Research Programmes
Chemistry & Molecular Pharmacology
Combinatorial chemistry for the discovery of new compounds
Fernando Albericio
Group Leader
Professor (Organic Chemistry Dept. - UB)
Office Tel : +34 93 40 37088
Lab Tel : +34 93 403 70 87 / +34 93 403 70 69
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
Acridine and quindoline oligomers linked through a 4-aminoproline backbone prefer G-quadruplex structures.
Ferreira R, Artali R, Farrera-Sinfreu J, Albericio F, Royo M, Eritja R, Mazzini S.
Biochim Biophys Acta., 1810 (8), 769-776 (2011)
Streamlined access to functionalized chromenes and quinolines using domino reactions of salicylic aldehydes and methyl 4-chloro-2-butynoate
Bello D, Ruiz-Rodríguez J, Albericio F, Ramón, R, Lavilla R.
Eur J Org Chem, 28, 5373-5379 (2010)
Solid-phase synthesis of aza-Kahalalide F analogues: (2R,3R)-2-amino-3-azidobutanoic acid as precursor of the aza-threonine
Izzo I, Acosta GA, Tulla-Puche J, Cupido T, Martin-Lopez MJ, Cuevas C, Albericio F.
Eur J Org Chem, 13, 2536-2543 (2010)
Sample preparation for sequencing hits from one-bead-one-peptide combinatorial libraries by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
Martínez-Ceron MC, Giudicessi SL, Marani MM, Albericio F, Cascone O, Erra-Balsells R, Camperi SA.
Anal Biochem., 400 (2), 295-297 (2010)
Engineering advanced capsosomes: maximizing the number of subcompartments, cargo retention, and temperature-triggered reaction.
Chandrawati R, Hosta-Rigau L, Vanderstraaten D, Lokuliyana SA, Städler B, Albericio F, Caruso F.
ACS Nano., 4 (3), 1351-1361 (2010)
A convenient microwave-enhanced solid-phase synthesis of short chain N-methyl-rich peptides.
Rodríguez H, Suarez M, Albericio F.
J Pept Sci., 16 (3), 136-140 (2010)
A hybrid indoloquinolizidine peptide as allosteric modulator of dopamine D1 receptors.
Soriano A, Vendrell M, Gonzalez S, Mallol J, Albericio F, Royo M, Lluís C, Canela EI, Franco R, Cortés A, Casadó V.
J Pharmacol Exp Ther., 332 (3), 876-885 (2010)
Targeted PLGA nano- but not microparticles specifically deliver antigen to human dendritic cells via DC-SIGN in vitro.
Cruz LJ, Tacken PJ, Fokkink R, Joosten B, Stuart MC, Albericio F, Torensma R, Figdor CG.
J Control Release., 144 (2), 118-126 (2010)
Multifunctionalized gold nanoparticles with peptides targeted to gastrin-releasing peptide receptor of a tumor cell line.
Hosta-Rigau L, Olmedo I, Arbiol J, Cruz LJ, Kogan MJ, Albericio F.
Bioconjug Chem., 21 (6), 1070-1078 (2010)
Oxime carbonates: Novel reagents for the introduction of Fmoc and alloc protecting groups, free of side reactions
Khattab SN, Subirós-Funosas R, El-Faham A, Albericio F
Eur J Org Chem, 17, 3275-3280 (2010)
Synthesis of orthogonally protected L-threo-beta-ethoxyasparagine
Spengler J, Pelay M, Tulla-Puche J, Albericio F.
Amino Acids, 39 (1), 161-165 (2010)
A novel family of onium salts based upon isonitroso meldrum's acid proves useful as peptide coupling reagents
El-Faham A, Subirós-Funosas R, Albericio F.
Eur J Org Chem, 19, 3641-3649 (2010)
2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran-5-methyl (Pbfm) as an alternative to the trityl group for the side-chain protection of cysteine and asparagine/glutamine
Garcia O, Bofill JM, Nicolas E, Albericio F.
