Pharmaceutical Substances Syntheses, Patents, Applications - Part 43. Reference containing a collection of 2267 active pharmaceutical ingredients, including those launched recently. Listed alphabetically according to their INNs and established a link between INNs, structure, synthesis and production processes, patent and literature situation, medical use, and trade names. For pharmacists and researchers | r Cetylpyridinium chloride c 421 Trade Name s r D Cetrotide ASTA Medica GB Cetrotide ASTA Medica J AWD 1999 i Cetylpyridinium chloride ATC B05CA01 DO8AJO3 D09AA07 R02AA06 Use disinfectant antiseptic RN 123-03-5 MF C2IH38C1N MW EINECS 204-593-9 Ị LDS0 10 mg kg M . 108 mg kg M . I 200 mg kg R . CN 1-hexadecylpyridinium chloride y ci- ch2 15-ch3 cetyl chloride Ceiylpyridinium chloride Reference s Budesinsky-Protiva 531-532. Formulation s eff. tabl. mg 3 mg lozenge mg sol. 5 mg 10 ml tab . 2 mg Trade Name s Dobendan Cassella-med Formamint N Beecham- Wiilfing Tyrosolvetten Byk Gulden Roland -comb. numerous combination preparations Alodont Warner-Lambert - comb. Broncorinol Roche Nicholas -comb. Cétylyre Oberlin Calgel Warner-Lambert Merocaine Seton -comb. Merocet Seton Borocaina Schiapparelli Salute Flu prim Roche Gola Sella Golagamma Avantgarde Neocepacol Lepetit Neocoricidin Schering- Plough Neoformitrol Sandoz Neogola Sella Noalcool Sella Penaten Johnson Johnson Ragaden Ganassini Vidermina Ganassini numerous combination preparations Colgen 123 Kowa -comb. Pabron Troche Taisho Suprol Iwaki USA Cepacol Lakeside -comb. wfm Cobrex Reid-Rowell -comb. wfm Chenodeoxycholic acid Chenodiol Acide chenodéoxycholique Chenodesoxycholsäure ATC A05AA01 Use choleretic choleretic anticholethithogenic dissolution of cholesterol gallstones RN 474-25-9 MF C24H40O4 MW EINECS 207-481-8 LD50 100 mg kg M . 3 g kg M . 106 mg kg R . 4 g kg R . 1 g kg dog . CN 3a 5ß 7a -3 7-dihydroxycholan-24-oic acid 422 C Chenodeoxycholic acid methyl 3a 7a-d ocetoxy- 12a-hydroxycholanate I methyl 3a 7a-diocetoxy-12-oxocholanote II 1. h2n-nh2 -H2O 200 c 2. HCI k 1. hydrozine hydrate Reference s Fieser . Rajagopalan S. J. Am. Chem. Soc. JACSAT 72 5530 1950 . Hauser E. et al. Helv. Chim. Acta HCACAV 43 1595 1960 . Hofmann . ActaChem. Scand. ACHSE7 17 173 1963 . Sato Y Ikekawa N. J. Org. Chem. JOCEAH 24 1367 1959 . purification DOS 2 302 744 Union .
