메뉴 건너뛰기




Volumn 75, Issue 3, 2009, Pages 227-229

Cytotoxicity and phytotoxicity of trichothecene macrolides from Myrothecium gramminum

Author keywords

Cytotoxicity; Myrothecium gramminum; Phytotoxicity; Trichothecene macrolides; Tuberculariaceae

Indexed keywords

2,4 DICHLOROPHENOXYACETIC ACID; ISORORIDINE E; MACROLIDE; MYROTHECIUM GRAMMIMUM EXTRACT; RORIDIN A; RORIDIN E; RORIDIN L; TRICHOTHECENE MACROLIDE DERIVATIVE; UNCLASSIFIED DRUG; VERRUCARIN A; VERRUCARIN B; VERRUCARIN M; CYTOTOXIN;

EID: 64549136253     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0028-1112196     Document Type: Article
Times cited : (9)

References (19)
  • 3
    • 4444268646 scopus 로고    scopus 로고
    • Cellular and molecular mechanisms for immune modulation by deoxynivalenol and other trichothecenes: Unraveling a paradox
    • DOI 10.1016/j.toxlet.2004.04.023, PII S0378427404002449
    • Pestka JJ, Zhou HR, Moon Y, Chung YJ. Cellular and molecular mechanisms for immune modulation by deoxynivalenol and other trichothecenes: unraveling a paradox. Toxicol Lett 2004; 153: 61-73 (Pubitemid 39165750)
    • (2004) Toxicology Letters , vol.153 , Issue.1 , pp. 61-73
    • Pestka, J.J.1    Zhou, H.-R.2    Moon, Y.3    Chung, Y.J.4
  • 4
    • 0033026397 scopus 로고    scopus 로고
    • Antimalarial activity of macrocyclic trichothecenes isolated from the fungus Myrothecium verrucaria
    • Isaka M, Punya J, Lertwerawat Y, Tanticharoen M, Thebtaranonth Y. Antimalarial activity of macrocyclic trichothecenes isolated from the fungus Myrothecium verrucaria. J Nat Prod 1999; 62: 329-331
    • (1999) J Nat Prod , vol.62 , pp. 329-331
    • Isaka, M.1    Punya, J.2    Lertwerawat, Y.3    Tanticharoen, M.4    Thebtaranonth, Y.5
  • 5
    • 14644426529 scopus 로고    scopus 로고
    • Metabolites inhibiting germination of Orobanche ramosa seeds produced by Myrothecium verrucaria and Fusarium compactum
    • DOI 10.1021/jf048339i
    • Andolfi A, Boari A, Evidente A, Vurro M. Metabolites inhibiting germination of Orobanche ramosa seeds produced by Myrothecium verrucaria and Fusarium compactum. J Agric Food Chem 2005; 53: 1598-1603 (Pubitemid 40322158)
    • (2005) Journal of Agricultural and Food Chemistry , vol.53 , Issue.5 , pp. 1598-1603
    • Andolfi, A.1    Boari, A.2    Evidente, A.3    Vurro, M.4
  • 6
    • 43249084944 scopus 로고    scopus 로고
    • Structure and conformational dynamics of trichothecenemycotoxins
    • Steinmetz WE, Robustelli P, Edens E, Heineman D. Structure and conformational dynamics of trichothecenemycotoxins. J Nat Prod 2008; 71: 589-594
    • (2008) J Nat Prod , vol.71 , pp. 589-594
    • Steinmetz, W.E.1    Robustelli, P.2    Edens, E.3    Heineman, D.4
  • 7
    • 37549039422 scopus 로고    scopus 로고
    • Penicidones A - C, three cytotoxic alkaloidal metabolites of an endophytic Penicillium sp.
    • Ge HM, Shen Y, Zhu CH, Tan SH, Ding H, Song YC. Penicidones A - C, three cytotoxic alkaloidal metabolites of an endophytic Penicillium sp. Phytochemistry 2008; 69: 571-576
    • (2008) Phytochemistry , vol.69 , pp. 571-576
    • Ge, H.M.1    Shen, Y.2    Zhu, C.H.3    Tan, S.H.4    Ding, H.5    Song, Y.C.6
  • 8
    • 33846304654 scopus 로고    scopus 로고
    • Chaetominine, a cytotoxic alkaloid produced by endophytic Chaetomium sp. IFB-E015
    • Jiao RH, Xu S, Liu JY, Ge HM, Ding H, Xu C. Chaetominine, a cytotoxic alkaloid produced by endophytic Chaetomium sp. IFB-E015. Org Lett 2006; 8: 5709-5712
    • (2006) Org Lett , vol.8 , pp. 5709-5712
    • Jiao, R.H.1    Xu, S.2    Liu, J.Y.3    Ge, H.M.4    Ding, H.5    Xu, C.6
  • 9
    • 53549105531 scopus 로고    scopus 로고
    • Unprecedented immunosuppressive polyketides from Daldinia eschscholzii, a mantis-associated fungus
    • Zhang YL, Ge HM, Zhao W, Dong H, Xu Q, Li SH. Unprecedented immunosuppressive polyketides from Daldinia eschscholzii, a mantis-associated fungus. Angew Chem Int Ed 2008; 47: 5823-5826
    • (2008) Angew Chem Int Ed , vol.47 , pp. 5823-5826
    • Zhang, Y.L.1    Ge, H.M.2    Zhao, W.3    Dong, H.4    Xu, Q.5    Li, S.H.6
  • 10
    • 33645130667 scopus 로고    scopus 로고
