메뉴 건너뛰기




Volumn 16, Issue 26, 2009, Pages 3414-3468

Prenylated isoflavonoids: Botanical distribution, structures, biological activities and biotechnological studies. An update (1995-2006)

Author keywords

Antimicrobial activity; Antitumor activity; Arylcoumarins; Biotechnology; Coumestans; Prenylated isoflavonoids; Pterocarpans; Rotenoids

Indexed keywords

AMORPHIGENIN; BITUCARPIN B; BOLUCARPAN A; BOLUCARPAN B; BOLUCARPAN C; BOLUSANTHOL B; BOLUSANTHOL C; DABINOL; DEGUELIN; DERRISIN; DIMETHYLALLYLTRANSFERASE; ERYBRAEDIN C; GLABRIDIN; ISOFLAVONE; ISOFLAVONOID; ISOPRENOID; LIQUIRITIN; METICILLIN; OXACILLIN; PERVILLEANONE; PLANT MEDICINAL PRODUCT; POMIFERIN; PSEUDOMONIC ACID; PSORALIDIN; PTEROCARPAN DERIVATIVE; ROTENONE; SCANDERONE; SILDENAFIL; UNCLASSIFIED DRUG; UNINDEXED DRUG; WARANGALONE;

EID: 70450221333     PISSN: 09298673     EISSN: None     Source Type: Journal    
DOI: 10.2174/092986709789057662     Document Type: Review
Times cited : (63)

References (248)
  • 1
    • 0023040739 scopus 로고
    • Enzymic synthesis of isoflavones
    • Kocks, G.; Griseback, H. Enzymic synthesis of isoflavones. Eur. J. Biochem. 1986, 155, 311-318;
    • (1986) Eur. J. Biochem. , vol.155 , pp. 311-318
    • Kocks, G.1    Griseback, H.2
  • 3
    • 0025163193 scopus 로고
    • Reaction mechanism of oxidative rearrangement of flavanone in isoflavone biosynthesis
    • DOI 10.1016/0014-5793(90)80410-K
    • c) Hashim, M.F.; Hakamatsuka, T.; Ebizuka, Y.; Sankawa, U. Reaction mechanism of oxidative rearrangement of flavanone in isoflavanone biosynthesis. FEBS Lett. 1990, 271, 219-222 (Pubitemid 20336243)
    • (1990) FEBS Letters , vol.271 , Issue.1-2 , pp. 219-222
    • Hashim, M.F.1    Hakamatsuka, T.2    Ebizuka, Y.3    Sankawa, U.4
  • 4
    • 0026772826 scopus 로고
    • The mechanism of the enzymic induced flavanone-isoflavanone change
    • d) Crombie, L; Whiting, D.A.The mechanism of the enzymic induced flavanone-isoflavanone change. Tetrahedron Lett. 1992, 33, 3663-3666.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 3663-3666
    • Crombie, L.1    Whiting, D.A.2
  • 5
    • 0029135787 scopus 로고
    • Prenylated isoflavonoids-An update
    • Tahara, S.; Ibrahim, R.K. Prenylated isoflavonoids-An update. Phytochemistry 1995, 38, 107-194.
    • (1995) Phytochemistry , vol.38 , pp. 107-194
    • Tahara, S.1    Ibrahim, R.K.2
  • 7
    • 0034931657 scopus 로고    scopus 로고
    • Chemistry and biosynthesis of prenylflavonoids
    • Nomura, T. Chemistry and biosynthesis of prenylflavonoids. Yakugaku Zasshi 2001, 121(7), 535-556.
    • (2001) Yakugaku Zasshi , vol.121 , Issue.7 , pp. 535-556
    • Nomura, T.1
  • 9
    • 0004132535 scopus 로고    scopus 로고
    • Harborne, J.B.; Baxter, H. Eds. Wiley, Chichester 2 vols.
    • Handbook of Natural Flavonoids" Harborne, J.B.; Baxter, H. Eds. Wiley, Chichester 1999 2 vols.
    • (1999) Handbook of Natural Flavonoids
  • 10
  • 12
    • 33646056981 scopus 로고    scopus 로고
    • Distribution of isoflavonoids in non-leguminous taxa: An update
    • Mackova, Z.; Kobloska, R.; Lapcik, O. Distribution of isoflavonoids in non-leguminous taxa: an update. Phytochemistry 2006, 67, 849-855.
    • (2006) Phytochemistry , vol.67 , pp. 849-855
    • Mackova, Z.1    Kobloska, R.2    Lapcik, O.3
  • 14
    • 0042855325 scopus 로고
    • Induced isoflavonoids from copper chloride-treated stems of Pueraria lobata
    • Hakamatsuka, T.; Ebizuka, Y.; Sankawa, U. Induced isoflavonoids from copper chloride-treated stems of Pueraria lobata. Phytochemistry 1991, 30, 1481-1482.
    • (1991) Phytochemistry , vol.30 , pp. 1481-1482
    • Hakamatsuka, T.1    Ebizuka, Y.2    Sankawa, U.3
  • 16
    • 0035849167 scopus 로고    scopus 로고
    • Flavonoids from the stem bark of Bolusanthus specious
    • Bojase, G.; Wanjala C.C.; Majinda, R.R. Flavonoids from the stem bark of Bolusanthus specious Phytochemistry 2001, 56, 837-841.
    • (2001) Phytochemistry , vol.56 , pp. 837-841
    • Bojase, G.1    Wanjala, C.C.2    Majinda, R.R.3
  • 17
  • 18
    • 1842817379 scopus 로고    scopus 로고
    • Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus specious
    • Erasto, P.; Bojase-Moleta, G.; Majinda, R.R.T. Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus specious. Phytochemistry 2004, 65, 875-880.
    • (2004) Phytochemistry , vol.65 , pp. 875-880
    • Erasto, P.1    Bojase-Moleta, G.2    Majinda, R.R.T.3
  • 19
    • 0036213452 scopus 로고    scopus 로고
    • New pterocarpanoids of Crotalaria pallida and Crotalaria assamica
    • Weng, J.-R.; Yen, M.-H.; Lin, C.-N. New pterocarpanoids of Crotalaria pallida and Crotalaria assamica. Helv. Chim. Acta 2002, 85, 847-851.
    • (2002) Helv. Chim. Acta , vol.85 , pp. 847-851
    • Weng, J.-R.1    Yen, M.-H.2    Lin, C.-N.3
  • 20
    • 0037349213 scopus 로고    scopus 로고
    • Anti-inflammatory constituents and new pterocarpanoid of Crotalaria pallida
    • Weng, J.-R.; Tsao, L.-T.; Yen, M.-H.; Wang, J.-P.; Lin, C.N. Anti-inflammatory constituents and new pterocarpanoid of Crotalaria pallida. J. Nat. Prod. 2003, 66, 404-407.
    • (2003) J. Nat. Prod. , vol.66 , pp. 404-407
    • Weng, J.-R.1    Tsao, L.-T.2    Yen, M.-H.3    Wang, J.-P.4    Lin, C.N.5
  • 21
    • 33645525847 scopus 로고    scopus 로고
    • Activity of isoflavans of Dalea aurea (Fabaceae) against the opportunistic ameba Naegleria
    • Belofsky G, Carreno R , Goswick SM, John DT. Activity of isoflavans of Dalea aurea (Fabaceae) against the opportunistic ameba Naegleria. Planta Med. 2006, 72, 383-386.
    • (2006) Planta Med. , vol.72 , pp. 383-386
    • Belofsky, G.1    Carreno, R.2    Goswick, S.M.3    John, D.T.4
  • 22
    • 0032030508 scopus 로고    scopus 로고
    • Three prenylated isoflavans from Maackia tenuifolia
    • Zeng, J.F., Wei, H.X.; Li, G.L.; Zu, D.Y. Three prenylated isoflavans from Maackia tenuifolia. Phytochemistry 1998, 47, 903-905.
    • (1998) Phytochemistry , vol.47 , pp. 903-905
    • Zeng, J.F.1    Wei, H.X.2    Li, G.L.3    Zu, D.Y.4
  • 23
    • 0035341550 scopus 로고    scopus 로고
    • Prenylated isoflonoids from Deguelia hatschbachii and their systematic significance in Deguelia
    • Magalhaes, A.F.; Tozzi, A.M.G.A., Magalhaes, E.G., de Souza Moraes, V.R. Prenylated isoflonoids from Deguelia hatschbachii and their systematic significance in Deguelia. Phytochemistry 2001, 57, 77-89.
    • (2001) Phytochemistry , vol.57 , pp. 77-89
    • Magalhaes, A.F.1    Tozzi, A.M.G.A.2    Magalhaes, E.G.3    De Souza Moraes, V.R.4
  • 24
    • 33645529006 scopus 로고    scopus 로고
    • New prenylated metabolites of Deguelia longeracemosa and evaluation of their antimicrobial potential
    • Magalhães, A.F.; Tozzi, A.M.; Magalhães, E.G.; Souza-Neta, L.C. New prenylated metabolites of Deguelia longeracemosa and evaluation of their antimicrobial potential. Planta Med. 2006, 72, 358-363.
    • (2006) Planta Med. , vol.72 , pp. 358-363
    • Magalhães, A.F.1    Tozzi, A.M.2    Magalhães, E.G.3    Souza-Neta, L.C.4
  • 25
    • 0036241807 scopus 로고    scopus 로고
    • Derrisin, a new rotenoid from Derris malaccensis plain and anti-helicobacter pylori activity of its related constituents
    • Takashima, J.; Chiba, N.; Yoneda, K.; Ohsaki, A. Derrisin, a new rotenoid from Derris malaccensis plain and anti-helicobacter pylori activity of its related constituents. J. Nat. Prod. 2002, 65, 611-613.
    • (2002) J. Nat. Prod. , vol.65 , pp. 611-613
    • Takashima, J.1    Chiba, N.2    Yoneda, K.3    Ohsaki, A.4
  • 26
    • 0032584097 scopus 로고    scopus 로고
    • Anticancer action of cube insecticide: Correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxoreductase and induced ornithine decarboxylase activities
    • Fang, N.; Casida, J.E. Anticancer action of cube insecticide: correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxoreductase and induced ornithine decarboxylase activities. Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 3380-3384.
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 3380-3384
    • Fang, N.1    Casida, J.E.2
  • 27
    • 0032585986 scopus 로고    scopus 로고
    • Cube Resin Insecticide: Identification and biological activity of 29 rotenoid constituents
    • Fang, N.; Casida, J.E. Cube Resin Insecticide: identification and biological activity of 29 rotenoid constituents. J. Agric. Food Chem. 1999, 47, 2130-2136.
    • (1999) J. Agric. Food Chem. , vol.47 , pp. 2130-2136
    • Fang, N.1    Casida, J.E.2
  • 29
    • 2142753011 scopus 로고    scopus 로고
    • A benzil and isoflavone derivatives from Derris scandens Benth
    • DOI 10.1016/j.phytochem.2004.03.006, PII S0031942204001050
    • Mahabusarakam, W.; Deachathai, S.; Phongpaichit, S., Jansakul, C.; Taylor, W.C. A benzil and isoflavano derivatives from Derris scandens Benth. Phytochemistry 2004, 65, 1185-1191 (Pubitemid 38542758)
    • (2004) Phytochemistry , vol.65 , Issue.8 , pp. 1185-1191
    • Mahabusarakam, W.1    Deachathai, S.2    Phongpaichit, S.3    Jansakul, C.4    Taylor, W.C.5
  • 32
    • 33646781910 scopus 로고    scopus 로고
    • The unusual rotenoid derivatives, 7a-O-methyl-12a-hydroxydeguelol and spiro-13-homo-13-oxaelliptone, from the seeds of Derris trifoliata
    • Yenesew, A.; Kipiagat, J.T.; Derese, S.; Midiwo, J.O.; Kabaru, J.M.; Heydenreich, M.; Peter, M.G. The unusual rotenoid derivatives, 7a-O-methyl-12a-hydroxydeguelol and spiro-13-homo-13-oxaelliptone, from the seeds of Derris trifoliata. Phytochemistry 2006, 67, 988-991.
