Bioorganic and Medicinal Chemistry Letters p. 3009 - 3014 (1999)
Update date:2022-08-04
Topics:
Vu, Chi B.
Corpuz, Evelyn G.
Pradeepan, Selvaluxmi G.
Violette, Shelia
Bartlett, Catherine
Sawyer, Tomi K.
The synthesis of a series of 1,2,4-oxadiazole analogs is discussed along with their ZAP-70 SH2 inhibitory activity. The tyrosine moiety in the original series has been replaced with nonpeptidic functional groups without a substantial loss of binding affin
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Doi:10.1016/S0040-4020(99)00301-4
(1999)Doi:10.1007/s11172-008-0117-5
(2008)Doi:10.1246/bcsj.66.2042
(1993)Doi:10.1016/j.jfluchem.2005.01.003
(2005)Doi:10.1021/om990216d
(1999)Doi:10.1016/S0040-4020(99)00548-7
(1999)
