Nanomateriais e Moléculas Bioactivas
NANOBIOMOL
Centre National de la Recherche Scientifique
París, FranciaPublicacións en colaboración con investigadores/as de Centre National de la Recherche Scientifique (18)
2023
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Compact CPL emitters based on a [2.2]paracyclophane scaffold: recent developments and future perspectives
Journal of Materials Chemistry C, Vol. 11, Núm. 6, pp. 2053-2062
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Corrigendum to “Lithocholic acid-based design of noncalcemic vitamin D receptor agonists” [Bioorg. Chem. 111 (2021) 104878] (Bioorganic Chemistry (2021) 111, (S0045206821002558), (10.1016/j.bioorg.2021.104878))
Bioorganic Chemistry
2022
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Correction: Stereomutation and chiroptical bias in the kinetically controlled supramolecular polymerization of cyano-luminogens (Chemical Science (2022) 13 (11577-11584) DOI: 10.1039/D2SC03449B)
Chemical Science
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Dithia[9]helicenes: Molecular design, surface imaging, and circularly polarized luminescence with enhanced dissymmetry factors
Journal of Materials Chemistry C, Vol. 10, Núm. 38, pp. 14306-14318
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Mutual Monomer Orientation to Bias the Supramolecular Polymerization of [6]Helicenes and the Resulting Circularly Polarized Light and Spin Filtering Properties
Journal of the American Chemical Society, Vol. 144, Núm. 17, pp. 7709-7719
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Planar Chiral Analogues of PRODAN Based on a [2.2]Paracyclophane Scaffold: Synthesis and Photophysical Studies
Journal of Organic Chemistry, Vol. 87, Núm. 1, pp. 147-158
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Site-Specific Reduction-Induced Hydrogenation of a Helical Bilayer Nanographene with K and Rb Metals: Electron Multiaddition and Selective Rb+ Complexation
Angewandte Chemie - International Edition, Vol. 61, Núm. 10
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Stereomutation and chiroptical bias in the kinetically controlled supramolecular polymerization of cyano-luminogens
Chemical Science
2021
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Design, Synthesis, Evaluation and Structure of Allenic 1α,25-Dihydroxyvitamin D3 Analogs with Locked Mobility at C-17
Chemistry - A European Journal, Vol. 27, Núm. 53, pp. 13384-13389
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Design, synthesis and evaluation of side-chain hydroxylated derivatives of lithocholic acid as potent agonists of the vitamin D receptor (VDR)
Bioorganic Chemistry, Vol. 115
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Distance Matters: Biasing Mechanism, Transfer of Asymmetry, and Stereomutation in N-Annulated Perylene Bisimide Supramolecular Polymers
Journal of the American Chemical Society, Vol. 143, Núm. 33, pp. 13281-13291
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Enantioenriched Ruthenium-Tris-Bipyridine Complexes Bearing One Helical Bipyridine Ligand: Access to Fused Multihelicenic Systems and Chiroptical Redox Switches
Inorganic Chemistry, Vol. 60, Núm. 16, pp. 11838-11851
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Lithocholic acid-based design of noncalcemic vitamin D receptor agonists
Bioorganic Chemistry, Vol. 111
2020
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Metal-Based Multihelicenic Architectures
Angewandte Chemie - International Edition, Vol. 59, Núm. 51, pp. 22840-22856
2011
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1α,25(OH)2-3-epi-vitamin D3, a natural physiological metabolite of vitamin D3: Its synthesis, biological activity and crystal structure with its receptor
PLoS ONE, Vol. 6, Núm. 3
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Synthesis, structure, and biological activity of des-side Chain analogues of 1α,25-Dihydroxyvitamin D3 with substituents at C18
ChemMedChem, Vol. 6, Núm. 5, pp. 788-793
2008
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Structure-Based Design of a Superagonist Ligand for the Vitamin D Nuclear Receptor
Chemistry and Biology, Vol. 15, Núm. 4, pp. 383-392
2007
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Crystal structure of the vitamin D nuclear receptor ligand binding domain in complex with a locked side chain analog of calcitriol
Archives of Biochemistry and Biophysics, Vol. 460, Núm. 2, pp. 172-176