    • (2006) Phytochemistry , vol.67 , pp. 988-991
    • Yenesew, A.1    Kipiagat, J.T.2    Derese, S.3    Midiwo, J.O.4    Kabaru, J.M.5    Heydenreich, M.6    Peter, M.G.7
  • 33
    • 0141794400 scopus 로고    scopus 로고
    • Three isoflavanones with cannabinoid-like moieties from Desmodium canum
    • DOI 10.1016/S0031-9422(03)00201-2
    • Botta, B.; Gàcs-Baitz, E, Vinciguerra, V.; Delle Monache, G. Three isoflavanones with cannabinoid-like moieties from Desmodium canum. Phytochemistry 2003, 64, 599-602 (Pubitemid 37168983)
    • (2003) Phytochemistry , vol.64 , Issue.2 , pp. 599-602
    • Botta, B.1    Gacs-Baitz, E.2    Vinciguerra, V.3    Delle Monache, G.4
  • 38
    • 0041880377 scopus 로고    scopus 로고
    • Flavonoids and isoflavonoids with antiplasmodial activities from the root bark of Erythrina abyssinica
    • DOI 10.1055/s-2003-41119
    • Yenesew, A.; Derese, S.; Irungu, B.; Midiwo, J.O.; Waters, N.C.; Liyala, P., Akala, H.; Heydenreich, M.; Peter, M.G. Flavonoids and isoflavonoids with antiplasmodial activities from the root bark of Erythrina abyssinica. Planta Med. 2003, 69, 658-661 (Pubitemid 37041064)
    • (2003) Planta Medica , vol.69 , Issue.7 , pp. 658-661
    • Yenesew, A.1    Derese, S.2    Irungu, B.3    Midiwo, J.O.4    Waters, N.C.5    Liyala, P.6    Akala, H.7    Heydenreich, M.8    Peter, M.G.9
  • 39
    • 33748592544 scopus 로고    scopus 로고
    • Inhibition of protein tyrosine phosphatase 1B by prenylated isoflava-noids isolated from the stem bark of Erythrina addisoniae
    • Bae, E.Y.; Na M.; Njamen, D.; Mbafor, J. T.; Fomum, Z. T.; Cui, L.; Choung D. H.; Kim, B. Y.; Oh, W. K.; Ahn, J. S. Inhibition of protein tyrosine phosphatase 1B by prenylated isoflava-noids isolated from the stem bark of Erythrina addisoniae. Planta Med. 2006, 72, 945-948.
    • (2006) Planta Med. , vol.72 , pp. 945-948
    • Bae, E.Y.1    Na, M.2    Njamen, D.3    Mbafor, J.T.4    Fomum, Z.T.5    Cui, L.6    Choung, D.H.7    Kim, B.Y.8    Oh, W.K.9    Ahn, J.S.10
  • 40
    • 0037138278 scopus 로고    scopus 로고
    • Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii
    • DOI 10.1016/S0031-9422(01)00459-9, PII S0031942201004599
    • Yenesew, A.; Midiwo, J.O.; Guchu, S.M.; Heidenreich, M.; Peter, M.G. Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burtii. Phytochemistry 2002, 59, 337-341 (Pubitemid 34145435)
    • (2002) Phytochemistry , vol.59 , Issue.3 , pp. 337-341
    • Yenesew, A.1    Midiwo, J.O.2    Guchu, S.M.3    Heydenreich, M.4    Peter, M.G.5
  • 44
    • 0034716825 scopus 로고    scopus 로고
    • Indicanines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica
    • DOI 10.1016/S0031-9422(99)00615-9, PII S0031942299006159
    • Ngengfack, A.E.; Waffo, A.K.; Azebaze, G.A.; Fomum, Z.T.; Meyer, M.; Bodo, B.; van Heerden F.R. Indicamines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica. Phytochemistry 2000, 53, 981-985 (Pubitemid 30233136)
    • (2000) Phytochemistry , vol.53 , Issue.8 , pp. 981-985
    • Waffo, A.K.1    Azebaze, G.A.2    Nkengfack, A.E.3    Fomum, Z.T.4    Meyer, M.5    Bodo, B.6    Van Heerden, F.R.7
  • 47
    • 70450131275 scopus 로고    scopus 로고
    • Constituents of Erythrina lysistemon, their brine shrimp lethality, antimicrobial and radical scavenging activities
    • Juma, B.F.; Majinda, R.R.T. Constituents of Erythrina lysistemon, their brine shrimp lethality, antimicrobial and radical scavenging activities. Nat. Prod. Commun. 2006, 1, 103-107.
    • (2006) Nat. Prod. Commun. , vol.1 , pp. 103-107
    • Juma, B.F.1    Majinda, R.R.T.2
  • 48
    • 0037665217 scopus 로고    scopus 로고
    • An arylbenzo-furan and four isoflavanoids from the roots of Erythrina poeppigiana
    • Tanaka, H.; Oh-Uchi, T.; Etoh, H.; Sako, M.; Sato, M.; Fukai, T.; Tateishi, T. An arylbenzo-furan and four isoflavanoids from the roots of Erythrina poeppigiana. Phytochemistry 2003, 63, 597-602.
    • (2003) Phytochemistry , vol.63 , pp. 597-602
    • Tanaka, H.1    Oh-Uchi, T.2    Etoh, H.3    Sako, M.4    Sato, M.5    Fukai, T.6    Tateishi, T.7
  • 49
    • 2442690155 scopus 로고    scopus 로고
    • Antibacterial properties of a new isoflavonoid from Erythrina poeppigiana against methicillin-resistant Staphylococcus aureus
    • DOI 10.1078/0944711041495137
    • Tanaka, H.; Sato, M.; Oh-Uchi, T.; Yamaguchi, R.; Shimizu, H.; Sako, M.; Takeuchi, H. Antibacterial properties of a new isoflavonoid from Erythrina poeppigiana against methicillum-resistant Staphilococcos aureus. Phytomedicine 2004, 11, 331-337 (Pubitemid 38657464)
    • (2004) Phytomedicine , vol.11 , Issue.4 , pp. 331-337
    • Tanaka, H.1    Sato, M.2    Oh-Uchi, T.3    Yamaguchi, R.4    Etoh, H.5    Shimizu, H.6    Sako, M.7    Takeuchi, H.8
  • 50
    • 0034727719 scopus 로고    scopus 로고
    • Two isoflavanones from the stem bark of Erythrina sacleuxii
    • DOI 10.1016/S0031-9422(00)00349-6, PII S0031942200003496
    • Yenesew, A.; Midiwo, J. O.; Heydenreich, M.; Schanzenbach, D.; Peter, M. G. Two isoflavanones from the stem bark of Erythrina sacleuxii. Phytochemistry 2000, 55, 457-459 (Pubitemid 30954022)
    • (2000) Phytochemistry , vol.55 , Issue.5 , pp. 457-459
    • Yenesew, A.1    Midiwo, J.O.2    Heydenreich, M.3    Schanzenbach, D.4    Peter, M.G.5
  • 54
    • 0025663417 scopus 로고
    • Erythrina studies. Part 18. A new prenylated isoflavone and long chain esters from two Erythrina species
    • Wandji, X.; Nkengfack, A.E.; Fomum, Z.T.; Ubillas, R.; Killday, K.B.; Tempesta, M.S. Erythrina studies. Part 18. A new prenylated isoflavone and long chain esters from two Erythrina species. J. Nat. Prod. 1990, 53, 1425-1429.
    • (1990) J. Nat. Prod. , vol.53 , pp. 1425-1429
    • Wandji, X.1    Nkengfack, A.E.2    Fomum, Z.T.3    Ubillas, R.4    Killday, K.B.5    Tempesta, M.S.6
  • 56
    • 0035815345 scopus 로고    scopus 로고
    • Erysubins C-F, four isoflavonoids from Erythrina tuberosa var. glabrescences
    • Tanaka, H.; Etoh, H.; Watanabe, N.; Shimizu, H.; Ahmad, M.; Rizwani, G.H. Erysubins C-F, four isoflavonoids from Erythrina tuberosa var. glabrescences. Phytochemistry 2001, 56, 769-773.
    • (2001) Phytochemistry , vol.56 , pp. 769-773
    • Tanaka, H.1    Etoh, H.2    Watanabe, N.3    Shimizu, H.4    Ahmad, M.5    Rizwani, G.H.6
  • 58
    • 0033897395 scopus 로고    scopus 로고
    • Two new isoflavonoids from Erythrina variegata
    • DOI 10.1055/s-2000-8602
    • Tanaka, H.; Etoh, H.; Shimizu, H; Makita, T.; Tateishi, Y. Two new isoflavonoids from Erythrina variegate. Planta Med. 2000, 66, 578-579 (Pubitemid 30626491)
    • (2000) Planta Medica , vol.66 , Issue.6 , pp. 578-579
    • Tanaka, H.1    Etoh, H.2    Shimizu, H.3    Makita, T.4    Tateishi, Y.5
  • 63
    • 33646884435 scopus 로고    scopus 로고
    • Two new isofla-vonoids and a new 2-aryl benzofuran from the roots of Erythrina variegate
    • Tanaka, H.; Sudo, M.; Hirata, M.; Sako, M.; Sato, M.; Chen, I.-S.; Fukai, T. Two new isofla-vonoids and a new 2-aryl benzofuran from the roots of Erythrina variegate. Heterocycles 2005, 65, 871-877.
    • (2005) Heterocycles , vol.65 , pp. 871-877
    • Tanaka, H.1    Sudo, M.2    Hirata, M.3    Sako, M.4    Sato, M.5    Chen, I.-S.6    Fukai, T.7
  • 64
  • 68
    • 0036668388 scopus 로고    scopus 로고
    • Coumaronochromones and flavanones from Euchresta formosana roots
    • Lo, W.-L.; Chan, F.-R.; Hsieh, T.-J.; Wu, Y.-C. Coumaronochromones and flavanones from Euchresta formosana roots. Phytochemistry 2002, 60, 839-845.
