13 articles for C Gardelli
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Dihydroxypyrimidine-4-carboxamides as novel potent and selective HIV integrase inhibitors.

P. Angeletti S.P.A. (Merck Research Laboratories)
The design and enzyme-bound crystal structure of indoline based peptidomimetic inhibitors of hepatitis C virus NS3 protease.

Mrl Rome
Capped dipeptide phenethylamide inhibitors of the HCV NS3 protease.

Irbm, Mrl Rome
Capped dipeptide alpha-ketoacid inhibitors of the HCV NS3 protease.

Irbm, Mrl Rome
Identification and Optimization of Pyrrolidine Derivatives as Highly Potent Ghrelin Receptor Full Agonists.

Astrazeneca
Development of 2-pyrrolidinyl-N-methyl pyrimidones as potent and orally bioavailable HIV integrase inhibitors.

Irbm-Mrl
Dihydroxy-pyrimidine and N-methylpyrimidone HIV-integrase inhibitors: improving cell based activity by the quaternarization of a chiral center.

Irbm-Merck Research Laboratories Rome
Identification and Pharmacological Profile of an Indane Based Series of Ghrelin Receptor Full Agonists.

Astrazeneca
Discovery of Highly Isoform Selective Orally Bioavailable Phosphoinositide 3-Kinase (PI3K)-γ Inhibitors.

Pharmaron-Beijing
Sulfonyl piperidine derivatives and their use for treating prokineticin mediated diseases

Takeda Pharmaceutical
Novel tacrine-melatonin hybrids as dual-acting drugs for Alzheimer disease, with improved acetylcholinesterase inhibitory and antioxidant properties.

Instituto De Quimica Medica (Csic)
SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylcholinesterase inhibitors: synthesis, enzyme inhibitory activity, QSAR, and structure-based CoMFA of tacrine analogues.

University of Bologna
Synthesis and evaluation of tacrine-E2020 hybrids as acetylcholinesterase inhibitors for the treatment of Alzheimer's disease.

Shanghai Institute of Materia Medica