Sökresultat - "decarboxylation"

Chalcogen-Bonding-Enabled, Light-Driven Decarboxylative Oxygenation of Amino Acid Derivatives and Short Peptides Using O 2 .

Li Y; School of Pharmacy and Key Laboratory of Molecular Pharmacology and Drug Evaluation (Ministry of Education), Yantai University, Yantai, 264005, China., Ye T; School of Pharmacy and Key Laboratory of Molecular Pharmacology and Drug Evaluation (Ministry of Education), Yantai University, Yantai, 264005, China., Li F; School of Pharmacy and Key Laboratory of Molecular Pharmacology and Drug Evaluation (Ministry of Education), Yantai University, Yantai, 264005, China., Tan S; School of Pharmacy and Key Laboratory of Molecular Pharmacology and Drug Evaluation (Ministry of Education), Yantai University, Yantai, 264005, China.

Journal Article , 2025

Highly-Selective Electrochemical Decarboxylative Late-Stage Functionalization of Amino Acids.

Ghosh A; Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India., Parida VK; Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India., von Münchow T; Institute for Organic and Biomolecular Chemistry, Georg-August-Universität Göttingen, Tammannstr. 2, 37077, Göttingen, Germany., Ackermann L; Institute for Organic and Biomolecular Chemistry, Georg-August-Universität Göttingen, Tammannstr. 2, 37077, Göttingen, Germany., Banerjee D; Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India.

Journal Article , 2025

Pyridoxal-Inspired Photo-Decarboxylase Catalysis: Photochemical Decarboxylation of Unprotected Amino Acids.

Tan DH; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA., Das A; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA., Huang V; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA., Schoch TD; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA., Mohammed AL; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA., Lipshultz JM; Department of Chemistry and Institute of Chemical Biology and Drug Discovery, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11794, USA.

Journal Article , 2025

Decarboxylative click cycloaddition: an emerging strategy towards substituted 1,2,3-triazole derivatives.

Kaur M; Laboratory of Organic Synthesis and Catalysis, Department of Chemistry, Central University of Punjab, Bathinda, 151401, India., Bharti D; Laboratory of Organic Synthesis and Catalysis, Department of Chemistry, Central University of Punjab, Bathinda, 151401, India., Kumar V; Laboratory of Organic Synthesis and Catalysis, Department of Chemistry, Central University of Punjab, Bathinda, 151401, India., Verma PK; School of Advanced Chemical Sciences, Shoolini University, Solan, Himachal Pradesh, 173229, India., Kumar R; Laboratory of Organic Synthesis and Catalysis, Department of Chemistry, Central University of Punjab, Bathinda, 151401, India. rakesh.kumar@cup.edu.in.

Journal Article; Review , 2025

Photodecarboxylase-assistant cascades for hydrolyzed and decarboxylation enrichment of PUFAs in a three-liquid-phase system.

Liang Q; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China., Li J; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China., Yang Z; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China., Chen H; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China; Guangdong Provincial Key Laboratory of Fermentation and Enzyme Engineering, South China University of Technology, Guangzhou 510006, China., Yang B; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China; Guangdong Provincial Key Laboratory of Fermentation and Enzyme Engineering, South China University of Technology, Guangzhou 510006, China., Wang Y; School of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China., Ma Y; State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640, China; School of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China. Electronic address: myj605740779@scut.edu.cn., Li Z; School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China. Electronic address: bizgl@scut.edu.cn.

Journal Article , 2025

Molecular characterization of histidine and tyrosine decarboxylating Enterococcus species isolated from some milk products.

Shanab O; Department of Biochemistry, Faculty of Veterinary Medicine, South Valley University, Qena, 83523, Egypt., Fareed F; Department of Biochemistry, Faculty of Veterinary Medicine, South Valley University, Qena, 83523, Egypt., Nassar AY; Department of Biochemistry, Faculty of Medicine, Assiut University, Assiut, 71526, Egypt., Abd-Elhafeez HH; Department of Cell and Tissues, Faculty of Veterinary Medicine, Assiut University, Assiut, 71526, Egypt. hhnnzz91@aun.edu.eg., Ahmed AS; Department of Food Hygiene and Control (Milk Hygiene), Faculty of Veterinary Medicine, South Valley University, Qena, 83523, Egypt., El-Zamkan MA; Department of Food Hygiene and Control (Milk Hygiene), Faculty of Veterinary Medicine, South Valley University, Qena, 83523, Egypt. m_zam@vet.svu.edu.eg.

Journal Article , 2025

Promiscuity Guided Evolution of Decarboxylative Aldolases for Synthesis of Tertiary γ-Hydroxy Amino Acids.

Campbell ME; Department of Chemistry, University of Wisconsin-Madison, USA, Madison, WI 53706., Ohler AR; Department of Chemistry, University of Wisconsin-Madison, USA, Madison, WI 53706., McGill MJ; Department of Chemistry, University of Wisconsin-Madison, USA, Madison, WI 53706., Buller AR; Department of Chemistry, University of Wisconsin-Madison, USA, Madison, WI 53706.