    • (2002) Phytochemistry , vol.60 , pp. 839-845
    • Lo, W.-L.1    Chan, F.-R.2    Hsieh, T.-J.3    Wu, Y.-C.4
  • 70
    • 27544447061 scopus 로고    scopus 로고
    • Structural study of glabrisoflavone, a novel isoflavone from Glycyrrhiza glabra L. Flavonoids of the aereal parts of Glycyrrhiza glabra L. grown in Uzbekistan
    • a) Yuldashev, M.P.; Batirov, E.Kh.; Vdovin, A.D.; Abdullaev, N.D. Structural study of glabrisoflavone, a novel isoflavone from Glycyrrhiza glabra L. Flavonoids of the aereal parts of Glycyrrhiza glabra L. grown in Uzbekistan. Russian J. Bioorg. Chem. 2000, 26, 784-786;
    • (2000) Russian J. Bioorg. Chem. , vol.26 , pp. 784-786
    • Yuldashev, M.P.1    Batirov, E.Kh.2    Vdovin, A.D.3    Abdullaev, N.D.4
  • 71
    • 70450153821 scopus 로고    scopus 로고
    • Flavonoids of the aereal parts of Glycyrrhiza glabra L. grown in Uzbekistan
    • b) Yuldashev, M. P.; Nigmatullaev, A. M.; Sultanov, S. Flavonoids of the aereal parts of Glycyrrhiza glabra L. grown in Uzbekistan. Rastitel'nye Resursy 2000, 36, 56-59;
    • (2000) Rastitel'nye Resursy , vol.36 , pp. 56-59
    • Yuldashev, M.P.1    Nigmatullaev, A.M.2    Sultanov, S.3
  • 72
    • 70450121832 scopus 로고    scopus 로고
    • Flavonoids of the aerial parts of Glycyrrhiza glabra L. Structural study of glabrisoflavone, a novel isoflavone from Glycyrrhiza glabra
    • c) Yuldashev, M. P.; Batirov, E. S.; Vdovin, A. D.; Abdullaev, N. D. Flavonoids of the aerial parts of Glycyrrhiza glabra L. Structural study of glabrisoflavone, a novel isoflavone from Glycyrrhiza glabra. Seriya Khimicheskaya 2000, 2, 67-71.
    • (2000) Seriya Khimicheskaya , vol.2 , pp. 67-71
    • Yuldashev, M.P.1    Batirov, E.S.2    Vdovin, A.D.3    Abdullaev, N.D.4
  • 73
  • 74
    • 32644432493 scopus 로고    scopus 로고
    • Antibacterial compounds from Glycyrrhiza uralensis
    • He, J.; Chen, L.; Heber, D.; Shi, W.; Lu, O.Y. Antibacterial compounds from Glycyrrhiza uralensis. J. Nat. Prod. 2006, 69, 121-124.
    • (2006) J. Nat. Prod. , vol.69 , pp. 121-124
    • He, J.1    Chen, L.2    Heber, D.3    Shi, W.4    Lu, O.Y.5
  • 76
    • 0346363609 scopus 로고    scopus 로고
    • New prenylated isoflavanones and other constituents of Lespedeza bicolor
    • Maximov, O.B.; Kulesh, N.I.; Stepanenko, L.S.; Dmitrenok, P.S. New prenylated isoflavanones and other constituents of Lespedeza bicolor. Fitoterapia 2004, 75, 96-98.
    • (2004) Fitoterapia , vol.75 , pp. 96-98
    • Maximov, O.B.1    Kulesh, N.I.2    Stepanenko, L.S.3    Dmitrenok, P.S.4
  • 77
    • 0033027321 scopus 로고    scopus 로고
    • New bioactive flavonoids and stilbenes in cubé resin insecticide
    • a) Fang, N.; Casida, J.E. New bioactive flavonoids and stilbenes in cubé resin insecticide. J. Nat. Prod. 1999, 62, 205-210;
    • (1999) J. Nat. Prod. , vol.62 , pp. 205-210
    • Fang, N.1    Casida, J.E.2
  • 78
    • 79953651061 scopus 로고    scopus 로고
    • erratum in
    • b) erratum in J. Nat. Prod. 2000, 63, 293.
    • (2000) J. Nat. Prod. , vol.63 , pp. 293
  • 79
    • 0032585986 scopus 로고    scopus 로고
    • Cubé resin insecticide: Identification and biological activity of 29 rotenoid constituents
    • Fang, N.; Casida, J.E. Cubé resin insecticide: identification and biological activity of 29 rotenoid constituents. J. Agric. Food Chem. 1999, 47, 2130-2136;
    • (1999) J. Agric. Food Chem. , vol.47 , pp. 2130-2136
    • Fang, N.1    Casida, J.E.2
  • 80
    • 19944397485 scopus 로고    scopus 로고
    • Comment on cube resin insecticide: Identification and biological activity of 29 rotenoid constituents
    • DOI 10.1021/jf048227r
    • b) Coll, J. Comment on cube resin insecticide: identification and biological activity of 29 rotenoid constituents. J. Agric. Food Chem. 2005, 53, 3749-3750 (Pubitemid 40758222)
    • (2005) Journal of Agricultural and Food Chemistry , vol.53 , Issue.9 , pp. 3749-3750
    • Coll, J.1
  • 81
    • 0442309833 scopus 로고    scopus 로고
    • Manuifolin Q, an unusual 4-aryl-substituted isoflavan from Maackia tenuifolia
    • Zeng J.F., Tan C.H., Zhu D.Y. Manuifolin Q, an unusual 4-aryl-substituted isoflavan from Maackia tenuifolia. J Asian Nat Prod Res. 2004, 6, 45-48.
    • (2004) J Asian Nat Prod Res. , vol.6 , pp. 45-48
    • Zeng, J.F.1    Tan, C.H.2    Zhu, D.Y.3
  • 82
    • 0034193612 scopus 로고    scopus 로고
    • Anti-tumor-promoting effects of isoflavonoids on Epstein-Barr virus activation and two-stage mouse skin carcinogenesis
    • DOI 10.1016/S0304-3835(00)00331-1, PII S0304383500003311
    • Ito, C.; Itoigawa, M.; Tan, H.T.; Tokuda, H.; Yang Mou, X.; Mukainaka, T.; Ishikawa, T.; Nishino, H.; Furukawa, H. Anti- tumour-promoting effects of isoflavonoids on Epstein-Barr virus activation and two-stage mouse skin carcinogenesis. Cancer Lett. 2000, 152, 187-192 (Pubitemid 30201501)
    • (2000) Cancer Letters , vol.152 , Issue.2 , pp. 187-192
    • Ito, C.1    Itoigawa, M.2    Tan, H.T.W.3    Tokuda, H.4    Yang Mou, X.5    Mukainaka, T.6    Ishikawa, T.7    Nishino, H.8    Furukawa, H.9
  • 88
    • 32644452994 scopus 로고
    • Second Edition, Huang, T.-C., Ed.; Editorial Committee of the Flora of Taiwan
    • Huang, T.-C.; Ohashi, H. In Flora of Taiwan, Second Edition, Vol.3; Huang, T.-C., Ed.; Editorial Committee of the Flora of Taiwan, 1993; p. 337.
    • (1993) Flora of Taiwan , vol.3 , pp. 337
    • Huang, T.-C.1    Ohashi, H.2
  • 89
    • 3242742751 scopus 로고    scopus 로고
    • Chemical constituents of Millettia taiwaniana: Structure elucidation of five new isoflavonoids and their cancer chemopreventive activity
    • DOI 10.1021/np030554q
    • Ito, C.; Itoigawa, M.; Kojima, N.; Tokuda, H.; Hirata, T.; Nishino, H.; Furukawa, H. Chemical Constituents of Millettia taiwaniana: structure elucidation of five New iso-flavonoids and their cancer chemopreventive activity. J. Nat. Prod. 2004, 67, 1125-1130 (Pubitemid 38971672)
    • (2004) Journal of Natural Products , vol.67 , Issue.7 , pp. 1125-1130
    • Ito, C.1    Itoigawa, M.2    Kojima, N.3    Tokuda, H.4    Hirata, T.5    Nishino, H.6    Furukawa, H.7
  • 90
    • 33645969315 scopus 로고    scopus 로고
    • Induction of apoptosis by isoflavonoids from the leaves of Millettia taiwaniana in human leukemia HL-60 cells
    • Ito, C.; Murata, T; Itoigawa, M.; Nakao, K; Kumagai, M.; Kaneda, N. Furukawa, H. Induction of apoptosis by isoflavonoids from the leaves of Millettia taiwaniana in human leukemia HL-60 cells. Planta Med. 2006, 72, 424-429.
    • (2006) Planta Med. , vol.72 , pp. 424-429
    • Ito, C.1    Murata, T.2    Itoigawa, M.3    Nakao, K.4    Kumagai, M.5    Kaneda, N.6    Furukawa, H.7
  • 94
    • 0031965075 scopus 로고    scopus 로고
    • Rotenoids, isoflavones and chalcones from the stem bark of Millettia usaramensis subspecies usaramensis
    • Yenesew, A.; Midiwo, J.O.; Waterman, P.G. Rotenoids, isoflavones and chalcones from the stem bark of Millettia usaramensis subspecies usaramensis. Phytochemistry 1998, 47, 295-300.
    • (1998) Phytochemistry , vol.47 , pp. 295-300
    • Yenesew, A.1    Midiwo, J.O.2    Waterman, P.G.3
  • 95
    • 37049052389 scopus 로고
    • The structure and stereochemistry of the rotenolones, rotenonols, isorotenolones, and isorotenonols
    • Crombie, L.; Godin, P.J. The structure and stereochemistry of the rotenolones, rotenonols, isorotenolones, and isorotenonols. J. Chem. Soc. 1961, 2861-2875.
    • (1961) J. Chem. Soc. , pp. 2861-2875
    • Crombie, L.1    Godin, P.J.2
  • 96
    • 16544395423 scopus 로고    scopus 로고
    • Estrogenic and antiestrogenic activities of the roots of Moghania philippinensis and their constituents
    • Ahn, E.M.; Nakamura, N.; Akao, T.; Nishihara, T.; Hattori, M. Estrogenic and antiestrogenic activities of the roots of Moghania philippinensis and their constituents. Biol. Pharm. Bull. 2004, 27, 548-553.
    • (2004) Biol. Pharm. Bull. , vol.27 , pp. 548-553
    • Ahn, E.M.1    Nakamura, N.2    Akao, T.3    Nishihara, T.4    Hattori, M.5
  • 98
    • 0034518615 scopus 로고    scopus 로고
    • Three new arylobenzofurans from Onobrychis ebenoides and evaluation of their binding affinity for the estrogen receptor
    • Halabalaki, M.;Aligiannis, N.; Papoutsi, Z.; Mitakou,S.; Moutsatsou, P.; Sekeris, C.; Skaltsounis, A.-L. Three new arylobenzofurans from Onobrychis ebenoides and evaluation of their binding affinity for the estrogen receptor. J. Nat. Prod. 2000, 63, 1672-1674.
    • (2000) J. Nat. Prod. , vol.63 , pp. 1672-1674
    • Halabalaki, M.1    Aligiannis, N.2    Papoutsi, Z.3    Mitakou, S.4    Moutsatsou, P.5    Sekeris, C.6    Skaltsounis, A.-L.7
  • 100
    • 32644445887 scopus 로고    scopus 로고
    • Isoflavonoids and others compounds from Psorothamnus arborescens with antiprotozoal activities
    • Salem, M.M.; Werbovetz, K.A. Isoflavonoids and others compounds from Psorothamnus arborescens with antiprotozoal activities. J. Nat. Prod. 2006, 69, 43-49.
    • (2006) J. Nat. Prod. , vol.69 , pp. 43-49
    • Salem, M.M.1    Werbovetz, K.A.2
  • 103
    • 0033996618 scopus 로고    scopus 로고
    • Identification of deoxymiroestrol as the actual rejuvenating principle "kwao keur", Pueraria mirifica. The known miroestrol may be an artefact
    • Chansakaow, S.; Ishikawa, T.; Seki, H.; Sekine, K.; Okada, M.; Chaichantipyuth, C. Identification of deoxymiroestrol as the actual rejuvenating principle "kwao keur", Pueraria mirifica. The known miroestrol may be an artefact. J. Nat. Prod. 2000, 63, 173-175.
