about
Novel styryl-indoles as small molecule inhibitors of 25-hydroxyvitamin D-24-hydroxylase (CYP24A1): Synthesis and biological evaluation.Design and Synthesis of Potent in Vitro and in Vivo Anticancer Agents Based on 1-(3',4',5'-Trimethoxyphenyl)-2-Aryl-1H-ImidazolePolyfluorinated groups in medicinal chemistry.Rational design and synthesis of novel anti-prostate cancer agents bearing a 3,5-bis-trifluoromethylphenyl moiety.Design and synthesis of novel bicalutamide and enzalutamide derivatives as antiproliferative agents for the treatment of prostate cancer.Small-molecule inhibitors of 25-hydroxyvitamin D-24-hydroxylase (CYP24A1): synthesis and biological evaluation.Discovery of novel multi-target indole-based derivatives as potent and selective inhibitors of chikungunya virus replication.Broad-spectrum non-nucleoside inhibitors for caliciviruses.Novel symmetrical phenylenediamines as potential anti-hepatitis C virus agents.Networks of enzymatically oxidized membrane lipids support calcium-dependent coagulation factor binding to maintain hemostasis.Synthesis and biological evaluation of 6-substituted-5-fluorouridine ProTides.Quercetin derivatives as novel antihypertensive agents: Synthesis and physiological characterization.In silico screening for human norovirus antivirals reveals a novel non-nucleoside inhibitor of the viral polymerase.3-Aryl/Heteroaryl-5-amino-1-(3′,4′,5′-trimethoxybenzoyl)-1,2,4-triazoles as antimicrotubule agents. Design, synthesis, antiproliferative activity and inhibition of tubulin polymerizationStructure-activity relationship study of itraconazole, a broad-range inhibitor of picornavirus replication that targets oxysterol-binding protein (OSBP)Combining bioinformatics, cheminformatics, functional genomics and whole organism approaches for identifying epigenetic drug targets in Schistosoma mansoniRational design and synthesis of novel phenylsulfonyl-benzamides as anti-prostate cancer agents.A new antiviral scaffold for human norovirus identified with computer-aided approaches on the viral polymeraseA new series of bicalutamide, enzalutamide and enobosarm derivatives carrying pentafluorosulfanyl (SF5) and pentafluoroethyl (C2F5) substituents: Improved antiproliferative agents against prostate cancerDesign, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors
P50
Q35266394-DA2414F8-4630-42B5-8B35-6F2BCB57272AQ36928505-F418A32A-210E-46F8-B933-29BD940BB095Q38421820-90A18571-BC29-4F5F-8E52-43D234C5FD89Q38764448-27E3CB33-4ABC-496D-A5BF-86214D26E90BQ38774262-2B902D5B-2BE6-4124-A012-C0EDFE37E866Q38963669-F3C04154-6ECC-42A5-AB8E-E42B86F1C793Q39180019-86F5F5C0-C3C0-4E2C-B139-8ED1F1006ED0Q40102135-C25914EB-634A-4C5E-8019-92A745333B1EQ40463230-65A8A6D8-4034-4C70-B621-B3E7D3811541Q46252434-8FF1058E-789E-4F62-AA2C-841271537764Q47560573-3D8DF2C8-8620-4D6D-8E12-3DB836F048CBQ51320238-AF5F2EFD-682E-4A41-9971-F1044EF75C7DQ52668531-EEBF8561-7725-4F0D-8932-2525F4275198Q57266027-9278D2F2-7796-427C-91D4-73FF788F0F28Q57266029-3CFD673B-52AA-4A23-81CE-F2D52A9BDCDCQ59171150-FF94737F-9F0B-49ED-8666-13307B3C040EQ64949057-52FB41A1-BC05-4AF9-ABF3-ECE3622DB12EQ91718477-2019A763-8155-4893-A192-AC075C26C869Q91745069-2AA7B48B-F812-4E3D-94FE-8D8EDAC7ACB3Q92541759-FA2B0687-CC3D-4A08-A2B5-EF01C585CF4C
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Salvatore Ferla
@ast
Salvatore Ferla
@en
Salvatore Ferla
@es
Salvatore Ferla
@nl
Salvatore Ferla
@sl
type
label
Salvatore Ferla
@ast
Salvatore Ferla
@en
Salvatore Ferla
@es
Salvatore Ferla
@nl
Salvatore Ferla
@sl
prefLabel
Salvatore Ferla
@ast
Salvatore Ferla
@en
Salvatore Ferla
@es
Salvatore Ferla
@nl
Salvatore Ferla
@sl
P1053
F-7976-2016
P106
P1153
56364921000
P21
P31
P3829
P496
0000-0002-5918-9237