.S.1    Sadowski, J.A.2    Suttie, J.W.3
  • 48
    • 0023730671 scopus 로고
    • Normal and warfarin-resistant rat hepatocyte metabolism of vitamin K 2,3-epoxide: Evidence for multiple pathways of hydroxyvitamin K formation
    • 2-s2.0-0023730671
    • Trivedi L. S., Rhee M., Galivan J. H., Fasco M. J., Normal and warfarin-resistant rat hepatocyte metabolism of vitamin K 2,3-epoxide: evidence for multiple pathways of hydroxyvitamin K formation. Archives of Biochemistry and Biophysics 1988 264 1 67 73 2-s2.0-0023730671
    • (1988) Archives of Biochemistry and Biophysics , vol.264 , Issue.1 , pp. 67-73
    • Trivedi, L.S.1    Rhee, M.2    Galivan, J.H.3    Fasco, M.J.4
  • 49
    • 0020396486 scopus 로고
    • Evidence that warfarin anticoagulant action involves two distinct reductase activities
    • Fasco M. J., Hildebrandt E. F., Suttie J. W., Evidence that warfarin anticoagulant action involves two distinct reductase activities. The Journal of Biological Chemistry 1982 257 19 11210 11212 2-s2.0-0020396486 (Pubitemid 13203353)
    • (1982) Journal of Biological Chemistry , vol.257 , Issue.19 , pp. 11210-11212
    • Fasco, M.J.1    Hildebrandt, E.F.2    Suttie, J.W.3
  • 51
    • 0017663278 scopus 로고
    • A spectrum of partially carboxylated prothrombins in the plasmas of coumarin-treated patients
    • Friedman P. A., Rosenberg R. D., Hauschka P. V., Fitz-James A., A spectrum of partially carboxylated prothrombins in the plasmas of coumarin-treated patients. Biochimica et Biophysica Acta 1977 494 1 271 276 2-s2.0-0017663278 (Pubitemid 8176034)
    • (1977) Biochimica et Biophysica Acta , vol.494 , Issue.1 , pp. 271-276
    • Friedman, P.A.1    Rosenberg, R.D.2    Hauschka, P.V.3    Fitz-James, A.4
  • 52
    • 0021915109 scopus 로고
    • The kinetics of activation of normal and γ-carboxyglutamic acid-deficient prothrombins
    • Malhotra O. P., Nesheim M. E., Mann K. G., The kinetics of activation of normal and γ -carboxyglutamic acid-deficient prothrombins. The Journal of Biological Chemistry 1985 260 1 279 287 2-s2.0-0021915109 (Pubitemid 15164047)
    • (1985) Journal of Biological Chemistry , vol.260 , Issue.1 , pp. 279-287
    • Malhotra, O.P.1    Nesheim, M.E.2    Mann, K.G.3
  • 53
    • 0017138587 scopus 로고
    • Role of γ carboxyglutamic acid. An unusual protein transition required for the calcium dependent binding of prothrombin to phospholipid
    • 2-s2.0-0017138587
    • Nelsestuen G. L., Role of γ carboxyglutamic acid. An unusual protein transition required for the calcium dependent binding of prothrombin to phospholipid. The Journal of Biological Chemistry 1976 251 18 5648 5656 2-s2.0-0017138587
    • (1976) The Journal of Biological Chemistry , vol.251 , Issue.18 , pp. 5648-5656
    • Nelsestuen, G.L.1
  • 54
    • 0017620084 scopus 로고
    • Differentiation of metal ion induced transitions of prothrombin fragment 1
    • Prendergast F. G., Mann K. G., Differentiation of metal ion induced transitions of prothrombin fragment 1. The Journal of Biological Chemistry 1977 252 3 840 850 2-s2.0-0017620084 (Pubitemid 8041872)