    • (2000) J. Nat. Prod. , vol.63 , pp. 173-175
    • Chansakaow, S.1    Ishikawa, T.2    Seki, H.3    Sekine, K.4    Okada, M.5    Chaichantipyuth, C.6
  • 106
    • 0032964965 scopus 로고    scopus 로고
    • Four isoflavanones from roots of Sophora tetraptera
    • DOI 10.1016/S0031-9422(98)00551-2, PII S0031942298005512
    • Shirataki, Y.; Matsuoka, S.; Komatsu, M.; Masayoshi, O.; Tanaka, T.; Iinuma, M. Four isofla-vanones from the roots of Sophora tetraptera. Phytochemistry 1999, 50, 695-701 (Pubitemid 29058506)
    • (1999) Phytochemistry , vol.50 , Issue.4 , pp. 695-701
    • Shirataki, Y.1    Matsuoka, S.2    Komatsu, M.3    Masayoshi, O.4    Tanaka, T.5    Iinuma, M.6
  • 111
    • 5044243216 scopus 로고    scopus 로고
    • Isoflavonoids in the Rutaceae family: 1. Fortunella obovata, Murraya paniculata and four citrus species
    • DOI 10.1002/pca.781
    • Lapcik, O.; Klejdus, B.; Davidova, M.; Kokoska, L.; Kuban, V., Moravcova, J. Isoflavonoids in the Rutaceae family: 1. Fortumella obovata, Murraya paniculata and four Citrus species. Phytochem. Anal. 2004, 15, 293-299 (Pubitemid 39341165)
    • (2004) Phytochemical Analysis , vol.15 , Issue.5 , pp. 293-299
    • Lapcik, O.1    Klejdus, B.2    Davidova, M.3    Kokoska, L.4    Kuban, V.5    Moravcova, J.6
  • 112
    • 0034735973 scopus 로고    scopus 로고
    • Distribution of flavonoids in Myristicaceae
    • Valderrama, J.M.C. Distribution of flavonoids in Myristicaceae. Phytochemistry 2000, 55, 505-511.
    • (2000) Phytochemistry , vol.55 , pp. 505-511
    • Valderrama, J.M.C.1
  • 113
    • 0036911164 scopus 로고    scopus 로고
    • Artoindonesianins N and O, new prenylated stilbene and prenylated arylbenzofuran derivatives from Artocarpus gomezianus
    • Hakim, E.H.; Ulinnuha, U.Z.; Syah, Y.M.; Ghisalberti, E.L. Artoindonesianins N and O, new prenylated stilbene and prenylated arylbenzofuran derivatives from Artocarpus gomezianus. Fitoterapia 2002, 73, 597-603.
    • (2002) Fitoterapia , vol.73 , pp. 597-603
    • Hakim, E.H.1    Ulinnuha, U.Z.2    Syah, Y.M.3    Ghisalberti, E.L.4
  • 116
    • 0035736545 scopus 로고    scopus 로고
    • Formation of novel bioactive metabolites from the reactions of pro-inflammatory oxidants with polyphenolics
    • Boersma, B.J.; Patel, R.P; Botting, N.; White, C.R.; Parks, D.; Barnes, S.; Darley-Usmar, V.M. Formation of novel bioactive metabolites from the reactions of pro-inflammatory oxidants with polyphenolics. Biofactors 2001, 15, 79-81.
    • (2001) Biofactors , vol.15 , pp. 79-81
    • Boersma, B.J.1    Patel, R.P.2    Botting, N.3    White, C.R.4    Parks, D.5    Barnes, S.6    Darley-Usmar, V.M.7
  • 117
    • 0029888128 scopus 로고    scopus 로고
    • Structure-antioxidant activity relationships of flavonoids and phenolic acids
    • DOI 10.1016/0891-5849(95)02227-9
    • Rice-Evans, C.A.; Miller, N.J.; Paganga, G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radical Biol. Med. 1996, 20, 933-956 (Pubitemid 26157509)
    • (1996) Free Radical Biology and Medicine , vol.20 , Issue.7 , pp. 933-956
    • Rice-Evans, C.A.1    Miller, N.J.2    Paganga, G.3
  • 119
    • 0029102006 scopus 로고
    • Use specific dyes in the detection of antimicrobial compounds from the crude plant extracts using a thin layer chromatography agar overlay technique
    • Saxena, G.; Farmer, S.; Towers, G.H.N.; Hancock, R.E.W. Use specific dyes in the detection of antimicrobial compounds from the crude plant extracts using a thin layer chromatography agar overlay technique. Phytochemical Analysis 1995, 6, 125-129.
    • (1995) Phytochemical Analysis , vol.6 , pp. 125-129
    • Saxena, G.1    Farmer, S.2    Towers, G.H.N.3    Hancock, R.E.W.4
  • 120
    • 0001426948 scopus 로고    scopus 로고
    • Ensayos biológicos com extractos obtenidos de raíces de Lonchocarpus latifolius (WILLD.) D. C. Y. de un nuevo dibenzoilmetano aislado
    • Magalhaes, A.F.; Tozzi, A.M.G.A., Magalhaes, E.G., Nogueira, M.A; Roncancio, V.J.F. Ensayos biológicos com extractos obtenidos de raíces de Lonchocarpus latifolius (WILLD.) D. C. Y. de un nuevo dibenzoilmetano aislado. Revista Ceres 1998, 45, 351-358.
    • (1998) Revista Ceres , vol.45 , pp. 351-358
    • Magalhaes, A.F.1    Tozzi, A.M.G.A.2    Magalhaes, E.G.3    Nogueira, M.A.4    Roncancio, V.J.F.5
  • 121
    • 0035341550 scopus 로고    scopus 로고
    • Crenulated flavonoids from Deguelia hatschbachii and their systematic significance in Deguelia
    • Magalhaes, A. F.; Tozzi, A. M. G. A.; Magalhaes, E. G.; Moraes, V. R. S. Crenulated flavonoids from Deguelia hatschbachii and their systematic significance in Deguelia. Phytochemistry 2001, 57(1), 77-89.
    • (2001) Phytochemistry , vol.57 , Issue.1 , pp. 77-89
    • Magalhaes, A.F.1    Tozzi, A.M.G.A.2    Magalhaes, E.G.3    Moraes, V.R.S.4
  • 123
    • 0027526094 scopus 로고
    • Methicillin-resistant Staphylococcus aureus: A consensus review of the microbiology, pathogenesis, and epidemiology with implications for prevention and management
    • Mulligan, M.E.; Murray-Lesure, K.A.; Ribner, B.S.; Standiford, H.C.; John, J.F.; Korvick, J.A. Kauffman, C.A.; Yu, V.L. Methicillin-resistant Staphylococcus aureus: a consensus review of the microbiology, pathogenesis, and epidemiology with implications for prevention and management. Am. J. Med. 1993, 94, 313-328.
    • (1993) Am. J. Med. , vol.94 , pp. 313-328
    • Mulligan, M.E.1    Murray-Lesure, K.A.2    Ribner, B.S.3    Standiford, H.C.4    John, J.F.5    Korvick, J.A.6    Kauffman, C.A.7    Yu, V.L.8
  • 125
    • 0003431765 scopus 로고
    • Dalziel, J.M. (ed.) Crown Agents For Colonies, London
    • Dalziel, J.M. (ed.) (1937) in The useful plants of West Tropical Africa, p. 612, Crown Agents For Colonies, London.
    • (1937) The Useful Plants of West Tropical Africa , pp. 612
  • 126
    • 0038141179 scopus 로고    scopus 로고
    • Erythrina poeppigiana-derived phytochemical exhibiting antimicrobial activity against Candida albicans and methicillin-resistant Staphylococcus aureus
    • DOI 10.1046/j.1472-765X.2003.01352.x
    • Sato, M.; Tanaka, H.; Yamaguchi, R.; Oh-Uchi, T.; Etoh, H. Erythrina poeppigiana-derived phytochemical exhibiting antimicrobial activity against Candida albicans and methicillin-resistant Staphylococcus aureus. Lett. Appl. Microbiol. 2003, 37, 81-85 (Pubitemid 36783086)
    • (2003) Letters in Applied Microbiology , vol.37 , Issue.1 , pp. 81-85
    • Sato, M.1    Tanaka, H.2    Yamaguchi, R.3    Oh-Uchi, T.4    Etoh, H.5
  • 127
    • 33747109421 scopus 로고    scopus 로고
    • Different antibacterial actions of isoflavones isolated from Erythrina poeppigiana against methicillin-resistant Staphylococcus aureus
    • DOI 10.1111/j.1472-765X.2006.01963.x
    • Sato, M. Tanaka, H.; Tani, N.; Nagayama, M.; Yamaguchi, R. Different antibacterial actions of isoflavones isolated from Erythrina poeppigiana against methicillin-resistant Staphylococcus aureus. Lett. Appl. Microbiol. 2006, 43, 243-248 (Pubitemid 44222152)
    • (2006) Letters in Applied Microbiology , vol.43 , Issue.3 , pp. 243-248
    • Sato, M.1    Tanaka, H.2    Tani, N.3    Nagayama, M.4    Yamaguchi, R.5
  • 128
    • 4344657761 scopus 로고    scopus 로고
    • Synergistic effects of mupirocin and an isoflavanone isolated from Erythrina variegata on growth and recovery of methicillin-resistant Staphylococcus aureus
    • Sato, M.; Tanaka, H.; Yamaguchi, R.; Kato, K.; Etoh, H. Synergistic effects of mupirocin and an isoflavanone isolated from Erythrina variegata on growth and recovery of methicillin-resistant Staphylococcus aureus. Int J. Antimicrob Agents 2004, 24, 241-246.
    • (2004) Int J. Antimicrob Agents , vol.24 , pp. 241-246
    • Sato, M.1    Tanaka, H.2    Yamaguchi, R.3    Kato, K.4    Etoh, H.5
  • 129
    • 0036368468 scopus 로고    scopus 로고
    • Antibacterial activity of isoflavonoids isolated from Erythrina variegata against methicillin-resistant Staphylococcus aureus
    • DOI 10.1046/j.1472-765X.2002.01222.x
    • Tanaka, H.; Sato, M.; Fujiwara, S.; Hirata, M.; Etoh, H.; Takeuchi, H. Antibacterial activity of isoflavonoids isolated from Erythrina variegata against methicillin-resistant Staphylococcus aureus. Lett. Appl. Microbiol. 2002, 35, 494-498 (Pubitemid 41724405)
    • (2002) Letters in Applied Microbiology , vol.35 , Issue.6 , pp. 494-498
    • Tanaka, H.1    Sato, M.2    Fujiwara, S.3    Hirata, M.4    Etoh, H.5    Takeuchi, H.6
  • 130
    • 11144235211 scopus 로고    scopus 로고
    • Antibacterial activity of phytochemicals isolated from Erythrina zeyheri against vancomycin-resistant enterococci and their combinations with vancomycin
    • Sato, M.; Tanaka, H.; Oh-Uchi, T.; Fukai, T.; Yamaguchi, R. Antibacterial activity of phytochemicals isolated from Erythrina zeyheri against vancomycin-resistant enterococci and their combinations with vancomycin. Phytother. Res. 2004, 18, 906-910.
