27 articles for B Bader
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Discovery of potent SOS1 inhibitors that block RAS activation via disruption of the RAS-SOS1 interaction.

Bayer AG
Novel Mps1 Kinase Inhibitors with Potent Antitumor Activity.

Bayer Pharma AG
Novel Class of Potent and Cellularly Active Inhibitors Devalidates MTH1 as Broad-Spectrum Cancer Target.

Bayer AG
BAY-8400: A Novel Potent and Selective DNA-PK Inhibitor which Shows Synergistic Efficacy in Combination with Targeted Alpha Therapies.

Bayer
Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 Kinase.

Bayer
Damage Incorporated: Discovery of the Potent, Highly Selective, Orally Available ATR Inhibitor BAY 1895344 with Favorable Pharmacokinetic Properties and Promising Efficacy in Monotherapy and in Combination Treatments in Preclinical Tumor Models.

Bayer
Discovery of BAY-985, a Highly Selective TBK1/IKKε Inhibitor.

Bayer
CRYSTAL FORM OF PYRROLOPYRIMIDINE COMPOUND AND PREPARATION METHOD FOR CRYSTAL FORM

Zhejiang Longcharm Bio-Tech Pharma. Co.
Compounds and probes for imaging huntingtin protein

CHDI Foundation, Inc.
Leucine-rich repeat kinase 2 (LRRK2) inhibitors

H. Lundbeck
SMALL-MOLECULE MODULATORS OF THE ORPHAN NUCLEAR RECEPTOR TLX

Baylor College of Medicine
GALECTIN-3 INHIBITING 2-HYDROXYCYCLOALKANE-1-CARBAMOYL DERIVATIVES

Idorsia Pharmaceuticals
Crystalline succinate salt of 6-(6-aminopyrazin-2-yl)-n-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyrazin-8-amine

Kronos Bio
Inhibitors of tryptophan dioxygenases (IDO1 and TDO) and their use in therapy

Auckland Uniservices
Substituted [5,6]cyclic-4(3H)-pyrimidinones as anticancer agents

Zenji Research Laboratories
Imidazolepyridine compounds and uses thereof

Novartis
GLS1 inhibitors for treating disease

The University of Texas System
Cinnoline derivatives useful as CB-1 receptor inverse agonists

Janssen Pharmaceutica
Molecular docking studies and biological evaluation of 1,3,4-thiadiazole derivatives bearing Schiff base moieties as tyrosinase inhibitors.

Shaoyang University
Fused heterocyclic derivative, medicinal composition containing the same, and medicinal use thereof

Kissei Pharmaceutical
Design, synthesis, biological evaluation, and molecular docking of novel benzopyran and phenylpyrazole derivatives as Akt inhibitors.

Zhejiang University
Selective androgen receptor modulators

Radius Health
Histone deacetylase inhibitors, process for preparation and uses thereof

Zhejiang Hisun Pharmaceutical
Heterocyclic pyrazole compounds, method for preparing the same and use thereof

Development Center For Biotechnology
Benzoxazines, benzothiazines, and related compounds having NOS inhibitory activity

Neuraxon
Urokinase inhibitors, production and use thereof

The Medicines