Combinatorial chemistry for the discovery of new compounds
Fernando Albericio
Principal Investigator
Professor (Organic Chemistry Dept. - UB)
Office Tel : +34 93 403 70 88
Lab Tel : +34 93 4037087-+34 93 4037069
e-mail : fernando.albericio
irbbarcelona.org
Background
This group applies sciences to obtain two types of new compounds: pharmacological agents (medicinal chemistry) and polymers (new materials field). Our research involves two complementary elements: the exploration of new methodologies for the preparation of libraries, and the application of these methodologies in the search for new compounds. In terms of methodology, we work on supports, handles, scaffolds and privileged structures that interact with two or more unrelated receptors. In the field of medicinal chemistry, our studies focus mainly on two types of processes: cancer and disorders of the central nervous system.
Research Lines
a) Synthesis and structural assignation of peptides with bioactivity
Marine Peptides. In this sub-project, we focus on structurally different compounds: kahalalide F (currently in Phase III clinical trials), cyclopeptides, and peptides with concatenated azols. Our main interests are: the analogingof natural compounds to increase the potency of natural compounds such as kahalalide F; the preparation of analog libraries to improve ADME properties; and the development of synthetic methodologies for these compounds.
Peptidic Cancer Vaccines: This project addresses the rational development of synthetic, peptide-based vaccines for the treatment of melanoma. To eliminate tumours and prevent their proliferation to other organs (metastasis), a cancer vaccine must have the capacity to selectively induce both cellular (cytotoxic T cells) and humoral (specific B lymphocytes) immune responses. The structural flexibility of the peptidic vaccines proposed would facilitate the development of cancer-specific and patient-specific therapeutic strategies. Furthermore, multiple antigens could be used on the same vaccine to increase its coverage and prevent the emergence of resistant variants.
b) Synthesis of polyheterocyclic nitrogen-containing systems
Marine invertebrates, such as sponges, tunicates, ascidians and corals, have provided a rich arsenal of new bioactive compounds. These compounds are characterized by unprecedented structures and are highly active against various tumour cell lines. We have synthesized several marine alkaloids (listed below) in solution or in solid-phase, and we are currently preparing libraries of related compounds and also developing total syntheses of new marine alkaloids. E.g.: Ascididemine, Variolin-B, Pyrrole Lamellarin derivatives, Pentacyclic Lamellarins
c) Solid-phase synthesis of bioactive libraries compounds
We use combinatorial chemistry to prepare medium-sized libraries, with a focus on improving the activity, physical properties or other characteristics of bioactive compounds.
d) New resins and linkers Solid-phase synthesis requires properly functionalized resins and linkers.
The resins can be used not only as supporting material for anchoring the scaffold and growing the compound but also as protecting group of a functionality of the reactive starting material. Our research in this field includes the modification of commercially available resins and the synthesis of new linkers.
e) The hexafluoroacetone chemistry (HFA)
The bi-functional application of HFA as protecting group and activating agent for a-hydroxyacids is useful for the preparation of depsipeptides and other compounds of biological interest. We are currently preparing depsipeptidic analogs of Cilengitide (Merck) and also libraries of peptides and glycosidic compounds.