    • (2004) Phytother. Res. , vol.18 , pp. 906-910
    • Sato, M.1    Tanaka, H.2    Oh-Uchi, T.3    Fukai, T.4    Yamaguchi, R.5
  • 131
    • 0037870319 scopus 로고    scopus 로고
    • Antibacterial property of isoflavonoids isolated from erythrina variegata against cariogenic oral bacteria
    • DOI 10.1078/0944-7113-00225
    • Sato, M.; Tanaka, H.; Fujiwara, S.; Hirata, M.; Yamaguchi, R.; Etoh, H.; Tokuda, C. Antibacterial property of isoflavonoids isolated from Erythrina variegata against cariogenic oral bacteria. Phytomedicine 2003, 10, 427-433 (Pubitemid 36745167)
    • (2003) Phytomedicine , vol.10 , Issue.5 , pp. 427-433
    • Sato, M.1    Tanaka, H.2    Fujiwara, S.3    Hirata, M.4    Yamaguchi, R.5    Etoh, H.6    Tokuda, C.7
  • 133
    • 0002630313 scopus 로고
    • Jacobson, M., Crosby, D.G. Eds.; Marcel Dekker: New York, Chapter 2
    • Fukai, H.; Nakajima, M. In Naturally Occurring Insecticides; Jacobson, M., Crosby, D.G. Eds.; Marcel Dekker: New York, 1971; Chapter 2, pp. 71-97.
    • (1971) Naturally Occurring Insecticides , pp. 71-97
    • Fukai, H.1    Nakajima, M.2
  • 134
    • 0034170336 scopus 로고    scopus 로고
    • Biotransformation of glycyrrhizin by human intestinal bacteria and its relation to biological activities
    • Kim, D.-H.; Hong, S.-V.; Kim, B.-T.; Bae, E.-A.; Park, H.-Y.; Han, M.J. Biotransformation of glycyrrhizin by human intestinal bacteria and its relation to biological activities. Arch. Pharmacol. Res. 2000, 23, 172-177.
    • (2000) Arch. Pharmacol. Res. , vol.23 , pp. 172-177
    • Kim, D.-H.1    Hong, S.-V.2    Kim, B.-T.3    Bae, E.-A.4    Park, H.-Y.5    Han, M.J.6
  • 135
    • 0037047461 scopus 로고    scopus 로고
    • Anti-Helicobacter pylori flavonoids from licorice extract
    • DOI 10.1016/S0024-3205(02)01864-7, PII S0024320502018647
    • Fukai, T.; Marumo, A.; Kaitou, K.; Kanda, T.; Terada, S.; Nomura, T. Anti-Helicobacter pylori flavonoids from licorice extract. Life Sci. 2002, 71(12), 1449-1463 (Pubitemid 34786288)
    • (2002) Life Sciences , vol.71 , Issue.12 , pp. 1449-1463
    • Fukai, T.1    Marumo, A.2    Kaitou, K.3    Kanda, T.4    Terada, S.5    Nomura, T.6
  • 136
    • 0031612262 scopus 로고    scopus 로고
    • Herz, W.; Kirby, G.W.; Moore, R.E.: Steglich, W.; Tamm, C., Eds., Springer: Vienna, and references cited therein
    • Nomura, T.; Fukai.T. In Progress in the Chemistry of Organic Natural Products Herz, W.; Kirby, G.W.; Moore, R.E.: Steglich, W.; Tamm, C., Eds., Springer: Vienna, 1998; vol.73, pp. 1-140 (and references cited therein).
    • (1998) Progress in the Chemistry of Organic Natural Products , vol.73 , pp. 1-140
    • Nomura, T.1    Fukai, T.2
  • 137
  • 139
    • 0025853376 scopus 로고
    • Invasive candida infections-evolution of a fungal pathogen
    • b) Edwards, J.E. Invasive candida infections-evolution of a fungal pathogen. New Engl. J. Med. 1991, 324, 1060-1062.
    • (1991) New Engl. J. Med. , vol.324 , pp. 1060-1062
    • Edwards, J.E.1
  • 140
    • 0037131103 scopus 로고    scopus 로고
    • On-line identification of the antifungal constituents of Erythrina vogelii by liquid chromatography with tandem mass spectrometry, ultraviolet absorbance detection and nuclear magnetic resonance spectrometry combined with liquid chromatographic micro-fractionation
    • Queiroz, E.F., Wolfender, J.L.; Atindehou, K.K.; Traore, D.; Hostettmann, K. J. On-line identification of the antifungal constituents of Erythrina vogelii by liquid chromatography with tandem mass spectrometry, ultraviolet absorbance detection and nuclear magnetic resonance spectrometry combined with liquid chromatographic micro-fractionation. J. Chromatogr. A 2002, 974, 123-134.
    • (2002) J. Chromatogr. A , vol.974 , pp. 123-134
    • Queiroz, E.F.1    Wolfender, J.L.2    Atindehou, K.K.3    Traore, D.4    Hostettmann, K.J.5
  • 142
  • 145
    • 12344318162 scopus 로고
    • The anthelmintic study of Tadehagi triquetrum
    • Guandong Pharmic Academy
    • c) Guandong Pharmic Academy. The anthelmintic study of Tadehagi triquetrum. Rev. Iatrical Sci. Technol. 1971, 12, 3-6.
    • (1971) Rev. Iatrical Sci. Technol. , vol.12 , pp. 3-6
  • 146
    • 0036188537 scopus 로고    scopus 로고
    • Clinical status and implications of antimalarial drug resistance
    • DOI 10.1016/S1286-4579(01)01523-4, PII S1286457901015234
    • Winstanley, P.A.; Ward, S.A.; Snow, R.W. Clinical status and implications of antimalarial drug resistance. Microbes Infect. 2002, 4, 157-164 (Pubitemid 34183489)
    • (2002) Microbes and Infection , vol.4 , Issue.2 , pp. 157-164
    • Winstanley, P.A.1    Ward, S.A.2    Snow, R.W.3
  • 147
    • 0036188538 scopus 로고    scopus 로고
    • Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs
    • DOI 10.1016/S1286-4579(01)01524-6, PII S1286457901015246
    • b) Hyde, J.E. Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs. Microbes Infect. 2002, 4, 165-174 (Pubitemid 34183490)
    • (2002) Microbes and Infection , vol.4 , Issue.2 , pp. 165-174
    • Hyde, J.E.1
  • 149
    • 0036194878 scopus 로고    scopus 로고
    • Antischistosomal bioactivity of isoflavonoids from Millettia thonningii (leguminosae)
    • Lyddlard, J.R.; Withfield, P.J.; Bartlett, A. Antischistosomal bioactivity of isoflavonoids from Millettia thonningii (Leguminosae). J. Parasitol. 2002, 88, 163-170 (Pubitemid 34250648)
    • (2002) Journal of Parasitology , vol.88 , Issue.1 , pp. 163-170
    • Lyddiard, J.R.A.1    Whitfield, P.J.2    Bartlett, A.3
  • 150
    • 0019795527 scopus 로고
    • Anti-inflammatory testing methods: Comparative evaluation of mice and rats
    • Sugishita, E.; Amagaya, S.; Ogihara, Y. Anti-inflammatory testing methods: comparative evaluation of mice and rats. J. Pharmacobiodyn. 1981, 4, 565-575.
    • (1981) J. Pharmacobiodyn. , vol.4 , pp. 565-575
    • Sugishita, E.1    Amagaya, S.2    Ogihara, Y.3
  • 152
    • 0027434789 scopus 로고
    • Differential effects of Mandevilla velutina compounds on paw oedema induced by phospholipase A2 and phospholipase C
    • Neves, P.C.A.; Neves, M.C.A.; Bella Cruz, A.; Sant'ana, A.E.G.; Yunes, R.A.; Calixto, J.B. Differential effects of Mandevilla velutina compounds on paw oedema induced by phospholipase A2 and phospholipase C. Eur. J. Pharmacol. 1993, 243, 213-219.
    • (1993) Eur. J. Pharmacol. , vol.243 , pp. 213-219
    • Neves, P.C.A.1    Neves, M.C.A.2    Bella Cruz, A.3    Sant'ana, A.E.G.4    Yunes, R.A.5    Calixto, J.B.6
  • 153
    • 0028013648 scopus 로고
    • Inhibitory effect of norathyriol, a xanthone from Tripterospermum lanceolatum, on cutaneous plasma extravasation
    • Wang, J.P.; Raung, S.L.; Lin, C.N.; Teng, C.M. Inhibitory effect of norathyriol, a xanthone from Tripterospermum lanceolatum, on cutaneous plasma extravasation. Eur. J. Pharmacol. 1994, 251, 35-42.
    • (1994) Eur. J. Pharmacol. , vol.251 , pp. 35-42
    • Wang, J.P.1    Raung, S.L.2    Lin, C.N.3    Teng, C.M.4
  • 154
    • 0028053465 scopus 로고
    • Inhibition by gomisin C (a lignan from Schizandra chinensis) of the respiratory burst of rat neutrophils
    • Wang, J.P.; Raung, S.L.; Hsu, M.F.; Chen, C.C. Inhibition by gomisin C (a lignan from Schizandra chinensis) of the respiratory burst of rat neutrophils. Br. J. Pharmacol. 1994, 113, 945-953.
    • (1994) Br. J. Pharmacol. , vol.113 , pp. 945-953
    • Wang, J.P.1    Raung, S.L.2    Hsu, M.F.3    Chen, C.C.4
  • 155
    • 0023706894 scopus 로고
    • Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production
    • a) Ding, A.H.; Nathan, C.F.; Stuehr, D.J. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production. J. Immunol. 1988, 141, 2407-2412;
    • (1988) J. Immunol. , vol.141 , pp. 2407-2412
    • Ding, A.H.1    Nathan, C.F.2    Stuehr, D.J.3
  • 157
    • 0023944339 scopus 로고
    • Tumor necrosis, cachexia, shock, and inflammation: A common mediator
    • c) Beutler, B.; Cerami, A. Tumor necrosis, cachexia, shock, and inflammation: a common mediator. Annu. Rev. Biochem. 1988, 57, 505-518 (Pubitemid 18171400)
    • (1988) Annual Review of Biochemistry , vol.57 , pp. 505-518
    • Beutler, B.1    Cerami, A.2
  • 158
    • 0842302970 scopus 로고    scopus 로고
    • Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica
    • Ko, H.-H.; Weng, J.-R.; Tsao, L.-T.; Yen, M.-H.; Wang, J.-P.; Lin, C.-N. Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica. Bioorg. Med. Chem. Lett. 2004, 14, 1011-1014.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 1011-1014
    • Ko, H.-H.1    Weng, J.-R.2    Tsao, L.-T.3    Yen, M.-H.4    Wang, J.-P.5    Lin, C.-N.6
  • 159
    • 29044432730 scopus 로고    scopus 로고
    • Inhibition of lipopolysaccharide-stimulated NO production by crotafuran B in RAW 264.7 macrophages involves the blockade of NF-kappaB activation through the increase in IkappaBalpha synthesis
    • Lin, M.-W.; Tsao, L.-T.; Huang, L.-J.; Kuo, S.-C.; Weng, J.-R.;Ko, H.-H.; Lee, M.-R.; Wang, J.-P. Inhibition of lipopolysaccharide-stimulated NO production by crotafuran B in RAW 264.7 macrophages involves the blockade of NF-kappaB activation through the increase in IkappaBalpha synthesis. Toxicol. Appl. Pharmacol. 2006, 210, 108-115.
