M. Carda

发表

Triclosan-caffeic acid hybrids: Synthesis, leishmanicidal, trypanocidal and cytotoxic activities.

S. Robledo, I. Velez, E. Otero, 2017, European journal of medicinal chemistry.

One drug for two targets: Biological evaluation of antiretroviral agents endowed with antiproliferative activity.

C. Zamperini, M. Chiariello, L. Botta, 2017, Bioorganic & medicinal chemistry letters.

2.14 Selected Diastereoselective Reactions: Enolate Alkylation

M. Carda, E. Falomir, J. Marco, 2012 .

Synthesis and biological evaluation of carbamates derived from aminocombretastatin A-4 as vascular disrupting agents.

S. Liekens, M. Carda, E. Falomir, 2018, European journal of medicinal chemistry.

Double diastereoselection in anti aldol reactions mediated by dicyclohexylchloroborane between an L-erythrulose derivative and chiral aldehydes.

M. Carda, E. Falomir, J. Marco, 2012, Organic & biomolecular chemistry.

Aldol reactions between L-erythrulose derivatives and chiral alpha-amino and alpha-fluoro aldehydes: competition between Felkin-Anh and Cornforth transition states.

M. Carda, E. Falomir, J. Marco, 2008, Chemistry.

Induction of protection against the necrotrophic pathogens Phytophthora citrophthora and Alternaria solani in Lycopersicon esculentum Mill. by a novel synthetic glycoside combined with amines

V. Flors, M. Carda, P. García-Agustín, 2003, Planta.

Synthesis and biological properties of the cytotoxic 14-membered macrolides aspergillide A and B.

M. Carda, E. Falomir, J. Marco, 2011, Chemistry.

Cytotoxic, Antiangiogenic and Antitelomerase Activity of Glucosyl‐ and Acyl‐ Resveratrol Prodrugs and Resveratrol Sulfate Metabolites

A. Zafra-Gómez, M. Carda, R. Martí-Centelles, 2016, Chembiochem : a European journal of chemical biology.

Stereoselective syntheses of naturally occurring 5,6-dihydropyran-2-ones

M. Carda, E. Falomir, J. Marco, 2007 .

The total synthesis and biological properties of the cytotoxic macrolide FD-891 and its non-natural (Z)-C12 isomer.

I. Barasoain, J. Díaz, J. F. Díaz, 2007, Chemistry.

Stereoselective synthesis of the C14–C26 fragment of the cytotoxic macrolide FD-891

M. Carda, J. Marco, J. Murga, 2004 .

Synthesis and evaluation of biphenyl derivatives as potential downregulators of VEGF protein secretion and telomerase-related gene expressions.

M. Carda, E. Falomir, J. Marco, 2016, Bioorganic & medicinal chemistry.

Current trends in the description of lanthanum-strontium-manganite oxygen electrode reaction mechanism in a high-temperature solid oxide cell

K. Bouzek, M. Paidar, M. Carda, 2021, Current Opinion in Electrochemistry.

Synthesis and in-vitro Evaluation of S-allyl Cysteine Ester - Caffeic Acid Amide Hybrids as Potential Anticancer Agents

M. Carda, M. Maldonado, T. Naranjo, 2019, Iranian journal of pharmaceutical research : IJPR.

Synthesis and antiproliferative activity of 3- and 7-styrylcoumarins

E. Otero, M. Carda, Raül Agut, 2018, Medicinal Chemistry Research.

Interactions of long-chain homologues of colchicine with tubulin.

G. Breuzard, P. Barbier, Diane Allegro, 2017, European journal of medicinal chemistry.

Synthesis and biological evaluation of truncated α-tubulin-binding pironetin analogues lacking alkyl pendants in the side chain or the dihydropyrone ring.

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2013, Organic & biomolecular chemistry.

Synthesis and Biological Evaluation of α‐Tubulin‐Binding Pironetin Analogues with Enhanced Lipophilicity

I. Barasoain, M. Carda, E. Falomir, 2013 .

Synthesis and biological evaluation as microtubule-active agents of several tetrahydrofuran and spiroacetal derivatives.

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2013, Current medicinal chemistry.

Design and synthesis of pironetin analogues with simplified structure and study of their interactions with microtubules.