    • Antifungal and new metabolites of Myrothecium sp. Z16, a fungus associated with white croaker Argyrosomus argentatus
    • Liu JY, Huang LL, Ye YH, Zou WX, Guo ZJ, Tan RX. Antifungal and new metabolites of Myrothecium sp. Z16, a fungus associated with white croaker Argyrosomus argentatus. J Appl Microbiol 2006; 100: 195-202
    • (2006) J Appl Microbiol , vol.100 , pp. 195-202
    • Liu, J.Y.1    Huang, L.L.2    Ye, Y.H.3    Zou, W.X.4    Guo, Z.J.5    Tan, R.X.6
  • 12
    • 0035206971 scopus 로고    scopus 로고
    • Roridin L, M and verrucarin M, new macrocyclic trichothecene group antitumor antibiotics, from Myrothecium verrucaria
    • Murakamo Y, Okuda T, Shindo K. Roridin L, M and verrucarin M, new macrocyclic trichothecene group antitumor antibiotics, from Myrothecium verrucaria. J Antibiot 2001; 54: 980-983
    • (2001) J Antibiot , vol.54 , pp. 980-983
    • Murakamo, Y.1    Okuda, T.2    Shindo, K.3
  • 13
    • 0016591292 scopus 로고
    • 13C-NMR-spectroscopy of the trichothecene derivatives verrucarol, verrucarins A and B and roridins A, D and H
    • 13C-NMR-spectroscopy of the trichothecene derivatives verrucarol, verrucarins A and B and roridins A, D and H. Helv Chim Acta 1975; 58: 1172-1180
    • (1975) Helv Chim Acta , vol.58 , pp. 1172-1180
    • Breitenstein, W.1    Tamm, C.2
  • 14
    • 0014902648 scopus 로고
    • Die Struktur des Antibiotikums Roridin E
    • Traxler P, Zurcher W, Tamm Ch. Die Struktur des Antibiotikums Roridin E. Helv Chim Acta 1970; 53: 2071-2085
    • (1970) Helv Chim Acta , vol.53 , pp. 2071-2085
    • Traxler, P.1    Zurcher, W.2    Tamm, Ch.3
  • 15
    • 0000553955 scopus 로고
    • Structures of isororidin E, epoxyisororidin E, and epoxy- and diepoxyroridin H, new metabolites isolated from cylindrocarpon species determined by carbon-13 and hydrogen-1 NMR spectroscopy. Revision of C-2′: C-3′ double bond configuration of the roridin group
    • Matsumoto M, Minato H, Tori K, Ueyama M. Structures of isororidin E, epoxyisororidin E, and epoxy- and diepoxyroridin H, new metabolites isolated from cylindrocarpon species determined by carbon-13 and hydrogen-1 NMR spectroscopy. Revision of C-2′: C-3′ double bond configuration of the roridin group. Tetrahedron Lett 1977; 18: 4093-4096
    • (1977) Tetrahedron Lett , vol.18 , pp. 4093-4096
    • Matsumoto, M.1    Minato, H.2    Tori, K.3    Ueyama, M.4
  • 16
    • 0037138273 scopus 로고    scopus 로고
    • Phytotoxicity and mammalian cytotoxicity of macrocyclic trichothecenemycotoxins from Myrothecium verrucaria
    • Abbas HK, Johnson BB, Shier WT, Tak H, Jarvis BB, Boyette CD. Phytotoxicity and mammalian cytotoxicity of macrocyclic trichothecenemycotoxins from Myrothecium verrucaria. Phytochemistry 2002; 59: 309-313
    • (2002) Phytochemistry , vol.59 , pp. 309-313
    • Abbas, H.K.1    Johnson, B.B.2    Shier, W.T.3    Tak, H.4    Jarvis, B.B.5    Boyette, C.D.6
  • 17
    • 0000423049 scopus 로고
    • Preliminary observations on the effects of macrocyclic trichothecenes on plant growth
    • Culter HG, Jarvis BB. Preliminary observations on the effects of macrocyclic trichothecenes on plant growth. Environ Exp Bot 1985; 25: 115-128
    • (1985) Environ Exp Bot , vol.25 , pp. 115-128
    • Culter, H.G.1    Jarvis, B.B.2
  • 18
    • 33845940774 scopus 로고    scopus 로고
    • Hopeanol: A potent cytotoxin with a novel skeleton from Hopea exalata
    • Ge HM, Xu C, Wang XT, Huang B, Tan RX. Hopeanol: a potent cytotoxin with a novel skeleton from Hopea exalata. Eur J Org Chem 2006; 24: 5551-5554
    • (2006) Eur J Org Chem , vol.24 , pp. 5551-5554
    • Ge, H.M.1    Xu, C.2    Wang, X.T.3    Huang, B.4    Tan, R.X.5
  • 19
    • 22544444508 scopus 로고    scopus 로고
    • Phytotoxins from Hofmeisteria schaffneri: Isolation and synthesis of 2′-(2″-hydroxy-4″-methylphenyl)-2′-oxoethyl acetate
    • Pérez-Vásquez A, Reyes A, Linares E, Bye R, Mata R. Phytotoxins from Hofmeisteria schaffneri: isolation and synthesis of 2′-(2″-hydroxy-4″-methylphenyl)-2′-oxoethyl acetate. J Nat Prod 2005; 68: 959-962
    • (2005) J Nat Prod , vol.68 , pp. 959-962
    • Pérez-Vásquez, A.1    Reyes, A.2    Linares, E.3    Bye, R.4    Mata, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.