Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

P-Amino salicylic acid

SYNS p-AMINOSALICYLATE SODIUM p-AMINO-SALICYLIC ACID SODIUxM SALT BACTYLAN LEPASEN NATRI-PAS NIPPAS PAMISYL SODIUM PASADE PASALON-RAKEET PASNAL PASSODICO SALVIS SANIPIROL SODIOPAS SODIUM AMINOSALICYLATE SODIUM p-AxMINOSALICYLIC ACID TUBERSAN... [Pg.1241]

Fig. 31.29 Different metabolic pathways of p-amino-salicylic acid. Several conjugating enzymes are involved glycine TV-acyltransferases (reaction 1), UDP-glucuro-nosyltransferases (acyl-, ether-, A/-glucuronides, reactions 2, 4 and 6, respectively), sulfotransferases (reactions 3 and 5), A/-acetyltransferases (reaction 7). Fig. 31.29 Different metabolic pathways of p-amino-salicylic acid. Several conjugating enzymes are involved glycine TV-acyltransferases (reaction 1), UDP-glucuro-nosyltransferases (acyl-, ether-, A/-glucuronides, reactions 2, 4 and 6, respectively), sulfotransferases (reactions 3 and 5), A/-acetyltransferases (reaction 7).
A good example of a compound undergoing a number of key conjugation reactions is p-amino-salicylic acid (Figure 6). [Pg.878]

Amino-3-nitrotoluene 1 b 415,419 Amino phases la 3 Aminophenazone lb312,314,354 2-Aminophenol lb 309, 310, 381 4-Aminophenol lb 309, 310, 381 Aminophenols lb 309,381,383,401 9-(p-Aminophenoxy)acridine lb 145 1-Aminopyrene la 61 4-Amino salicylic acid lb 309,310 Amino sugars lb 47,232-235,354 Aminotrimethylenephosphonic acid la 172... [Pg.479]

Erdmann and Uhrich (2000 Erdmann et al., 2000) recently synthesized novel poly(anhydride-co-ester)s containing salicylic acid in the backbone, by melt polycondensation of the disalicylic acid ester of sebacic acid, poly[bis(o-carboxyphenoxy)sebacate] (PCPS) and the copolymer P(CPH-CPS). The release of salicylic acid (the active form of aspirin) from the former was studied in vitro and from the latter was studied in vivo (Erdmann and Uhrich, 2000 Erdmann et al., 2000). Similar polymers that release 5-amino salicylic acid, and p-nitro salicylic acid have been prepared... [Pg.186]

Simultaneous aspirin, p-aminophenol, 3-0-acetylascorbic acid, 2-0-acetylascorbic acid. Vitamin C, saccharin, 0-acetyl-p-aminophenol, salicylic acid (UV 280), diacetyl-p-amino-phenol (UV 280)... [Pg.14]

Catechol, hydroquinone, resorcinol, dihydroxy-phenylalaninc, p-hydroxydiphenyl, guaiacol, va-nillan, p-crcsol, mcsitol, durenol, pyrogallol Benzoic, salicylic, protocatechuic, gallic, p-amino benzoic acids... [Pg.105]

Sulfasalazine Sulfasalazine, 5-[p-[(4,6-dimethyl-2-pyridinyl)sulfamoyl]phenylazo]sali-cylic acid (33.1.22), is a derivative of sulfapyridine drug described above and one of the few sulfanilamides in which the free amino group in the benzene ring is modified, and it is synthesized by an azo-coupling reaction of a diazo salt, which is synthesized by reacting sulfapyridine (33.1.21) with nitrous acid and salicylic acid alkaline media [24,25]. [Pg.505]

See other pages where P-Amino salicylic acid is mentioned: [Pg.69]    [Pg.91]    [Pg.112]    [Pg.247]    [Pg.113]    [Pg.69]    [Pg.69]    [Pg.193]    [Pg.91]    [Pg.79]    [Pg.469]    [Pg.1079]    [Pg.230]    [Pg.476]    [Pg.267]    [Pg.929]    [Pg.69]    [Pg.91]    [Pg.112]    [Pg.247]    [Pg.113]    [Pg.69]    [Pg.69]    [Pg.193]    [Pg.91]    [Pg.79]    [Pg.469]    [Pg.1079]    [Pg.230]    [Pg.476]    [Pg.267]    [Pg.929]    [Pg.1613]    [Pg.374]    [Pg.6]    [Pg.256]    [Pg.1613]    [Pg.231]    [Pg.252]    [Pg.231]    [Pg.1613]    [Pg.176]    [Pg.199]    [Pg.376]    [Pg.202]    [Pg.45]    [Pg.91]    [Pg.125]    [Pg.102]    [Pg.37]    [Pg.141]    [Pg.147]    [Pg.64]    [Pg.79]   
See also in sourсe #XX -- [ Pg.112 ]



SEARCH



4-Amino salicylic acid

Acids salicylic acid

P-amino acids

Salicylic acid

Salicylic acid acidity

© 2024 chempedia.info