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Dive into the research topics where Jeannette E. Brown is active.

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Featured researches published by Jeannette E. Brown.


Cellular and Molecular Life Sciences | 1977

Anticoccidial riboflavine antagonists.

Donald W. Graham; Jeannette E. Brown; Wallace T. Ashton; Ronald D. Brown; Edward F. Rogers

4 types of riboflavine antagonists have broad-spectrum activity in poultry coccidiosis. 5-Deazariboflavine is most effective. 10-Benzyl analogs of riboflavine control intestinal species of coccidia.


Bioorganic & Medicinal Chemistry Letters | 1994

Structure-activity relationships of the non-peptidyl growth hormone secretagogue L-692,429

Dong Ok; William R. Schoen; Paul J. Hodges; Robert J. DeVita; Jeannette E. Brown; Kang Cheng; Wanda W.-S. Chan; Bridget Butler; Roy G. Smith; Michael H. Fisher; Matthew J. Wyvratt

Abstract Systematic investigation of the amino acid sidechain of L-692,429, the prototype of a novel class of benzolactam growth hormone (GH) secretagogues, has led to the preparation of L-692,585, a 2(R)-hydroxypropyl amino analog, which is twenty times more potent in vitro than L-692,429. Additional amino modifications reported here further define the structure-activity profile for L-692,429.


Bioorganic & Medicinal Chemistry Letters | 1995

Aliphatic replacements of the biphenyl moiety of the nonpeptidyl growth hormone secretagogues L-692,429 and L-692,585

Lin Chu; Helmut Mrozik; Michael H. Fisher; Jeannette E. Brown; Kang Cheng; Wanda W.-S. Chan; William R. Schoen; Matthew J. Wyvratt; Bridget Butler; Roy G. Smith

Abstract Replacement of the central phenyl ring of the biphenyl moiety in the novel growth hormone (GH) secretagogues L-692,429 and L-692,585 with partially or completely saturated surrogates has been investigated. The cyclohexenyl analogue 37 displayed GH releasing activity comparable to L-692,585, indicating that the aromaticity of this central ring is not critical for bioactivity and that this ring may serve primarily to orient the benzolactam and phenyltetrazole pharmacophores.


Biochemistry | 1978

Chemical and enzymatic properties of riboflavin analogues.

Christopher T. Walsh; Jed F. Fisher; Rob Spencer; Donald W. Graham; Wallace T. Ashton; Jeannette E. Brown; Ronald D. Brown; Edward F. Rogers


Journal of Medicinal Chemistry | 1987

Inhibition of the mammalian .beta.-lactamase renal dipeptidase (dehydropeptidase-I) by Z-2-(acylamino)-3-substituted-propenoic acids

Donald W. Graham; Wallace T. Ashton; Louis Barash; Jeannette E. Brown; Ronald D. Brown; Laura F. Canning; Anna Chen; James P. Springer; Edward F. Rogers


Journal of Medicinal Chemistry | 1991

Benzylated 1,2,3-triazoles as anticoccidiostats.

Richard J. Bochis; John C. Chabala; Ellwood Harris; Louis H. Peterson; Louis Barash; Thomas R. Beattie; Jeannette E. Brown; Donald W. Graham; Frank S. Waksmunski


Archive | 1989

Z-omega-substituted thio-2-(2,2-dimethylcyclopropanecarboxamido)-2-alkenoic acids, a process for preparing and an antibacterial composition containing the same

Wallace T. Ashton; Louis Barash; Jeannette E. Brown; Donald W. Graham


Archive | 1976

Anticoccidial cyclicamino ethanols and esters thereof

Richard A. Dybas; Donald W. Graham; Jeannette E. Brown


Archive | 1981

Acides 2-alcénoiques Z-2-(2,2-diméthylcyclopropanecarboxamido)-oméga-thio substitué, procédé pour leur préparation et composition antibactérienne les contenant

Wallace T. Ashton; Louis Barash; Jeannette E. Brown; Donald W. Graham


Archive | 1981

Process for the preparation of traumatin

Jeannette E. Brown; Edward F. Rogers; Donald W. Graham

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