引用次数
引用: 3,818
H-指数: 32
I10-指数 : 62
出版物: 127
One-pot synthesis of polycyclic nucleosides with unusual molecular skeletons.
María-Cruz Bonache , Alessandra Cordeiro , Paula Carrero , Ernesto Quesada
Journal of Organic Chemistry 74 ( 23) 9071 -9081
4
2009
Targeting HIV Entry through Interaction with Envelope Glycoprotein 120 (gp120): Synthesis and Antiviral Evaluation of 1,3,5-Triazines with Aromatic Amino Acids
Virginia Lozano , Leire Aguado , Bart Hoorelbeke , Marleen Renders
Journal of Medicinal Chemistry 54 ( 15) 5335 -5348
27
2011
Exploitation of the low fidelity of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase and the nucleotide composition bias in the HIV-1 genome to alter the drug resistance development of HIV.
Jan Balzarini , Maria-José Camarasa , Maria-Jesus Pérez-Pérez , Ana San-Félix
Journal of Virology 75 ( 13) 5772 -5777
18
2001
Synthesis of 3′‐Spiro‐Substituted Nucleosides: Chemistry of TSAO Nucleoside Derivatives
María‐José Camarasa , Sonsoles Velázquez , Ana San‐Félix , María‐Jesús Pérez‐Pérez
Chemical Synthesis of nucleoside analogues 427 -472
3
2013
TSAO Analogues. Part 3. Synthesis and Anti-HIV-1 Activity of 2′,5′-Bis- O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl 3′-Spiro-5′′-(4′′- amino-1′′,2′′-oxathiole 2′′,2′′-dioxide) Purine and Purine-Modified Nucleosides.
S VELAZQUEZ , A SAN‐FELIX , MJ PEREZ‐PEREZ , J BALZARINI
ChemInform 25 ( 11)
1994
Síntesis de análogos de nucleosidodifosfatohexosas con actividad antiviral potencial.
Ana Rosa San Félix García
Universidad Complutense de Madrid (Spain)
1986
Un nuevo procedimiento para la preparación de isotiocianatos de azúcares
Ana San-Félix , María Teresa García López , Federico Gómez de las Heras Martín-Maestro , Piedad Fernández Resa
1
1985
A new class of dual HIV and EV71 entry inhibitors: tri and tetrapodal tryptophan derivatives
Ana San-Félix , Leen Delang , Carmen Mirabelli , Dominique Schols
2019
A second-generation of tryptophan-containing small molecules extremely potent against HIV and EV-A71 clinical isolates
Ana San-Félix , Leen Delang , Carmen Mirabelli , Dominique Schols
2019
Exploring nanoparticle approaches for in vivo delivery of a potent class of EV-A71 inhibitors
Ana San-Félix , Fernando Herranz , Belén Martínez-Gualda , Olaia Martí-Marí
2019
Multivalent Tryptophan- and Tyrosine-Containing [60]Fullerene Hexa-Adducts as Dual HIV and Enterovirus A71 Entry Inhibitors.
Ana San-Félix , Johan Neyts , Nazario Martin , Beatriz M. Illescas
Chemistry: A European Journal
2021
TSAO derivatives the first non-peptide inhibitors of HIV-1 RT dimerization.
María-José Camarasa , Sonsoles Velázquez , Ana San-Félix , María-Jesús Pérez-Pérez
Antiviral Chemistry & Chemotherapy 16 ( 3) 147 -153
5
2005
Structure-activity relationship studies on a novel family of specific HIV-1 reverse transcriptase inhibitors.
María-Cruz Bonache , Cristina Chamorro , Esther Lobatón , Erik De Clercq
Antiviral Chemistry & Chemotherapy 14 ( 5) 249 -262
3
2003
Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides
Ana-Isabel Hernández , Jan Balzarini , Fátima Rodrı́guez-Barrios , Ana San-Félix
Bioorganic & Medicinal Chemistry Letters 13 ( 18) 3027 -3030
14
2003
Synthesis of novel Bi-, Tri-, and tetracyclic nucleosides by reaction of a common cyclic enamine derived from TSAO-T with nucleophiles.
María-Cruz Bonache , Cristina Chamorro , Alessandra Cordeiro , María-José Camarasa
Journal of Organic Chemistry 69 ( 25) 8758 -8766
8
2004
Galloyl Carbohydrates with Antiangiogenic Activity Mediated by Capillary Morphogenesis Gene 2 (CMG2) Protein Binding.
Elisa G.-Doyagüez , Paula Carrero , Andrés Madrona , Patricia Rodriguez-Salamanca
Journal of Medicinal Chemistry 62 ( 8) 3958 -3970
4
2019
Linear and branched alkyl-esters and amides of gallic acid and other (mono-, di- and tri-) hydroxy benzoyl derivatives as promising anti-HCV inhibitors
Eva Rivero-Buceta , Paula Carrero , Elisa G. Doyagüez , Andrés Madrona
European Journal of Medicinal Chemistry 92 656 -671
21
2015
A Cyclic Enamine Derived from 1,2-O-Isopropylidene-α-d-xylofuranose As a Novel Carbohydrate Intermediate To Achieve Skeletal Diversity
Alessandra Cordeiro , Ernesto Quesada , María-Cruz Bonache , Sonsoles Velázquez
Journal of Organic Chemistry 71 ( 19) 7224 -7235
10
2006
Unprecedented Lability of the 5‘-O-tert-Butyldimethylsilyl Group from 3‘-Spiro-5‘ ‘-(4‘ ‘-acylamino-1‘ ‘,2‘ ‘-oxathiole-2‘ ‘,2‘ ‘-dioxide) Nucleoside Derivatives via Neighboring Group Participation of the 4‘ ‘-Acylamino Residue
Sonia de Castro , Angel Lozano , María-Luisa Jimeno , María-Jesús Pérez-Pérez
Journal of Organic Chemistry 71 ( 4) 1407 -1415
7
2006
Viral engagement with host receptors blocked by a novel class of tryptophan dendrimers that targets the 5-fold-axis of the enterovirus-A71 capsid
Liang Sun , Hyunwook Lee , Hendrik Jan Thibaut , Kristina Lanko
PLOS Pathogens 15 ( 5) e1007760
24
2019