    • (1977) Journal of Biological Chemistry , vol.252 , Issue.3 , pp. 840-850
    • Prendergast, F.G.1    Mann, K.G.2
  • 55
    • 0023020122 scopus 로고
    • Prothrombin requires two sequential metal-dependent conformational transitions to bind phospholipid. Conformation-specific antibodies directed against the phospholipid-binding site on prothrombin
    • Borowski M., Furie B. C., Bauminger S., Furie B., Prothrombin requires two sequential metal-dependent conformational transitions to bind phospholipid. Conformation-specific antibodies directed against the phospholipid-binding site on prothrombin. The Journal of Biological Chemistry 1986 261 32 14969 14975 2-s2.0-0023020122 (Pubitemid 17218059)
    • (1986) Journal of Biological Chemistry , vol.261 , Issue.32 , pp. 14969-14975
    • Borowski, M.1    Furie, B.C.2    Bauminger, S.3    Furie, B.4
  • 56
    • 0034302969 scopus 로고    scopus 로고
    • Furanocoumarins from the root of Angelica dahurica
    • 2-s2.0-0034302969
    • Baek N. I., Ahn E. M., Kim H. Y., Park Y. D., Furanocoumarins from the root of Angelica dahurica. Archives of Pharmacal Research 2000 23 5 467 470 2-s2.0-0034302969
    • (2000) Archives of Pharmacal Research , vol.23 , Issue.5 , pp. 467-470
    • Baek, N.I.1    Ahn, E.M.2    Kim, H.Y.3    Park, Y.D.4
  • 57
    • 82755187437 scopus 로고    scopus 로고
    • Imperatorin a furocoumarin inhibits periplasmic Cu-Zn SOD of Shigella dysenteriae their by modulates its resistance towards phagocytosis during host pathogen interaction
    • Raja S. B., Murali M. R., Roopa K., Imperatorin a furocoumarin inhibits periplasmic Cu-Zn SOD of Shigella dysenteriae their by modulates its resistance towards phagocytosis during host pathogen interaction. Biomedicine & Pharmacotherapy 2011 65 8 560 568
    • (2011) Biomedicine & Pharmacotherapy , vol.65 , Issue.8 , pp. 560-568
    • Raja, S.B.1    Murali, M.R.2    Roopa, K.3
  • 58
    • 2442754064 scopus 로고
    • Synthesis of sucrose and other β -D-fructofuranosyl aldosides by levansucrase
    • 2-s2.0-2442754064
    • Hestrin S., Feingold D. S., Avigad G., Synthesis of sucrose and other β -D-fructofuranosyl aldosides by levansucrase. Journal of the American Chemical Society 1955 77 24 6710 2-s2.0-2442754064
    • (1955) Journal of the American Chemical Society , vol.77 , Issue.24 , pp. 6710
    • Hestrin, S.1    Feingold, D.S.2    Avigad, G.3
  • 59
    • 0028038864 scopus 로고
    • The relaxant action of osthole isolated from Angelica pubescens in guinea-pig trachea
    • 2-s2.0-0028038864
    • Teng C. M., Lin C. H., Ko F. N., Wu T. S., Huang T. F., The relaxant action of osthole isolated from Angelica pubescens in guinea-pig trachea. Naunyn-Schmiedeberg's Archives of Pharmacology 1994 349 2 202 208 2-s2.0-0028038864
    • (1994) Naunyn-Schmiedeberg's Archives of Pharmacology , vol.349 , Issue.2 , pp. 202-208
    • Teng, C.M.1    Lin, C.H.2    Ko, F.N.3    Wu, T.S.4    Huang, T.F.5
  • 60
    • 33947581715 scopus 로고    scopus 로고
    • Antitumor effects of osthol from Cnidium monnieri: An in vitro and in vivo study
