21 articles for I Mochalkin
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Exploration of 4,4-disubstituted pyrrolidine-1,2-dicarboxamides as potent, orally active Factor Xa inhibitors with extended duration of action.

Pfizer
Identification of Clinical Candidate M2698, a Dual p70S6K and Akt Inhibitor, for Treatment of PAM Pathway-Altered Cancers.

Emd Serono Research & Development Institute
Discovery of 4-aminopyrimidine analogs as highly potent dual P70S6K/Akt inhibitors.

Emd Serono Research and Development Institute
Discovery of Evobrutinib: An Oral, Potent, and Highly Selective, Covalent Bruton's Tyrosine Kinase (BTK) Inhibitor for the Treatment of Immunological Diseases.

Merck
Structure based design of an in vivo active hydroxamic acid inhibitor of P. aeruginosa LpxC.

Pfizer
Discovery of a novel series of pyridine and pyrimidine carboxamides as potent and selective covalent inhibitors of Btk.

Emd Serono Research & Development Institute
Optimization of the efflux ratio and permeability of covalent irreversible BTK inhibitors.

Emd Serono Research & Development Institute
Discovery of potent, highly selective covalent irreversible BTK inhibitors from a fragment hit.

Emd Serono Research & Development Institute
Recent progress towards clinically relevant ATP-competitive Akt inhibitors.

Merck
Fluorinated tetrahydronaphthyridinyl nonanoic acid derivatives and uses thereof

Ocuterra Therapeutics
Heteroaryl inhibitors of PAD4

Padlock Therapeutics
ASK1 inhibitor and preparation method and use thereof

Fuijan Cosunter Pharmaceutical
Compounds as inhibitors of DNA methyltransferases

FundaciÓN Para La InvestigaciÓN MÉDica Aplicada
Pyridyl analogs of 1-(2-cyano-3,12-dioxooleana-1,9(11)dien-28-oyl) imidazole

Dartmouth College
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH

Novartis
Inhibitors of SYK

Hoffmann-La Roche
Amino pyridine derivatives as phosphatidylinositol 3-kinase inhibitors

Novartis
Substituted [1,2,4]triazolo[4,3-a]pyrazines as PARP-1 inhibitors

Shanghai Institute of Material Medica, Chinese Academy of Sciences
Pyrimidooxazocine derivatives as mTOR-inhibitors

Sanofi
Benzoxazepin compounds selective for PI3K P110 delta and methods of use

Genentech
Cyclic inhibitors of 11BETA-hydroxysteroid dehydrogenase 1

Vitae Pharmaceuticals