Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maxime, Munch"'
Autor:
Odey Bsharat, Michael G. J. Doyle, Maxime Munch, Braeden A. Mair, Christopher J. C. Cooze, Volker Derdau, Armin Bauer, Duanyang Kong, Benjamin H. Rotstein, Rylan J. Lundgren
Publikováno v:
Nature Chemistry. 14:1367-1374
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87cb406c34e6006ff898999e60974cbc
https://doi.org/10.1038/s41557-022-01074-0
https://doi.org/10.1038/s41557-022-01074-0
Autor:
Maxime Munch, Erika Colombain, Timothée Stoerkler, Pauline M. Vérité, Denis Jacquemin, Gilles Ulrich, Julien Massue
Publikováno v:
Journal of Physical Chemistry B
Journal of Physical Chemistry B, 2022, 126 (10), pp.2108-2118. ⟨10.1021/acs.jpcb.2c00383⟩
Journal of Physical Chemistry B, 2022, 126 (10), pp.2108-2118. ⟨10.1021/acs.jpcb.2c00383⟩
International audience; This article describes the synthesis, spectroscopic studies, and theoretical calculations of nine original fluorophores based on the 2-(2′-hydroxyphenyl)benzazole (HBX) scaffold, functionalized at the 4-position of the pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d672be9517ade9b6f67e6be33cb0f895
https://doi.org/10.1021/acs.jpcb.2c00383
https://doi.org/10.1021/acs.jpcb.2c00383
Publikováno v:
Molecules, Vol 25, Iss 24, p 6042 (2020)
Recent progress realized in the development of optical imaging (OPI) probes and devices has made this technique more and more affordable for imaging studies and fluorescence-guided surgery procedures. However, this imaging modality still suffers from
Externí odkaz:
https://doaj.org/article/cc2c5ad1bbd346deac290d9cfcf4ac68
Publikováno v:
Organic & Biomolecular Chemistry. 20:4640-4649
This article describes the synthetic efforts towards the solubilization of organic fluorescent emitters based on a 2-(2'-hydroxybenzofuranyl)benzazole (HBBX) scaffold in aqueous media under physiological conditions (PBS, pH 7.4). These dyes are well-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::928c3e6db991f0ec6ed78b7a22854ced
https://doi.org/10.1039/d2ob00691j
https://doi.org/10.1039/d2ob00691j
Autor:
Xiaoling Zhao, Ariel Buchler, Eadan Farber, Maxime Munch, Rami Al-Haddad, Benjamin H. Rotstein, Gedaliah Farber
Publikováno v:
Molecular Imaging and Biology. 24:93-103
Overexpression and activation of matrix metalloproteinase-13 (MMP-13) within atheroma increases susceptibility to plaque rupture, a major cause of severe cardiovascular complications. In comparison to pan-MMP targeting [18F]BR-351, we evaluated the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b0e074747da651dfb5c65e733842e7
https://doi.org/10.1007/s11307-021-01626-9
https://doi.org/10.1007/s11307-021-01626-9
Publikováno v:
Chemical Communications. 57:5266-5269
A direct CO2-fixation methodology couples structurally diverse iminophosphoranes with various nucleophiles to synthesize ureas, carbamates, thiocarbamates, and amides, and is amenable for 11C radiolabeling. This methodology is practical, as demonstra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a15962964704003a6312803c54f881fc
https://doi.org/10.1039/d1cc01016f
https://doi.org/10.1039/d1cc01016f
Publikováno v:
Organic Letters. 22:2746-2750
Amides were prepared using rhodium-catalyzed coupling of organozinc iodides and carbon-11 (11C, t1/2 = 20.4 min) isocyanates. Nonradioactive isocyanates and sp3 or sp2 organozinc iodides generated ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d483c9ae7b807be244955148ee1ff0
https://doi.org/10.1021/acs.orglett.0c00729
https://doi.org/10.1021/acs.orglett.0c00729
Autor:
Odey, Bsharat, Michael G J, Doyle, Maxime, Munch, Braeden A, Mair, Christopher J C, Cooze, Volker, Derdau, Armin, Bauer, Duanyang, Kong, Benjamin H, Rotstein, Rylan J, Lundgren
Publikováno v:
Nature chemistry. 14(12)
The isotopic labelling of small molecules is integral to drug development and for understanding biochemical processes. The preparation of carbon-labelled α-amino acids remains difficult and time consuming, with established methods involving label in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ace9d9aa4f66dbc16751504b0e2ce20f
https://pubmed.ncbi.nlm.nih.gov/36344821
https://pubmed.ncbi.nlm.nih.gov/36344821
Autor:
Braeden Mair, Michael G. J. Doyle, Rylan J. Lundgren, Armin Bauer, Benjamin H. Rotstein, Volker Derdau, Odey Bsharat, Christopher Cooze, Duanyang Kong, Maxime Munch
a-Amino acids are among the essential chemical building blocks of life. These structures are embedded in many small molecule pharmaceuticals and are the primary components of peptide-based therapeutics and biologics. Isotopically labeled a-amino acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1f37e4b611dd33f43bf34c4835c8bf1
https://doi.org/10.26434/chemrxiv-2021-j4prf
https://doi.org/10.26434/chemrxiv-2021-j4prf
Publikováno v:
Chemical communications (Cambridge, England). 57(43)
A direct CO2-fixation methodology couples structurally diverse iminophosphoranes with various nucleophiles to synthesize ureas, carbamates, thiocarbamates, and amides, and is amenable for 11C radiolabeling. This methodology is practical, as demonstra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aed0615190540d77d1c5d57cfed2fea0
https://pubmed.ncbi.nlm.nih.gov/33942043
https://pubmed.ncbi.nlm.nih.gov/33942043