The Design of Amino Hydroxamic Metal Chelates and Their Activity in Biological Systems. Formation Constants between 2-Amino-4-methylpentanehydroxamic Acid with Proton, Copper(II), and Iron(III) in Aqueous Solution
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/64/8/64_8_2488/_pdf
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4. Hydroxamic acid inhibitors of 5-lipoxygenase
5. Rationally designed, potent competitive inhibitors of leukotriene biosynthesis
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2. Solid-state complexes of poly(L-histidine) with metal chlorides from the first row of thed-block;Journal of Polymer Science Part B: Polymer Physics;1999-02-15
3. FORMATION EQUILIBRIA OF COPPER(II) TERNARY COMPLEXES WITH (S)-LEUCINEHYDROXAMIC ACID AND (R)- OR (S)-AMINO ACIDS IN AQUEOUS SOLUTION;Journal of Coordination Chemistry;1998-07-01
4. CHARACTERIZATION OF AMINO HYDROXAMIC METAL CHELATES AND THEIR ACTIVITY IN BIOLOGICAL SYSTEMS. FORMATION CONSTANTS BETWEEN 2-AMINO-N, 3-DIHYDROXYPROPANAMIDE AND 2-AMINO-N, 3-DIHYDROXYBUTANAMIDE AND IRON(III) IONS IN AQUEOUS SOLUTION;Journal of Coordination Chemistry;1994-09
5. AMINOHYDROXAMIC ACIDS AS SEQUESTERING AGENTS IN LIVING SYSTEMS. POTENTIOMETRIC DETERMINATION OF PROTONATION AND FORMATION CONSTANTS FOR 2,6-DIAMINO-N-HYDROXYHEXANAMIDE AND COPPER(II), NICKEL(II), COBALT(II), AND HYDROGEN IONS IN AQUEOUS SOLUTION;Journal of Coordination Chemistry;1993-04
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