BindingDB logo
myBDB logout

15 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
25757604 2 (18)F-AmBF3-MJ9: a novel radiofluorinated bombesin derivative for prostate cancer imaging.EBI Bc Cancer Agency
23992105 4 Studies toward the development of new silicon-containing building blocks for the direct (18)F-labeling of peptides.EBI Institute Of Technology (Eth) Zurich
23265893 7 Heterobivalent dual-target probe for targeting GRP and Y1 receptors on tumor cells.EBI The Ohio State University
18329268 2 Targeting gastrin-releasing peptide receptors of prostate cancer cells for photodynamic therapy with a phthalocyanine-bombesin conjugate.EBI Universit£
9873586 50 PD 176252--the first high affinity non-peptide gastrin-releasing peptide (BB2) receptor antagonist.EBI Cambridge University Forvie Site
 42 PD 165929 the first high affinity non-peptide neuromedin-B (NMB) receptor selective antagonistEBI TBA
24900253 28 Discovery of MK-5046, a Potent, Selective Bombesin Receptor Subtype-3 Agonist for the Treatment of ObesityEBI TBA
20219372 114 Synthesis and SAR of derivatives based on 2-biarylethylimidazole as bombesin receptor subtype-3 (BRS-3) agonists for the treatment of obesity.EBI Merck Research Laboratories
20167483 90 Discovery of substituted biphenyl imidazoles as potent, bioavailable bombesin receptor subtype-3 agonists.EBI Merck Research Laboratories
19553112 39 Discovery and optimization of a novel Neuromedin B receptor antagonist.EBI Amgen
19522464 3 Structural assessment and biological evaluation of two N3S bombesin derivatives.EBI Institutes Of Radioisotopes-Radiodiagnostic Products And Biology
18818070 28 Discovery of small molecule agonists for the bombesin receptor subtype 3 (BRS-3) based on an omeprazole lead.EBI Glaxosmithkline
15634004 20 Potent bombesin-like peptides for GRP-receptor targeting of tumors with 99mTc: a preclinical study.EBI National Center For Scientific Research Demokritos
12723954 47 Design of selective peptidomimetic agonists for the human orphan receptor BRS-3.EBI Technische UniversitäT MüNchen
26833890 18 Synthesis, Biological Evaluation, and Molecular Docking of 8-imino-2-oxo-2H,8H-pyrano[2,3-f]chromene Analogs: New Dual AChE Inhibitors as Potential Drugs for the Treatment of Alzheimer's Disease.BDB Yogi Vemana University