C. Neagu

发表

Discovery of potent and selective reversible Bruton's tyrosine kinase inhibitors.

A. Bender, A. Goutopoulos, Xiaohua Zhu, 2021, Bioorganic & medicinal chemistry.

Large-Scale Assessment of Binding Free Energy Calculations in Active Drug Discovery Projects

Catherine Jorand Lebrun, Andrea Unzue Lopez, Daniel Kuhn, 2020, J. Chem. Inf. Model..

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

T. E. Richardson, F. Rohdich, B. Huck, 2021, Journal of medicinal chemistry.

Induction of sister chromatid exchange by 3,4-expoxybutane-1,2-diol in cultured human lymphocytes of different GSTT1 and GSTM1 genotypes.

H. Järventaus, H. Norppa, K. Pelin, 1996, Mutation research.

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

A. Follis, A. Goutopoulos, R. Grenningloh, 2018, Bioorganic & medicinal chemistry letters.

1-((3S,4S)-4-amino-1-(4-substituted-1,3,5-triazin-2-yl) pyrrolidin-3-yl)-5,5-difluoropiperidin-2-one inhibitors of DPP-4 for the treatment of type 2 diabetes.

R. McPherson, J. Treadway, D. Beebe, 2011, Bioorganic & medicinal chemistry letters.

Optimization of the efflux ratio and permeability of covalent irreversible BTK inhibitors.

A. Goutopoulos, R. Grenningloh, A. Gardberg, 2018, Bioorganic & medicinal chemistry letters.

Design and Synthesis of a Transition State Analog for the Ene Reaction between Maleimide and 1-Alkenes

Ari Yliniemelä, Gösta Brunow, Olle Teleman, 1995 .

N-benzylimidazole carboxamides as potent, orally active stearoylCoA desaturase-1 inhibitors.

C. Steppan, J. Litchfield, R. Trilles, 2011, Bioorganic & medicinal chemistry letters.

Synthesis and enzymatic incorporation of a novel, bicyclic pyrimidine nucleoside: a thymidine mimic

M. Mcdougall, D. Loakes, Daniel M. Brown, 2003 .

Synthesis and Some Biochemical Properties of a Novel 5,6,7,8‐Tetrahydropyrimido[4,5‐c]pyridazine Nucleoside

M. Mcdougall, D. Loakes, Daniel M. Brown, 2003 .

The discovery of novel calcium sensing receptor negative allosteric modulators.

J. Bauman, David A. Price, A. Kalgutkar, 2009, Bioorganic & medicinal chemistry letters.

Discovery of potent, highly selective covalent irreversible BTK inhibitors from a fragment hit.

A. Follis, A. Goutopoulos, R. Grenningloh, 2018, Bioorganic & medicinal chemistry letters.

Synthesis of enantiomerically pure 3-butene-1,2-diol derivatives via a sharpless asymmetric epoxidation route.

T. Hase, C. Neagu, 1993 .

Synthesis of Enantiomerically Pure 3‐Butene‐1,2‐diol Derivatives via a Sharpless Asymmetric Epoxidation Route.

T. Hase, C. Neagu, 1993 .

Butadiene monoxide and deoxyguanosine alkylation products at the N7-position.

K. Peltonen, R. Kostiainen, P. Koivisto, 1995, Carcinogenesis.

Discovery of 4-Aminopyrimidine Analogs as highly Potent Dual P70S6K/Akt Inhibitors.

Xuliang Jiang, B. Huck, E. Wilker, 2021, Bioorganic & medicinal chemistry letters.

The discovery of novel calcium sensing receptor negative allosteric modulators.

J. Bauman, A. Kalgutkar, V. Paralkar, 2009, Bioorganic & medicinal chemistry letters.