    • DOI 10.1002/ptr.2044
    • Chou S. Y., Hsu C. S., Wang K. T., Wang M. C., Wang C. C., Antitumor effects of osthol from Cnidium monnieri: an in vitro and in vivo study. Phytotherapy Research 2007 21 3 226 230 2-s2.0-33947581715 10.1002/ptr.2044 (Pubitemid 46479671)
    • (2007) Phytotherapy Research , vol.21 , Issue.3 , pp. 226-230
    • Chou, S.-Y.1    Hsu, C.-S.2    Wang, K.-T.3    Wang, M.-C.4    Wang, C.-C.5
  • 62
    • 0001763261 scopus 로고
    • The structure of costatolide
    • 2-s2.0-0001763261
    • Stout G. H., Stevens K. L., The structure of costatolide. Journal of Organic Chemistry 1964 29 12 3604 3609 2-s2.0-0001763261
    • (1964) Journal of Organic Chemistry , vol.29 , Issue.12 , pp. 3604-3609
    • Stout, G.H.1    Stevens, K.L.2
  • 64
    • 83755182761 scopus 로고    scopus 로고
    • Anticancer effects of imperatorin isolated from Angelica dahurica: Induction of apoptosis in HepG2 cells through both death-receptor and mitochondria-mediated pathways
    • 10.1159/000331641
    • Luo K. W., Sun J. G., Chan J. Y., Anticancer effects of imperatorin isolated from Angelica dahurica: induction of apoptosis in HepG2 cells through both death-receptor and mitochondria-mediated pathways. Chemotherapy 2011 57 6 449 459 10.1159/000331641
    • (2011) Chemotherapy , vol.57 , Issue.6 , pp. 449-459
    • Luo, K.W.1    Sun, J.G.2    Chan, J.Y.3
  • 65
    • 77955210698 scopus 로고    scopus 로고
    • Effects of osthole on migration and invasion in breast cancer cells
    • 2-s2.0-77955210698 10.1271/bbb.100110
    • Yang D., Gu T., Wang T., Tang Q., Ma C., Effects of osthole on migration and invasion in breast cancer cells. Bioscience, Biotechnology and Biochemistry 2010 74 7 1430 1434 2-s2.0-77955210698 10.1271/bbb.100110
    • (2010) Bioscience, Biotechnology and Biochemistry , vol.74 , Issue.7 , pp. 1430-1434
    • Yang, D.1    Gu, T.2    Wang, T.3    Tang, Q.4    Ma, C.5
  • 66
    • 84860398973 scopus 로고    scopus 로고
    • P38 MAPK activation is required for esculetin-induced inhibition of vascular smooth muscle cells proliferation
    • 10.1016/j.tiv.2011.05.001
    • Yun E. S., Park S. S., Shin H. C., p38 MAPK activation is required for esculetin-induced inhibition of vascular smooth muscle cells proliferation. Toxicology in Vitro 2011 25 7 1335 1342 10.1016/j.tiv.2011.05.001
    • (2011) Toxicology in Vitro , vol.25 , Issue.7 , pp. 1335-1342
    • Yun, E.S.1    Park, S.S.2    Shin, H.C.3
  • 67
    • 84862009408 scopus 로고    scopus 로고
    • Esculetin inhibits N-methyl-D-aspartate neurotoxicity via glutathione preservation in primary cortical cultures
    • 10.5625/lar.2011.27.3.259
    • Lee C. R., Shin E. J., Kim H. C., Esculetin inhibits N-methyl-D-aspartate neurotoxicity via glutathione preservation in primary cortical cultures. Laboratory Animal Research 2011 27 3 259 263 10.5625/lar.2011.27.3.259
    • (2011) Laboratory Animal Research , vol.27 , Issue.3 , pp. 259-263
    • Lee, C.R.1    Shin, E.J.2    Kim, H.C.3
  • 68
    • 0000223316 scopus 로고
