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Dimalonic acid

Okuda K, Mashino T, Hirobe M (1996) Superoxide radical quenching and cytochrome C peroxidase-like activity of C60-dimalonic acid, C62(COOH)4. Bioorg. Med. Chem. Lett. 6 539-542. [Pg.77]

Satoh, M., et al. (1997), Inhibitory effects of a fullerene derivative, dimalonic acid C60, on nitric oxide-induced relaxation of rabbit aorta, Eur. J. Pharmacol, 327, 175-181. [Pg.1316]

Diamino-2-hydroxypropane-N,N -dipropanedioic acid (2-hydroxy-l,3-propylenediamine-N,N -dimalonic acid)... [Pg.50]

Figure 10.10 Normal (left) and short contact time (right) N CP/MAS NMR spectra of free base (1), sesquisuccinic acid co-crystal (2), dimalonic acid mixed ionic/zwitterionic complex (3) and dimaleate salt (4) forms of an ErbB2 inhibitor. Only N atoms attached to appear in the short contact time spectra (Adapted from Li et al, ref. 65 Copyright 2006 American Chemical Society). Figure 10.10 Normal (left) and short contact time (right) N CP/MAS NMR spectra of free base (1), sesquisuccinic acid co-crystal (2), dimalonic acid mixed ionic/zwitterionic complex (3) and dimaleate salt (4) forms of an ErbB2 inhibitor. Only N atoms attached to appear in the short contact time spectra (Adapted from Li et al, ref. 65 Copyright 2006 American Chemical Society).
Ethvlenediiminodipropanedioic acid (ethvlenediamine-N.N -dimalonic acid. EDDM) (other references in Vol.2, p.90 and Vol.5, p.456)... [Pg.42]

See other pages where Dimalonic acid is mentioned: [Pg.92]    [Pg.214]    [Pg.44]    [Pg.18]    [Pg.877]    [Pg.46]    [Pg.48]    [Pg.220]    [Pg.235]    [Pg.236]    [Pg.46]    [Pg.47]    [Pg.48]   
See also in sourсe #XX -- [ Pg.236 ]



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