I. Barasoain, J. Díaz, M. Carda, 2011, European journal of medicinal chemistry.

Recent Advances in the Field of Naturally Occurring 5,6‐Dihydropyran‐2‐ones

M. Carda, J. Marco, 2013 .

An ab initio study of the unimolecular decomposition mechanism of formamidine. 4‐31G Characterization of potential energy hypersurface

E. Silla, J. Andrés, M. Carda, 1991 .

Three novel synthetic amides of adipic acid protect Capsicum anuum plants against the necrotrophic pathogen Alternaria solani.

V. Flors, M. Carda, P. García-Agustín, 2003 .

The widespread presence of a family of fish virulence plasmids in Vibrio vulnificus stresses its relevance as a zoonotic pathogen linked to fish farms

F. González-Candelas, M. Carda, B. Fouz, 2021, Emerging microbes & infections.

Enantiotoposelective PLE-catalyzed hydrolysis of cis-5-substituted-1,3-diacyloxycyclohexanes. Preparation of some useful chiral building blocks

M. Carda, J. V. D. Eycken, M. Vandewalle, 1990 .

Synthesis and biological evaluation of cyclic derivatives of combretastatin A-4 containing group 14 elements.

M. Carda, E. Falomir, S. Royo, 2018, Organic & biomolecular chemistry.

The Mechanism of the Interactions of Pironetin Analog/Combretastatin A‐4 Hybrids with Tubulin

M. Redondo-Horcajo, I. Barasoain, J. Díaz, 2015, Archiv der Pharmazie.

Stereoselective synthesis of (-)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis

M. Carda, J. Marco, S. Díaz-Oltra, 2003 .

Erythrulose derivatives as functionalized chiral d3 and d4 synthons

M. Carda, E. Falomir, J. Marco, 2002 .

Stereoselective synthesis of (−)-cytoxazone

M. Carda, J. Marco, F. González, 2002 .

Synthesis of (±)-(E)-2,6-dimethyl-6-hydroxyocta-2,7-dienoic acid and the corresponding amide (“acacialactam”)

M. Carda, J. Marco, J. Murga, 1994 .

Arylpyridines, arylpyrimidines and related compounds as potential modulator agents of the VEGF, hTERT and c-Myc oncogenes.

M. Carda, E. Falomir, J. Marco, 2019, Bioorganic & medicinal chemistry.

Furanchalcone–biphenyl hybrids: synthesis, in silico studies, antitrypanosomal and cytotoxic activities

S. Robledo, I. Velez, E. García, 2019, Medicinal Chemistry Research.

Synthesis and Biological Evaluation of Imines Structurally Related to Resveratrol as Dual Inhibitors of VEGF Protein Secretion and hTERT Gene Expression1

M. Carda, R. Martí-Centelles, E. Falomir, 2017, Natural product communications.

2-Aza-2,4-cyclopentadienone. Existence and reactivity

S. Luis, M. Carda, A. Costero, 1988 .

Diastereoselective additions of organolithium and organomagnesium reagents to the CN bond of a chiral, cyclic nitrone derived from erythrulose

J. Lex, M. Carda, E. Falomir, 1998 .

Diastereoselective additions of organolithium reagents to the CN bond of protected erythrulose oxime ethers. Synthesis of enantiopure α,α-disubstituted α-aminiacids

M. Carda, E. Falomir, J. Marco, 1997 .

Chemical constituents and standardization of Piper piedecuestanum TREL & YUNCK. With antiplasmodial and cytotoxic activity

Carlos Alberto Peláez Jaramillo, M. Carda, S. B. Trujillo, 2019, Cogent Food & Agriculture.

Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck

Carlos Alberto Peláez Jaramillo, M. Carda, A. Cardona, 2018 .

Carbon-13 NMR spectroscopy of sesquiterpenes. 3. Synthesis and carbon-13 NMR spectral data of 4.alpha.,5.alpha.- and 4.beta.,5.beta.-epoxyeudesmanolides. Configuration and .gamma. effect of the oxirane ring

M. Carda, J. Marco, J. F. Sanz, 1992 .

Xanthanolides from Xanthium: absolute configuration of xanthanol, isoxanthanol and their C-4 epimers

M. Carda, J. Marco, Julia Corral, 1993 .

Design, synthesis and antimalarial evaluation of novel thiazole derivatives.