Funding
This group receives financial support from the following sources:
- Comisión Interministerial de Ciencia y Tecnología (Interministerial Commission for Science and Technology)
- Fundació La Marató de TV3 ("La Marató de TV3" Foundation)
- Secretaría de Estado de Cooperación Internacional (AECI)(Spanish Agency for International Cooperation)
More info
Combinatorial chemistry for the discovery of new compounds
Solid-phase combinatorial synthesis of a lysyl-tRNA synthetase (LysRS) inhibitory library
Farrera-Sinfreu J, Español Y, Geslain R, Guitart T, Albericio F, Ribas de Pouplana L and Royo M
J Comb Chem, 10 (3), 391-400 (2008)
Synthesis of oligonucleotide derivatives using ChemMatrix supports
Mazzini S, García-Martin F, Alvira M, Aviñó A, Manning B, Albericio F and Eritja R
Chem Biodivers, 5 (1), 209-218 (2008)
Solid-phase synthesis of oligomers carrying several chromophore units linked by phosphodiester backbones
Aviñó A, Navarro I, Farrera-Sinfreu J, Royo M, Aymamí J, Delgado A, Llebaria A, Albericio F and Eritja R
Bioorg Med Chem Lett, 18 (7), 2306-2310 (2008)
Design, synthesis and antiproliferative properties of oligomers with chromophore units linked by amide backbones
Farrera-Sinfreu J, Aviñó A, Navarro I, Aymamí J, Beteta NG, Varón S, Pérez-Tomás R, Castillo-Avila W, Eritja R, Albericio F and Royo M
Bioorg Med Chem Lett, 18 (7), 2440-2444 (2008)
A nonacid degradable linker for solid-phase synthesis
Colombo A, De la Figuera N, Fernàndez JC, Fernández-Forner D, Albericio F and Forns P
Org Lett, 9 (21), 4319-4322 (2007)
Novel proton acceptor immonium-type coupling reagents: application in solution and solid-phase peptide synthesis
Ayman El-Faham and Fernando Albericio
Org Lett, 9 (22), 4475-4477 (2007)
Simple machine-assisted protocol for solid-phase synthesis of depsipeptides
Spengler J, Koksch B and Albericio F
Biopolymers, 88 (6), 823-828 (2007)
Design and synthesis of indole-based peptoids as potent noncompetitive antagonists of transient receptor potential vanilloid 1
Quintanar-Audelo M, Fernández-Carvajal A, Van Den Nest W, Carreño C, Ferrer-Montiel A and Albericio F
J Med Chem, 50 (24), 6133-6143 (2007)
The synthesis of naturally occurring peptides and their analogs
Cupido T, Tulla-Puche J, Spengler J and Albericio F
Curr Opin Drug Discov Devel, 10 (6), 768-783 (2007)
Enolase as a plasminogen binding protein in Leishmania mexicana
Vanegas G, Quiñones W, Carrasco-López C, Concepción JL and Albericio F and Avilán L
Parasitol Res, 101 (6), 1511-1516 (2007)
Formation of dihydrouracils via cyclization of N-Substituted 3-Thioureidopropanoic acids and facile desulfurization
Carina ML, Delpiccolo, Albericio F, Schiksnis R A and Michelotti EL
Tetrahedron, 63, 8949-8953 (2007)
Identification of protein-binding peptides by direct MALDI-TOF-MS analysis of peptide beads selected from the screening of one-bead-one peptide combinatorial libraries
Marani MM, Oliveira E, Côte S, Camperi SA, Albericio F and Cascone O
Anal Biochem, 370 (2), 215-222 (2007)
Solid-phase synthesis of oxathiocoraline by a key intermolecular disulfide dimer
Tulla-Puche J, Bayó-Puxan N, Moreno JA, Francesch AM, Cuevas C, Álvarez M and Albericio F
J Am Chem Soc, 129 (17), 5322-5323 (2007)
Smallest peptoids with antiproliferative activity on human neoplastic cells
Mas-Moruno C, Cruz LJ, Mora P, Messeguer A, Pérez-Payá E and Albericio F
J Med Chem, 50 (10), 2443-2449 (2007)
Solid-phase synthesis of sulfamate peptidomimetics
Farrera-Sinfreu J, Albericio F and Royo M
