المؤلفون: Marx, Lisa, Ríos‐Lombardía, Nicolás, Süss, Philipp, Höhne, Matthias, Morís, Francisco, González‐Sabín, Javier, Berglund, Per

المصدر: European Journal of Organic Chemistry. 2020(4):510-513

مصطلحات موضوعية: Asymmetric catalysis, Biocatalysis, Ketoreductases, Medicinal chemistry, Synthetic methods, Bioteknologi, Biotechnology

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-266975Test
https://doi.org/10.1002/ejoc.201901810Test
https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201901810Test

المؤلفون: Moreno, Carlos J., Hernández, Karel, Gittings, Samantha, Bolte, Michael, Joglar, Jesús, Bujons, Jordi, Parella, Teodor, Clapés Saborit, Pere

المساهمون: Ministerio de Ciencia e Innovación (España), orcid

مصطلحات موضوعية: Ketoreductases, 2-hydroxy acids, 2-hydroxy-4-butyrolactones, 2-oxoacid aldolase, Aldol addition, Biocatalysis, http://metadata.un.org/sdg/3Test, Ensure healthy lives and promote well-being for all at all ages

العلاقة: #PLACEHOLDER_PARENT_METADATA_VALUE#; info:eu-repo/grantAgreement/MCIN/AEI/10.13039/501100011033; ACS Catalysis; Publisher's version; https://doi.org/10.1021/acscatal.3c00367Test; Sí; ACS Catalysis 13 (8): 5348–5357 (2023); http://hdl.handle.net/10261/307046Test; http://dx.doi.org/10.13039/501100004837Test; 2-s2.0-85152201605; https://api.elsevier.com/content/abstract/scopus_id/85152201605Test

الإتاحة: https://doi.org/10.1021/acscatal.3c0036710.13039/501100004837Test
http://hdl.handle.net/10261/307046Test
https://api.elsevier.com/content/abstract/scopus_id/85152201605Test

المؤلفون: Vega, Kimberly B., Cruz, Daniel M. V., Oliveira, Artur R. T., Silva, Marcos R. da, Lemos, Telma L. G. de, Oliveira, Maria C. F., Bernardo, Ricardo D. S., Sousa, Jackson R. de, Zanatta, Geancarlo, Nasário, Fábio D., Marsaioli, Anita J., Mattos, Marcos C. de

المصدر: Journal of the Brazilian Chemical Society. May 2021 32(5)

مصطلحات موضوعية: apremilast, biocatalysis, ketoreductases, lipases, enzymatic kinetic resolution

وصف الملف: text/html

الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021000501100Test

المؤلفون: Marx, Lisa, Rios-Lombardia, Nicolas, Farnberger, Judith F., Kroutil, Wolfgang, Benitez-Mateos, Ana I., Lopez-Gallego, Fernando, Moris, Francisco, Gonzalez-Sabin, Javier, Berglund, Per

المصدر: Biocascades Advanced Synthesis and Catalysis. 360(11):2157-2165

مصطلحات موضوعية: Cinacalcet, Transaminases, Ketoreductases, Asymmetric synthesis, Biocatalysis, Bioteknologi, Biotechnology

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-224455Test
https://doi.org/10.1002/adsc.201701485Test
https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.201701485Test

المؤلفون: Coto-Cid, Juan M., de Gonzalo, Gonzalo, Carmona, José A., Iglesias-Sigüenza, Javier, Rodríguez-Salamanca, Patricia, Fernández, Rosario, Hornillos, Valentín, Lassaletta, José M.

المساهمون: Ministerio de Ciencia e Innovación (España), Junta de Andalucía, European Commission, Agencia Estatal de Investigación (España)

مصطلحات موضوعية: Asymmetric catalysis, Axial chirality, Dynamic kinetic resolution, Ketoreductases, Quinolines

وصف الملف: application/pdf

العلاقة: #PLACEHOLDER_PARENT_METADATA_VALUE#; info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB−C22; info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106358GB−C2; info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC-2017-22294; Advanced Synthesis and Catalysis; Sí; Advanced Synthesis and Catalysis 366 (4): 909-915 (2024); http://hdl.handle.net/10261/356103Test; http://dx.doi.org/10.13039/501100011033Test; http://dx.doi.org/10.13039/501100000780Test; http://dx.doi.org/10.13039/501100011011Test; http://dx.doi.org/10.13039/501100004837Test; 2-s2.0-85181742989; https://api.elsevier.com/content/abstract/scopus_id/85181742989Test

الإتاحة: https://doi.org/10.1002/adsc.20230131010.13039/50110001103310.13039/50110000078010.13039/50110001101110.13039/501100004837Test
http://hdl.handle.net/10261/356103Test
https://api.elsevier.com/content/abstract/scopus_id/85181742989Test

المؤلفون: Patricia Rodríguez-Salamanca (14295076), Gonzalo de Gonzalo (12076635), José A. Carmona (14295079), Joaquín López-Serrano (1522171), Javier Iglesias-Sigüenza (1502572), Rosario Fernández (1502575), José M. Lassaletta (1502569), Valentín Hornillos (1433788)