Eur J Org Chem, 19, 3631-3640 (2010)
Solid-phase synthesis of new Trp(Nps)-containing dipeptide derivatives as TRPV1 channel blockers
Pérez de Vega MJ, García-López MT, Zaccaro L, Royo M, Albericio F, Fernández-Carvajal A, Ferrer-Montiel A, González-Muñiz R.
Molecules, 15 (7), 4924-4933 (2010)
Amphiphilic peptides and their cross-disciplinary role as building blocks for nanoscience.
Cavalli S, Albericio F, Kros A.
Chem Soc Rev., 39 (1), 241-263 (2010)
COMU: a third generation of uronium-type coupling reagents.
El-Faham A, Albericio F.
J Pept Sci., 16 (1), 6-9 (2010)
Capsosomes with multilayered subcompartments: Assembly and loading with hydrophobic cargo
Hosta-Rigau L, Städler B, Yan Y, Collins Nice E, Heath JK, Albericio F, Caruso F.
Adv Funct Mater, 20 (1), 59-66 (2010)
Microwave assisted SPPS of amylin and its toxicity of the pure product to RIN-5F cells
Muthusamy K, Albericio F, Arvidsson PI, Govender P, Kruger HG, Maguire GE, Govender T.
Biopolymers, 64 (3), 323-330 (2010)
Postsynthetic modification of peptides: chemoselective C-arylation of tryptophan residues
Ruiz-Rodríguez J, Albericio F, Lavilla R.
Chemistry, 16 (4), 1124-1127 (2010)
A novel dipeptidomimetic containing a cyclic threonine.
Sicherl F, Cupido T, Albericio F.
Chem Commun (Camb)., 46 (8), 1266-1268 (2010)
Synthesis of 2-(4,6-dimethoxy-1,3,5-triazin-2-yloxyimino) derivatives: application in solution peptide synthesis.
Al-Warhi TI, Al-Hazimi HM, El-Faham A, Albericio F.
Molecules, 15 (12), 9403-9417 (2010)
ChemMatrix(®) for complex peptides and combinatorial chemistry.
García-Ramos Y, Paradís-Bas M, Tulla-Puche J, Albericio F.
J Pept Sci., 16 (12), 675-678 (2010)
Improving the brain delivery of gold nanoparticles by conjugation with an amphipathic peptide.
Guerrero S, Araya E, Fiedler JL, Arias JI, Adura C, Albericio F, Giralt E, Arias JL, Fernández MS, Kogan MJ.
Nanomedicine (Lond)., 5 (6), 897-913 (2010)
Improved antimicrobial activity of h-lysozyme (107-115) by rational Ala substitution.
González R, Albericio F, Cascone O, Iannucci NB.
J Pept Sci., 16 (8), 424-429 (2010)
Antioxidant, cytotoxic and apoptotic activity of Drosophyllum lusitanicum extracts
Gonçalves S, Xavier C, Costa P, Alberício F, Romano A.
J Med Plants Res, 4 (15), 1601-1608 (2010)
Total regioselective control of tartaric acid
Spengler J, Fernández-Llamazares AI, Ruiz-Rodríguez J, Burger K, Albericio F.
J Org Chem., 75 (16), 5746-5769 (2010)
PyOxP and PyOxB: the Oxyma-based novel family of phosphonium salts
Subirós-Funosas R, El-Faham A, Albericio F.
Org Biomol Chem., 8 (16), 3665-3673 (2010)
Amide-to-ester substitution allows fine-tuning of the cyclopeptide conformational ensemble.
Cupido T, Spengler J, Ruiz-Rodriguez J, Adan J, Mitjans F, Piulats J, Albericio F.
Angew Chem Int Ed Engl., 49 (15), 2732-2737 (2010)
Synthesis and aminolysis of N,N-diethyl carbamic esters of HOBt derivatives
Khattab SN, Hassan SY, Hamed EA, Albericio F, El-Faham A.
