17 articles for IV Efremov
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
11
Discovery and optimization of a novel spiropyrrolidine inhibitor ofß-secretase (BACE1) through fragment-based drug design.

Pfizer
34
1-[(1-methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 positive allosteric modulators for the treatment of psychosis.

Pfizer
6
Discovery of Clinical Candidate PF-06648671: A Potent γ-Secretase Modulator for the Treatment of Alzheimer's Disease.

Pfizer
14
Design and optimization of a series of 4-(3-azabicyclo[3.1.0]hexan-3-yl)pyrimidin-2-amines: Dual inhibitors of TYK2 and JAK1.

Pfizer
19
Dual Inhibition of TYK2 and JAK1 for the Treatment of Autoimmune Diseases: Discovery of (( S)-2,2-Difluorocyclopropyl)((1 R,5 S)-3-(2-((1-methyl-1 H-pyrazol-4-yl)amino)pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl)methanone (PF-06700841).

Pfizer
20
Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active γ-secretase inhibitor.

Pfizer
23
Metabolism-directed design of oxetane-containing arylsulfonamide derivatives as γ-secretase inhibitors.

Pfizer
92
N-((HET)arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors

Kalvista Pharmaceuticals
5
Synthesis and biological activity of progesterone derivatives as 5alpha-reductase inhibitors, and their effect on hamster prostate weight.

Universidad Nacional Autonoma De Mexico
9
Phosphonate derivatives and methods of use thereof in the treatment of Alzheimer's disease

University of Kansas
62
Structural determinants of Tau aggregation inhibitor potency.

The Ohio State University
2
Trifluoromethyl pyrazolyl guanidine F1F0-ATPase inhibitors and therapeutic uses thereof

Lycera
87
5-substituted indazoles as kinase inhibitors

Abbvie
70
1,3,5-triazine-2-amine derivatives, preparation thereof and diagnostic and therapeutic use thereof

Sanofi
130
5-alkynyl-pyridines

Boehringer Ingelheim International
1
Novel cyclic peptide agonist of high potency and selectivity for the type II vasoactive intestinal peptide receptor.

University of California San Francisco