مصطلحات موضوعية: Biophysics, Biochemistry, Molecular Biology, Cancer, Infectious Diseases, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Information Systems not elsewhere classified, takes place thanks, carbonyl group catalyzed, broad substrate scope, >- arylindole aminoalcohols, >- arylindole aldehydes, biocatalytic atroposelective synthesis, corresponding axially chiral, 2 , axially chiral, n <, atroposelective bioreduction, strategy relies, stereogenic axis, protocol features, optical purities, mild conditions, excellent conversions, configurationally labile, commercial ketoreductases, aldehyde groups

العلاقة: https://figshare.com/articles/journal_contribution/Biocatalytic_Atroposelective_Synthesis_of_Axially_Chiral_i_N_i_Arylindoles_via_Dynamic_Kinetic_Resolution/21772297Test

الإتاحة: https://doi.org/10.1021/acscatal.2c06175.s001Test

المؤلفون: Erica Elisa Ferrandi, Ivan Bassanini, Susanna Bertuletti, Sergio Riva, Chiara Tognoli, Marta Vanoni, Daniela Monti

المصدر: International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12153

مصطلحات موضوعية: enzyme discovery, biocatalysis, metagenomics, steroids, ketoreductases, stereoselectivity, functional characterization

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Biochemistry; https://dx.doi.org/10.3390/ijms232012153Test

الإتاحة: https://doi.org/10.3390/ijms232012153Test

المؤلفون: Hongjun Dong (367231), Michelle C. Y. Chang (7480244)

مصطلحات موضوعية: Biochemistry, Genetics, Evolutionary Biology, Cancer, Inorganic Chemistry, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, α- methyl, M 258, vivo screening, 3- oxo-butyryl-CoA, substrate selectivity, oxidoreductase family, α- methyl group, Structural Basis, acyl-CoA substrate, OB-CoA substrate, α- methyl group selectivity, substrate lid, Ascaris suum, saturation mutagenesis, mitochondrial ketoreductase AsHadh 2, R 213S mutation, crystal structure, 14 positions, impact substrate selectivity, Branched Substrate Selectivity, alkyl substituents, docking studies, Ascaris suum Ketoreductases

العلاقة: https://figshare.com/articles/journal_contribution/Structural_Basis_for_Branched_Substrate_Selectivity_in_a_Ketoreductase_from_Ascaris_suum/14924567Test

الإتاحة: https://doi.org/10.1021/acscatal.1c01642.s001Test

المؤلفون: Asif Fazal (6565232), Glyn R. Hemsworth (1295010), Michael E. Webb (4419319), Ryan F. Seipke (211124)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Biotechnology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, uncharacterized standalone β- ketor., anticancer compounds, Tyr 185, Aromatic checkpoint residues, substrate access, Mutational analysis, Antimycin Scaffold Antimycins, NRPS, PKS acyl carrier protein, standalone β- ketoreductases, antimycin scaffold, AntM acts, combinatorial biosynthesis, acid residues, terminal biosynthetic, C 8 carbonyl, standalone β- ketoreductase enzyme AntM

العلاقة: https://figshare.com/articles/journal_contribution/Standalone_Ketoreductase_Acts_Concomitantly_with_Biosynthesis_of_the_Antimycin_Scaffold/14813006Test

الإتاحة: https://doi.org/10.1021/acschembio.1c00229.s001Test

المؤلفون: Γιαννόπουλος, Βασίλειος Π

المساهمون: Σμόνου, Ιουλία, Στρατάκης, Εμμανουήλ, Κατερινόπουλος, Χαράλαμπος, Βασιλικογιαννάκης, Γεώργιος, Νεοχωρίτης, Κωνσταντίνος, Σπύρος, Απόστολος, Παυλίδης, Ιωάννης

مصطلحات موضوعية: Βιοκατάλυση, Φωτοκατάλυση, Βιοκαταλυτική αναγωγή, Κετορεδουκτάσες, Ρεδουκτάσες ενίου, Αρυλο αλκοόλες, Μηχανιστικές μελέτες, Διχλωρίωση, α,α-διχλωρο-β-κετοεστέρες, Biocatalysis, Photocatalysis, Biocatalytic reduction, Ketoreductases, Ene reductases, NADPH, CD-C3N4, One-pot, Aryl alcohols, Mechanistic studies, Oxone/AlCl3, Dichlorination, α,α-dichloro-β-ketoesters

وصف الملف: 320 σ. : πίν., σχήμ., εικ. (μερ. εγχρ.); 30 εκ.

العلاقة: http://elocus.lib.uoc.gr:443/dlib/3/1/9/metadata-dlib-1687244171-639233-15709.tklTest; 000456425

الإتاحة: http://elocus.lib.uoc.gr:443/dlib/3/1/9/metadata-dlib-1687244171-639233-15709.tklTest