J Comb Chem, 9 (3), 501-506 (2007)
From the one-bead-one-compound concept to one-bead-one-reactor
Marani MM, Paradís-Bas M, Tulla-Puche J, Côté S, Camperi SA, Cascone O and Albericio F
J Comb Chem, 9 (3), 395-398 (2007)
Cell-penetrating proline-rich peptidomimetics
Farrera-Sinfreu J, Giralt E, Royo M and Albericio F
Methods Mol Biol, 386, 241-267 (2007)
Synthesis of IB-01211, a cyclic peptide containing 2,4-concatenated thia- and oxazoles, via Hantzsch macrocyclization
Hernández D, Vilar G, Riego E, Cañedo LM, Cuevas C, Albericio F and Alvarez M
Org Lett, 9 (5), 809-811 (2007)
Understanding the mechanism of action of the novel SSAO substrate (C7NH10)6(V10O28).2H2O, a prodrug of peroxovanadate insulin mimetics
Yraola F, García-Vicente S, Marti L, Albericio F, Zorzano A and Royo M
Chem Biol Drug Des, 69 (6), 423-428 (2007)
Novel ergopeptides as dual ligands for adenosine and dopamine receptors
Vendrell M, Angulo E, Casado V, Lluis C, Franco R, Albericio F and Royo M
J Med Chem, 50 (13), 3062-3069 (2007)
Peptides and metallic nanoparticles for biomedical applications
Kogan MJ, Olmedo I, Hosta L, Guerrero AR, Cruz LJ and Albericio F
Nanomed, 2 (3), 287-306 (2007)
Beyond azathicoraline synthesis. Synthesis of analogues
Bayó-Puxan N, Fernández A, Tulla-Puche J, Riego E, Álvarez M and Albericio F
Int J Pept Res Ther, 13 (1-2), 205-306 (2007)
Synthesis and structure-activity relationship of cytotoxic marine cyclodepsipeptide IB-01212 analogues
Cruz LJ, Francesch A, Cuevas C and Albericio F
ChemMedChem, 2 (7), 1076-1084 (2007)
ds-Oligonucleotide-peptide conjugates featuring peptides from the leucine-zipper region of Fos as switchable receptors for the oncoprotein Jun
Portela C, Albericio F, Eritja R, Castedo L and Mascareñas JL
ChemBiochem, 8 (10), 1110-1114 (2007)
Advances in solid-phase cycloadditions for heterocyclic synthesis
Feliu L, Vera-Luque P, Albericio F and Alvarez M
J Comb Chem, 9 (4), 521-565 (2007)
Oral insulin-mimetic compounds that act independently of insulin
Garcia-Vicente S, Yraola F, Marti L, González-Muñoz E, García-Barrado MJ, Canto C, Abella A, Bour S, Artuch R, Sierra C, Brandi N, Carpene C, Moratinos J, Camps M, Palacín M, Testar X, Guma A, Albericio F, Royo M, Mian A and Zorzano A
Diabetes, 56 (2), 486-493 (2007)
Inhibition of VAP1: quickly gaining ground as an anti-inflammatory therapy
Yraola F, Albericio F and Royo M
ChemMedChem, 2 (2), 173-174 (2007)
p-Nitromandelic acid as a highly acid-stable safety-catch linker for solid-phase synthesis of peptide and depsipeptide acids
Isidro-Llobet A, Alvarez M, Burger K, Spengler J and Albericio F
Org Lett, 9 (8), 1429-1432 (2007)
New developments on the synthesis of oligonucleotide-peptide conjugates
Portela C, Mascareñas JL, Albericio F, Mazzini S, Caminal C, Ramos R, Ocampo SM and Eritja R
Nucleosides Nucleotides Nucleic Acids, 26 (8-9), 963-967 (2007)
Amide-to-ester substitution in coiled coils: the effect of removing hydrogen bonds on protein structure
Scheike JA, Baldauf C, Spengler J, Albericio F, Pisabarro MT and Koksch B
Angew Chem Int Ed Engl, 46 (41), 7766-7769 (2007)
Efficient regioselective monobromination of highly activated benzenes
Pla D, Albericio F and Álvarez M
Eur J Org Chem, 12, 1921-1924 (2007)
Chlorotrityl chloride (CTC) resin as a convenient reusable protecting group
García MF, Puxan NB , Cruz LJ, Bohling CJ and Albericio F
QSAR & Comb Sci, 26, 1027-1035 (2007)
Preparation of penta-azole containing cyclopeptides: challenges in macrocyclization