    • (2006) Toxicol. Appl. Pharmacol. , vol.210 , pp. 108-115
    • Lin, M.-W.1    Tsao, L.-T.2    Huang, L.-J.3    Kuo, S.-C.4    Weng, J.-R.5    Ko, H.-H.6    Lee, M.-R.7    Wang, J.-P.8
  • 161
    • 0000782975 scopus 로고
    • The effecys of aggregation, electric shock and adrenergic blocking drugs on inhibition of the "writhing" syndrome
    • Okun, R.; Liddon, S.C.; Lasagnal, L. The effecys of aggregation, electric shock and adrenergic blocking drugs on inhibition of the "writhing" syndrome. J. Pharmacol. Exp. Ther. 1963, 139, 107-109.
    • (1963) J. Pharmacol. Exp. Ther. , vol.139 , pp. 107-109
    • Okun, R.1    Liddon, S.C.2    Lasagnal, L.3
  • 162
    • 33747331967 scopus 로고    scopus 로고
    • Anti-inflammatory and antinociceptive potential of Maclura pomifera (Rafin.) Schneider fruit extracts and its major isoflavonoids, scandenone and auriculasin
    • a) Kupeli, E.; Orhan, I.; Toker, G.; Yesilada, E. Anti-inflammatory and antinociceptive potential of Maclura pomifera (Rafin.) Schneider fruit extracts and its major isoflavonoids, scandenone and auriculasin. J. Ethnopharmacol. 2006, 107, 169-174.
    • (2006) J. Ethnopharmacol. , vol.107 , pp. 169-174
    • Kupeli, E.1    Orhan, I.2    Toker, G.3    Yesilada, E.4
  • 163
    • 0141566388 scopus 로고    scopus 로고
    • Griffonianone D, an isoflavanone with anti-inflammatory activity from the root bark of Millettia griffoniana
    • b) J.C.; Giner, R.M.; Recio, M.C.; Manez, S.; Rios, J.L. Griffonianone D, an isoflavanone with anti-inflammatory activity from the root bark of Millettia griffoniana. J. Nat. Prod. 2003, 66, 1288-1290.
    • (2003) J. Nat. Prod. , vol.66 , pp. 1288-1290
    • Giner, R.M.1    Recio, M.C.2    Manez, S.3    Rios, J.L.4
  • 164
    • 0029035973 scopus 로고
    • Mechanism of 5- Lypoxygenase inhibition by acetyl-11-keto-β- boswellic acid
    • Safayhi, H.; Sailer, S.; Ammon, H.P. Mechanism of 5- lypoxygenase inhibition by acetyl-11-keto-β-boswellic acid. Mol. Pharmacol. 1995, 47(6), 1212-1216.
    • (1995) Mol. Pharmacol. , vol.47 , Issue.6 , pp. 1212-1216
    • Safayhi, H.1    Sailer, S.2    Ammon, H.P.3
  • 165
    • 0001116265 scopus 로고
    • In vitro test system for the evaluation of dual cyclooxygenase and 5-lipoxygenase inhibitors
    • Laufer, S.; Neher,K.; Bayer, B.; Homman, J.; Reutter, E.; Tries, S. In vitro test system for the evaluation of dual cyclooxygenase and 5-lipoxygenase inhibitors. Pharm. Pharmacol. Lett. 1995, 4, 166-169.
    • (1995) Pharm. Pharmacol. Lett. , vol.4 , pp. 166-169
    • Laufer, S.1    Neher, K.2    Bayer, B.3    Homman, J.4    Reutter, E.5    Tries, S.6
  • 166
    • 0027434789 scopus 로고
    • Differential effects of Mandevilla velutina compounds on paw oedema induced by phosphor-lipase A2 and phospholipase C
    • Neves, P.C.A.; Neves, M.C.A.; Bella Cruz, A.; Sant' ana, A.E.G.; Yunes, R.A.; Calixto, J.B.; Differential effects of Mandevilla velutina compounds on paw oedema induced by phosphor-lipase A2 and phospholipase C. Eur. J. Pharmacol. 1993, 243, 213-219.
    • (1993) Eur. J. Pharmacol. , vol.243 , pp. 213-219
    • Neves, P.C.A.1    Neves, M.C.A.2    Bella Cruz, A.3    Sant'ana, A.E.G.4    Yunes, R.A.5    Calixto, J.B.6
  • 169
    • 0030889085 scopus 로고    scopus 로고
    • The estrogenic and antiestrogenic activities of phytochemicals with the human estrogen receptor expressed in yeast
    • a) Collins, M.B.; McLachlan, J.A.; Arnold, S.F. The estrogenic and antiestrogenic activities of phytochemicals with the human estrogen receptor expressed in yeast. Steroids 1997, 62, 365-372;
    • (1997) Steroids , vol.62 , pp. 365-372
    • Collins, M.B.1    McLachlan, J.A.2    Arnold, S.F.3
  • 171
    • 0032827059 scopus 로고    scopus 로고
    • Bioassay of phytoestrogen in herbal medicine used for postmenopausal disorder using transformed MCF-7 cells
    • c) Shilzaki, K.; Goto, K.; Ishige, A.; Komatsu, Y.; Bioassay of phytoestrogen in herbal medicine used for postmenopausal disorder using transformed MCF-7 cells. Phytother. Res. 1999, 13, 498-503.
    • (1999) Phytother. Res. , vol.13 , pp. 498-503
    • Shilzaki, K.1    Goto, K.2    Ishige, A.3    Komatsu, Y.4
  • 173
    • 0032445310 scopus 로고    scopus 로고
    • O-geranylated isoflavones and a 3-phenylcoumarin from Millettia griffoniana
    • DOI 10.1016/S0031-9422(98)00392-6, PII S0031942298003926
    • Yankep, E.; Fomum, Z.T.; Bisrat, D.; Dagne, E.; Hellwig, V.; Steglich, W. O-Geranylated isoflavones and a 3-phenylcoumarin from Millettia griffoniana. Phytochemistry 1998, 49, 2521-2523 (Pubitemid 29016267)
    • (1998) Phytochemistry , vol.49 , Issue.8 , pp. 2521-2523
    • Yankep, E.1    Fomum, Z.T.2    Bisrat, D.3    Dagne, E.4    Hellwig, V.5    Steglich, W.6
  • 174
    • 33645520496 scopus 로고    scopus 로고
    • Anti-estrogenic activity of prenylated isoflavones from Millettia pachycarpa: Implications for pharmacophores and unique mechanisms
    • Okamoto, Y.; Suzuki, A.; Ueda, K.; Ito, C.; Itogawa, M.; Furukawa, H.; Nishihara, T.; Kojima, T. Anti-estrogenic activity of prenylated isoflavones from Millettia pachycarpa: implications for pharmacophores and unique mechanisms. J. Health Sci. 2006, 52, 186-191.
    • (2006) J. Health Sci. , vol.52 , pp. 186-191
    • Okamoto, Y.1    Suzuki, A.2    Ueda, K.3    Ito, C.4    Itogawa, M.5    Furukawa, H.6    Nishihara, T.7    Kojima, T.8
  • 175
    • 0024988751 scopus 로고
    • 1-(Aminoalkyl)-2-phenylindoles as novel pure estrogen antagonists
    • DOI 10.1021/jm00171a045
    • a) von Angerer, E.; Knebel, N.; Kager, M.; Ganss, B. 1-(aminoalkyl)-2- phenylindoles as novel pure estrogen antagonists. J. Med. Chem. 1990, 33, 2635-2644 (Pubitemid 20274225)
    • (1990) Journal of Medicinal Chemistry , vol.33 , Issue.9 , pp. 2635-2640
    • Von Angerer, E.1    Knebel, N.2    Kager, M.3    Ganss, B.4
  • 176
    • 0033047550 scopus 로고    scopus 로고
    • In vitro test systems for the evaluation of the estrogenic activity of natural products
    • DOI 10.1055/s-1999-13980
    • b) Diel, P.; Smolnikar, K.; Michna, H. In vitro test systems for the evaluation of the estrogenic activity of natural Products. Planta Med. 1999, 65, 197-203 (Pubitemid 29186069)
    • (1999) Planta Medica , vol.65 , Issue.3 , pp. 197-203
    • Diel, P.1    Smolnikar, K.2    Michna, H.3
  • 178
    • 0346849610 scopus 로고    scopus 로고
    • Phytoestrogens modulate binding response of estrogen receptors alpha and beta to the estrogen response element
    • Kostelac, D.; Rechkemmer, G.; Briviba, K. Phytoestrogens modulate binding response of estrogen receptors alpha and beta to the estrogen response element. J. Agric. Food Chem. 2003, 51, 7632-7635.
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 7632-7635
    • Kostelac, D.1    Rechkemmer, G.2    Briviba, K.3
  • 179
    • 0001386750 scopus 로고
    • Miroestrol: An oestrogen from the plant Pueraria mirifica
    • a) Cain, J.C. Miroestrol: an oestrogen from the plant Pueraria mirifica. Nature 1960, 188, 774-777;
    • (1960) Nature , vol.188 , pp. 774-777
    • Cain, J.C.1
  • 180
    • 0008469076 scopus 로고
    • The X-ray christallographic determination of the structure of bromomiroestrol
    • b) Taylor, N.E.; Hodgkin, D.C.; Rollet, J.S.The X-ray christallographic determination of the structure of bromomiroestrol. J. Chem. Soc. 1960, 3685-3695;
    • (1960) J. Chem. Soc. , pp. 3685-3695
    • Taylor, N.E.1    Hodgkin, D.C.2    Rollet, J.S.3
  • 181
    • 37049050651 scopus 로고
    • Light absorption and chemical properties of mi roestrol, the estrogenic substance of Pueraria mirifica
    • c) Bounds, D.G.; Pope, G.S. Light absorption and chemical properties of mi roestrol, the estrogenic substance of Pueraria mirifica. J. Chem. Soc. 1960, 3696-3704.
    • (1960) J. Chem. Soc. , pp. 3696-3704
    • Bounds, D.G.1    Pope, G.S.2
  • 182
    • 73049129066 scopus 로고
    • A method for the isolation of miroestrol from Pueraria mirifica
    • Jones, H.E.M.; Pope, H. A method for the isolation of miroestrol from Pueraria mirifica. J. Endocrinol. 1961, 22, 303-312.
