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Kinase Inhibitory sentence examples within Raf Kinase Inhibitory



Limited inhibition of multiple nodes in a driver network blocks metastasis


Integrated computational approaches on pyrazoline derivatives as B-Raf kinase inhibitors for the development of novel anticancer agents

Kinase Inhibitory sentence examples within Protein Kinase Inhibitory



Evaluation of Novel Substituted Furopyridines as Inhibitors of Protein Kinases Related to Tau Pathology in Alzheimer´s Disease.


Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor

Kinase Inhibitory sentence examples within Tyrosine Kinase Inhibitory



Musarin, a novel protein with tyrosine kinase inhibitory activity from Trametes versicolor, accepted inhibits colorectal cancer stem cell growth.


Persicoimidate isolated from Allium ampeloprasum Subsp. Persicum with Apoptotic effects against Breast cancer cell lines



Kinase Inhibitory sentence examples within 1 Kinase Inhibitory



Protective effect of Raf-1 kinase inhibitory protein on diabetic retinal neurodegeneration through P38-MAPK pathway.


Possible biomarkers for predicting lymph node metastasis of esophageal squamous cell carcinoma: a review

Kinase Inhibitory sentence examples within E Kinase Inhibitory



Chiral Pyrazolo[4,3-e][1,2,4]triazine Sulfonamides—Their Biological Activity, Lipophilicity, Protein Affinity, and Metabolic Transformations


Synthesis of 4,6-disubstituted pyrazolo[3,4-d]pyrimidine analogues: Cyclin-dependent kinase 2 (CDK2) inhibition, molecular docking and anticancer evaluation

Kinase Inhibitory sentence examples within 1r Kinase Inhibitory



Discovery of 3-(thiophen/thiazole-2-ylthio)pyridine derivatives as multitarget anticancer agents


Design, synthesis, and biological evaluation of novel 3‐(thiophen‐2‐ylthio)pyridine derivatives as potential multitarget anticancer agents

Kinase Inhibitory sentence examples within Excellent Kinase Inhibitory



Design, synthesis and biological evaluation of aminopyrimidine derivatives bearing a 4,5,6,7-tetrahydrothieno [3,2-c]pyridine as potent EGFR inhibitors.


Design, synthesis and biological evaluation of AZD9291 derivatives as selective and potent EGFRL858R/T790M inhibitors.

Kinase Inhibitory sentence examples within Egfr Kinase Inhibitory



New picolinic acid derivatives: Synthesis, docking study and anti-EGFR kinase inhibitory effect


Design, synthesis and docking studies of benzimidazole derivatives as potential EGFR inhibitors.

Kinase Inhibitory sentence examples within Met Kinase Inhibitory



Transforming Type II to Type I c-Met kinase inhibitors via combined scaffold hopping and structure-guided synthesis of new series of 1,3,4-thiadiazolo[2,3-c]-1,2,4-triazin-4-one derivatives.


Novel Crizotinib–GnRH Conjugates Revealed the Significance of Lysosomal Trapping in GnRH-Based Drug Delivery Systems

Kinase Inhibitory sentence examples within Dual Kinase Inhibitory



Design, synthesis, biological evaluation, and docking studies of novel (imidazol-5-yl)pyrimidine-based derivatives as dual BRAFV600E/p38α inhibitors.


Structure based designing of triazolopyrimidone-based reversible inhibitors for kinases involved in NSCLC.

Kinase Inhibitory sentence examples within Selective Kinase Inhibitory



The synthesis and bioactivity of pyrrolo[2,3-d]pyrimidine derivatives as tyrosine kinase inhibitors for NSCLC cells with EGFR mutations.


The Intraocular Pressure Lowering Effect of a Dual Kinase Inhibitor (ITRI-E-(S)4046) in Ocular Hypertensive Animal Models.

Kinase Inhibitory sentence examples within Abl1 Kinase Inhibitory



Structure-Based Design, Synthesis, and Evaluation of Anti-CML Activity of the Quinolinequinones as LY83583 Analogs.


Design, synthesis and investigation of the mechanism of action underlying anti-leukemic effects of the quinolinequinones as LY83583 analogs.

Kinase Inhibitory sentence examples within kinase inhibitory activity



Anti-inflammatory and Anti-anemic Properties of Nanocomplex Based on C60 Fullerenes and Pyrrole Core under Acute Ulcerative Colitis in Rats


The synthesis and bioactivity of pyrrolo[2,3-d]pyrimidine derivatives as tyrosine kinase inhibitors for NSCLC cells with EGFR mutations.

Kinase Inhibitory sentence examples within kinase inhibitory protein



New Insights into CDK Regulators: Novel Opportunities for Cancer Therapy.


Limited inhibition of multiple nodes in a driver network blocks metastasis

Kinase Inhibitory sentence examples within kinase inhibitory potency



Cyclic Peptides as Protein Kinase Inhibitors: Structure-Activity Relationship and Molecular Modeling


Chiral Pyrazolo[4,3-e][1,2,4]triazine Sulfonamides—Their Biological Activity, Lipophilicity, Protein Affinity, and Metabolic Transformations

Kinase Inhibitory sentence examples within kinase inhibitory effect



Target modulation and pharmacokinetics/pharmacodynamics translation of the BTK inhibitor poseltinib for model-informed phase II dose selection


Antitumor effects of berberine against EGFR, ERK1/2, P38 and AKT in MDA-MB231 and MCF-7 breast cancer cells using molecular modelling and in vitro study.

Kinase Inhibitory sentence examples within kinase inhibitory potential



Structure based designing of thiazolidinone-pyrimidine derivatives as ERK2 inhibitors: Synthesis and in vitro evaluation


Phytochemical analysis and versatile in vitro evaluation of antimicrobial, cytotoxic and enzyme inhibition potential of different extracts of traditionally used Aquilegia pubiflora Wall. Ex Royle

Kinase Inhibitory sentence examples within kinase inhibitory region



Corneal Application of R9-SOCS1-KIR Peptide Alleviates Endotoxin-Induced Uveitis


Suppressor of cytokine signaling-1 mimetic peptides attenuate lymphocyte activation in the MRL/lpr mouse autoimmune model

Kinase Inhibitory sentence examples within kinase inhibitory property



3-Alkenyl-2-oxindoles: Synthesis, antiproliferative and antiviral properties against SARS-CoV-2


Evaluation of Novel Substituted Furopyridines as Inhibitors of Protein Kinases Related to Tau Pathology in Alzheimer´s Disease.

Kinase Inhibitory sentence examples within kinase inhibitory assay



Synthesis, characterization, in vitro biological and computational evaluation of 5-benzyl-4-(benzylideneamino)-2H-1,2,4-triazole-3(4H)-thiones


20(S)-Protopanaxadiol blocks cell cycle progression by targeting epidermal growth factor receptor.


Safety of FLT3 inhibitors in patients with acute myeloid leukemia


Kinase Inhibitory 키나제 억제


Kinase Inhibitory 키나제 억제
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