메뉴 건너뛰기




Volumn 14, Issue 8, 2014, Pages 1014-1021

Antitrypanosomal activity & docking studies of isolated constituents from the lichen Cetraria islandica: Possibly multifunctional scaffolds

Author keywords

Antitrypanosomal activity; Cetraria islandica; Grip docking; Iceland moss; Phytoconstituents

Indexed keywords

FUMARPROTOCETRARIC ACID; GLUTATHIONE SYNTHASE; LICHESTERINIC ACID; PLANT MEDICINAL PRODUCT; PROTOCETRARIC ACID; PROTOLICHESTERINIC ACID; RIBOFLAVIN KINASE; ROHEDSAIN; STEROL 14ALPHA DEMETHYLASE; SURAMIN; UNCLASSIFIED DRUG; ANTITRYPANOSOMAL AGENT;

EID: 84903722768     PISSN: 15680266     EISSN: 18734294     Source Type: Journal    
DOI: 10.2174/1568026614666140324122323     Document Type: Article
Times cited : (24)

References (29)
  • 1
    • 58149498819 scopus 로고    scopus 로고
    • In vitro antiprotozoal activity of some xanthones isolated from roots of Andrographis paniculata
    • Dua, V.K.; Verma, G.; Dash, A.P. In vitro antiprotozoal activity of some xanthones isolated from roots of Andrographis paniculata. Phytother. Res., 2009, 23, 126-128.
    • (2009) Phytother. Res , vol.23 , pp. 126-128
    • Dua, V.K.1    Verma, G.2    Dash, A.P.3
  • 2
    • 78650881109 scopus 로고    scopus 로고
    • Isolation and characterization of phytoconstituents from the stem of Ichnocarpus frutescens
    • Aggarwal, B.; Ali, M.; Singh, V.; Singla, R.K. Isolation and characterization of phytoconstituents from the stem of Ichnocarpus frutescens. Chin. J. Nat. Med., 2010, 8, 401-404.
    • (2010) Chin. J. Nat. Med , vol.8 , pp. 401-404
    • Aggarwal, B.1    Ali, M.2    Singh, V.3    Singla, R.K.4
  • 3
    • 84872073082 scopus 로고    scopus 로고
    • Antitrypanosomal properties of Panax ginseng C.A. meyer: New possibilities for a remarkable traditional drug
    • Herrmann, F.; Sporer, F.; Tahrani, A.; Wink, M. Antitrypanosomal properties of Panax ginseng C.A. meyer: new possibilities for a remarkable traditional drug. Phytother. Res., 2013, 27, 86-98.
    • (2013) Phytother. Res , vol.27 , pp. 86-98
    • Herrmann, F.1    Sporer, F.2    Tahrani, A.3    Wink, M.4
  • 8
    • 0002722616 scopus 로고
    • Ahmadjian, V., Hale, M. E., Eds, New York: The Lichens Academic Press Inc
    • Vartia, K.O. Antibiotics in lichens. In; Ahmadjian, V., Hale, M. E., Eds.; New York: The Lichens Academic Press Inc, 1973; pp. 547-561.
    • (1973) Antibiotics In Lichens , pp. 547-561
    • Vartia, K.O.1
  • 12
    • 34447643379 scopus 로고    scopus 로고
    • Separation of a mixture of paraconic acids from Cetraria islandica (L.) Ach. employing a fluorous tag-catch and release strategy
    • Horhant, D.; Lamer, A-C.L.; Boustie, J.; Uriac, P.; Gouault, N. Separation of a mixture of paraconic acids from Cetraria islandica (L.) Ach. employing a fluorous tag-catch and release strategy. Tetrahedron Lett., 2007, 48, 6031-6033.
    • (2007) Tetrahedron Lett , vol.48 , pp. 6031-6033
    • Horhant, D.1    Lamer, A.-C.L.2    Boustie, J.3    Uriac, P.4    Gouault, N.5
  • 14
    • 0029165982 scopus 로고
    • Concise Syntheses of natural gamma-butyrolactones, (+)-trans-whisky lactone, (+)-trans-cognac lactone, (-)-methylenolactocin, (+)-nephrosteranic Acid, and (+)-roccellaric acid using novel chiral butenolide synthons
    • 5628
    • Takahata, H.; Uchida, Y.; Momose, T. Concise Syntheses of natural gamma-butyrolactones, (+)-trans-whisky lactone, (+)-trans-cognac lactone, (-)-methylenolactocin, (+)-nephrosteranic Acid, and (+)-roccellaric acid using novel chiral butenolide synthons. J. Org. Chem., 1995, 60, 5628 5633.
    • (1995) J. Org. Chem , vol.60 , pp. 5633
    • Takahata, H.1    Uchida, Y.2    Momose, T.3
  • 16
    • 34548027730 scopus 로고    scopus 로고
    • Stictic acid derivatives from the lichen Usnea articulata and their antioxidant activities
    • Lohezic-Le, D.F.; Tomasi, S.; Elix, J.A.; Bernard, A.; Rouaud, I.; Uriac, P.; Boustie, J. Stictic acid derivatives from the lichen Usnea articulata and their antioxidant activities. J. Nat. Prod., 2007, 70, 1218-1220.
    • (2007) J. Nat. Prod , vol.70 , pp. 1218-1220
