Hydroxamic acid inhibitors of 5-lipoxygenase: quantitative structure-activity relationships
β Scribed by Summers, James B.; Kim, Ki H.; Mazdiyasni, Hormoz; Holms, James H.; Ratajczyk, James D.; Stewart, Andrew O.; Dyer, Richard D.; Carter, George W.
- Book ID
- 118183003
- Publisher
- American Chemical Society
- Year
- 1990
- Tongue
- English
- Weight
- 982 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2623
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Background: Clinical symptoms of prostatitis, prostatodynia, and benign prostatic hyperplasia are relieved by the pollen extract cernilton, and the water-soluble fraction of this extract selectively inhibits growth of some prostate cancer cells. a cyclic hydroxamic acid, diboa, has been isolated
N-Hydroxyurea and Hydroxamic Acid Inhibitors of Cyclooxygenase and 5-Lipoxygenase. -Among the prepared two series of N-hydroxyurea (XII) and hydroxamic acids (XVIII) potent both COX and 5-LO inhibitors are evaluated. The desired long duration inhibition of 5-LO could not be achieved. - (CONNOLLY,