Korean J Chem Eng, 31, 75-81 (2010)
Solid-phase synthesis of chiral bicyclic guanidinium oligomers
Martos V, Castreño P, Royo M, Albericio F and Mendoza JD
J Comb Chem (2009)
Synthesis of the pyrrolo[2,3-c]carbazole core of the dictyodendrins
Ayats C, Soley R, Albericio F and Alvarez M
Org Biomol Chem, 7 (5), 860-862 (2009)
NMe amide as a synthetic surrogate for the thioester moiety in thiocoraline
Tulla-Puche J, Marcucci E, Prats-Alfonso E, Bayó-Puxan N and Albericio F
J Med Chem, 52 (3), 834-839 (2009)
Conjugation of Kahalalide F with gold nanoparticles to enhance in vitro antitumoral activity
Hosta L, Pla-Roca M, Arbiol J, López-Iglesias C, Samitier J, Cruz LJ, Kogan MJ and Albericio F
Bioconjug Chem, 20 (1), 138-146 (2009)
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)
Design and synthesis of FAJANU: a de novo C(2) symmetric cyclopeptide family
Garcia-Martin F, Cruz LJ, Rodriguez-Mias RA, Giralt E and Albericio F
J Med Chem, 51 (11), 3194-3202 (2008)
Structure-activity relationship of kahalalide F synthetic analogues
Jiménez JC, López-Macià A, Gracia C, Varón S, Carrascal M, Caba JM, Royo M, Francesch AM, Cuevas C, Giralt E and Albericio F
J Med Chem, 51 (16), 4920-4931 (2008)
Asymmetric synthesis of α-unsubstituted β-hydroxy acids
Spengler J and Albericio F
Curr Org Chem, 5 (2), 151-161 (2008)
[{Cu(pzPh)(Opo)}2(?-Cl)2]: A new dinuclear copper(II) complex with a chloride bridge and mixed blocking ligands
Yraola F, Albericio F, Corbella M and Royo M
Inorg Chim Acta, 36 (8), 2455-2461 (2008)
A 6H-Pyran-3-one scaffold derived from a C-Glycoside
de la Figuera N, Fiol S, Fernández JC, Forns P, Fernández-Forner D and Albericio F
Lett Org Chem, 5 (5), 374-378 (2008)
A novel protecting/activating strategy for beta-hydroxy acids and its use in convergent peptide synthesis
Spengler J, Ruíz-Rodríguez J, Yraola F, Royo M, Winter M, Burger K and Albericio F
J Org Chem, 73 (6), 2311-2314 (2008)
Conformationally restricted hydantoin-based peptidomimetics as inhibitors of caspase-3 with basic groups allowed at the S3 enzyme subsite
Vázquez J, García-Jareño A, Mondragón L, Rubio-Martinez J, Pérez-Payá E and Albericio F
ChemMedChem, 3 (6), 979-985 (2008)
Crystal structure of hexakis(4-fluorophenylethylammonium)decavanadate(
Yraola F, Albericio F, Royo M and Solans X
Kristallogr, 223, 45-47 (2008)
Cysteine-S-trityl a key derivative to prepare N-methyl cysteines
Marcucci E, Bayó-Puxan N, Tulla-Puche J, Spengler J and Albericio F
J Comb Chem, 10 (1), 69-78 (2008)
EDOTn and MIM, new peptide backbone protecting groups
Isidro-Llobet A, Just-Baringo X, Alvarez M and Albericio F
Biopolymers, 90 (3), 444-449 (2008)
Morpholine-based immonium and halogenoamidinium salts as coupling reagents in Peptide synthesis1
El-Faham A and Albericio F
J Org Chem, 73 (7), 2731-2737 (2008)
N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate (TCFH), a powerful coupling reagent for bioconjugation
Tulla-Puche J, Torres A, Calvo P, Royo M and Albericio F
Bioconjug Chem, 19 (10), 1968-1971 (2008)
Nanostructure formation enhances the activity of LPS-neutralizing peptides
Mas-Moruno C, Cascales L, Cruz LJ, Mora P, Pérez-Payá E and Albericio F
ChemMedChem, 3 (11), 1748-1755 (2008)
Peptides
Tulla-Puche J and Albericio F
