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Substituted N-(3,5-dichlorobenzenesulfonyl)-L-prolyl-phenylalanine analogues as potent VLA-4 antagonists.

Bioorganic & medicinal chemistry letters (2002-02-15)
Ihor E Kopka, David N Young, Linus S Lin, Richard A Mumford, Plato A Magriotis, Malcolm MacCoss, Sander G Mills, Gail Van Riper, Ermengilda McCauley, Linda E Egger, Usha Kidambi, John A Schmidt, Kathryn Lyons, Ralph Stearns, Stella Vincent, Adria Colletti, Zhen Wang, Sharon Tong, Junying Wang, Song Zheng, Karen Owens, Dorothy Levorse, William K Hagmann
RESUMEN

A series of substituted N-(3,5-dichlorobenzenesulfonyl)-L-prolyl- and alpha-methyl-L-prolyl-phenylalanine derivatives was prepared as VLA-4/VCAM antagonists. The compounds showed excellent potency with a wide variety of neutral, polar, electron withdrawing or donating groups on the phenylalanine ring (IC50 approximately 1 nM). Heteroaryl ring substitution for phenylalanine was also well tolerated. Pharmacokinetic studies in rat were performed on a representative set of compounds in both series.

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Sigma-Aldrich
Benzenesulfonyl chloride, 99%
Sigma-Aldrich
Benzenesulfonyl chloride, 96%
Sigma-Aldrich
Benzenesulfonyl chloride, for HPLC derivatization