    • (1961) J. Endocrinol. , vol.22 , pp. 303-312
    • Jones, H.E.M.1    Pope, H.2
  • 183
    • 0001385370 scopus 로고
    • Puerarin 6-O-β-apiofuranoside A, C-glycosyloisoflavone O-glucoside from Pueraria mirifica
    • a) Ingham, J.L.; Markham, K.R.; Dziedzic, S.Z.; Pope, G.S. Puerarin 6-O-β-apiofuranoside A, C-glycosyloisoflavone O-glucoside from Pueraria mirifica. Phytochemistry 1986, 25, 1772-1775;
    • (1986) Phytochemistry , vol.25 , pp. 1772-1775
    • Ingham, J.L.1    Markham, K.R.2    Dziedzic, S.Z.3    Pope, G.S.4
  • 184
    • 84890205068 scopus 로고
    • A chemical investigation of Pueraria mirifica roots
    • b) Ingham, J.L.; Tahara, S.; Dziedzic, S.Z. A chemical investigation of Pueraria mirifica roots. Z. Naturforsch. 1986, 41C, 403-408;
    • (1986) Z. Naturforsch. , vol.41 C , pp. 403-408
    • Ingham, J.L.1    Tahara, S.2    Dziedzic, S.Z.3
  • 185
    • 0008508938 scopus 로고
    • Structure elucidation of kwakhurin, a new prenylated isoflavone form Pueraria mirifica roots
    • c) Tahara, S.; Ingham, J.L.; Dziedzic, S.Z. Structure elucidation of kwakhurin, a new prenylated isoflavone form Pueraria mirifica roots. Z. Naturforsch. 1987, 42C, 510-518;
    • (1987) Z. Naturforsch. , vol.42 C , pp. 510-518
    • Tahara, S.1    Ingham, J.L.2    Dziedzic, S.Z.3
  • 186
    • 84945736954 scopus 로고
    • Coumestans from the roots of Pueraria mirifica
    • d) Ingham, J.L.; Tahara, S.; Dziedzic, S.Z. Coumestans from the roots of Pueraria mirifica. Z. Naturforsch. 1988, 43C, 5-10;
    • (1988) Z. Naturforsch. , vol.43 C , pp. 5-10
    • Ingham, J.L.1    Tahara, S.2    Dziedzic, S.Z.3
  • 187
    • 80053991580 scopus 로고
    • Minor isoflavones from the roots of Pueraria mirifica
    • e) Ingham, J.L.; Tahara, S.; Dziedzic, S.Z. Minor isoflavones from the roots of Pueraria mirifica. Z. Naturforsch. 1989, 44C, 724-726.
    • (1989) Z. Naturforsch. , vol.44 C , pp. 724-726
    • Ingham, J.L.1    Tahara, S.2    Dziedzic, S.Z.3
  • 188
    • 0043198624 scopus 로고    scopus 로고
    • Requirement of metabolic activation for estrogenic activity of Pueraria mirifica
    • Lee, Y.S.; Park, J.S.; Cho, S.D.; Son, J.K.; Cherdshewasart, W.; Kang, K.S. Requirement of metabolic activation for estrogenic activity of Pueraria mirifica. J. Vet. Sci. 2002, 3, 273-277.
    • (2002) J. Vet. Sci. , vol.3 , pp. 273-277
    • Lee, Y.S.1    Park, J.S.2    Cho, S.D.3    Son, J.K.4    Cherdshewasart, W.5    Kang, K.S.6
  • 189
    • 3242730521 scopus 로고    scopus 로고
    • The differential anti-proliferation effect of white (Pueraria mirifica), red (Butea superba), and black (Mucuna collettii) Kwao Krua plants on the growth of MCF-7 cells
    • Cherdshewasart, W.; Cheewasopit, W.; Picha, P. The differential anti-proliferation effect of white (Pueraria mirifica), red (Butea superba), and black (Mucuna collettii) Kwao Krua plants on the growth of MCF-7 cells. J. Ethnopharmacol. 2004, 93, 255-260.
    • (2004) J. Ethnopharmacol. , vol.93 , pp. 255-260
    • Cherdshewasart, W.1    Cheewasopit, W.2    Picha, P.3
  • 192
    • 0035377141 scopus 로고    scopus 로고
    • Cytotoxic constituents of Psoralea corylifolia
    • Mar, W, Je, K.H.; Seo, E.K. Cytotoxic constituents of Psoralea corylifolia. Arch. Pharm. Res. 2001, 24, 211-213.
    • (2001) Arch. Pharm. Res. , vol.24 , pp. 211-213
    • Mar, W.1    Je, K.H.2    Seo, E.K.3
  • 198
    • 0001249286 scopus 로고
    • Inhibitors of respiratory complex I: Mechanisms, pesticidal actions and toxicology
    • Hollingsworth, R.M.; Ahammadsahib, K.I. Inhibitors of respiratory complex I: mechanisms, pesticidal actions and toxicology. Rev. Pestic. Toxicol. 1995, 3, 277-302.
    • (1995) Rev. Pestic. Toxicol. , vol.3 , pp. 277-302
    • Hollingsworth, R.M.1    Ahammadsahib, K.I.2
  • 201
    • 0008904099 scopus 로고    scopus 로고
    • Novel bioactive cube insecticide constituents: Isolation and preparation of 13-homo-13-oxa-6a,12a-dehydrorotenoid
    • Fang, N.; Casida. J.E. Novel bioactive cube insecticide constituents: isolation and preparation of 13-homo-13-oxa-6a,12a-dehydrorotenoid. J.Org. Chem. 1997, 62, 350-353.
    • (1997) J.Org. Chem. , vol.62 , pp. 350-353
    • Fang, N.1    Casida, J.E.2
  • 202
    • 0030800144 scopus 로고    scopus 로고
    • Anomalous structure activity relationship of 13-homo-13-oxarotenoids and 13-homo-13-oxadeydrorotenoids
    • Fang, N.; Rowlands, J.C.; Casida, J.E. Anomalous structure activity relationship of 13-homo-13-oxarotenoids and 13-homo-13-oxadeydrorotenoids. Chem. Res. Toxicol. 1997, 10, 853-858.
    • (1997) Chem. Res. Toxicol. , vol.10 , pp. 853-858
    • Fang, N.1    Rowlands, J.C.2    Casida, J.E.3
  • 203
    • 0032584097 scopus 로고    scopus 로고
    • Anticancer action of cubé insecticide: Correlation for rotenoid constituents between inhibition of NADH: ubiquinone oxidoreductase and induced ornithine decarboxilase activities
    • Fang, N.; Casida, J.E. Anticancer action of cubé insecticide: correlation for rotenoid constituents between inhibition of NADH: ubiquinone oxidoreductase and induced ornithine decarboxilase activities. Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 3380-3384.
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 3380-3384
    • Fang, N.1    Casida, J.E.2
  • 206
    • 0041859233 scopus 로고    scopus 로고
    • Regulation of ornithine decarboxylase induction by deguelin, a natural product cancer chemopreventive agent
    • b) Gerhäuser, C.; Lee, S.K.; Kosmeder, J.W.; Moriarty, R.M.; Hamel, E..; Mehta, R.G.; Moon, R.C.; Pezzuto, J.M. Regulation of ornithine decarboxylase induction by deguelin, a natural product cancer chemopreventive agent. Cancer Res. 1997, 57, 3429-3435 (Pubitemid 27355488)
    • (1997) Cancer Research , vol.57 , Issue.16 , pp. 3429-3435
    • Gerhauser, C.1    Lee, S.K.2    Kosmeder, J.W.3    Moriarty, R.M.4    Hamel, E.5    Mehta, R.G.6    Moon, R.C.7    Pezzuto, J.M.8
  • 207
    • 33749524818 scopus 로고    scopus 로고
    • Deguelin, an Akt inhibitor, suppresses IkappaBalpha kinase activation leading to suppression of NF-kappaB-regulated gene expression, potentiation of apoptosis, and inhibition of cellular invasion
    • Nair, A.S.; Shishodia, S., Ahn, K.S.; Kunnumakkara, A.B.; Sethi, G.; Aggarwal, B.B. Deguelin, an Akt inhibitor, suppresses Ikappa-Balpha kinase activation leading to suppression of NF-kappaB-regulated gene expression, potentiation of apoptosis and inhibition of cellular invasion. J. Immunol. 2006, 177, 5612-5622 (Pubitemid 44527636)
    • (2006) Journal of Immunology , vol.177 , Issue.8 , pp. 5612-5622
    • Nair, A.S.1    Shishodia, S.2    Ahn, K.S.3    Kunnumakkara, A.B.4    Sethi, G.5    Aggarwal, B.B.6
  • 209
    • 0033002127 scopus 로고    scopus 로고
    • Inhibitory effect of munetone, an isoflavonoid, on 12-O- tetradecanoylphorbol 13-acetate-induced ornithine decarboxylase activity
    • DOI 10.1016/S0304-3835(98)00309-7, PII S0304383598003097
    • Lee, S.K.; Luvengi, L.; Gerhäuser, C.; Mar, W.; Lee, K.; Mehta, R.G.; Kinghorn, A.D.; Pezzuto, J.M. Inhibitory effect of munetone, an isoflavonoid, on 12-O-tetradecanoylphorbol 13-acetate induced ornithine decarboxylase activity. Cancer Lett. 1999, 136, 59-65 (Pubitemid 29142303)
    • (1999) Cancer Letters , vol.136 , Issue.1 , pp. 59-65
    • Lee, S.K.1    Luyengi, L.2    Gerhauser, C.3    Mar, W.4    Lee, K.5    Mehta, R.G.6    Kinghorn, A.D.7    Pezzuto, J.M.8
  • 210
    • 0035055786 scopus 로고    scopus 로고
    • Phospholipase Cγ as a target for the development of new anticancer agent from natural sources
    • Lee, J.S.; Kim, J.; Phospholipase Cγ as a target for the development of new anticancer agent from natural sources. Drugs of the Future 2001, 26, 163-173.
    • (2001) Drugs of the Future , vol.26 , pp. 163-173
    • Lee, J.S.1    Kim, J.2
  • 211
    • 0029077640 scopus 로고
    • Dihydrolicoisoflavone, a new isoflavanone from Swartzia polyphylla
    • DuBois, J.L.; Sneden, A.T. Dihydrolicoisoflavone, a new isoflavanone from Swartzia polyphylla. J. Nat. Prod. 1995, 58, 629-632.
    • (1995) J. Nat. Prod. , vol.58 , pp. 629-632
    • DuBois, J.L.1    Sneden, A.T.2
  • 212
    • 0031106692 scopus 로고    scopus 로고
    • Specific inhibition of cyclic AMP-dependent protein kinase by warangalone and robustic acid
    • DOI 10.1016/S0031-9422(96)00664-4, PII S0031942296006644
    • Wang, B.H., Ternai, B.; Polya, G. Specific inhibition of cyclic AMP-dependent protein kinase by warangalone and robustic acid. Phytochemistry 1997, 44, 787-796 (Pubitemid 27093151)
    • (1997) Phytochemistry , vol.44 , Issue.5 , pp. 787-796
    • Wang, B.H.1    Ternai, B.2    Polya, G.3
  • 214
    • 33646937440 scopus 로고    scopus 로고
    • Antioxidant and 15-lipoxygenase inhibitory activity of rotenoids, isoflavones and phenolic Glycosides from Sarcolobus globosus
    • Wangensteen, H.; Miron, A.; Alamgir, M.; Rajia, S.; Samuelsen, A.B.; Malterud, K.E. Antioxidant and 15-lipoxygenase inhibitory activity of rotenoids, isoflavones and phenolic Glycosides from Sarcolobus globosus. Fitoterapia 2006, 77, 290-295.
    • (2006) Fitoterapia , vol.77 , pp. 290-295
    • Wangensteen, H.1    Miron, A.2    Alamgir, M.3    Rajia, S.4    Samuelsen, A.B.5    Malterud, K.E.6
  • 215
    • 33845916144 scopus 로고    scopus 로고
    • Protein tyrosine phosphatase-1B inhibitory activity of isoprenylated flavonoids isolated from Erythrina mildbraedii
    • Na, MK.; Jang, JP.; Njamen, D.; Mbafor, J.T.; Fomum, Z.T.; Kim, B.Y. Protein tyrosine phosphatase-1B inhibitory activity of isoprenylated flavonoids isolated from Erythrina mildbraedii. J. Nat. Prod. 2006, 69, 1572-1576.