    • Lohezic-Le, D.F.1    Tomasi, S.2    Elix, J.A.3    Bernard, A.4    Rouaud, I.5    Uriac, P.6    Boustie, J.7
  • 18
    • 74849132388 scopus 로고    scopus 로고
    • Structure of trypanosome brucei glutathione synthetase: Domain and loop alterations in the catalytic cycle of a highly conserved enzyme
    • Fyfe, P.K.; Alphey, M.S.; Hunter, W.N. Structure of trypanosome brucei glutathione synthetase: domain and loop alterations in the catalytic cycle of a highly conserved enzyme. Mol. Biochem. Para-sitol, 2010, 170, 93.
    • (2010) Mol. Biochem. Para-sitol , vol.170 , pp. 93
    • Fyfe, P.K.1    Alphey, M.S.2    Hunter, W.N.3
  • 21
    • 80053920610 scopus 로고    scopus 로고
    • Dihydro-quinazolines as novel class of Trypanosoma brucei trypanothione reductase inhibitors: Discovery, synthesis, and characterization of their binding mode by protein crystallography
    • Patterson, S.; Alphey, M.S.; Jones, D.C.; Shanks, E.J.; Street, I.P.; Frearson, J.A.; Wyatt, P.G.; Gilbert, I.H.; Fairlamb, A.H. Dihydro-quinazolines as novel class of Trypanosoma brucei trypanothione reductase inhibitors: Discovery, synthesis, and characterization of their binding mode by protein crystallography. J. Med. Chem., 2011, 54, 6514.
    • (2011) J. Med. Chem , vol.54 , pp. 6514
    • Patterson, S.1    Alphey, M.S.2    Jones, D.C.3    Shanks, E.J.4    Street, I.P.5    Frearson, J.A.6    Wyatt, P.G.7    Gilbert, I.H.8    Fairlamb, A.H.9
  • 22
    • 77955768742 scopus 로고    scopus 로고
    • Synthesis, anticancer activity and docking of some substituted benzothiazoles as tyrosine kinase inhibitor
    • Bhuva, H.A.; Kini, S.G. Synthesis, anticancer activity and docking of some substituted benzothiazoles as tyrosine kinase inhibitor. J. Mol. Graphics Modell., 2010, 29, 32-37.
    • (2010) J. Mol. Graphics Modell , vol.29 , pp. 32-37
    • Bhuva, H.A.1    Kini, S.G.2
  • 23
    • 84884818663 scopus 로고    scopus 로고
    • A comparative QSAR analysis and molecular docking studies of quinazoline derivatives as tyrosine kinase (EGFR) inhibitors: A rationale approach to anticancer drug design
    • Malleshappa, N.N.; Patel, H.M. A comparative QSAR analysis and molecular docking studies of quinazoline derivatives as tyrosine kinase (EGFR) inhibitors: A rationale approach to anticancer drug design. J. Saudi Chem. Soc., 2013, 17, 361-379.
    • (2013) J. Saudi Chem. Soc , vol.17 , pp. 361-379
    • Malleshappa, N.N.1    Patel, H.M.2
  • 24
    • 77956028811 scopus 로고    scopus 로고
    • QSAR model for predicting the fungicidal action of 1,2,4-triazole derivatives against candida albicans
    • Singla, R.K.; Bhat, V.G. QSAR model for predicting the fungicidal action of 1,2,4-triazole derivatives against candida albicans. J. Enzyme Inhib. Med. Chem., 2010, 25, 696-701.
    • (2010) J. Enzyme Inhib. Med. Chem , vol.25 , pp. 696-701
    • Singla, R.K.1    Bhat, V.G.2
  • 25
    • 84889640830 scopus 로고    scopus 로고
    • VLife Sciences Technologies Pvt. Ltd., Pune, India
    • VLifeMDS: Molecular Design Suite. VLife Sciences Technologies Pvt. Ltd., Pune, India, 2010. URL: www.vlifesciences.com/
    • (2010) VLifeMDS: Molecular Design Suite
  • 26
    • 0027749503 scopus 로고
    • Synthesis and absolute stereochemistry of (-)-protolichesterinic acid, antitumor antibiotic lactone from Cetraria islandica
    • Murta, M.M.; Azavedo, M.B.M.; Greene, A.E. Synthesis and absolute stereochemistry of (-)-protolichesterinic acid, antitumor antibiotic lactone from Cetraria islandica. J. Org. Chem., 1993, 58, 7536-7537.
    • (1993) J. Org. Chem , vol.58 , pp. 7536-7537
    • Murta, M.M.1    Azavedo, M.B.M.2    Greene, A.E.3
  • 27
    • 77956015176 scopus 로고    scopus 로고
    • General approach to 2,4-dialkyl-3-carboxybutyrolactones: An efficient synthesis of (±)-striatisporolide A and (±)-lichesterinic acid
    • Patel, R.M.; Argade, N.P. General approach to 2,4-dialkyl-3-carboxybutyrolactones: An efficient synthesis of (±)-striatisporolide A and (±)-lichesterinic acid. Ind. J. Chem., 2010, 49B, 1071-1075.
    • (2010) Ind. J. Chem , vol.49 B , pp. 1071-1075
    • Patel, R.M.1    Argade, N.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.