    • Dihydromammea C/OB: A new coumarin from the seed of Mammea africana
    • 2-s2.0-0000223316
    • Crichton E. G., Waterman P. G., Dihydromammea C/OB: a new coumarin from the seed of Mammea africana. Phytochemistry 1978 17 10 1783 1786 2-s2.0-0000223316
    • (1978) Phytochemistry , vol.17 , Issue.10 , pp. 1783-1786
    • Crichton, E.G.1    Waterman, P.G.2
  • 70
    • 42749094233 scopus 로고    scopus 로고
    • Anti-hypertensive effects of the methanol/methylene chloride stem bark extract of Mammea africana in l-NAME-induced hypertensive rats
    • 2-s2.0-42749094233 10.1016/j.jep.2008.02.028
    • Nguelefack-Mbuyo P. E., Nguelefack T. B., Dongmo A. B., Afkir S., Azebaze A. G. B., Dimo T., Legssyer A., Kamanyi A., Ziyyat A., Anti-hypertensive effects of the methanol/methylene chloride stem bark extract of Mammea africana in l-NAME-induced hypertensive rats. Journal of Ethnopharmacology 2008 117 3 446 450 2-s2.0-42749094233 10.1016/j.jep.2008.02.028
    • (2008) Journal of Ethnopharmacology , vol.117 , Issue.3 , pp. 446-450
    • Nguelefack-Mbuyo, P.E.1    Nguelefack, T.B.2    Dongmo, A.B.3    Afkir, S.4    Azebaze, A.G.B.5    Dimo, T.6    Legssyer, A.7    Kamanyi, A.8    Ziyyat, A.9
  • 72
    • 0023722721 scopus 로고
    • Studies on cardio-active crude drugs; I. Effect of coumarins on cultured myocardial cells
    • 2-s2.0-0023722721
    • Namba T., Morita O., Huang S. L., Goshima K., Hattori M., Kakiuchi N., Studies on cardio-active crude drugs; I. Effect of coumarins on cultured myocardial cells. Planta Medica 1988 54 4 277 282 2-s2.0-0023722721
    • (1988) Planta Medica , vol.54 , Issue.4 , pp. 277-282
    • Namba, T.1    Morita, O.2    Huang, S.L.3    Goshima, K.4    Hattori, M.5    Kakiuchi, N.6
  • 73
    • 34250122297 scopus 로고
    • Khellactone derivatives from Phlojodicarpus sibiricus
    • 2-s2.0-34250122297 10.1007/BF00574597
    • Gantimur D., Syrchina A. I., Semenov A. A., Khellactone derivatives from Phlojodicarpus sibiricus. Chemistry of Natural Compounds 1986 22 1 103 104 2-s2.0-34250122297 10.1007/BF00574597
    • (1986) Chemistry of Natural Compounds , vol.22 , Issue.1 , pp. 103-104
    • Gantimur, D.1    Syrchina, A.I.2    Semenov, A.A.3
  • 74
    • 67650450222 scopus 로고    scopus 로고
    • Anticonvulsant and acute neurotoxic effects of imperatorin, osthole and valproate in the maximal electroshock seizure and chimney tests in mice: A comparative study
    • 2-s2.0-67650450222 10.1016/j.eplepsyres.2009.03.027
    • Luszczki J. J., Wojda E., Andres-Mach M., Cisowski W., Glensk M., Glowniak K., Czuczwar S. J., Anticonvulsant and acute neurotoxic effects of imperatorin, osthole and valproate in the maximal electroshock seizure and chimney tests in mice: a comparative study. Epilepsy Research 2009 85 2-3 293 299 2-s2.0-67650450222 10.1016/j.eplepsyres.2009.03.027
    • (2009) Epilepsy Research , vol.85 , Issue.2-3 , pp. 293-299
    • Luszczki, J.J.1    Wojda, E.2    Andres-Mach, M.3    Cisowski, W.4    Glensk, M.5    Glowniak, K.6    Czuczwar, S.J.7
  • 75
    • 74149092176 scopus 로고    scopus 로고