M. Carda, Benigno Crespo, María L León, 2016, Bioorganic & medicinal chemistry letters.

A practical procedure of low valent tin mediated Barbier allylation of aldehydes in wet solvent

M. Carda, B. Dhotare, A. Chattopadhyay, 2013 .

Synthesis, leishmanicidal, trypanocidal and cytotoxic activities of quinoline-chalcone and quinoline-chromone hybrids

S. Robledo, I. Velez, E. García, 2017 .

Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids

S. Robledo, I. Velez, M. Carda, 2014, Molecules.

Synthesis and antiproliferative activity of 3- and 7-styrylcoumarins

M. Carda, Raül Agut, M. Maldonado, 2018, Medicinal Chemistry Research.

Influence of the protecting groups on the syn/anti stereoselectivity of boron aldol additions with erythrulose derivatives. A theoretical and experimental study

M. Carda, E. Falomir, Juan Murga, 2002 .

Boron aldol additions with erythrulose derivatives: dependence of stereoselectivity on the type of protecting group

M. Carda, E. Falomir, J. Marco, 1999 .

Erythrulose as a multifunctional chiron: Highly stereoselective boron aldol additions

A. Linden, M. Carda, E. Falomir, 1999 .

Diastereoselectivity of the reactions of organolithium reagents with protected erythrulose oximes

M. Carda, E. Falomir, J. Marco, 1998 .

Synthesis of conjugated δ-lactams using ring-closing metathesis

M. Carda, J. Marco, S. Rodríguez, 2002 .

Stereoselective synthesis of (+)-boronolide.

M. Carda, J. Marco, S. Rodríguez, 2002, The Journal of organic chemistry.

Stereoselective indium-mediated allylation of erythrulose derivatives in aqueous media

M. Carda, J. Marco, J. Murga, 1998 .

Stereoselective Synthesis of Five Biologically Active, Naturally Occurring Medium and Large Ring Lactones

M. Carda, J. Marco, 2011 .

A Practical Procedure of Low Valent Tin Mediated Barbier Allylation of Aldehydes in Wet Solvent.

M. Carda, B. Dhotare, A. Chattopadhyay, 2014 .

Inhibition of VEGF expression in cancer cells and endothelial cell differentiation by synthetic stilbene derivatives.

M. Carda, R. Martí-Centelles, E. Falomir, 2013, Bioorganic & medicinal chemistry.

Stereoselective synthesis of hyptolide and 6-epi-hyptolide

M. Carda, J. Marco, J. Murga, 2004 .

Asymmetric synthesis of passifloricin A: a correction in structure

M. Carda, J. Marco, J. Murga, 2003 .

On the structure of passifloricin A: asymmetric synthesis of the delta-lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)tetrahydroxyhexacos-2-enoic acid.

M. Carda, J. Marco, J. Murga, 2003, Organic letters.

Stereoselective synthesis of (+)-hyptolide

M. Carda, J. Marco, J. Murga, 2003 .

Stereoselective synthesis of spicigerolide

M. Carda, E. Falomir, J. Marco, 2003 .

Stereoselective synthesis of the cytotoxic macrolide aspergillide B

M. Carda, M. Kneeteman, J. Marco, 2009 .

Antiparasite and antimycobacterial activity of passifloricin analogues

S. Robledo, F. Echeverri, I. Velez, 2006 .

Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M.

M. Carda, E. Falomir, J. Murga, 2009, Organic & biomolecular chemistry.

Synthesis of conjugated γ- and δ-lactones from aldehydes and ketones via a vinylation(allylation)-ring closing metathesis–oxidation sequence

M. Carda, M. Kneeteman, J. Marco, 2003 .

Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3

M. Carda, E. Falomir, J. Marco, 2009 .

Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategy.

M. Carda, E. Falomir, J. Marco, 2007, Organic letters.

Stereoselective addition of organometallic reagents to a chiral acyclic nitrone derived from l-erythrulose

M. Carda, E. Falomir, J. Marco, 2005 .

Synthesis of α,α-Disubstituted α-Amino Acid Derivatives in Enantiopure Form via Stereoselective Addition of Grignard Reagents to a Chiral Acyclic Nitrone Derived from l-Erythrulose

M. Carda, E. Falomir, S. Uriel, 2002 .

Synthesis, leishmanicidal, trypanocidal and cytotoxic activity of quinoline-hydrazone hybrids.

