Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Roland H. Nearn"'
Autor:
Matthew Pollard, Linda Howell, Brian J. O’Driscoll, George O. Lovrecz, Ross Fernley, Julian Grusovin, Peter J. James, Andris J. Liepa, Christa Leitner, Ronald J. Hill, Dionne A. Jones, Lloyd D. Graham, Wynona M. Johnson, Louis Lu, Kathleen A. Turner, Roland H. Nearn, Albert Hofmann, Woldeamanuel Birru, David A. Winkler, Karen E. Jarvis, Tram Phan
Publikováno v:
ResearcherID
Nuclear hormone receptors, such as the ecdysone receptor, often display a large amount of induced fit to ligands. The size and shape of the binding pocket in the EcR subunit changes markedly on ligand binding, making modelling methods such as docking
Publikováno v:
ChemInform. 32
Dilithiation of 1-hydroxy-5-aryltetrazoles with 2 equiv. of butyllithium in the presence of N,N,N´N´-tetra-methylethylenediamine enables the introduction of ortho-substituents into the aryl ring to form compounds (6a–e). The hydroxy group of 1-hy
Publikováno v:
Australian Journal of Chemistry. 53:619
Dilithiation of 1-hydroxy-5-aryltetrazoles with 2 equiv. of butyllithium in the presence of N,N,N´N´-tetra-methylethylenediamine enables the introduction of ortho-substituents into the aryl ring to form compounds (6a–e). The hydroxy group of 1-hy
Autor:
Charles Hetru, Dennis H.S. Horn, Jules A. Hoffmann, Roland H. Nearn, Luu Bang, Christine Kappler
Publikováno v:
Molecular and cellular endocrinology. 26(1-2)
Ovaries of adult females of Locusta migratoria synthesize impressive amounts of the steroid hormone ecdysone (and related ecdysteroids) during the late phases of vitellogenesis. The present study, aimed at elucidating the sequence of the biosynthetic
Autor:
John W. Loder, Roland H. Nearn
Publikováno v:
Chemischer Informationsdienst. 6
Norerythrostachaldine (1) and its naturally occurring 3β-acetate (2) are highly cytotoxic aldehydic bases considered to be 19- oxonorcassaidine and its 3β-acetate. The carbon skeleton, stereochemistry and position of oxygen substituents were establ
Publikováno v:
Chemischer Informationsdienst. 6
Unstable 2-methylaminoethyl esters from E. chlorostachys can be isolated with careful pH control and then manipulated as their stable hydrochlorides. A large-scale extraction and counter- current distribution separated two new crystalline alkaloid hy
Autor:
John W. Loder, Roland H. Nearn
Publikováno v:
HETEROCYCLES. 7:113
Autor:
Roland H. Nearn, John W. Loder
Publikováno v:
Australian Journal of Chemistry. 28:651
Norerythrostachaldine (1) and its naturally occurring 3β-acetate (2) are highly cytotoxic aldehydic bases considered to be 19- oxonorcassaidine and its 3β-acetate. The carbon skeleton, stereochemistry and position of oxygen substituents were establ
Publikováno v:
Australian Journal of Chemistry. 31:1011
Racemic and optical isomers of 7-hydroxy-3-(p-hydroxyphenyl)-3,4- dihydronaphthalen-1(2H)-one (1) have been synthesized and the configurations of the optical isomers assigned by o.r.d. spectrometry. Derivatives of these 3,4-dihydronaphthalen-1(2H)-on
Publikováno v:
Australian Journal of Chemistry. 28:645
Unstable 2-methylaminoethyl esters from E. chlorostachys can be isolated with careful pH control and then manipulated as their stable hydrochlorides. A large-scale extraction and counter- current distribution separated two new crystalline alkaloid hy