Hernández D, Riego E, Francesch A, Cuevas C, Albericio F and Álvarez M
Tetrahedron, 63, 9862-9870 (2007)
Chemical synthesis of 19F-labeled HIV-1 protease using fmoc-chemistry and ChemMatrix Resin
Frutos S, Tulla-Puche J, Albericio F and Giralt E
Int J Pept Res Ther, 13, 221-227 (2007)
Partially fluorinated heterocycles from 4,4-Bis(trifluoromethyl)-hetero-1,3-dienes via C-F bond activation
Burger K, Helmreich B, Henning L, Spengler J, Albericio F and Fuchs A
Monatshefte fuer Chemie/Chemical Monthly, 138, 227-236 (2007)
Novel synthesis of bisaryl acetylenes
Soley R, Albericio F and Álvarez M
Synthesis, 10, 1559-1565 (2007)
Fmoc-2-mercaptobenzothiazole, for the introduction of the Fmoc moiety free of side-reactions
Isidro-Llobet A, Just-Baringo X, Ewenson A, Alvarez M and Albericio F
Biopolymers, 88, 733-737 (2007)
Total solid-phase synthesis of marine cyclodepsipeptide IB-01212
Cruz LJ, Cuevas C, Cañedo LM, Giralt E and Albericio F
J Org Chem, 71 (9), 3339-3344 (2006)
IB-01212, a new cytotoxic cyclodepsipeptide isolated from the marine fungus Clonostachys sp. ESNA-A009
Cruz LJ, Insua MM, Baz JP, Trujillo M, Rodriguez-Mias RA, Oliveira E, Giralt E, Albericio F and Cañedo LM
J Org Chem, 71 (9), 3335-3338 (2006)
A convenient semicarbazide resin for the solid-phase synthesis of peptide ketones and aldehydes
Vázquez J and Albericio F
Tetrahedron Lett, 47 (10), 1657-1661 (2006)
A straightforward synthesis of 5'-peptide oligonucleotide conjugates using N(alpha)-Fmoc-protected amino acids
Ocampo SM, Albericio F, Fernández I, Vilaseca M and Eritja R
Org Lett, 7 (20), 4349-4352 (2005)
Peptide and amide bond-containing dendrimers
Crespo L, Sanclimens G, Pons M, Giralt E, Royo M and Albericio F
Chem Rev, 105 (5), 1663-1681 (2005)
Cell-penetrating cis-gamma-amino-l-proline-derived peptides
Farrera-Sinfreu J, Giralt E, Castel S, Albericio F and Royo M
J Am Chem Soc, 127 (26), 9459-9468 (2005)
Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines
Carranco I, Díaz JL, Jiménez O, Vendrell M, Albericio F, Royo M and Lavilla R
J Comb Chem, 7 (1), 33-41 (2005)
A new strategy for solid-phase depsipeptide synthesis using recoverable building blocks
Albericio F, Burger K, Ruíz-Rodríguez J and Spengler J
Org Lett, 7 (4), 597-600 (2005)
Preparation of de novo globular proteins based on proline dendrimers
Sanclimens G, Crespo L, Giralt E, Albericio F and Royo M
J Org Chem, 70 (16), 6274-6281 (2005)
Solid-phase synthesis of second-generation polyproline dendrimers
Sanclimens G, Crespo L, Giralt E, Royo M and Albericio F
Biopolymers, 76 (4), 283-297 (2004)
Solid-phase combinatorial synthesis of peptide-biphenyl hybrids as calpain inhibitors
Montero A, Albericio F, Royo M and Herradón B
Org Lett, 6 (22), 4089-4092 (2004)
A new class of foldamers based on cis-gamma-amino-L-proline
Farrera-Sinfreu J, Zaccaro L, Vidal D, Salvatella X, Giralt E, Pons M, Albericio F and Royo M
J Am Chem Soc, 126 (19), 6048-6057 (2004)
Developments in peptide and amide synthesis
Albericio F
Curr Opin Chem Biol, 8 (3), 211-221 (2004)
From production of peptides in milligram amounts for research to multi-tons quantities for drugs of the future
Bruckdorfer T, Marder O and Albericio F
Curr Pharm Biotechnol, 5 (1), 29-43 (2004)
Solid-phase syntheses of furopyridine and furoquinoline systems
Cironi P, Tulla-Puche J, Barany G, Albericio F and Alvarez M
Org Lett, 6 (9), 1405-1408 (2004)
Bicyclic homodetic peptide libraries: comparison of synthetic strategies for their solid-phase synthesis
