Search Results - "Chang, ChiehYing J"
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Small Molecule Reversible Inhibitors of Bruton’s Tyrosine Kinase (BTK): Structure–Activity Relationships Leading to the Identification of 7‑(2-Hydroxypropan-2-yl)-4-[2-methyl-3-(4-oxo-3,4-dihydroquinazolin-3-yl)phenyl]‑9H‑carbazole-1-carboxamide (BMS-935177)
Published in Journal of medicinal chemistry (08-09-2016)“…Bruton’s tyrosine kinase (BTK) belongs to the TEC family of nonreceptor tyrosine kinases and plays a critical role in multiple cell types responsible for…”
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Journal Article -
2
The structure of human tau-tubulin kinase 1 both in the apo form and in complex with an inhibitor
Published in Acta crystallographica. Section F, Structural biology communications (01-02-2014)“…Tau‐tubulin kinase 1 (TTBK1) is a dual‐specificity (serine/threonine and tyrosine) kinase belonging to the casein kinase 1 superfamily. TTBK1 is a…”
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Journal Article -
3
Design of LFA-1 antagonists based on a 2,3-dihydro-1H-pyrrolizin-5(7aH)-one scaffold
Published in Bioorganic & medicinal chemistry letters (01-04-2007)“…A new class of lymphocyte function-associated antigen-1 (LFA-1) antagonists is described. Elaboration of the 2,3-dihydro-1H-pyrrolizin-5(7aH)-one scaffold…”
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4
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffold
Published in Bioorganic & medicinal chemistry letters (15-02-2005)“…LFA-1 is a member of the β2-integrin family and is expressed on all leukocytes. This paper describes the de novo design, synthesis, and in vitro activity of…”
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5
Small Molecule Reversible Inhibitors of Bruton’s Tyrosine Kinase (BTK): Structure–Activity Relationships Leading to the Identification of 7-(2-Hydroxypropan-2-yl)-4-[2-methyl-3-(4-oxo-3,4-dihydroquinazolin-3-yl)phenyl]-9 H -carbazole-1-carboxamide (BMS-935177)
Published in Journal of medicinal chemistry (08-09-2016)“…Bruton’s tyrosine kinase (BTK) belongs to the TEC family of nonreceptor tyrosine kinases and plays a critical role in multiple cell types responsible for…”
Get full text
Journal Article -
6
Design of LFA-1 antagonists based on a 2,3-dihydro-1 H-pyrrolizin-5(7aH)-one scaffold
Published in Bioorganic & medicinal chemistry letters (2007)“…A new class of lymphocyte function-associated antigen-1 (LFA-1) antagonists is described. Elaboration of the 2,3-dihydro-1 H-pyrrolizin-5(7aH)-one scaffold…”
Get full text
Journal Article