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Kinases are signalling proteins which have proven to be successful targets for the treatment of a variety of diseases, predominantly in cancers. However, only a small proportion of kinases (<20%) have been investigated for their therapeutic viability, likely due to the lack of available chemical tools across the kinome. In this work we describe initial efforts in the development of a selective chemical tool for protein kinase N2 (PKN2), a relatively unexplored kinase of interest in several types of cancer. The most successful compound, 5, has a measured IC50 of 0.064 μM against PKN2, with ca. 17-fold selectivity over close homologue, PKN1.

More information Original publication

DOI

10.1016/j.bmcl.2020.127040

Type

Journal article

Publication Date

2020-04-01T00:00:00+00:00

Volume

30

Addresses

S, u, s, s, e, x, , D, r, u, g, , D, i, s, c, o, v, e, r, y, , C, e, n, t, r, e, ,, , U, n, i, v, e, r, s, i, t, y, , o, f, , S, u, s, s, e, x, ,, , S, u, s, s, e, x, , H, o, u, s, e, ,, , F, a, l, m, e, r, ,, , B, r, i, g, h, t, o, n, , B, N, 1, , 9, R, H, ,, , U, n, i, t, e, d, , K, i, n, g, d, o, m, ., , E, l, e, c, t, r, o, n, i, c, , a, d, d, r, e, s, s, :, , f, ., s, c, o, t, t, @, s, u, s, s, e, x, ., a, c, ., u, k, .

Keywords

Humans, Neoplasms, Benzimidazoles, Protein Kinase C, Antineoplastic Agents, Protein Kinase Inhibitors, Crystallography, X-Ray, Molecular Structure, Structure-Activity Relationship, Dose-Response Relationship, Drug, Models, Molecular, Drug Development