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Francesca Blasco
Observed names:
Blasco, Francesca,
F. BLASCO
Observed institutions:
Roche (Switzerland),
Novartis (Switzerland),
Novartis (Singapore),
Novartis Institutes for BioMedical Research,
Novartis Institute For Tropical Diseases,
Politecnico di Milano
show all 6
OpenAlex ID:
A5024405486
Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation
2013
·
Pascal Furet
, Vito Guagnano
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
483
Implementation of pharmacokinetic and pharmacodynamic strategies in early research phases of drug discovery and development at Novartis Institute of Biomedical Research
2014
·
Tove Tuntland
, Brian Ethell
, et al.
·
Frontiers in Pharmacology
·
238
PDF
A Cryptosporidium PI(4)K inhibitor is a drug candidate for cryptosporidiosis
2017
·
Ujjini H. Manjunatha
, Sumiti Vinayak
, et al.
·
Nature
·
207
PDF
Indolcarboxamide Is a Preclinical Candidate for Treating Multidrug-Resistant Tuberculosis
2013
·
Srinivasa P. S. Rao
, Suresh B. Lakshminarayana
, et al.
·
Science Translational Medicine
·
147
Direct inhibitors of InhA are active against Mycobacterium tuberculosis
2015
·
Ujjini H. Manjunatha
, Srinivasa P. S. Rao
, et al.
·
Science Translational Medicine
·
136
Potent and Selective Inhibition of Polycythemia by the Quinoxaline JAK2 Inhibitor NVP-BSK805
2010
·
Fabienne Baffert
, Catherine H. Régnier
, et al.
·
Molecular Cancer Therapeutics
·
120
Discovery of Dengue Virus NS4B Inhibitors
2015
·
Qing-Yin Wang
, Hongping Dong
, et al.
·
Journal of Virology
·
105
PDF
NITD-688, a pan-serotype inhibitor of the dengue virus NS4B protein, shows favorable pharmacokinetics and efficacy in preclinical animal models
2021
·
Stephanie A. Moquin
, Oliver Simon
, et al.
·
Science Translational Medicine
·
103
Activation of Peripheral Blood Mononuclear Cells by Dengue Virus Infection Depotentiates Balapiravir
2013
·
Yen-Liang Chen
, Nahdiyah Abdul Ghafar
, et al.
·
Journal of Virology
·
82
Lead Optimization of Spiropyrazolopyridones: A New and Potent Class of Dengue Virus Inhibitors
2015
·
Bin Zou
, Wai Ling Chan
, et al.
·
ACS Medicinal Chemistry Letters
·
73
The kinetic deuterium isotope effect as applied to metabolic deactivation of imatinib to the des-methyl metabolite, CGP74588
2013
·
Paul W. Manley
, Francesca Blasco
, et al.
·
Bioorganic & Medicinal Chemistry
·
52
Modulation of inflammation and pathology during dengue virus infection by p38 MAPK inhibitor SB203580
2014
·
Yilong Fu
, Andy Yip
, et al.
·
Antiviral Research
·
43
Discovery and SAR of potent, orally available 2,8-diaryl-quinoxalines as a new class of JAK2 inhibitors
2010
·
Carole Pissot-Soldermann
, Marc Gerspacher
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
41
Optimised method to estimate octanol water distribution coefficient (logD) in a high throughput format
2016
·
Ying Wei (Ivan) Low
, Francesca Blasco
, et al.
·
European Journal of Pharmaceutical Sciences
·
40
Trifluoromethyl vs. methyl ability to direct enantioselection in microbial reduction of carbonyl substrates.
1998
·
Alberto Arnone
, Rosanna Bernardi
, et al.
·
Tetrahedron
·
39
Design of novel aminopyrrolidine factor Xa inhibitors from a screening hit
2009
·
Katrin Groebke Zbinden
, Lilli Anselm
, et al.
·
European Journal of Medicinal Chemistry
·
37
Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: Optimising brain penetration
2007
·
Jens-Uwe Peters
, Thomas Lübbers
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
30
A Cyclic Phosphoramidate Prodrug of 2′-Deoxy-2′-Fluoro-2′- C -Methylguanosine for the Treatment of Dengue Virus Infection
2020
·
Ratna Karuna
, Fumiaki Yokokawa
, et al.
·
Antimicrobial Agents and Chemotherapy
·
29
PDF
Discovery of the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine scaffold as a novel, potent and selective GABAA α5 inverse agonist series
2009
·
Guido Achermann
, Theresa M. Ballard
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
28
Pharmacokinetics-Pharmacodynamics Analysis of Bicyclic 4-Nitroimidazole Analogs in a Murine Model of Tuberculosis
2014
·
Suresh B. Lakshminarayana
, Helena I. M. Boshoff
, et al.
·
PLoS ONE
·
25
PDF
2-Amino-aryl-7-aryl-benzoxazoles as potent, selective and orally available JAK2 inhibitors
2010
·
Marc Gerspacher
, Pascal Furet
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
22
Identification and optimisation of 4,5-dihydrobenzo[1,2-d:3,4-d]bisthiazole and 4,5-dihydrothiazolo[4,5-h]quinazoline series of selective phosphatidylinositol-3 kinase alpha inhibitors
2015
·
Robin A. Fairhurst
, Marc Gerspacher
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Pharmacokinetic-Pharmacodynamic Analysis of Spiroindolone Analogs and KAE609 in a Murine Malaria Model
2014
·
Suresh B. Lakshminarayana
, Céline Freymond
, et al.
·
Antimicrobial Agents and Chemotherapy
·
17
PDF
Corrigendum to “Discovery of NVP-BYL719 a potent and selective phosphatidylinositol-3 kinase alpha inhibitor selected for clinical evaluation” [Bioorg. Med. Chem. Lett. 23 (2013) 3741–3748]
2013
·
Pascal Furet
, Vito Guagnano
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: Structure–activity relationship elucidation
2007
·
Jens-Uwe Peters
, Thomas Lübbers
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
13
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Works count:
41
Citation count:
2,173
H-index:
21
I10-index:
26
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