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Volumn 85, Issue , 2014, Pages 58-64

Biological activities of new monohydroxylated brassinosteroid analogues with a carboxylic group in the side chain

Author keywords

Anticancer activity; Brassinosteroids; Molecular docking; Organic synthesis; Plant bioassays; Receptor kinase BRI1

Indexed keywords

24 EPIBRASSINOLIDE; 28 HOMOCASTASTERONE; 2ALPHA HYDROXY 6 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLIC ACID; 2ALPHA HYDROXY 7 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLIC ACID; 3ALPHA HYDROXY 6 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLIC ACID; 3ALPHA HYDROXY 7 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLIC ACID; ANTINEOPLASTIC AGENT; BRASSINOLIDE; BRASSINOSTEROID; CARBOXYLIC ACID; CASTASTERONE; METHYL 2ALPHA HYDROXY 6 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 2ALPHA HYDROXY 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 2ALPHA HYDROXY 7 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 3ALPHA (4 NITROBENZOYLOXY) 6 OXO 5ALPHA PREGNANE 2 CARBOXYLATE; METHYL 3ALPHA (4 NITROBENZOYLOXY) 7 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 3ALPHA (4 NITROBENZOYLOXY) 7 OXO 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 3ALPHA HYDROXY 6 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 3ALPHA HYDROXY 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; METHYL 3ALPHA HYDROXY 7 OXA 7ALPHA HOMO 6 OXO 5ALPHA PREGNANE 20 CARBOXYLATE; UNCLASSIFIED DRUG; CHOLESTANOL; CYTOTOXIN; HETEROCYCLIC STEROID;

EID: 84899798673     PISSN: 0039128X     EISSN: 18785867     Source Type: Journal    
DOI: 10.1016/j.steroids.2014.04.007     Document Type: Article
Times cited : (21)