S. Robledo, I. Velez, M. Carda, 2015, European journal of medicinal chemistry.

A stereoselective synthesis of (+)-malyngolide via a ring-closing olefin metathesis

M. Carda, J. Marco, S. Rodríguez, 2000 .

Stereoselective allylations of erythrulose derivatives under anhydrous conditions

M. Carda, J. Marco, F. González, 2001 .

The Stereoselective Synthesis of the Nonnatural Enantiomers of Communiols A-C. A Stereochemical Correction

M. Carda, E. Falomir, J. Marco, 2006 .

Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers.

M. Carda, E. Falomir, J. Marco, 2003, The Journal of organic chemistry.

Revision of the enantiotoposelective PLE-catalyzed hydrolysis of cis-5-substituted-1,3-diacyloxycyclohexanes

M. Carda, J. V. D. Eycken, L. Dumortier, 1991 .

Synthesis and biological evaluation of simplified pironetin analogues with modifications in the side chain and the lactone ring.

M. Carda, E. Falomir, J. Marco, 2016, Organic & biomolecular chemistry.

Título artículo / Títol article: Design and Synthesis of Pironetin Analogue/Colchicine Hybrids and Study of Their Cytotoxic Activity and Mechanisms of Interaction with Tubulin

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2014 .

Design and synthesis of pironetin analogue/combretastatin A-4 hybrids containing a 1,2,3-triazole ring and evaluation of their cytotoxic activity.

M. Carda, E. Falomir, S. Torijano-Gutiérrez, 2014, European journal of medicinal chemistry.

Design and Synthesis of Pironetin Analogue/Combretastatin A‐4 Hybrids and Evaluation of Their Cytotoxic Activity

M. Carda, E. Falomir, S. Torijano-Gutiérrez, 2014 .

Stereoselective Synthesis of the Naturally Occurring Lactones(−)‐Osmundalactone and (−)‐Muricatacine Using Ring‐Closing Metathesis

M. Carda, J. Marco, F. González, 2002 .

Boron Aldol Additions with Erythrulose Derivatives: Dependence of Stereoselectivity on the Type of Protecting Group.

M. Carda, E. Falomir, J. Marco, 1999 .

An ab initio study of the enolboration of 3-pentanone mediated by boron monochlorides L2BCl

M. Carda, E. Falomir, Juan Murga, 2001 .

SYNTHESIS OF (E)-2,6-DIMETHYL-6-HYDROXYOCTA-2,7-DIENOIC ACID AND THE CORRESPONDING AMIDE ( ACACIALACTAM ) IN OPTICALLY ACTIVE FORM

M. Carda, J. Marco, J. Murga, 1995 .

Diastereoselective synthesis of enantiomeric tertiary alcohols via nucleophilic additions to protected D- and L-erythrulose derivatives

M. Carda, J. Marco, F. González, 1992 .

Stereoselective synthesis of pachastrissamine (jaspine B)

M. Carda, E. Falomir, J. Marco, 2006 .

Stereoselective synthesis of microcarpalide.

M. Carda, E. Falomir, J. Marco, 2002, Organic letters.

Stereoselective synthesis of the cytotoxic macrolide FD-891.

M. Carda, J. Marco, J. Murga, 2006, Organic letters.

Diastereoselectivity of the Reactions of Organolithium Reagents with Protected Erythrulose Oximes.

M. Carda, E. Falomir, J. Marco, 1998 .

Synthesis of Conjugated δ‐Lactams Using Ring‐Closing Metathesis.

M. Carda, J. Marco, S. Rodríguez, 2002 .

Synthesis of Conjugated γ- and δ-Lactones from Aldehydes and Ketones via a Vinylation/Allylation-Ring Closing Metathesis-Oxidation Sequence

M. Carda, S. Uriel, J. Marco, 1999 .

A formal synthesis of the syributins and secosyrins and a synthetic approach towards the syringolides

M. Carda, E. Falomir, J. Marco, 1998 .

Stereoselective synthesis of α-substituted serines from protected erythrulose oximes

M. Carda, J. Marco, J. Murga, 1998 .

AN EFFICIENT PREPARATION OF SILYLATED DERIVATIVES OF L-ERYTHRULOSE 3,4-O-ACETALS

M. Carda, E. Falomir, J. Marco, 1999 .

Stereoselective Indium‐Mediated Allylation of Erythrulose Derivatives in Aqueous Media.

