Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michèle Reboud-Ravaux

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Antiviral Chemistry & Chemotherapy|October 28, 2006
AZT and AZT-monophosphate prodrugs incorporating HIV-protease substrate fragment: synthesis and evaluation as specific drug delivery systemsJean-François Liotard, Mohamed Mehiri, Audrey Di Giorgio, et al.
Journal of Medicinal Chemistry|November 30, 2004
New constrained "molecular tongs" designed to dissociate HIV-1 protease dimerNaïma Merabet, Julien Dumond, Bruno Collinet, et al.
Biochemistry|December 25, 2008
Dimer disruption and monomer sequestration by alkyl tripeptides are successful strategies for inhibiting wild-type and multidrug-resistant mutated HIV-1 proteasesLudovic Bannwarth, Thierry Rose, Laure Dufau, et al.
Journal of Medicinal Chemistry|November 19, 2009
Novel organic proteasome inhibitors identified by virtual and in vitro screeningNicolas Basse, Matthieu Montes, Xavier Maréchal, et al.
Journal of Medicinal Chemistry|May 22, 2007
Linear TMC-95-based proteasome inhibitorsNicolas Basse, Sandrine Piguel, David Papapostolou, et al.
Bioorganic & Medicinal Chemistry Letters|February 19, 2014
New C(4)- and C(1)-derivatives of furo[3,4-c]pyridine-3-ones and related compounds: evidence for site-specific inhibition of the constitutive proteasome and its immunoisoformAnna Hovhannisyan, The Hien Pham, Dominique Bouvier, et al.
Chemmedchem|August 18, 2010
20S proteasome inhibition: designing noncovalent linear peptide mimics of the natural product TMC-95AMichael Groll, Nerea Gallastegui, Xavier Maréchal, et al.
Journal of Medicinal Chemistry|November 14, 2003
Dimerization inhibitors of HIV-1 protease based on a bicyclic guanidinium subunitPerla Breccia, Nicole Boggetto, Ruth Pérez-Fernández, et al.
Biochemical and Biophysical Research Communications|January 23, 2018
Piperlongumine and some of its analogs inhibit selectively the human immunoproteasome over the constitutive proteasomeElodie Bosc, Jhennifer Nastri, Valérie Lefort, et al.
Journal of Medicinal Chemistry|December 10, 2014
Toward the first class of suicide inhibitors of kallikreins involved in skin diseasesXiao Tan, Feryel Soualmia, Laetitia Furio, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Antiviral Chemistry & Chemotherapy|October 28, 2006
AZT and AZT-monophosphate prodrugs incorporating HIV-protease substrate fragment: synthesis and evaluation as specific drug delivery systemsJean-François Liotard, Mohamed Mehiri, Audrey Di Giorgio, et al.
Journal of Medicinal Chemistry|November 30, 2004
New constrained "molecular tongs" designed to dissociate HIV-1 protease dimerNaïma Merabet, Julien Dumond, Bruno Collinet, et al.
Biochemistry|December 25, 2008
Dimer disruption and monomer sequestration by alkyl tripeptides are successful strategies for inhibiting wild-type and multidrug-resistant mutated HIV-1 proteasesLudovic Bannwarth, Thierry Rose, Laure Dufau, et al.
Journal of Medicinal Chemistry|November 19, 2009
Novel organic proteasome inhibitors identified by virtual and in vitro screeningNicolas Basse, Matthieu Montes, Xavier Maréchal, et al.
Journal of Medicinal Chemistry|May 22, 2007
Linear TMC-95-based proteasome inhibitorsNicolas Basse, Sandrine Piguel, David Papapostolou, et al.
Bioorganic & Medicinal Chemistry Letters|February 19, 2014
New C(4)- and C(1)-derivatives of furo[3,4-c]pyridine-3-ones and related compounds: evidence for site-specific inhibition of the constitutive proteasome and its immunoisoformAnna Hovhannisyan, The Hien Pham, Dominique Bouvier, et al.
Chemmedchem|August 18, 2010
20S proteasome inhibition: designing noncovalent linear peptide mimics of the natural product TMC-95AMichael Groll, Nerea Gallastegui, Xavier Maréchal, et al.
Journal of Medicinal Chemistry|November 14, 2003
Dimerization inhibitors of HIV-1 protease based on a bicyclic guanidinium subunitPerla Breccia, Nicole Boggetto, Ruth Pérez-Fernández, et al.
Biochemical and Biophysical Research Communications|January 23, 2018
Piperlongumine and some of its analogs inhibit selectively the human immunoproteasome over the constitutive proteasomeElodie Bosc, Jhennifer Nastri, Valérie Lefort, et al.
Journal of Medicinal Chemistry|December 10, 2014
Toward the first class of suicide inhibitors of kallikreins involved in skin diseasesXiao Tan, Feryel Soualmia, Laetitia Furio, et al.
Pageof 5