S. Leclerc

发表

Pyrazolo[3,4-b]quinoxalines. A new class of cyclin-dependent kinases inhibitors.

L. Meijer, A. Monge, I. Aldana, 2002, Bioorganic & medicinal chemistry.

Synthesis of a new series of purine derivatives and their anti‐cyclin‐dependent kinase activities

L. Meijer, M. Legraverend, S. Leclerc, 2001 .

Properties and potential-applications of chemical inhibitors of cyclin-dependent kinases.

L Meijer, L. Meijer, M. Leost, 1999, Pharmacology & therapeutics.

Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases

Doris Marko, Ralph Hoessel, Gerhard Eisenbrand, 1999, Nature Cell Biology.

Indirubins Inhibit Glycogen Synthase Kinase-3β and CDK5/P25, Two Protein Kinases Involved in Abnormal Tau Phosphorylation in Alzheimer's Disease

P. Greengard, G. Snyder, J. Bibb, 2001, The Journal of Biological Chemistry.

Synthesis of a New Series of Purine Derivatives and Their Anti-Cyclin-Dependent Kinase Activities.

L. Meijer, M. Legraverend, S. Leclerc, 2001 .

Alkyl and alkoxyethyl antineoplastic phospholipids.

H. Fiebig, A. Tsotinis, T. Calogeropoulou, 1996, Journal of medicinal chemistry.

Screening the active constituents of Chinese medicinal herbs as potent inhibitors of Cdc25 tyrosine phosphatase, an activator of the mitosis-inducing p34cdc2 kinase.

L. Meijer, J. Cheng, Su-zhan Zhang, 2005, Journal of Zhejiang University. Science. B.

Direct investigation of halogen bonds by solid-state multinuclear magnetic resonance spectroscopy and molecular orbital analysis.

D. L. Bryce, I. Korobkov, Jasmine Viger‐Gravel, 2014, Journal of the American Chemical Society.

Correlation between 13C chemical shifts and the halogen bonding environment in a series of solid para-diiodotetrafluorobenzene complexes

D. L. Bryce, I. Korobkov, Jasmine Viger‐Gravel, 2013 .

Flavonoids as cycline-dependent kinase inhibitors: inhibition of cdc 25 phosphatase activity by flavonoids belonging to the quercetin and kaempferol series.

S. Leclerc, S. Mitaku, N. Aligiannis, 2001, Planta medica.

Antitumor and Hypoglycemic Activities of Polysaccharides from the Sclerotia and Mycelia of Inonotus obliquus (Pers.: Fr.) Pil. (Aphyllophoromycetideae)

Laurent Meijer, Cun Zhuang, Takashi Mizuno, 1999 .

Indirubins inhibit glycogen synthase kinase-3 beta and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors?

G L Snyder, G Eisenbrand, L Meijer, 2001, The Journal of biological chemistry.

Cyclin-Dependent Kinases and Their Chemical Inhibitors: New Targets and Tools for the Study of the Testis?

L. Meijer, M. Leost, M. Garnier, 2000 .

Correlation of 3-isobutyl-2-methoxypyrazine to 3-isobutyl-2-hydroxypyrazine during maturation of bell pepper (Capsicum annuum) and wine grapes (Vitis vinifera).

G. Sacks, Imelda Ryona, S. Leclerc, 2010, Journal of agricultural and food chemistry.

Inhibition of cyclin-dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitine.

S H Kim, L Meijer, L. Meijer, 1997, European journal of biochemistry.

Structure-activity relationships and inhibitory effects of various purine derivatives on the in vitro growth of Plasmodium falciparum.

L. Meijer, N. Gray, S. Leclerc, 2001, Biochemical pharmacology.

Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors.

S H Kim, N S Gray, L Wodicka, 1998, Science.

Inhibition of cyclin-dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitine.

L. Meijer, Sung-Hou Kim, M. Strnad, 1997, European journal of biochemistry.

Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors.

L. Meijer, S. Leclerc, V. Favaudon, 1999, Bioorganic & medicinal chemistry.

Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors.

E. Bisagni, M. Legraverend, N. Giocanti, 1999, Bioorganic & medicinal chemistry.