Journal Article , 2025

Detoxification of Ustiloxin A Through Oxidative Deamination and Decarboxylation by Endophytic Fungus Petriella setifera .

Li P; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China., Gu G; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China., Hou X; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China., Xu D; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China., Dai J; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100050, China., Kuang Y; Department of Basic Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China., Wang M; Innovation Center of Pesticide Research, Department of Applied Chemistry, College of Science, China Agricultural University, Beijing 100193, China., Lai D; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China., Zhou L; Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China.

Journal Article; Research Support, Non-U.S. Gov't , 2025

Amide Synthesis from Decarboxylative Coupling of Isocyanates and Carboxylic Acids.

Wang R; School of Chemistry, Sun Yat-sen University, Guangzhou, 510006, China., Liu WH; School of Chemistry, Sun Yat-sen University, Guangzhou, 510006, China.

Journal Article; Review , 2025

Tryptamine accumulates in cheese mainly via the decarboxylation of tryptophan by lactic acid bacteria.

Arranz D; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain; Molecular Microbiology Research Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Avenida del Hospital Central de Asturias, Oviedo 33005, Spain. Electronic address: david.arranz@ipla.csic.es., Fernández E; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain; Molecular Microbiology Research Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Avenida del Hospital Central de Asturias, Oviedo 33005, Spain. Electronic address: eva.fernandez@ipla.csic.es., Szekeres B; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain., Carvalho A; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain., Rio BD; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain; Molecular Microbiology Research Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Avenida del Hospital Central de Asturias, Oviedo 33005, Spain. Electronic address: beadelrio@ipla.csic.es., Redruello B; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain; Molecular Microbiology Research Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Avenida del Hospital Central de Asturias, Oviedo 33005, Spain. Electronic address: bredruel@ipla.csic.es., Alvarez MA; Molecular Microbiology Research Laboratory, Department of Technology and Biotechnology of Dairy Products, Dairy Research Institute (IPLA-CSIC), Villaviciosa 33300, Spain; Molecular Microbiology Research Group, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Avenida del Hospital Central de Asturias, Oviedo 33005, Spain. Electronic address: maag@ipla.csic.es.

Journal Article , 2025

Continuous site mutagenesis of fatty acid photodecarboxylase enables a highly thermostable enzyme for co-solvent-free decarboxylation.

Wang M; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China., Wang Y; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China., Huang H; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China., Cao X; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China., Ren J; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China., Feng Y; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China. Electronic address: afyb@dlut.edu.cn., Xue S; MOE Key Laboratory of Bio-Intelligent Manufacturing, School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, China. Electronic address: xuesong@dlut.edu.cn.

Journal Article , 2025

Regulation of ferryl reactivity by the cytochrome P450 decarboxylase OleT.

Gering HE; Department of Structural and Molecular Biochemistry, North Carolina State University, Raleigh, NC 27695, United States., Manley OM; Department of Structural and Molecular Biochemistry, North Carolina State University, Raleigh, NC 27695, United States., Holwerda AJ; Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, United States., Grant JL; Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, United States., Ratigan SC; Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, United States., Makris TM; Department of Structural and Molecular Biochemistry, North Carolina State University, Raleigh, NC 27695, United States; Department of Chemistry, North Carolina State University, Raleigh, NC 27695, United States. Electronic address: tmmakris@ncsu.edu.

Journal Article , 2025

Enabling electrochemical, decarboxylative C(sp ² )-C(sp ³ ) cross-coupling for parallel medicinal chemistry.

Morvan J; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Tang B; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Ryabchuk P; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Renders E; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Last S; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Van Eynde L; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Bartkowiak K; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Buijnsters PJJA; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium., Jones AX; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium. Electronic address: ajones40@its.jnj.com., Carvalho MA; Global Discovery Chemistry, Janssen Research and Development, Turnhoutseweg 30, Beerse, 2340 Belgium. Electronic address: mcarva11@its.jnj.com., Diccianni JB; Global Discovery Chemistry, Janssen Research & Development LLC, 1400 McKean Road, Spring House, PA 19477, United States. Electronic address: jdiccian@its.jnj.com.

Journal Article , 2025

Cascade synthesis of miltirone derivatives via arylation, decarboxylation, and aromatization for their potential as antitumor agents.

Huang H; Key Laboratory of Modern Preparation of TCM, Ministry of Education, Jiangxi University of Chinese Medicine, Nanchang 330004, China., Yin F; School of Pharmaceutical Science, University of South China, Heng Yang 421001, People's Republic of China; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China. Electronic address: yinfucheng1994@163.com., Zhang Y; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China., Luo Z; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China., Wan S; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China., Ma L; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China., Wang X; State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China. Electronic address: xbwang@cpu.edu.cn.

Journal Article , 2025

Coordinated conformational changes in P450 decarboxylases enable hydrocarbons production from renewable feedstocks.

