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26 articles for M Teng


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design.EBI
Trius Therapeutics
Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors.EBI
Biogen Idec
Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1.EBI
Biogen Idec
Small-molecule agonists for the glucagon-like peptide 1 receptor.EBI
Novo Nordisk Als
Structure-based design and synthesis of (5-arylamino-2H-pyrazol-3-yl)-biphenyl-2',4'-diols as novel and potent human CHK1 inhibitors.EBI
Pfizer
Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I).EBI
Biogen Idec
 
Synthesis and biological activity of 1,2,3,4-tetrahydroquinoline and 3,4-(1H)-dihydroquinolin-2-one analogs of retinoic acidEBI
TBA
Small molecule ago-allosteric modulators of the human glucagon-like peptide-1 (hGLP-1) receptor.EBI
Pfizer
Unlocking DCAFs To Catalyze Degrader Development: An Arena for Innovative Approaches.EBI
Baylor College of Medicine
The Pursuit of Enzyme Activation: A Snapshot of the Gold Rush.EBI
Baylor College of Medicine
Optimization of alkylidene hydrazide based human glucagon receptor antagonists. Discovery of the highly potent and orally available 3-cyano-4-hydroxybenzoic acid [1-(2,3,5,6-tetramethylbenzyl)-1H-indol-4-ylmethylene]hydrazide.EBI
Novo Nordisk
Synthesis and biological activity of retinoic acid receptor-alpha specific amides.EBI
Allergan
Rationally Designed Covalent BCL6 Inhibitor That Targets a Tyrosine Residue in the Homodimer Interface.EBI
Dana-Farber Cancer Institute
Identification of a retinoic acid receptor alpha subtype specific agonist.EBI
Allergan
Identification of highly potent retinoic acid receptor alpha-selective antagonists.EBI
Allergan
Discovery of aminocyclohexene analogues as selective and orally bioavailable hNav1.7 inhibitors for analgesia.EBI
Wuxi Apptec (Shanghai)
The discovery of tetrahydropyridine analogs as hNav1.7 selective inhibitors for analgesia.EBI
Wuxi Apptec (Shanghai)
Isoquinolinone derivatives, method for preparing the same, and pharmaceutical composition for preventing or treating poly(ADP-ribose) polymerase-1-related diseases, comprising the same as active ingredientBDB
Digmbio
Heteroaromatic amide derivative and medicament containing the sameBDB
Kaken Pharmaceutical Co.
TLR8 agonistBDB
Chia Tai Tianqing Pharmaceutical Group
PYRIMIDINE SMALL-MOLECULE COMPOUND AND APPLICATION THEREOFBDB
Wenzhou Medical University
1-Pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and compositions thereof for inhibiting the activity of SHP2BDB
Novartis
Linear glycosidase inhibitorsBDB
Asceneuron
Heterocyclic inhibitors of PTPN11BDB
University Of Texas
1-(4-Methane(amino)sulfonylphenyl)-3-(4-substituted-phenyl)-5-(4-trifluoromethylphenyl)-1H-2-pyrazolines/pyrazoles as potential anti-inflammatory agents.BDB
Beni-Suef University
Development of new and selective Trypanosoma cruzi trans-sialidase inhibitors from sulfonamide chalcones and their derivatives.BDB
University of British Columbia