102 related articles for article (PubMed ID: 24769247)
1. Biological activities of new monohydroxylated brassinosteroid analogues with a carboxylic group in the side chain.
Kvasnica M; Oklestkova J; Bazgier V; Rarova L; Berka K; Strnad M
Steroids; 2014 Jul; 85():58-64. PubMed ID: 24769247
[TBL] [Abstract][Full Text] [Related]
2. Brassinosteroids: synthesis and activity of some fluoro analogues.
Slavikova B; Kohout L; Budesinsky M; Swaczynova J; Kasal A
J Med Chem; 2008 Jul; 51(13):3979-84. PubMed ID: 18557605
[TBL] [Abstract][Full Text] [Related]
3. Syntheses of new androstane brassinosteroids with 17beta-ester groups--butyrates, heptafluorobutyrates, and laurates.
Sísa M; Hnilicková J; Swaczynová J; Kohout L
Steroids; 2005 Oct; 70(11):755-62. PubMed ID: 15921713
[TBL] [Abstract][Full Text] [Related]
4. BRI1 is a critical component of a plasma-membrane receptor for plant steroids.
Wang ZY; Seto H; Fujioka S; Yoshida S; Chory J
Nature; 2001 Mar; 410(6826):380-3. PubMed ID: 11268216
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and biological activity of ring-A difluorinated brassinosteroids.
Acebedo SL; Alonso F; Galagovsky LR; Ramírez JA
Steroids; 2011; 76(10-11):1016-20. PubMed ID: 21515297
[TBL] [Abstract][Full Text] [Related]
6. Synthesis of [26-2H(3)]brassinosteroids.
Khripach VA; Zhabinskii VN; Konstantinova OV; Antonchick AP; Schneider B
Steroids; 2002 Jun; 67(7):587-95. PubMed ID: 11996931
[TBL] [Abstract][Full Text] [Related]
7. Effect of chain length and ring size of alkyl and cycloalkyl side-chain substituents upon the biological activity of brassinosteroids. Preparation of novel analogues with activity exceeding that of brassinolide.
Back TG; Janzen L; Nakajima SK; Pharis RP
J Org Chem; 2000 May; 65(10):3047-52. PubMed ID: 10814196
[TBL] [Abstract][Full Text] [Related]
8. Anticancer and antiproliferative activity of natural brassinosteroids.
Malíková J; Swaczynová J; Kolár Z; Strnad M
Phytochemistry; 2008 Jan; 69(2):418-26. PubMed ID: 17869317
[TBL] [Abstract][Full Text] [Related]
9. Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment.
Eignerová B; Slavíková B; Budĕsínský M; Dracínský M; Klepetárová B; St'astná E; Kotora M
J Med Chem; 2009 Sep; 52(18):5753-7. PubMed ID: 19719120
[TBL] [Abstract][Full Text] [Related]
10. Design, synthesis, and bioactivity of the first nonsteroidal mimetics of brassinolide.
Andersen DL; Back TG; Janzen L; Michalak K; Pharis RP; Sung GC
J Org Chem; 2001 Oct; 66(21):7129-41. PubMed ID: 11597241
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and biological activity of brassinosteroids fluorinated at C-2.
Acebedo SL; Ramírez JA; Galagovsky LR
Steroids; 2009; 74(4-5):435-40. PubMed ID: 19150620
[TBL] [Abstract][Full Text] [Related]
12. Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain.
Diachkov MV; Ferrer K; Oklestkova J; Rarova L; Bazgier V; Kvasnica M
Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33375728
[TBL] [Abstract][Full Text] [Related]
13. Preparation and synthetic application of partially protected brassinosteroids.
Khripach VA; Zhabinskii VN; Zhiburtovich YY; Ivanova GV; Konstantinova OV; Tsavlovskii DV; Lorenz S; Schneider B
Steroids; 2010 Jan; 75(1):27-33. PubMed ID: 19786042
[TBL] [Abstract][Full Text] [Related]
14. Binding of brassinosteroids to the extracellular domain of plant receptor kinase BRI1.
Kinoshita T; Caño-Delgado A; Seto H; Hiranuma S; Fujioka S; Yoshida S; Chory J
Nature; 2005 Jan; 433(7022):167-71. PubMed ID: 15650741
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and biological activities of new brassinosteroid analogues with a phenyl group in the side chain.
Kvasnica M; Oklestkova J; Bazgier V; Rárová L; Korinkova P; Mikulík J; Budesinsky M; Béres T; Berka K; Lu Q; Russinova E; Strnad M
Org Biomol Chem; 2016 Sep; 14(37):8691-8701. PubMed ID: 27714217
[TBL] [Abstract][Full Text] [Related]
16. Brassinolide activities of 2alpha,3alpha-diols versus 3alpha,4alpha-diols in the bean second internode bioassay: explanation by molecular modeling methods.
Sísa M; Vilaplana-Polo M; Ballesteros CB; Kohout L
Steroids; 2007 Oct; 72(11-12):740-50. PubMed ID: 17719069
[TBL] [Abstract][Full Text] [Related]
17. Synthesis and biological activity of brassinolide and its 22 beta, 23 beta-isomer: novel plant growth-promoting steroids.
Thompson MJ; Mandava NB; Meudt WJ; Lusby WR; Spaulding DW
Steroids; 1981 Nov; 38(5):567-80. PubMed ID: 7324086
[TBL] [Abstract][Full Text] [Related]
18. Synthesis and Biological Activity of New Brassinosteroid Analogs of Type 24-Nor-5β-Cholane and 23-Benzoate Function in the Side Chain.
Soto N; Ferrer K; Díaz K; González C; Taborga L; Olea AF; Carrasco H; Espinoza L
Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34062717
[TBL] [Abstract][Full Text] [Related]
19. Brassinolide-2,3-acetonide: a brassinolide-induced rice lamina joint inclination antagonist.
Muto T; Todoroki Y
Bioorg Med Chem; 2013 Jul; 21(14):4413-9. PubMed ID: 23673217
[TBL] [Abstract][Full Text] [Related]
20. Recent developments in the field of plant steroid hormones.
McMorris TC
Lipids; 1997 Dec; 32(12):1303-8. PubMed ID: 9438241
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