    • Attenuation of experimental autoimmune encephalomyelitis in C57 BL/6 mice by osthole, a natural coumarin
    • 2-s2.0-74149092176 10.1016/j.ejphar.2009.12.008
    • Chen X., Pi R., Zou Y., Liu M., Ma X., Jiang Y., Mao X., Hu X., Attenuation of experimental autoimmune encephalomyelitis in C57 BL/6 mice by osthole, a natural coumarin. European Journal of Pharmacology 2010 629 1-3 40 46 2-s2.0-74149092176 10.1016/j.ejphar.2009.12.008
    • (2010) European Journal of Pharmacology , vol.629 , Issue.1-3 , pp. 40-46
    • Chen, X.1    Pi, R.2    Zou, Y.3    Liu, M.4    Ma, X.5    Jiang, Y.6    Mao, X.7    Hu, X.8
  • 76
    • 0023137262 scopus 로고
    • Inactivation of human liver cytochrome P-450 by the drug methoxsalen and other psoralen derivatives
    • DOI 10.1016/0006-2952(87)90190-0
    • Tinel M., Belghiti J., Descatoire V., Inactivation of human liver cytochrome P-450 by the drug methoxsalen and other psoralen derivatives. Biochemical Pharmacology 1987 36 6 951 955 2-s2.0-0023137262 (Pubitemid 17038045)
    • (1987) Biochemical Pharmacology , vol.36 , Issue.6 , pp. 951-955
    • Tinel, M.1    Belghiti, J.2    Descatoire, V.3
  • 77
    • 0032693240 scopus 로고    scopus 로고
    • In vitro inducible nitric oxide synthesis inhibitory active constituents from Fraxinus rhynchophylla
    • DOI 10.1055/s-2006-960840
    • Kim N. Y., Pae H. O., Ko Y. S., Yoo J. C., Choi B. M., Jun C. D., Chung H. T., Inagaki M., Higuchi R., Kim Y. C., In vitro inducible nitric oxide synthesis inhibitory active constituents from Fraxinus rhynchophylla. Planta Medica 1999 65 7 656 658 2-s2.0-0032693240 10.1055/s-2006-960840 (Pubitemid 29503236)
    • (1999) Planta Medica , vol.65 , Issue.7 , pp. 656-658
    • Kim, N.-Y.1    Pae, H.-O.2    Ko, Y.-S.3    Yoo, J.-C.4    Choi, B.-M.5    Jun, C.-D.6    Chung, H.-T.7    Inagaki, M.8    Higuchi, R.9    Kim, Y.-C.10
  • 78
    • 0033630150 scopus 로고    scopus 로고
    • Antihyperglycemic activity of Teramnus labialis (Fabaceae)
    • 2-s2.0-0033630150
    • Fort D. M., Rao K., Jolad S. D., Luo J., Carlson T. J., King S. R., Antihyperglycemic activity of Teramnus labialis (Fabaceae). Phytomedicine 2000 6 6 465 467 2-s2.0-0033630150
    • (2000) Phytomedicine , vol.6 , Issue.6 , pp. 465-467
    • Fort, D.M.1    Rao, K.2    Jolad, S.D.3    Luo, J.4    Carlson, T.J.5    King, S.R.6
  • 79
    • 55149124015 scopus 로고    scopus 로고
    • Protective effect of esculetin against oxidative stress-induced cell damage via scavenging reactive oxygen species
    • 2-s2.0-55149124015 10.1111/j.1745-7254.2008.00878.x
    • Kim S. H., Kang K. A., Zhang R., Piao M. J., Ko D. O., Wang Z. H., Chae S. W., Kang S. S., Lee K. H., Kang H. K., Kang H. W., Hyun J. W., Protective effect of esculetin against oxidative stress-induced cell damage via scavenging reactive oxygen species. Acta Pharmacologica Sinica 2008 29 11 1319 1326 2-s2.0-55149124015 10.1111/j.1745-7254.2008.00878.x
    • (2008) Acta Pharmacologica Sinica , vol.29 , Issue.11 , pp. 1319-1326