M. Carda, J. Marco, J. Murga, 1998 .

Short, stereoselective synthesis of the naturally occurring pyrrolidine radicamine B and a formal synthesis of nectrisine.

M. Carda, E. Falomir, J. Marco, 2008, The Journal of organic chemistry.

Stereoselective anti aldol reactions of erythrulose derivatives. Functionalized chiral d3 and d4 synthons.

M. Carda, E. Falomir, J. Marco, 2004, The Journal of organic chemistry.

Double diastereoselection in aldol reactions mediated by dicyclohexylchloroborane between L-erythrulose derivatives and chiral aldehydes. The Felkin-Anh versus Cornforth dichotomy.

M. Carda, E. Falomir, J. Marco, 2003, The Journal of organic chemistry.

Stereoselective synthesis of syn-α-methyl-β-hydroxy esters

M. Carda, E. Falomir, J. Marco, 2000 .

Chlorodicyclohexylborane-Mediated Aldol Additions of α,α‘-Dioxygenated Ketones

M. Carda, E. Falomir, J. Marco, 2001 .

Synthesis of Protected Enantiopure Erythrulose Derivatives

M. Carda, J. Marco, J. Murga, 1996 .

Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives

M. Carda, J. Marco, F. González, 1993 .

Stereoselective synthesis of a C19–C26 fragment of amphidinolides G and H

M. Carda, P. Formentin, J. Marco, 2006 .

Aldol Reactions with Erythrulose Derivatives: Stereoselective Synthesis of Differentially Protected syn-α,β-Dihydroxy Esters

M. Carda, E. Falomir, J. Marco, 2000 .

Synthesis and antiprotozoal activity of furanchalcone–quinoline, furanchalcone–chromone and furanchalcone–imidazole hybrids

S. Robledo, I. Velez, E. García, 2017, Medicinal Chemistry Research.

Stereoselective synthesis of the naturally occurring styryllactones (+)-goniofufurone and (+)-cardiobutanolide.

M. Carda, J. Marco, J. Murga, 2005, The Journal of organic chemistry.

Synthesis, Binding Properties, and Differences in Cell Uptake of G-Quadruplex Ligands Based on Carbohydrate Naphthalene Diimide Conjugates.

J. M. Pérez-Victoria, J. Mergny, E. Belmonte-Reche, 2017, Chemistry.

13C NMR spectra of eudesmane derivatives

M. Carda, J. Marco, J. F. Sanz, 1992 .

Sesquiterpene lactones fromArtemisia barrelieri

M. Carda, J. Marco, J. Jakupovic, 1991 .

Synthesis and leishmanicidal activity of cinnamic acid esters: structure–activity relationship

D. Muñoz, S. Robledo, I. Velez, 2013, Medicinal Chemistry Research.

13C NMR spectra of eudesmanolides I—eudesman‐12,6‐olides

M. Carda, J. Marco, 1987 .

The Stereochemistry and Solid State Conformation of the Eudesmanolides Torrentin and 11-epi-Torrentin

J. Lex, M. Carda, J. Marco, 1992 .

Revision of the structure of torrentin

M. Carda, J. Marco, J. F. Sanz, 1989 .

Sesquiterpenes from Centaurea aspera.

F. Sancenón, M. Carda, J. Marco, 2005, Phytochemistry.

Influence of conformational factors on acid‐catalyzed cyclizations of germacranolides: Molecular structure of the cyclization products of gallicin and 8α‐hydroxygallicin (shonachalin a)

L. Domingo, J. Lex, M. Carda, 1995 .

Sesquiterpene lactones from Picris echioides

M. Carda, J. Marco, J. F. Sanz, 1992 .

Total syntheses of rothin-A and rothin-B

M. Carda, J. Marco, M. Arnó, 1986 .

Synthesis of umbellifolide and three natural eudesman-12,8-olides from (-)-artemisin

M. Carda, J. Marco, 1987 .

New germacranolides and eudesmanolides from North African Artemisia herba-alba

M. Carda, J. Marco, S. Rodríguez, 1994 .

Oxygenated germacranes from Santolina chamaecyparissus

J. Lex, M. Carda, J. Marco, 1993 .

Synthesis of yomogin, 1-deoxyivangustin, and 1-deoxy-8-epiivangustin

M. Carda, J. Marco, M. Arnó, 1987 .

Total synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone

M. Carda, J. Marco, 1992 .

Total synthesis of (−)-mintlactone

M. Carda, J. Marco, 1991 .

Total Synthesis of the Monoterpenes (-)-Mintlactone and (+)- Isomintlactone.