References (28)
  • 1
    • 33947287133 scopus 로고    scopus 로고
    • Metabolism of brassinosteroids in plants
    • A. Bajguz Metabolism of brassinosteroids in plants Plant Physiol Biochem 45 2007 95 107
    • (2007) Plant Physiol Biochem , vol.45 , pp. 95-107
    • Bajguz, A.1
  • 3
    • 0442313180 scopus 로고    scopus 로고
    • Structure-activity studies of brassinosteroids and the search for novel analogues and mimetics with improved bioactivity
    • T.G. Back, and R.P. Pharis Structure-activity studies of brassinosteroids and the search for novel analogues and mimetics with improved bioactivity J Plant Growth Regul 22 2003 350 361
    • (2003) J Plant Growth Regul , vol.22 , pp. 350-361
    • Back, T.G.1    Pharis, R.P.2
  • 5
    • 0031793484 scopus 로고    scopus 로고
    • Brassinosteroids: Essential regulators of plant growth and development
    • S.D. Clouse, and J.M. Sasse Brassinosteroids: essential regulators of plant growth and development Ann Rev Plant Physiol Plant Mol Biol 49 1998 427 451
    • (1998) Ann Rev Plant Physiol Plant Mol Biol , vol.49 , pp. 427-451
    • Clouse, S.D.1    Sasse, J.M.2
  • 6
    • 0030866902 scopus 로고    scopus 로고
    • A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction
    • J.M. Li, and J. Chory A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction Cell 90 1997 929 938
    • (1997) Cell , vol.90 , pp. 929-938
    • Li, J.M.1    Chory, J.2
  • 8
    • 84878939828 scopus 로고    scopus 로고
    • Structural basis for differential recognition of brassinolide by its receptors
    • J. She, Z.F. Han, B. Zhou, and J.J. Chai Structural basis for differential recognition of brassinolide by its receptors Protein Cell 4 2013 475 482
    • (2013) Protein Cell , vol.4 , pp. 475-482
    • She, J.1    Han, Z.F.2    Zhou, B.3    Chai, J.J.4
  • 9
    • 79959535565 scopus 로고    scopus 로고
    • Structural insight into brassinosteroid perception by BRI1
    • J. She, Z.F. Han, T.W. Kim, J.J. Wang, W. Cheng, and J.B. Chang et al. Structural insight into brassinosteroid perception by BRI1 Nature 474 2011 472 476
    • (2011) Nature , vol.474 , pp. 472-476
    • She, J.1    Han, Z.F.2    Kim, T.W.3    Wang, J.J.4    Cheng, W.5    Chang, J.B.6
  • 15
    • 37549043140 scopus 로고    scopus 로고
    • Anticancer and antiproliferative activity of natural brassinosteroids
    • J. Malikova, J. Swaczynova, Z. Kolar, and M. Strnad Anticancer and antiproliferative activity of natural brassinosteroids Phytochemistry 69 2008 418 426
    • (2008) Phytochemistry , vol.69 , pp. 418-426
    • Malikova, J.1    Swaczynova, J.2    Kolar, Z.3    Strnad, M.4
  • 19
    • 76149120388 scopus 로고    scopus 로고
    • Software News and Update AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
    • O. Trott, and A.J. Olson Software News and Update AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading J Comput Chem 31 2010 455 461
    • (2010) J Comput Chem , vol.31 , pp. 455-461
    • Trott, O.1    Olson, A.J.2
  • 21
    • 23844490599 scopus 로고    scopus 로고
    • Syntheses of new androstane brassinosteroids with 17β-ester group - Butyrates, heptafluorobutyrates, and laurates
    • M. Sisa, J. Hnilickova, J. Swaczynova, and L. Kohout Syntheses of new androstane brassinosteroids with 17β-ester group - butyrates, heptafluorobutyrates, and laurates Steroids 70 2005 755 762
    • (2005) Steroids , vol.70 , pp. 755-762
    • Sisa, M.1    Hnilickova, J.2    Swaczynova, J.3    Kohout, L.4
  • 22
    • 70349417952 scopus 로고    scopus 로고
    • Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment
    • B. Eignerova, B. Slavikova, M. Budesinsky, M. Dracinsky, B. Klepetarova, E. Stastna, and M. Kotora Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment J Med Chem 52 2009 5753 5757
    • (2009) J Med Chem , vol.52 , pp. 5753-5757
    • Eignerova, B.1    Slavikova, B.2    Budesinsky, M.3    Dracinsky, M.4    Klepetarova, B.5    Stastna, E.6    Kotora, M.7
  • 24
    • 0008174309 scopus 로고
    • Remote substituent effect on the regioselectivity in the Baeyer-Villiger oxidation of 5α-cholestan-6-one derivatives
    • S. Takatsuto, and N. Ikekawa Remote substituent effect on the regioselectivity in the Baeyer-Villiger oxidation of 5α-cholestan-6-one derivatives Tetrahedron Lett 24 1983 917 920
    • (1983) Tetrahedron Lett , vol.24 , pp. 917-920
    • Takatsuto, S.1    Ikekawa, N.2
  • 25
    • 0037630478 scopus 로고
    • Preparation of 2α, 3α-dihydroxy-7-oxa-6-oxo-23,24-dinor-B- homo-5α-cholanic acid, its esters and amides as brassinolide analogs
    • V. Cerny, M. Strnad, and M. Kaminek Preparation of 2α, 3α-dihydroxy-7-oxa-6-oxo-23,24-dinor-B-homo-5α-cholanic acid, its esters and amides as brassinolide analogs Collect Czech Chem Commun 51 1986 687 697
    • (1986) Collect Czech Chem Commun , vol.51 , pp. 687-697
    • Cerny, V.1    Strnad, M.2    Kaminek, M.3
  • 26
    • 83655167089 scopus 로고    scopus 로고
    • Brassinosteroids and analogs as neuroprotectors: Synthesis and structure-activity relationships
    • J. Ismaili, M. Boisvert, F. Longpre, J. Carange, C.L. Gall, M.G. Martinoli, and B. Daoust Brassinosteroids and analogs as neuroprotectors: synthesis and structure-activity relationships Steroids 77 2012 91 99
    • (2012) Steroids , vol.77 , pp. 91-99
    • Ismaili, J.1    Boisvert, M.2    Longpre, F.3    Carange, J.4    Gall, C.L.5    Martinoli, M.G.6    Daoust, B.7


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