Synthesis and structure–activity relationship of (1-halo-2-naphthyl) carbamate-based inhibitors of KIAA1363 (NCEH1/AADACL1)-Reference-Cited by-同舟云学术

Synthesis and structure–activity relationship of (1-halo-2-naphthyl) carbamate-based inhibitors of KIAA1363 (NCEH1/AADACL1)

Published:2012-09 Issue:17 Volume:22 Page:5748-5751
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shreder Kevin R.,Lin Emme C.K.,Wu Jiangyue,Cajica Julia,Amantea Christopher M.,Hu Yi,Okerberg Eric,Brown Heidi E.,Pham Lan M.,Chung De Michael,Fraser Allister S.,McGee Ethel,Rosenblum Jonathan S.,Kozarich John W.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference15 articles.

1. Enzyme activity profiles of the secreted and membrane proteome that depict cancer cell invasiveness

2. A streamlined platform for high-content functional proteomics of primary human specimens

3. An Enzyme that Regulates Ether Lipid Signaling Pathways in Cancer Annotated by Multidimensional Profiling

4. A Potent and Selective Inhibitor of KIAA1363/AADACL1 that Impairs Prostate Cancer Pathogenesis

5. Discovering potent and selective reversible inhibitors of enzymes in complex proteomes

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