    • Kim, S.H.1    Kang, K.A.2    Zhang, R.3    Piao, M.J.4    Ko, D.O.5    Wang, Z.H.6    Chae, S.W.7    Kang, S.S.8    Lee, K.H.9    Kang, H.K.10    Kang, H.W.11    Hyun, J.W.12
  • 80
    • 0036137906 scopus 로고    scopus 로고
    • Fraxin and esculin: Two coumarins specific to Actinidia chinensis and A. deliciosa (kiwifruit)
    • DOI 10.1016/S0305-1978(01)00064-3, PII S0305197801000643
    • Hirsch A. M., Longeon A., Guyot M., Fraxin and esculin: two coumarins specific to Actinidia chinensis and A. deliciosa (kiwifruit). Biochemical Systematics and Ecology 2002 30 1 55 60 2-s2.0-0036137906 10.1016/S0305-1978(01) 00064-3 (Pubitemid 34042351)
    • (2002) Biochemical Systematics and Ecology , vol.30 , Issue.1 , pp. 55-60
    • Hirsch, A.-M.1    Longeon, A.2    Guyot, M.3
  • 81
    • 84862011705 scopus 로고    scopus 로고
    • A natural coumarin derivative esculetin offers neuroprotection on cerebral ischemia/reperfusion injury in mice
    • 10.1111/j.1471-4159.2012.07744.x
    • Wang C., Pei A., Chen J., A natural coumarin derivative esculetin offers neuroprotection on cerebral ischemia/reperfusion injury in mice. Journal of Neurochemistry 2012 121 6 1007 1013 10.1111/j.1471-4159.2012.07744.x
    • (2012) Journal of Neurochemistry , vol.121 , Issue.6 , pp. 1007-1013
    • Wang, C.1    Pei, A.2    Chen, J.3
  • 82
    • 0035851021 scopus 로고    scopus 로고
    • Cytotoxic coumarins from Calophyllum dispar
    • DOI 10.1016/S0031-9422(01)00285-0, PII S0031942201002850
    • Guilet D., Séraphin D., Rondeau D., Richomme P., Bruneton J., Cytotoxic coumarins from Calophyllum dispar. Phytochemistry 2001 58 4 571 575 2-s2.0-0035851021 10.1016/S0031-9422(01)00285-0 (Pubitemid 32904874)
    • (2001) Phytochemistry , vol.58 , Issue.4 , pp. 571-575
    • Guilet, D.1    Seraphin, D.2    Rondeau, D.3    Richomme, P.4    Bruneton, J.5
  • 83
    • 37049129970 scopus 로고
    • Extractives of Mammea americana L - Part III: Identification of new coumarin relatives of mammea B/BA, B/BB, and B/BC having 5,6-annulation and higher oxidation levels
    • 2-s2.0-37049129970 10.1039/P19720002241
    • Crombie L., Games D. E., Haskins N. J., Reed G. F., Extractives of Mammea americana L-part III: Identification of new coumarin relatives of mammea B/BA, B/BB, and B/BC having 5,6-annulation and higher oxidation levels. Journal of the Chemical Society, Perkin Transactions 1 1972 1972 2241 2248 2-s2.0-37049129970 10.1039/P19720002241
    • (1972) Journal of the Chemical Society, Perkin Transactions 1 , vol.1972 , pp. 2241-2248
    • Crombie, L.1    Games, D.E.2    Haskins, N.J.3    Reed, G.F.4
  • 85
    • 33750920871 scopus 로고    scopus 로고
    • Natural coumarins: Methods of isolation and analysis
    • DOI 10.1007/s11094-006-0123-6
    • Lozhkin A. V., Sakanyan E. I., Natural coumarins: methods of isolation and analysis. Pharmaceutical Chemistry Journal 2006 40 6 337 346 2-s2.0-33750920871 10.1007/s11094-006-0123-6 (Pubitemid 44724886)
    • (2006) Pharmaceutical Chemistry Journal , vol.40 , Issue.6 , pp. 337-346
    • Lozhkin, A.V.1    Sakanyan, E.I.2


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