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Grupo de investigación en antimitóticos. Peláez y MedardeAntimitóticos inhibidores de la tubulinaÚltimas publicacionesMiembros del grupoContacta con nosotrosVisítanos en Facebook

ÚLTIMAS PUBLICACIONES

 

 
Año
Título
Referencia (Revista vol, pág.)
 
         
    Microtubule Destabilizing Sulfonamides as An Alternative to Taxane-Based Chemotherapy
Int J Mol Sci 22, 1907
 
 
2021
Methylsulfanylpyridine based diheteroaryl isocombretastatin analogs as potent anti-proliferative agents
Eur J Med Chem 209, 112933
 
         
 
2020
Potent colchicine-site ligands with improved intrinsic solubility by replacement of the 3, 4, 5-trimethoxyphenyl ring with a 2-methylsulfanyl-6-methoxypyridine ring
Bioorg Chem 98, 103755
 
         
 
Antitubulin sulfonamides: The successful combination of an established drug class and a multifaceted target.
Med Res Revs 39, 775
 
 
2019
The Bateman domain of IMP dehydrogenase is a binding target for dinucleoside polyphosphates.
J Biol Chem 294, 14768
 
 
In Silico Molecular Studies of Antiophidic Properties of the Amazonian Tree Cordia nodosa Lam.
Molecules 24, E4160
 
    The Masked Polar Group Incorporation (MPGI) Strategy in Drug Design: Effects of Nitrogen Substitutions on Combretastatin and Isocombretastatin Tubulin Inhibitors
Molecules 24, E4319
 
         
 
2018
Substitution at the indole 3 position yields highly potent indolecombretastatins against human tumor cells
Eur J Med Chem 158, 167
 
    Bioactive Heterometallic CuII-ZnII Complexes with Potential Biomedical Applications
ACS OMEGA 3, 13343
 
         
 
2017
JADOPPT: java based AutoDock preparing and processing tool
Bioinformatics 33, 583
 
         
 
2016
N-(2-methyl-indol-1H-5-yl)-1-naphthalenesulfonamide: A novel reversible antimitotic agent inhibiting cancer cell motility
Biochem Pharm 115, 28-42
 
 
Pyridine based antitumor compounds acting at the colchicine site

Curr Med Chem 23, 1100

 
         
 
2015
Exploring the size adaptability of the B ring binding zone of the colchicine site of tubulin with para-nitrogen substituted isocombretastatins
Eur J Med Chem 100, 210
 
         
         
 
2014

p,p-Dihydroxydihydrostilbenophanes Related to Antimitotic Combretastatins. Conformational Analysis and Its Relationship to Tubulin Inhibition

J Org Chem 79, 6840
 
    New Ligands of Tubulin Colchicine Site Based on X-Ray Structures
Curr Top Med Chem, 14, 2231
 
         
 
2013

Endowing Indole-Based Tubulin Inhibitors with an Anchor for Derivatization: Highly Potent 3-Substituted Indolephenstatins and Indoleisocombretastatins

J. Med. Chem. 56, 2813
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Bis-amidocarbazolyl urea receptor for short-chain dicarboxylate anions
Org Biomol Chem 10, 1181
 
 
2012
Total Synthesis of (+)-seco-C-Oleanane via Stepwise Controlled Radical Cascade Cyclization
J Org Chem 77, 341
 
    Lipid composition of Silybum marianum cell cultures treated with methyl jasmonate
Biol Plantar 56, 221
 
         
 
2011
New para–para Stilbenophanes: Synthesis by McMurry Coupling, Conformational Analysis and Inhibition of Tubulin Polymerisation
Chem Eur J 17, 3406
 
         
 
2010
Exploring the effect of 2,3,4-trimethoxy-phenyl moiety as a component of indolephenstatins
Eur J Med Chem 45, 588
 
         
 
2009
Design of New Chemoinformatic Tools for the Analysis of Virtual Screening Studies: Application to Tubulin Inhibitors
Adv Soft Comp 49, 189
 
    Isocombretastatins A: 1,1-Diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds
Bioorg. Med. Chem. 11, 8999
 
         
 
2008
Naphthylphenstatins as tubulin ligands: Synthesis and biological evaluation
Bioorg. Med. Chem. 11, 8999
 
 
Diarylmethyloxime and hydrazone derivatives with 5-indolyl moieties as potent inhibitors of tubulin polymerization
Bioorg. Med. Chem. 11, 5952
 
    An arabinogalactan protein isolated from medium of cell suspension cultures of Silybum marianum (L.)Gaernt
Carboh. Polym. 71, 634
 
 
Imino-Diels–Alder Reactions of 1-Aryl-3-(trialkylsiloxy)-1,3-butadienes in
Solution and the Solid Phase

Eur. J. Org. Chem. 23, 4004
 
         
 
2007
New dicyclopentadiene-based scaffolds
Tetrahedron 63, 2132
 
    Synthesis and biological activity of naphthalene analogues of phenstatins: Naphthylphenstatins
Bioorg. Med. Chem. Lett. 17, 3417
 
 
Synthesis and Conformational Analysis of Macrocyclic Dihydroxystilbenes linked up between para-para positions.
Chem. Eur. J. 13, 7246
 
    Conformationally restricted macrocyclic analogues of combretastatins
Bioorg. Med. Chem. Lett. 17, 6316
 
 
Application of Chemoinformatic Tools for the Analysis of Virtual Screening Studies of Tubulin Inhibitors
Adv Soft Comp 44, 411
 
   
   
 
2006
Macrocyclic Chiral Receptors toward Enantioselective Recognition of Naproxen
Org. Lett. 8, 4679
 
     
 
 
2005
Stilbenophane Analogues of Deoxycombretastatin A-4
J. Org. Chem. 70, 6544
3,46
 
Synthesis of a Conformationally Restricted Polyoxygenated Crownophane
Tetrahedron Lett. 46, 7055
2,48
 
Further naphthylcombretastatins. An investigation on the role of the naphthalene moiety
J. Med. Chem. 48, 556
4,82
 
New naphthylcombretastatins. Modifications on the ethylene bridge
Bioorg. Med. Chem. 13, 2097
2,19
 
Intrisically Fluorescent Cytotoxic Cisplatin Analogues as DNA Marker Molecules
Bioconjugate Chem. 19, 275
3,55
 
Diels-Alder reactivity of 4-aryl-1-phthalimido-2-siloxy-1,3-butadienes
Tetrahedron 61, 6871
2,64
 
 
 
2004
A new family of quinoline and quinoxaline analogues of combretastatins
Bioorg. Med. Chem. Lett. 14, 3771
2,33
    Naproxen: Hydroxypropyl-b-Cyclodextrin. Polyvinylpyrrolidone Ternary Complex Formation
J. Incl. Phenom. & Macroc. 48, 157
0,8
    1-Phthalimido-4-(3-indolyl)-2-siloxy-1,3-butadienes: synthesis and Diels-Alder reactivity
Tetrahedron Lett. 45, 1631
2,5
     
 
 
2003
Naphthalene Analogues of Lignans
J. Org. Chem. 68, 854
3,3