Generoso WC; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Alvarenga AHS; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Simões IT; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Miyamoto RY; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Melo RR; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Guilherme EPX; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Mandelli F; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Santos CA; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Prata R; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Santos CRD; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Colombari FM; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Morais MAB; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Pimentel Fernandes R; Sinochem Petróleo Brasil Ltda, Rio de Janeiro, RJ, Brazil., Persinoti GF; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Murakami MT; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil., Zanphorlin LM; Brazilian Biorenewables National Laboratory, Brazilian Center for Research in Energy and Materials, Campinas, SP, Brazil. leticia.zanphorlin@lnbr.cnpem.br.

Journal Article , 2025

Complex molecule synthesis by electrocatalytic decarboxylative cross-coupling.

Zhang B; Department of Chemistry, Scripps Research, La Jolla, CA, USA., He J; Department of Chemistry, Scripps Research, La Jolla, CA, USA., Gao Y; Department of Chemistry, Scripps Research, La Jolla, CA, USA., Levy L; Department of Chemistry, Scripps Research, La Jolla, CA, USA., Oderinde MS; Department of Discovery Synthesis, Bristol Myers Squibb Research & Early Development, Princeton, NJ, USA., Palkowitz MD; Small Molecule Drug Discovery, Bristol Myers Squibb Research & Early Development, Cambridge, MA, USA., Dhar TGM; Bristol Myers Squibb Research & Early Development, Princeton, NJ, USA., Mandler MD; Bristol Myers Squibb Research & Early Development, Princeton, NJ, USA., Collins MR; Oncology Medicinal Chemistry Department, Pfizer Pharmaceuticals, San Diego, CA, USA., Schmitt DC; Medicine Design, Pfizer Worldwide Research and Development, Groton, CT, USA.; Discovery Chemistry Research and Technologies, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, USA., Bolduc PN; Biogen Inc., Cambridge, MA, USA., Chen T; Biogen Inc., Cambridge, MA, USA., Clementson S; Research and Early Development, LEO Pharma A/S, Ballerup, Denmark., Petersen NN; Research and Early Development, LEO Pharma A/S, Ballerup, Denmark., Laudadio G; Department of Chemistry, Scripps Research, La Jolla, CA, USA., Bi C; Department of Chemistry, Scripps Research, La Jolla, CA, USA., Kawamata Y; Department of Chemistry, Scripps Research, La Jolla, CA, USA. yukawama@scripps.edu., Baran PS; Department of Chemistry, Scripps Research, La Jolla, CA, USA. pbaran@scripps.edu.

Journal Article , 2023

Decarboxylation of the Catalytic Lysine Residue by the C5α-Methyl-Substituted Carbapenem NA-1-157 Leads to Potent Inhibition of the OXA-58 Carbapenemase.

Toth M; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, United States., Stewart NK; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, United States., Maggiolo AO; Stanford Synchrotron Radiation Lightsource, Stanford University, Menlo Park, California 94025, United States., Quan P; Department of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States., Khan MMK; Department of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States., Buynak JD; Department of Chemistry, Southern Methodist University, Dallas, Texas 75275, United States., Smith CA; Stanford Synchrotron Radiation Lightsource, Stanford University, Menlo Park, California 94025, United States.; Department of Chemistry, Stanford University, Stanford, California 94305, United States., Vakulenko SB; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, United States.

Journal Article , 2024

Aldehyde-based Activation of C2α-lactylthiamin Diphosphate Decarboxylation on Bacterial 1-deoxy-d-xylulose 5-phosphate Synthase.

Toci EM; Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205, United States., Majumdar A; Biomolecular NMR Center, Johns Hopkins University, Baltimore, Maryland, 21218, United States., Meyers CLF; Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205, United States.

Journal Article , 2024

Identification of a chlorosalicylic acid decarboxylase (CsaD) involved in decarboxylation of 3,6-DCSA from an anaerobic dicamba-degrading sludge.

Zhang X; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China., Wu N; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China., Geng K; College of Rural Revitalization, Jiangsu Open University, Nanjing, China., Yuan C; College of Rural Revitalization, Jiangsu Open University, Nanjing, China., Wang B; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China., Shi J; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China., Qiu J; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China., He J; Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing, China.; Agricultural Microbial Resources Protection and Germplasm Innovation and Utilization Center of Jiangsu Province, Nanjing, Jiangsu, China.

Journal Article , 2024

Parahydrogen-enhanced pH measurements using [1- ¹³ C]bicarbonate derived from non-enzymatic decarboxylation of [1- ¹³ C]pyruvate-d 3 .

Santi MD; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Hune TLK; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Rodriguez GG; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Fries LM; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Mei R; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Sternkopf S; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Elsaßer J; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German., Glöggler S; NMR Signal Enhancement Group, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany. stefan.gloeggler@mpinat.mpg.de.; Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Von-Siebold-Str. 3A, 37075 Göttigen, German.

Journal Article , 2024