    • (2006) J. Nat. Prod. , vol.69 , pp. 1572-1576
    • Na, M.K.1    Jang, J.P.2    Njamen, D.3    Mbafor, J.T.4    Fomum, Z.T.5    Kim, B.Y.6
  • 217
    • 0036244676 scopus 로고    scopus 로고
    • The specificity of lipoxygenase-catalyzed lipid peroxidation and the effects of radical-scavenging antioxidants
    • DOI 10.1515/BC.2002.064
    • Nogushi, N.; Yamashita, H.; Hamahara, J.; Nakamura, A.; Kuhn, H; Niki, E. The specificity of lipoxygenase-catalyzed lipid peroxidation and the effects of radical-scavenging antioxidants. Biol. Chem. 2002, 383, 619-626 (Pubitemid 34506299)
    • (2002) Biological Chemistry , vol.383 , Issue.3-4 , pp. 619-626
    • Noguchi, N.1    Yamashita, H.2    Hamahara, J.3    Nakamura, A.4    Kuhn, H.5    Niki, E.6
  • 220
    • 0016263953 scopus 로고
    • Assay using brain homogenate for measuring the antioxidant activity of biological fluids
    • Stocks, J.; Gutteridge, J.M.C.; Sharp, R.J.; Dormandy, T.L. Assay using brain homogenate for measuring the antioxidant activity of biological fluids. Clin. Sci. Mol. Med. 1974, 47, 215-222.
    • (1974) Clin. Sci. Mol. Med. , vol.47 , pp. 215-222
    • Stocks, J.1    Gutteridge, J.M.C.2    Sharp, R.J.3    Dormandy, T.L.4
  • 221
    • 0015530358 scopus 로고
    • The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen
    • Nishikimi, M.; Rao, N.A.; Yagi, K. The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochem. Biophys. Res. Comm. 1972, 46, 849-854.
    • (1972) Biochem. Biophys. Res. Comm. , vol.46 , pp. 849-854
    • Nishikimi, M.1    Rao, N.A.2    Yagi, K.3
  • 222
    • 0005281217 scopus 로고
    • A colorimetric determination of tea tannin with ferreous tartrate
    • Iwasa K.; Torii, H. A colorimetric determination of tea tannin with ferreous tartrate. Study Tea 1962, 26, 87-91.
    • (1962) Study Tea , vol.26 , pp. 87-91
    • Iwasa, K.1    Torii, H.2
  • 223
    • 0346433748 scopus 로고    scopus 로고
    • Antioxidant isoflavones in Osage orange, Maclura pomifera (Raf) Schneid
    • Tsao, R.; Yang, R.; Young, J.C. Antioxidant isoflavones in Osage orange, Maclura pomifera (Raf) Schneid. J. Agric. Food Chem. 2003, 51, 6445-6451.
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 6445-6451
    • Tsao, R.1    Yang, R.2    Young, J.C.3
  • 227
    • 0024578841 scopus 로고
    • New Soluble- Formazan Assay for HIV-1 Cytopathic Effects: Application to high-flux screening of synthetic and natural products for AIDS-antiviral activity
    • Weislow, O.S.; Kiser, R.; Fine, D.L.; Bader, J.; Shoemaker, R.H.; Boyd, M.R. New Soluble- formazan Assay for HIV-1 Cytopathic Effects: Application to high-flux screening of synthetic and natural products for AIDS-antiviral activity. J. Natl. Cancer Inst. 1989, 81, 577-586.
    • (1989) J. Natl. Cancer Inst. , vol.81 , pp. 577-586
    • Weislow, O.S.1    Kiser, R.2    Fine, D.L.3    Bader, J.4    Shoemaker, R.H.5    Boyd, M.R.6
  • 228
    • 11944274965 scopus 로고    scopus 로고
    • New isoflavones and pterocarpane with hepatoprotective activity from the stems of Erycibe expansa
    • Matsuda, H.; Morikawa, T.; Xu, F.; Ninomiya, K. Yoshikawa, M. New isoflavones and pterocarpane with hepatoprotective activity from the stems of Erycibe expansa. Planta Med. 2004, 70, 1201-1209.
    • (2004) Planta Med. , vol.70 , pp. 1201-1209
    • Matsuda, H.1    Morikawa, T.2    Xu, F.3    Ninomiya, K.4    Yoshikawa, M.5
  • 229
    • 2442669734 scopus 로고    scopus 로고
    • Apoptosis induction by the natural product cancer chemopreventive agent deguelin is mediated through the inhibition of mitochondrial bioenergetics
    • DOI 10.1023/B:APPT.0000031449.57551.e1
    • Hail, N.; Lotan, R. Apoptosis induction by the natural product cancer chemopreventive agent deguelin is mediated through the inhibition of mitochondrial bioenergetics. Apoptosis 2004, 9, 437-447 (Pubitemid 38987580)
    • (2004) Apoptosis , vol.9 , Issue.4 , pp. 437-447
    • Hail Jr., N.1    Lotan, R.2
  • 231
    • 32644458203 scopus 로고    scopus 로고
    • Vasodilatory and hypoglycemic effects of two pyrano-isoflavone extractives from Eriosema kraussianum N.E.Br. [Fabaceae] rootstock in experimental rat models
    • Ojewole, J.A.O.; Drewes, S.E.; Khan, F. Vasodilatory and hypoglycemic effects of two pyrano-isoflavone extractives from Eriosema kraussianum N.E.Br. [Fabaceae] rootstock in experimental rat models. Phytochemistry 2006, 67, 610-617.
    • (2006) Phytochemistry , vol.67 , pp. 610-617
    • Ojewole, J.A.O.1    Drewes, S.E.2    Khan, F.3
  • 232
    • 70450141142 scopus 로고    scopus 로고
    • Application of compounds of Erythrina variegata and isoflavones for treating osteoporis
    • Yao, X.; Wang, N.; Li, X. Application of compounds of Erythrina variegata and isoflavones for treating osteoporis. Faming Zhuanli Shenqing Gongkai Shuomingshu 2006.
    • (2006) Faming Zhuanli Shenqing Gongkai Shuomingshu
    • Yao, X.1    Wang, N.2    Li, X.3
  • 234
    • 0028896173 scopus 로고
    • Comparison between metabolite production in cell culture and in whole plant of Maclura Pomifer
    • a) Delle Monache G.; Scurria, R.; Vitali, A.; Botta, B.; Monacelli, B.; Pasqua, G.; Cuteri, A. Comparison between metabolite production in cell culture and in whole plant of Maclura Pomifer. Phytochemistry 1995, 39(3), 575-580.
    • (1995) Phytochemistry , vol.39 , Issue.3 , pp. 575-580
    • Delle Monache, G.1    Scurria, R.2    Vitali, A.3    Botta, B.4    Monacelli, B.5    Pasqua, G.6    Cuteri, A.7
  • 235
    • 70450129166 scopus 로고
    • Maclura pomifera (Osage orange): In vitro culture and the formation of flavonoids and other secondary Metabolites
    • (ed. by Y.P.S Bajaj) Springer Verlag, Berlin, Heidelberg, Chapter XV
    • b) Botta, B.; Delle Monache, G. Maclura pomifera (Osage orange): in vitro culture and the formation of flavonoids and other secondary Metabolites. In: Biotechnology in Agriculture and Forestry, Vol.33. Medicinal and Aromatic Plants, VIII (ed. by Y.P.S Bajaj) 1995, Springer Verlag, Berlin, Heidelberg, Chapter XV.
    • (1995) Biotechnology in Agriculture and Forestry, Vol.33. Medicinal and Aromatic Plants
    • Botta, B.1    Delle Monache, G.2
  • 236
    • 0032007860 scopus 로고    scopus 로고
    • Isoprenylated flavonoids from hairy root cultures of Glycyrrhiza glabra
    • DOI 10.1016/S0031-9422(97)00591-8, PII S0031942297005918
    • Asaday, Y.; Li, W.; Yoshikawa, T. Isoprenylated flavonoids from hairy root cultures of Glycyrrhiza glabra. Phytochemistry 1998, 47, 389-392 (Pubitemid 28045813)
    • (1998) Phytochemistry , vol.47 , Issue.3 , pp. 389-392
    • Asada, Y.1    Li, W.2    Yoshikawa, T.3
  • 237
    • 0032435506 scopus 로고    scopus 로고
    • Antimicrobial flavonoids from Glycyrrhiza glabra hairy root cultures
    • DOI 10.1055/s-2006-957571
    • Li, W.; Asada,Y.; Yoshikawa, T. Antimicrobial flavonoids from Glycyrrhiza glabra hairy root cultures. Planta Med. 1998, 64, 746-747 (Pubitemid 29021575)
    • (1998) Planta Medica , vol.64 , Issue.8 , pp. 746-747
    • Li, W.1    Asada, Y.2    Yoshikawa, T.3
  • 241
    • 0001411498 scopus 로고
    • Fungitoxic dihydrofurano-isoflavone and related compounds in white lupin, Lupinus albus
    • Tahara, S. Ingham, J.L.; Nakahara, S. Mizutani, J. Harborne J.B., Fungitoxic dihydrofurano-isoflavone and related compounds in white lupin, Lupinus albus. Phytochemistry 1984, 23, 1889-1890.
    • (1984) Phytochemistry , vol.23 , pp. 1889-1890
    • Tahara, S.1    Ingham, J.L.2    Nakahara, S.3    Mizutani, J.4    Harborne, J.B.5
  • 242
    • 0000196973 scopus 로고
    • Enzymatic prenylation of isofavones in white lupin
    • and references cited therein
    • Laflamme, P.; Khouri, H.; Gulick, P.; Ibrahim, R.K. Enzymatic prenylation of isofavones in white lupin. Phytochemistry 1993, 34, 147-151 and references cited therein.
    • (1993) Phytochemistry , vol.34 , pp. 147-151
    • Laflamme, P.1    Khouri, H.2    Gulick, P.3    Ibrahim, R.K.4
  • 245
    • 27744589213 scopus 로고    scopus 로고
    • Novel prenyltransferase enzymes as a tool for flavonoid prenylation
    • DOI 10.1016/j.tips.2005.09.012, PII S0165614705002518
    • Botta, B.; Delle Monache, G.; Menendez, P.; Boffi, A. Novel prenyltransferase enzymes as a tool for flavonoid prenylation. Trends Pharmacol. Sci. 2005, 26, 606-608 (Pubitemid 41636304)
    • (2005) Trends in Pharmacological Sciences , vol.26 , Issue.12 , pp. 606-608
    • Botta, B.1    Monache, G.D.2    Menendez, P.3    Boffi, A.4
  • 246
    • 85004613197 scopus 로고
    • Metabolites of 7-O-methylluteone from Botrytis cinerea
    • Tahara, S.; Ingham, J.L.; Mizutani, J. Metabolites of 7-O-methylluteone from Botrytis cinerea. Nippon Nogei Kagaku Zashi 1989, 63, 999-1007.
    • (1989) Nippon Nogei Kagaku Zashi , vol.63 , pp. 999-1007
    • Tahara, S.1    Ingham, J.L.2    Mizutani, J.3
  • 248
    • 0030867423 scopus 로고    scopus 로고
    • Fad-dependent epoxidase as a key enzyme in fungal metabolism of prenylated flavonoids
    • DOI 10.1016/S0031-9422(97)00322-1, PII S0031942297003221
    • b) Tanaka, M.; Tahara, S. FAD-dependent epoxidase as a key enzyme in fungal metabolism of prenylated flavonoid. Phytochemistry 1997, 46, 433-439 (Pubitemid 27414920)
    • (1997) Phytochemistry , vol.46 , Issue.3 , pp. 433-439
    • Tanaka, M.1    Tahara, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.