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- Cholic acid-based fluorescent probes for enantioselective recognition of trifunctional amino acids. Hao Wang, Wing-Hong Chan, Albert W. M. Lee
, Org. Biomol. Chem.
, 2008
, 6
, 929
- Immobilization of O-acetylserine sulfhydrylase as a highly active and recyclable nanobiocatalyst: efficient synthesis of β-pyrazol-1-yl-l-alanine. Akbar K. Vahidi, Zunsheng Wang, William S. Y. Wong, Zhi Li
, Catal. Sci. Technol.
, 2016
, 6
, 6286
- Squaric acid as a new chemoselective moiety for mass spectrometry-based metabolomics analysis of amines. Weifeng Lin, Zhen Yang, Amanpreet Kaur, Annika Block, Miroslav Vujasinovic, J.-Matthias Löhr, Daniel Globisch
, RSC Chem. Biol.
, 2021
, 2
, 1479
- Mechanisms and stereochemistry of the activation of (2S)- and (2R)-serine O-sulfate as suicide inhibitors for Escherichia coli glutamic acid decarboxylase. Janet E. Rose, Paul D. Leeson, David Gani
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 3089
- A new fluorogenic reagent aimed at simultaneous determination of peptides or proteins in two different samples. Hiroshi Saimaru, Mayumi Masuda, Chifuyu Toriumi, Tomofumi Santa, Eiko Ichikawa, Norio Takamura, Kazuhiro Imai
, J. Mater. Chem.
, 2005
, 15
, 2865
- Targeted metabolomics reveals dynamic portrayal of amino acids and derivatives in triple-negative breast cancer cells and culture media. Fang Kou, Bangjie Zhu, Wenbin Zhou, Chunming Lv, Yu Cheng, Hai Wei
, Mol. Omics
, 2021
, 17
, 142
- A study of the reactivity of S(VI)–F containing warheads with nucleophilic amino-acid side chains under physiological conditions. H. Mukherjee, J. Debreczeni, J. Breed, S. Tentarelli, B. Aquila, J. E. Dowling, A. Whitty, N. P. Grimster
, Org. Biomol. Chem.
, 2017
, 15
, 9685
- Microbiome–metabolomics analysis reveals the potential effect of verbascoside in alleviating cognitive impairment in db/db mice. Zheng Ran, Bowei Ju, Lin Cao, Qiang Hou, Limei Wen, Ruoyu Geng, Yucheng Liao, Junping Hu, Jianhua Yang
, Food Funct.
, 2023
, 14
, 3488
- The biosynthesis of pramanicin in Stagonospora sp. ATCC 74235: a modified acyltetramic acid. Paul H. M. Harrison, Petar A. Duspara, Stephen I. Jenkins, Salima A. Kassam, David K. Liscombe, Donald W. Hughes
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 4390
- Amino acid-accepting ketosynthase domain from a trans-AT polyketide synthase exhibits high selectivity for predicted intermediate. Christoph Kohlhaas, Matthew Jenner, Annette Kampa, Geoff S. Briggs, José P. Afonso, Jörn Piel, Neil J. Oldham
, Chem. Sci.
, 2013
, 4
, 3212