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Authors:
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Citation: Ab. Shahripour et al., Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamide, BIOORG MED, 11(20), 2001, pp. 2779-2782
Authors:
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Citation: N. Kawahata et al., A novel phosphotyrosine mimetic 4 '-carboxymethyloxy-3 '-phosphonophenylalanine (Cpp): Exploitation in the design of nonpeptide inhibitors of pp60(Src) SH2 domain, BIOORG MED, 11(17), 2001, pp. 2319-2323
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Citation: Rs. Bohacek et al., X-ray structure of citrate bound to Src SH2 leads to a high-affinity, bone-targeted Src SH2 inhibitor, J MED CHEM, 44(5), 2001, pp. 660-663
Authors:
Metcalf, CA
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Citation: Ca. Metcalf et al., Structure-based design and solid-phase parallel synthesis of phosphorylated nonpeptides to explore hydrophobic binding at the Src SH2 domain, J COMB CHEM, 2(4), 2000, pp. 305-313
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Azimioara, MD
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Luke, GP
Dalgarno, DC
Hatada, MH
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Citation: Wc. Shakespeare et al., Structure-based design of novel bicyclic nonpeptide inhibitors for the SrcSH2 domain, J MED CHEM, 43(21), 2000, pp. 3815-3819
Authors:
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Merry, TJ
Pradeepan, SG
Bartlett, C
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Citation: Cb. Vu et al., Discovery of potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70, J MED CHEM, 42(20), 1999, pp. 4088-4098