45 articles for U Bömer
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
HEXAHYDROPYRIDO[4,3-B]INDOLYL KETONE DERIVATIVES USEFUL AS CGAS MODULATORS

Ventus Therapeutics U.S.
SALT OF 3,4-DIHYDROISOQUINOLINE COMPOUND AND USE THEREOF

CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang)
HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS

Chiesi Farmaceutici
Compounds and probes for imaging huntingtin protein

CHDI Foundation, Inc.
PREPARATION OF BIARYL RING-LINKED AROMATIC HETEROCYCLIC DERIVATIVE AS IMMUNOMODULATOR AND USE THEREOF

Shanghai Longwood Biopharmaceuticals
Pyrazolopyridine Compounds and Methods of Inhibiting IRE1 Using Same

Optikira
PYRROLO[2,1-F][1,2,4]TRIAZINES AND PREPARATION AND USES THEREOF

Biosplice Therapeutics
CaMKII inhibitors and uses thereof

The Johns Hopkins University
Bicyclic amide compounds and methods of use thereof

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

Auckland Uniservices
Spirocycle compounds and methods of making and using same

Lundbeck La Jolla Research Center
Imidazolepyridine compounds and uses thereof

Novartis
Kinase inhibitors

Topivert Pharma
C2-azaspiro iminothiazine dioxides as BACE inhibitors, compositions, and their use

Merck Sharp & Dohme
Synthesis and characterization of 5,7-dihydroxyflavanone derivatives as novel protein tyrosine phosphatase 1B inhibitors.

Yanbian University College of Pharmacy
Compounds as tyrosine kinase modulators

Allergan
Design, synthesis, cyclooxygenase inhibition and biological evaluation of new 1,3,5-triaryl-4,5-dihydro-1H-pyrazole derivatives possessing amino/methanesulfonyl pharmacophore.

Beni-Suef University
Structural Insights into the Inhibition of Tubulin by the Antitumor Agent 4ß-(1,2,4-triazol-3-ylthio)-4-deoxypodophyllotoxin.

Huazhong Agricultural University
Role of the two structural domains from the periplasmic Escherichia coli histidine-binding protein HisJ.

University of Calgary
Identification of human T2R receptors that respond to bitter compounds that elicit the bitter taste in compositions, and the use thereof in assays to identify compounds that inhibit (block) bitter taste in compositions and use thereof

Senomyx
Synthesis of novel bisindolylmethanes: New carbonic anhydrase II inhibitors, docking, and 3D pharmacophore studies.

Universiti Teknologi Mara (Uitm)
Sepiapterin reductase inhibitors for the treatment of pain

Solace Pharmaceuticals
N1/N2-lactam acetyl-CoA carboxylase inhibitors

Pfizer
Selective androgen receptor modulators

Radius Health
Heterocyclic derivatives

Novartis
Triazinoindole analogs as potent inhibitors of a-glucosidase: synthesis, biological evaluation and molecular docking studies.

Hazara University
Nitrogen heterocycle derivatives, preparation thereof and application thereof in human therapeutics

Pierre Fabre Medicament
Selective glycosidase inhibitors and uses thereof

Simon Fraser University
Substituted bicyclic heteroaryl compounds

Bristol-Myers Squibb
Pyridyl piperidine orexin receptor antagonists

Merch Sharp & Dohme
Inhibitors of JNK

Roche Palo Alto
Pyrazolothiazole compound

Eisai R&D Management
Pyrrolidine derivatives

Hoffmann-La Roche
Adenosine compounds and their use thereof

Inotek Pharmaceuticals
Selective indole-based ECE inhibitors: synthesis and pharmacological evaluation.

Bayer Healthcare
Stable expression of a synthetic gene for the human motilin receptor: use in an aequorin-based receptor activation assay.

Kosan Biosciences
Pharmacological profile of YM087, a novel potent nonpeptide vasopressin V1A and V2 receptor antagonist, in vitro and in vivo.

Yamanouchi Pharmaceutical
Biochemical and pharmacological characterization of mu, delta and kappa 3 opioid receptors expressed in BE(2)-C neuroblastoma cells.

Memorial Sloan-Kettering Cancer Center
Stable expression of human H1-histamine-receptor cDNA in Chinese hamster ovary cells. Pharmacological characterisation of the protein, tissue distribution of messenger RNA and chromosomal localisation of the gene.

UniversitÉ
Dynamic deconvolution of a pre-equilibrated dynamic combinatorial library of acetylcholinesterase inhibitors.

UniversitÉ
Specific binding of prostaglandin D2 to rat brain synaptic membrane. Occurrence, properties, and distribution.

Kyoto University
Affinities of fluoxetine, its enantiomers, and other inhibitors of serotonin uptake for subtypes of serotonin receptors.

Eli Lilly