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- Publications
- Influence
Phosphorylated tubulin adaptor protein CRMP‐2 as prognostic marker and candidate therapeutic target for NSCLC
- Erik Oliemuller, R. Peláez, +7 authors A. Rouzaut
- Biology, Medicine
- International journal of cancer
- 1 May 2013
Collapsin response mediator protein‐2 (CRMP‐2) is the first described and most studied member of a family of proteins that mediate the addition of tubulin dimers to the growing microtubule. CRMPs… Expand
Further naphthylcombretastatins. An investigation on the role of the naphthalene moiety.
- A. B. Maya, Concepción Pérez-Melero, +7 authors M. Medarde
- Chemistry, Medicine
- Journal of medicinal chemistry
- 27 January 2005
By synthesis and biological studies of new naphthalene analogues of combretastatins, we have found that the naphthalene is a good surrogate for the isovanillin moiety (3-hydroxy-4-methoxyphenyl) of… Expand
A new family of quinoline and quinoxaline analogues of combretastatins.
- Concepción Pérez-Melero, A. B. Maya, B. del Rey, R. Peláez, E. Caballero, M. Medarde
- Chemistry, Medicine
- Bioorganic & medicinal chemistry letters
- 16 July 2004
The 3-hydroxy-4-methoxyphenyl ring of combretastatin A-4 can be replaced by a 2-naphthyl moiety without significant loss of cytotoxicity and inhibition of tubulin polymerization potency. In this… Expand
Isocombretastatins A: 1,1-diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds.
- R. Álvarez, Concepción Álvarez, F. Mollinedo, B. G. Sierra, M. Medarde, R. Peláez
- Chemistry, Medicine
- Bioorganic & medicinal chemistry
- 1 September 2009
Isocombretastatins A are 1,1-diarylethene isomers of combretastatins A. We have synthesized the isomers of combretastatin A-4, deoxycombretastatin A-4, 3-amino-deoxycombretastatin A-4 (AVE-8063),… Expand
The Bateman domain of IMP dehydrogenase is a binding target for dinucleoside polyphosphates
- D. Fernández-Justel, R. Peláez, J. L. Revuelta, R. M. Buey
- Chemistry, Medicine
- The Journal of Biological Chemistry
- 15 August 2019
IMP dehydrogenase (IMPDH) is an essential enzyme that catalyzes the rate-limiting step in the de novo guanine nucleotide biosynthetic pathway. Because of its involvement in the control of cell… Expand
The Masked Polar Group Incorporation (MPGI) Strategy in Drug Design: Effects of Nitrogen Substitutions on Combretastatin and Isocombretastatin Tubulin Inhibitors
- M. Gonzalez, Younes Ellahioui, +8 authors R. Peláez
- Chemistry, Medicine
- Molecules
- 26 November 2019
Colchicine site ligands suffer from low aqueous solubility due to the highly hydrophobic nature of the binding site. A new strategy for increasing molecular polarity without exposing polar… Expand
Lipid composition of Silybum marianum cell cultures treated with methyl jasmonate
- M. Cacho, R. Peláez, P. Corchete
- Chemistry
- Biologia Plantarum
- 3 March 2012
Elicitation of cell cultures of Silybum marianum with methyl jasmonate (MeJA) increases the production and release of the secondary metabolite silymarin into the culture medium and this process seems… Expand
Naphthylphenstatins as tubulin ligands: synthesis and biological evaluation.
- Concepción Álvarez, R. Álvarez, P. Corchete, Concepción Pérez-Melero, R. Peláez, M. Medarde
- Chemistry, Medicine
- Bioorganic & medicinal chemistry
- 1 October 2008
A new family of naphthalenic analogues of phenstatins with modifications on the ketone-bridge has been synthesised. The synthesised compounds have been assayed for tubulin polymerisation inhibitory… Expand
Exploring the effect of 2,3,4-trimethoxy-phenyl moiety as a component of indolephenstatins.
- Concepción Álvarez, R. Alvarez, P. Corchete, Concepción Pérez-Melero, R. Peláez, M. Medarde
- Chemistry, Medicine
- European journal of medicinal chemistry
- 1 February 2010
A new family of phenstatin analogues has been synthesized and assayed. This family simultaneously incorporates modifications of the A-ring (replacement of the 3,4,5-trimethoxyphenyl by the… Expand
Endowing indole-based tubulin inhibitors with an anchor for derivatization: highly potent 3-substituted indolephenstatins and indoleisocombretastatins.
- R. Álvarez, P. Puebla, +7 authors R. Peláez
- Chemistry, Medicine
- Journal of medicinal chemistry
- 20 March 2013
Colchicine site ligands with indole B rings are potent tubulin polymerization inhibitors. Structural modifications at the indole 3-position of 1-methyl-5-indolyl-based isocombretastatins… Expand