M. Carda, J. Marco, 1993 .

Total Synthesis of (‐)‐Mintlactone (I).

M. Carda, J. Marco, 1992 .

Synthesis, In Silico Studies, Antiprotozoal and Cytotoxic Activities of Quinoline‐Biphenyl Hybrids

S. Robledo, M. Carda, Wilson Cardona‐G, 2020 .

Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D

M. Carda, E. Falomir, J. Marco, 2006 .

Enantioselective synthesis and absolute configurations of aculeatins A and B

M. Carda, E. Falomir, J. Marco, 2005 .

Stereoselective synthesis of anamarine

M. Carda, E. Falomir, J. Marco, 2004 .

Effects of Curcuminoid Pyrazoles on Cancer Cells and on the Expression of Telomerase Related Genes

Carla I. Nieto, M. Carda, R. Martí-Centelles, 2016, Archiv der Pharmazie.

Synthesis of honokiol analogues and evaluation of their modulating action on VEGF protein secretion and telomerase‐related gene expressions

M. Carda, E. Falomir, J. Marco, 2017, Chemical biology & drug design.

Synthesis of combretastatin A-4 O-alkyl derivatives and evaluation of their cytotoxic, antiangiogenic and antitelomerase activity.

M. Carda, E. Falomir, S. Torijano-Gutiérrez, 2013, Bioorganic & medicinal chemistry.

Synthesis and leishmanicidal activity of cinnamic acid esters: structure–activity relationship

D. Muñoz, S. Robledo, I. Velez, 2014, Medicinal Chemistry Research.

Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer

M. Carda, J. Marco, J. García-Fortanet, 2007 .

Synthesis of Combretastatin A-4 and 3′-Aminocombretastatin A-4 derivatives with Aminoacid Containing Pendants and Study of their Interaction with Tubulin and as Downregulators of the VEGF, hTERT and c-Myc Gene Expression

M. Carda, Raül Agut, E. Falomir, 2020, Molecules.

Synthesis and biological evaluation as antiangiogenic agents of ureas derived from 3'-aminocombretastatin A-4.

M. Carda, E. Falomir, J. Marco, 2019, European journal of medicinal chemistry.

Inhibitory effect of cytotoxic stilbenes related to resveratrol on the expression of the VEGF, hTERT and c-Myc genes.

M. Carda, R. Martí-Centelles, E. Falomir, 2015, European journal of medicinal chemistry.

Inhibitory effect of cytotoxic nitrogen-containing heterocyclic stilbene analogues on VEGF protein secretion and VEGF, hTERT and c-Myc gene expression

M. Carda, R. Martí-Centelles, E. Falomir, 2015 .

Arylureas derived from colchicine: Enhancement of colchicine oncogene downregulation activity.

M. Carda, E. Falomir, J. Marco, 2018, European journal of medicinal chemistry.

Inhibitory effect of pironetin analogue/colchicine hybrids on the expression of the VEGF, hTERT and c-Myc genes.

M. Carda, E. Falomir, J. Marco, 2015, Bioorganic & medicinal chemistry letters.

New N,C-Diaryl-1,2,4-triazol-3-ones: Synthesis and Evaluation as Anticancer Agents.

J. Elguero, M. Carda, E. Falomir, 2019, Medicinal chemistry (Shariqah (United Arab Emirates)).

2-Aza-2,4-cyclopentadienone. Existence and Reactivity.

S. Luis, M. Carda, A. Costero, 1988 .

Stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A.

M. Carda, J. Marco, J. Murga, 2010, The Journal of organic chemistry.

Exploring BenzylethoxyAryl Urea Scaffolds for Multitarget Immunomodulation Therapies

A. Serrels, M. Carda, E. Falomir, 2023, International journal of molecular sciences.

Diastereoselectivity in Organometallic Additions to the Carbonyl Group of Protected Erythrulose Derivatives.

