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The binding of metal ions by captopril (SQ 14225). Part II. Complexation of copper(II)
Institution:1. School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002, China;2. Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, 400714, China;1. Department of Chemistry, Hemvati Nandan Bahuguna Garhwal University, Srinagar-247174, India;2. Department of Chemistry, Ramjas College, University of Delhi, University Enclave, Delhi-110007, India;3. Department of Chemistry, Faculty of Natural and Agricultural Sciences, North-West University, 2735, South Africa;1. Department of Chemistry, Science Faculty, Selcuk University, Turkey;2. Department of Biology, Science Faculty, Selcuk University, Turkey;3. Department of Medical Services and Techniques, Vocational School of Health Services, Selcuk University, Turkey;1. National Research Tomsk Polytechnic University, Lenin Avenue 30, 634050, Tomsk, Russian Federation;2. Laboratory of Organometallics, Catalysis and Ordered Materials, State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Center for Chemical and Material Engineering, Wuhan University of Technology, Wuhan, 430070, PR China;3. College of Arts and Sciences, Khalifa University of Science and Technology, PO Box 127788, Abu Dhabi, United Arab Emirates;4. School of Chemical Engineering, Suranaree University of Technology, Nakhon Ratchasima, 30000, Thailand
Abstract:Formation constants for the interaction of copper(II) with captopril have been measured using (i) histidine and (ii) 2,3-diaminopropionic acid monohydrochloride as competing ligands to prevent redoxing. The main species present in both the binary and ternary experimental systems are reported. Blood plasma models based upon these new formation constants indicate that captopril at high doses may mobilise copper(II) from blood plasma.
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