In The Power of Functional Resins in Organic Chemistry (Tulla-Puche J, Albericio J), Wiley-VCH Verlag GmbH & Co, 495-527 (2008)
Phenyl-EDOTn derivatives as super acid labile carboxylic acid protecting groups for peptide synthesis
Isidro-Llobet A, Álvarez M and Albericio F
Tetrahedron Lett, 49 (20), 3304-3307 (2008)
Protection by conformationally restricted mobility: first solid-phase synthesis of triostin A
Tulla-Puche J, Marcucci E, Fermin M, Bayó-Puxan N and Albericio F
Chemistry, 14 (15), 4475-4478 (2008)
PyClocK, the phosphonium salt derived from 6-Cl-HOBt
Subiros-Funosas R, Moreno JA, Bayó-Puxan N, Abu-Rabeah K, Ewenson A and Albericio F
Chem Today, 26 (4), 10-12 (2008)
Recent advances in lamellarin alkaloids: isolation, synthesis and activity
Pla D, Albericio F and Alvarez M
Anticancer Agents Med Chem, 8 (7), 746-760 (2008)
Solid phase preparation of 1,3-disubstituted indazole derivatives
de la Figuera N, Fiol S, Fernández JC, Forns P, Eastwood P and Albericio F
QSAR & Comb Sci, 27 (11-12), 1267-1273 (2008)
Solid supports for the synthesis of peptides. From first used resin to the most sophisticated in the market
García-Martin F and Albericio F
Chem Today, 26 (4), 29-34 (2008)
Stereomeric studies on the oxidation and alkylation of 4-thiazolidinones
Colombo A, Fernández JC, Fernández-Forner D, de la Figuera N, Albericio F and Forns P
Tetrahedron Lett, 49 (10), 1569-1572 (2008)
Synthesis and antitumor activity of mechercharmycin A analogues
Hernández D, Altuna M, Cuevas C, Aligué R, Albericio F and Alvarez M
J Med Chem, 51 (18), 5722-5730 (2008)
Synthesis of natural product derivatives containing 2,4-concatenated oxazoles
Hernandez D, Riego E, Albericio F and Álvarez M
Eur J Org, 19, 3389-3396 (2008)
THAL, a sterically unhindered linker for the solid-phase synthesis of acid-sensitive protected peptide acids
Isidro-Llobet A, Boas U, Jensen KJ, Alvarez M and Albericio F
J Org Chem, 73 (18), 7342-7344 (2008)
The (classic concept of) solid support
Albericio F and Tulla-Puche J
In The Power of Functional Resins in Organic Chemistry (Tulla-Puche J, Albericio J), Wiley-VCH Verlag GmbH & Co, 3-14 (2008)
Tiratricol neutralizes bacterial endotoxins and reduces lipopolysaccharide-induced TNF-alpha production in the cell
Cascales L, Mas-Moruno C, Tamborero S, Aceña JL, Sanz-Cervera JF, Fustero S, Cruz LJ, Mora P, Albericio F and Pérez-Payá E
Chem Biol Drug Des, 72 (4), 320-328 (2008)
Use of N-methylpiperazine for the preparation of piperazine-based unsymmetrical bis-ureas as anti-HIV agents
El-Faham A, Armand-Ugón M, Esté JA and Albericio F
ChemMedChem, 3 (7), 1034-1037 (2008)
Trishomocubane amino acid as a beta-turn scaffold
Albericio F, Arvidson PI, Bisetty K, Giralt E, Govender T, Jali S, Kongsaeree P, Kruger HG and Prabpai S
Chem Biol Drug Des, 71 (2), 125-130 (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)
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)
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)
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)
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 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)
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
Group Leader
Professor (Organic Chemistry Dept. - UB)
