26 articles for M Teng
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Identification of bacteria-selective threonyl-tRNA synthetase substrate inhibitors by structure-based design.

Trius Therapeutics
Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors.

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.

Biogen Idec
Small-molecule agonists for the glucagon-like peptide 1 receptor.

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.

Pfizer
Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I).

Biogen Idec
Synthesis and biological activity of 1,2,3,4-tetrahydroquinoline and 3,4-(1H)-dihydroquinolin-2-one analogs of retinoic acid

TBA
Small molecule ago-allosteric modulators of the human glucagon-like peptide-1 (hGLP-1) receptor.

Pfizer
Unlocking DCAFs To Catalyze Degrader Development: An Arena for Innovative Approaches.

Baylor College of Medicine
The Pursuit of Enzyme Activation: A Snapshot of the Gold Rush.

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.

Novo Nordisk
Synthesis and biological activity of retinoic acid receptor-alpha specific amides.

Allergan
Rationally Designed Covalent BCL6 Inhibitor That Targets a Tyrosine Residue in the Homodimer Interface.

Dana-Farber Cancer Institute
Identification of a retinoic acid receptor alpha subtype specific agonist.

Allergan
Identification of highly potent retinoic acid receptor alpha-selective antagonists.

Allergan
Discovery of aminocyclohexene analogues as selective and orally bioavailable hNav1.7 inhibitors for analgesia.

Wuxi Apptec (Shanghai)
The discovery of tetrahydropyridine analogs as hNav1.7 selective inhibitors for analgesia.

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 ingredient

Digmbio
Heteroaromatic amide derivative and medicament containing the same

Kaken Pharmaceutical Co.
TLR8 agonist

Chia Tai Tianqing Pharmaceutical Group
PYRIMIDINE SMALL-MOLECULE COMPOUND AND APPLICATION THEREOF

Wenzhou Medical University
1-Pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and compositions thereof for inhibiting the activity of SHP2

Novartis
Linear glycosidase inhibitors

Asceneuron
Heterocyclic inhibitors of PTPN11

University Of Texas
1-(4-Methane(amino)sulfonylphenyl)-3-(4-substituted-phenyl)-5-(4-trifluoromethylphenyl)-1H-2-pyrazolines/pyrazoles as potential anti-inflammatory agents.

Beni-Suef University
Development of new and selective Trypanosoma cruzi trans-sialidase inhibitors from sulfonamide chalcones and their derivatives.

University of British Columbia