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Año |
Título |
Referencia
(Revista vol, pág.) |
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Microtubule Destabilizing Sulfonamides as An Alternative to Taxane-Based Chemotherapy |
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2021 |
Methylsulfanylpyridine based diheteroaryl isocombretastatin analogs as potent anti-proliferative agents |
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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 |
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Antitubulin sulfonamides: The successful combination of an established drug class and a multifaceted target. |
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2019 |
The Bateman domain of IMP dehydrogenase is a binding target for dinucleoside polyphosphates. |
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In Silico Molecular Studies of Antiophidic Properties of the Amazonian Tree Cordia nodosa Lam. |
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The Masked Polar Group Incorporation (MPGI) Strategy in Drug Design: Effects of Nitrogen Substitutions on Combretastatin and Isocombretastatin Tubulin Inhibitors |
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2018 |
Substitution at the indole 3 position yields highly potent indolecombretastatins against human tumor cells |
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Bioactive Heterometallic CuII-ZnII Complexes with Potential Biomedical Applications |
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2017 |
JADOPPT: java based AutoDock preparing and processing tool |
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2016 |
N-(2-methyl-indol-1H-5-yl)-1-naphthalenesulfonamide: A novel reversible antimitotic agent inhibiting cancer cell motility |
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Pyridine based antitumor compounds acting at the colchicine site |
Curr Med Chem 23, 1100 |
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2015 |
Exploring the size adaptability of the B ring binding zone of the colchicine site of tubulin with para-nitrogen substituted isocombretastatins |
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2014 |
p,p-Dihydroxydihydrostilbenophanes Related to Antimitotic Combretastatins. Conformational Analysis and Its Relationship to Tubulin Inhibition |
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New Ligands of Tubulin Colchicine Site Based on X-Ray Structures |
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2013 |
Endowing Indole-Based Tubulin Inhibitors with an Anchor for Derivatization: Highly Potent 3-Substituted Indolephenstatins and Indoleisocombretastatins |
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Bis-amidocarbazolyl urea receptor for short-chain dicarboxylate anions |
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2012 |
Total Synthesis of (+)-seco-C-Oleanane via Stepwise Controlled Radical Cascade Cyclization
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Lipid composition of Silybum marianum cell cultures treated with methyl jasmonate |
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2011 |
New para–para Stilbenophanes: Synthesis by McMurry Coupling, Conformational Analysis and Inhibition of Tubulin Polymerisation |
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2010 |
Exploring the effect of 2,3,4-trimethoxy-phenyl moiety as a component of indolephenstatins |
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2009 |
Design of New Chemoinformatic
Tools for the Analysis of Virtual Screening Studies: Application to Tubulin
Inhibitors |
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Isocombretastatins A: 1,1-Diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds |
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2008 |
Naphthylphenstatins as tubulin
ligands: Synthesis and biological evaluation |
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Diarylmethyloxime and hydrazone
derivatives with 5-indolyl moieties as potent inhibitors of tubulin polymerization |
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An arabinogalactan protein
isolated from medium of cell suspension cultures of Silybum marianum (L.)Gaernt |
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Imino-Diels–Alder Reactions
of 1-Aryl-3-(trialkylsiloxy)-1,3-butadienes in
Solution and the Solid Phase
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2007 |
New dicyclopentadiene-based
scaffolds |
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Synthesis and biological
activity of naphthalene analogues of phenstatins: Naphthylphenstatins |
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Synthesis and Conformational
Analysis of Macrocyclic Dihydroxystilbenes linked up between para-para positions.
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Conformationally restricted
macrocyclic analogues of combretastatins |
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Application of Chemoinformatic
Tools for the Analysis of Virtual Screening Studies of Tubulin Inhibitors
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Adv Soft
Comp 44, 411 |
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2006 |
Macrocyclic Chiral Receptors
toward Enantioselective Recognition of Naproxen |
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2005 |
Stilbenophane
Analogues of Deoxycombretastatin A-4 |
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3,46 |
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Synthesis
of a Conformationally Restricted Polyoxygenated Crownophane |
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2,48 |
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Further
naphthylcombretastatins. An investigation on the role of the naphthalene
moiety |
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4,82 |
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New
naphthylcombretastatins. Modifications on the ethylene bridge |
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2,19 |
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Intrisically
Fluorescent Cytotoxic Cisplatin Analogues as DNA Marker Molecules
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3,55 |
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Diels-Alder
reactivity of 4-aryl-1-phthalimido-2-siloxy-1,3-butadienes |
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2,64 |
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2004 |
A new family of quinoline
and quinoxaline analogues of combretastatins
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2,33 |
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Naproxen: Hydroxypropyl-b-Cyclodextrin.
Polyvinylpyrrolidone Ternary Complex Formation |
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0,8 |
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1-Phthalimido-4-(3-indolyl)-2-siloxy-1,3-butadienes:
synthesis and Diels-Alder reactivity |
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2,5 |
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2003 |
Naphthalene Analogues of
Lignans |
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3,3 |
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