Office Tel : +34 93 40 37088
Lab Tel : +34 93 403 70 87 / +34 93 403 70 69
e-mail : fernando.albericio
irbbarcelona.org
Research Associates
Jan Spengler
tel +34 93 40 37127
e-mail: jan.spengler
irbbarcelona.org
Mercedes álvarez
tel +34 93 40 37086
e-mail: mercedes.alvarez
irbbarcelona.org
Postdoctoral Fellows
Hortensia María Rodríguez
tel +34 93 40 37127
e-mail: hortensia.rodriguez
irbbarcelona.org
Juan Bautista Blanco
tel +34 93 40 37127
e-mail: juanbautista.blanco
irbbarcelona.org
Judit Tulla
tel +34 93 40 37127
e-mail: judit.tulla
irbbarcelona.org
Markus Muttenthaler
e-mail: markus.muttenthaler
irbbarcelona.org
Paolo Bruno
e-mail: paolo.bruno
irbbarcelona.org
Salvatore Bongarzone
tel +34 93 40 34869
e-mail: salvatore.bongarzone
irbbarcelona.org
PhD Students
Adriana Lorente
tel +34 93 40 34869
e-mail: adriana.lorente
irbbarcelona.org
Anna-Iris Fernández-Llamazares
tel +34 93 40 37127
e-mail: anna-iris.fernandez
irbbarcelona.org
Daniel Carbajo
tel +34 93 40 37127
e-mail: daniel.carbajo
irbbarcelona.org
Janire Lamariano
tel +34 93 40 34869
e-mail: janire.lamariano
irbbarcelona.org
Laia Miret
tel +34 93 40 37127
e-mail: laia.miret
irbbarcelona.org
Marta Pelay
tel +34 93 40 37087
e-mail: marta.pelay
irbbarcelona.org
Peter Fransen
tel +34 93 40 37127
e-mail: peter.fransen
irbbarcelona.org
Ramón Subirós
tel +34 93 40 37127
e-mail: ramon.subiros
irbbarcelona.org
Rubí Zamudio
tel +34 93 40 37127
e-mail: rubi.zamudio
irbbarcelona.org
Tobias Maria Postma
tel +34 93 40 37127
e-mail: tobias.postma
irbbarcelona.org
Vida De La Paz Del Mar Castro
tel +34 93 40 37127
e-mail: vida.castro
irbbarcelona.org
Xavier Just
tel +34 93 40 37087
e-mail: xavier.just
irbbarcelona.org
MSc Students
Clàudia Roca
tel + 34 93 40 37127
e-mail: claudia.roca
irbbarcelona.org
Research Assistants
Gerardo Acosta
tel +34 93 40 34869
e-mail: gerardo.acosta
irbbarcelona.org
Marta Paradís
tel +34 93 40 34869
e-mail: marta.paradis
irbbarcelona.org
Miriam Góngora
tel +34 93 40 34869
e-mail: miriam.gongora
irbbarcelona.org
Visiting Students
David Meunier
e-mail: david.meunier
irbbarcelona.org
Combinatorial chemistry for the discovery of new compounds
- 7 July 2011
Institute News
Fernando Albericio presented with the “Vincent du Vigneaud Award” by the American Peptide Society - 2 February 2011
Institute News
Fernando Albericio, doctor “honoris causa” by the University of Buenos Aires - 22 July 2009
Science News
Project given the go-ahead to develop new anti-cancer drugs“Bisthiazol” is funded by the Agency for Assessing and Marketing Research Results, run by the University of Barcelona (UB), and the Santander Bank.
- 15 March 2007
Mi Salud online
Generan una nueva familia de compuestos con potentes propiedades antidiabéticas - 15 March 2007
Doyma
Investigadores españoles descubren una línea de sustancias para tratar varios tipos de diabetes - 15 March 2007
Diario Médico
Hallados nuevos agentes con propiedades antidiabéticas - 14 March 2007
Science News
Development of a new family of compounds with potent anti-diabetic propertiesResearchers at IRB Barcelona and the Barcelona Science Park have transferred the patent to the biotech enterprise Genmedica Therapeutics








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