M. Carda, J. Marco, J. Murga, 1998, The Journal of organic chemistry.

Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine

M. Carda, E. Falomir, J. Marco, 2008 .

Aryl Urea Based Scaffolds for Multitarget Drug Discovery in Anticancer Immunotherapies

M. Carda, Raül Agut, E. Falomir, 2021, Pharmaceuticals.

Novel multitarget inhibitors with antiangiogenic and immunomodulator properties.

M. Carda, E. Falomir, J. Marco, 2019, European journal of medicinal chemistry.

A dopamine transport inhibitor with markedly low abuse liability suppresses cocaine self-administration in the rat

J. Canales, M. Carda, V. Merino, 2009, Psychopharmacology.

Effects on tubulin polymerization and down-regulation of c-Myc, hTERT and VEGF genes by colchicine haloacetyl and haloaroyl derivatives.

M. Carda, E. Falomir, J. Marco, 2018, European journal of medicinal chemistry.

The high affinity dopamine uptake inhibitor, JHW 007, blocks cocaine-induced reward, locomotor stimulation and sensitization

J. Canales, M. Carda, J. Murga, 2010, European Neuropsychopharmacology.

Antiplasmodials soulattrolide derivatives from Calophyllum brasiliense and its mechanism of activity

M. Carda, S. B. Trujillo, Ana María Vanegas, 2019, Journal of King Saud University - Science.

Título artículo / Títol article: Synthesis and Leishmanicidal Activity of Cinnamic Acid Esters: Structure-Activity Relationship

D. Muñoz, S. Robledo, M. Carda, 2015 .

The Dopamine Uptake Inhibitor 3α-[bis(4′-fluorophenyl)metoxy]-tropane Reduces Cocaine-Induced Early-Gene Expression, Locomotor Activity, and Conditioned Reward

J. Canales, M. Carda, V. Merino, 2009, Neuropsychopharmacology.

Stereoselective synthesis of ent-communiols A-C

M. Carda, E. Falomir, J. Marco, 2005 .

Stereoselective Synthesis of ent-Communiols A—C.

M. Carda, J. Marco, J. Murga, 2006 .

Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids

S. Robledo, I. Velez, Lina M Yepes, 2017, Medicinal Chemistry Research.

N-alpha-Aminoacyl Colchicines as Promising Anticancer Agents.

S. Noppen, S. Liekens, M. Carda, 2019, Medicinal chemistry (Shariqah (United Arab Emirates)).

Stereoselective total synthesis and absolute configuration of the natural decanolides (-)-microcarpalide and (+)-lethaloxin. Identity of (+)-lethaloxin and (+)-pinolidoxin.

M. Carda, E. Falomir, J. Marco, 2005, The Journal of organic chemistry.

A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D

M. Carda, E. Falomir, J. Marco, 2010 .

Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and B.

M. Carda, J. Marco, J. Murga, 2006, The Journal of organic chemistry.

Synthesis of N-acyl Derivatives of Aminocombretastatin A-4 and Study of their Interaction with Tubulin and downregulation of c-Myc.

M. Carda, Raül Agut, E. Falomir, 2020, Medicinal chemistry.

Unveiling the Potential of BenzylethyleneAryl–Urea Scaffolds for the Design of New Onco Immunomodulating Agents

M. Carda, E. Falomir, S. Royo, 2023, Pharmaceuticals.

Synthesis and Biological Evaluation of Potential Oncoimmunomodulator Agents

M. Carda, E. Falomir, Raquel Gil-Edo, 2023, International journal of molecular sciences.

Synthesis and Biological Evaluation of Small Molecules as Potential Anticancer Multitarget Agents

M. Carda, E. Falomir, Olaya García-Pedrero, 2022, International journal of molecular sciences.

Stereoselective synthesis and structural correction of the naturally occurring lactone stagonolide G.

M. Carda, J. Marco, J. Murga, 2010, Organic letters.

Styryl carbamates backbones for the discovery of TME-disruptors agents

M. Carda, E. Falomir, Amelia Bou-Puerto, 2024, Results in Chemistry.

Tetrazole derivatives as potent immunomodulatory agents in tumor microenvironment.

M. Carda, E. Falomir, Alberto Pla-López, 2023, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Aryl azoles based scaffolds for disrupting tumor microenvironment.

M. Carda, E. Falomir, Jose C. Orellana-Palacios, 2023, Bioorganic & medicinal chemistry.