His scientific interests lie mostly in Virology, Virus, Stereochemistry, Chemical synthesis and Structure–activity relationship. All of his Virology and Human cytomegalovirus, Cidofovir, Viral replication, Thymidine kinase and Ganciclovir investigations are sub-components of the entire Virology study. His work carried out in the field of Virus brings together such families of science as Vaccinia and Microbiology.
His research in Stereochemistry intersects with topics in Biological activity, DNA, Purine and Stereoisomerism. His Chemical synthesis study combines topics from a wide range of disciplines, such as Phosphonate, Bicyclic molecule and Pyrimidine. His Structure–activity relationship research focuses on subjects like Deoxyribonucleoside, which are linked to Deoxyuridine and Substituent.
His primary scientific interests are in Virology, Stereochemistry, Virus, Nucleoside and Cidofovir. His Virology study is mostly concerned with Herpes simplex virus, Human cytomegalovirus, Thymidine kinase, Viral replication and Foscarnet. His Stereochemistry research incorporates themes from Biological activity, Structure–activity relationship and Chemical synthesis.
Robert Snoeck has included themes like Vaccinia, In vitro and Cell culture in his Virus study. His Nucleoside research is multidisciplinary, incorporating elements of Prodrug and Cytotoxicity. Robert Snoeck regularly links together related areas like Cytosine in his Cidofovir studies.
His main research concerns Stereochemistry, Virology, Virus, DNA and RNA. He interconnects Cell culture, HeLa, Uracil, Nucleotide and Prodrug in the investigation of issues within Stereochemistry. His studies in Prodrug integrate themes in fields like Protide, Guanine, Pyrimidine, Phosphoramidate and Nucleoside.
Virology is represented through his Herpes simplex virus, Human cytomegalovirus, Varicella zoster virus, Viral replication and Cidofovir research. Robert Snoeck studies Virus, focusing on Thymidine kinase in particular. His DNA study integrates concerns from other disciplines, such as Phosphonate, IC50, Structure–activity relationship and Nitrone.
His primary areas of study are Stereochemistry, Virology, DNA, Virus and RNA. His Stereochemistry research is multidisciplinary, incorporating perspectives in Phosphonate, IC50, Prodrug, HeLa and Structure–activity relationship. Virology is closely attributed to Macrophage activation syndrome in his research.
His studies deal with areas such as Thymidine kinase and Potency as well as DNA. His research integrates issues of Combinatorial chemistry, Amino acid and Gene in his study of Virus. His Herpes simplex virus study which covers Human cytomegalovirus that intersects with DNA polymerase, Varicella zoster virus and Pyrimidine.
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Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
Rudi Pauwels;Jan Balzarini;Masanori Baba;Robert Snoeck.
Journal of Virological Methods (1988)
Sulfated polysaccharides are potent and selective inhibitors of various enveloped viruses, including herpes simplex virus, cytomegalovirus, vesicular stomatitis virus, and human immunodeficiency virus.
M Baba;R Snoeck;R Pauwels;E de Clercq.
Antimicrobial Agents and Chemotherapy (1988)
Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo antiretrovirus activities of (R)-9-(2-phosphonomethoxypropyl)-2,6-diaminopurine.
J Balzarini;A Holy;J Jindrich;L Naesens.
Antimicrobial Agents and Chemotherapy (1993)
Synthesis and antiviral activity of new pyrazole and thiazole derivatives
Osama I. El-Sabbagh;Mohamed M. Baraka;Samy M. Ibrahim;Christophe Pannecouque.
European Journal of Medicinal Chemistry (2009)
Treatment of Severe Laryngeal Papillomatosis With Intralesional Injections of Cidofovir ((S)-1-(3-Hydroxy-2-Phosphonylmethoxypropyl) Cytosine)
Robert Snoeck;Willy Wellens;Christian Desloovere;Mark Van Ranst.
Journal of Medical Virology (1998)
HPMPC (cidofovir), PMEA (adefovir) and related acyclic nucleoside phosphonate analogues: a review of their pharmacology and clinical potential in the treatment of viral infections
L Naesens;R Snoeck;G Andrei;J Balzarini.
Antiviral Chemistry & Chemotherapy (1997)
(S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine, a potent and selective inhibitor of human cytomegalovirus replication.
R Snoeck;T Sakuma;E De Clercq;I Rosenberg.
Antimicrobial Agents and Chemotherapy (1988)
Activities of various compounds against murine and primate polyomaviruses.
G Andrei;R Snoeck;M Vandeputte;E De Clercq.
Antimicrobial Agents and Chemotherapy (1997)
Potent and selective inhibition of varicella-zoster virus (VZV) by nucleoside analogues with an unusual bicyclic base.
Christopher McGuigan;Christopher J. Yarnold;Garry Jones;Sonsoles Velázquez.
Journal of Medicinal Chemistry (1999)
Structure-antiviral activity relationship in the series of pyrimidine and purine N-[2-(2-phosphonomethoxy)ethyl] nucleotide analogues. 1. Derivatives substituted at the carbon atoms of the base
Antonín Holý;Jaroslav Günter;Hana Dvořáková;Milena Masojídková.
Journal of Medicinal Chemistry (1999)
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