Bahar M, Kim H, Kim D
Signal Transduct Target Ther. 2023; 8(1):455.
PMID: 38105263
PMC: 10725898.
DOI: 10.1038/s41392-023-01705-z.
Luukkonen S, Meijer E, Tricarico G, Hofmans J, Stouten P, van Westen G
J Chem Inf Model. 2023; 63(12):3688-3696.
PMID: 37294674
PMC: 10302492.
DOI: 10.1021/acs.jcim.3c00132.
Ismail M, Abusaif M, El-Gaby M, Ammar Y, Ragab A
RSC Adv. 2023; 13(18):12589-12608.
PMID: 37101951
PMC: 10123497.
DOI: 10.1039/d3ra01635h.
Khine M, Sakurai K
Cancers (Basel). 2023; 15(7).
PMID: 37046746
PMC: 10093635.
DOI: 10.3390/cancers15072086.
Zhong Y, Shen C, Wu H, Xu T, Luo L
Interdiscip Sci. 2022; 14(3):775-785.
PMID: 35536538
DOI: 10.1007/s12539-022-00523-1.
Protein Flexibility and Dissociation Pathway Differentiation Can Explain Onset of Resistance Mutations in Kinases.
Shekhar M, Smith Z, Seeliger M, Tiwary P
Angew Chem Int Ed Engl. 2022; 61(28):e202200983.
PMID: 35486370
PMC: 9256798.
DOI: 10.1002/anie.202200983.
Identification of Sorafenib as a Treatment for Type 1 Diabetes.
Zeng Q, Song J, Wang D, Sun X, Xiao Y, Zhang H
Front Immunol. 2022; 13:740805.
PMID: 35242127
PMC: 8886732.
DOI: 10.3389/fimmu.2022.740805.
Stereochemistry of the methyl-idene-bridged quinazoline-iso-quinoline alkaloid 3-{[6,7-dimeth-oxy-1-(4-nitro-phen-yl)-1,2,3,4-tetra-hydro-isoquinolin-2-yl]methyl-idene}-1,2,3,9-tetra-hydro-pyrrolo-[2,1-]quinazolin-9-one methanol monosolvate.
Tojiboev A, Zhurakulov S, Vinogradova V, Englert U, Wang R
Acta Crystallogr E Crystallogr Commun. 2020; 76(Pt 6):914-919.
PMID: 32523763
PMC: 7273985.
DOI: 10.1107/S2056989020006696.
Lenvatinib in Management of Solid Tumors.
Hao Z, Wang P
Oncologist. 2020; 25(2):e302-e310.
PMID: 32043789
PMC: 7011622.
DOI: 10.1634/theoncologist.2019-0407.
Controlling the Circadian Clock with High Temporal Resolution through Photodosing.
Kolarski D, Sugiyama A, Breton G, Rakers C, Ono D, Schulte A
J Am Chem Soc. 2019; 141(40):15784-15791.
PMID: 31509406
PMC: 6787957.
DOI: 10.1021/jacs.9b05445.
Kinase inhibitors: the road ahead.
Ferguson F, Gray N
Nat Rev Drug Discov. 2018; 17(5):353-377.
PMID: 29545548
DOI: 10.1038/nrd.2018.21.
Discovery of a series of novel phenylpiperazine derivatives as EGFR TK inhibitors.
Sun J, Wang X, Lv P, Zhu H
Sci Rep. 2015; 5:13934.
PMID: 26349898
PMC: 4563558.
DOI: 10.1038/srep13934.
Crystal structure of 2-benzamido-N-(2,2-di-eth-oxy-eth-yl)benzamide.
Ouahrouch A, Taourirte M, Lazrek H, Engels J, Bolte M
Acta Crystallogr E Crystallogr Commun. 2015; 71(Pt 3):o214-5.
PMID: 25844255
PMC: 4350703.
DOI: 10.1107/S2056989015003370.
Structural basis of valmerins as dual inhibitors of GSK3β/CDK5.
Li X, Wang X, Tian Z, Zhao H, Liang D, Li W
J Mol Model. 2014; 20(9):2407.
PMID: 25142337
DOI: 10.1007/s00894-014-2407-1.
International Union of Basic and Clinical Pharmacology. XC. multisite pharmacology: recommendations for the nomenclature of receptor allosterism and allosteric ligands.
Christopoulos A, Changeux J, Catterall W, Fabbro D, Burris T, Cidlowski J
Pharmacol Rev. 2014; 66(4):918-47.
PMID: 25026896
PMC: 11060431.
DOI: 10.1124/pr.114.008862.
New frontiers in kinases: special issue.
Botta M
ACS Med Chem Lett. 2014; 5(4):270.
PMID: 24900819
PMC: 4027606.
DOI: 10.1021/ml500071m.
Modeling CaMKII in cardiac physiology: from molecule to tissue.
Onal B, Unudurthi S, Hund T
Front Pharmacol. 2014; 5:9.
PMID: 24550832
PMC: 3912431.
DOI: 10.3389/fphar.2014.00009.
Optimization of substituted 6-salicyl-4-anilinoquinazoline derivatives as dual EGFR/HER2 tyrosine kinase inhibitors.
Li D, Qin Y, Sun J, Li J, Fang F, Du Q
PLoS One. 2013; 8(8):e69427.
PMID: 23936329
PMC: 3731256.
DOI: 10.1371/journal.pone.0069427.
New Test System for Serine/Threonine Protein Kinase Inhibitors Screening: E. coli APHVIII/Pk25 design.
Bekker O, Alekseeva M, Osolodkin D, Palyulin V, Elizarov S, Zefirov N
Acta Naturae. 2012; 2(3):110-21.
PMID: 22649658
PMC: 3347566.
N⁴-Aryl-6-substitutedphenylmethyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamines as receptor tyrosine kinase inhibitors.
Gangjee A, Kurup S, Ihnat M, Thorpe J, Disch B
Bioorg Med Chem. 2011; 20(2):910-4.
PMID: 22204741
PMC: 3276368.
DOI: 10.1016/j.bmc.2011.11.058.