Teixido M, Altamura M, Quartara L, Giolitti A, Maggi CA, Giralt E and Albericio F
J Comb Chem, 5 (6), 760-768 (2003)
Solid-phase synthesis of the cyclic lipononadepsipeptide [N-Mst(Ser1), d-Ser4, L-Thr6, L-Asp8, L-Thr9]syringotoxin
Bayó N, Jiménez JC, Rivas L, Nicolás E and Albericio F
Chemistry, 9 (5), 1096-1103 (2003)
Tentoxin as a scaffold for drug discovery. Total solid-phase synthesis of tentoxin and a library of analogues
Jiménez JC, Chavarría B, López-Macià A, Royo M, Giralt E and Albericio F
Org Lett, 5 (12), 2115-2118 (2003)
Synthesis and SAR of alpha-acylaminoketone ligands for control of gene expression
Tice CM, Hormann RE, Thompson CS, Friz JL, Cavanaugh CK, Michelotti EL, Garcia J, Nicolas E and Albericio F
Bioorg Med Chem Lett, 13 (3), 475-478 (2003)
Saturated resins or stress of the resin
Sanclimens G, Crespo L, Pons M, Giralt E, Albericio F and Royo M
Tetrahedron Letters, 44 (9), 1751-1754 (2003)
Synthesis and NMR structure of p41icf, a potent inhibitor of human cathepsin L
Chiva C, Barthe P, Codina A, Gairí M, Molina F, Granier C, Pugnière M, Inui T, Nishio H, Nishiuchi Y, Kimura T, Sakakibara S, Albericio F and Giralt E
J Am Chem Soc, 125 (6), 1508-1517 (2003)
Solid-phase total synthesis of the pentacyclic system lamellarins U and L
Cironi P, Manzanares I, Albericio F and Alvarez M
Org Lett, 5 (16), 2959-2962 (2003)
Qualitative colorimetric tests for solid phase synthesis
Vázquez J, Qushair G and Albericio F
Methods Enzymol, 369, 21-35 (2003)
Combinatorial chemistry for the discovery of new compounds
Fernando Albericio
Principal Investigator
Professor (Organic Chemistry Dept. - UB)
Office Tel : +34 93 403 70 88
Lab Tel : +34 93 4037087-+34 93 4037069
e-mail : fernando.albericio
irbbarcelona.org
Managing Director
Mercedes Álvarez
tel +34 93 403 70 86
mercedes.alvarez
irbbarcelona.org
Postdoctoral Fellow
Jan Spengler
tel +34 93 403 71 27
jan.spengler
irbbarcelona.org
Judit Tulla
tel +34 93 403 48 69
judit.tulla
irbbarcelona.org
Svetlana Savina
tel +34 93 403 78 07
fax +34 93 403 71 26
Miroslav Sisa
tel +34 93 403 78 07
miroslav.sisa
irbbarcelona.org
PhD Student
Tommaso Cupido
tel +34 93 403 71 27
tommaso.cupido
irbbarcelona.org
Yésica García
tel +34 93 403 48 69
yesica.garcia
irbbarcelona.org
Letícia Hosta
tel +34 93 403 48 69
leticia.hosta
irbbarcelona.org
Albert Isidro
tel +34 93 403 71 27
albert.isidro
irbbarcelona.org
Carles Mas
tel +34 93 403 48 69
carles.mas
irbbarcelona.org
Marta Pelay
marta.pelay
irbbarcelona.org
Daniel Pla
tel +34 93 403 70 87
daniel.pla
irbbarcelona.org
Elisabet Prats
tel +34 93 403 48 69
elisabet.prats
irbbarcelona.org
Lorena Simón
tel +34 93 403 48 69
lorena.simon
irbbarcelona.org
Gemma Vilar
tel +34 93 403 70 87
gemma.vilar
irbbarcelona.org
Ramón Subiros Funosas
tel +34 93 403 71 27
ramon.subiros
irbbarcelona.org
Pau Ruiz Sanchís
tel +34 93 403 70 87
pau.ruiz
irbbarcelona.org
Xavier Just Baringo
tel +34 93 403 70 87
xavier.just
irbbarcelona.org
Peter Fransen
tel +34 93 403 71 27
peter.fransen
irbbarcelona.org
Anna-Iris Fernández
tel +34 93 403 70 87
anna-iris.fernandez
irbbarcelona.org
Laia Miret
tel +34 93 403 70 69
laia.miret
irbbarcelona.org
Project Manager
Eva Poca
tel +34 93 403 71 24
eva.poca
irbbarcelona.org
Research Assistant
Gerardo Alexis Acosta
tel +34 93 403 70 87
gerardo.acosta
irbbarcelona.org
Marta Paradís
tel +34 93 403 48 69
mparadis
pcb.ub.es
Miriam Góngora Benitez
tel +34 93 403 48 69
miriam.gongora
irbbarcelona.org
Visiting Professor
Sukhendu Dev
ken.dev
irbbarcelona.org