tailieunhanh - Pharmaceutical Substances Syntheses, Patents, Applications - Part 135

Pharmaceutical Substances Syntheses, Patents, Applications - Part 135. 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 | Minocycline M 1341 Minocycline ATC J01AA08 Use antibiotic RN 10118-90-8 MF C23H27N3O7 MW LDS0 140 rng kg M . 3100 mg kg M . CN 4S- 4a 4aa 5aa 12aa -4 7-bis dimethylarnino -l 4 4a 5 5a 6 l l 12a-octahydro-3 10 12 12a-tetrahydroxy-1 11 -dioxo-2-naphthacenecarboxamide monohydrochloride RN 13614-98-7 MF C23H27N3O7 HCl MW EINECS 237-099-7 LDS0 154 mg kg M . 3600 mg kg M . 164 mg kg R . 2380 mg kg R . 6-demethyltetrocycline KNOj liq. HF -------------- 1 in Reference s US 3 148 212 American Cyanamid appl. . US 3 226 436 American Cyanamid prior. . US 3 345 410 American Cyanamid prior. . Church . et al. J. Org. Chem. JOCEAH 36 723 1971 . DE 1 245 942 American Cyanamid appl. USA-prior. . DE 1 643 767 American Cyanamid prior. . intermediates US 3 403 179 American Cyanamid prior. . US 3 483 251 American Cyanamid prior. . 1342 M Minoxidil purification DOS 2 309 582 American Cyanamid appl. USA-prior. . Formulations cps. 50 mg 100 mg f. c. tabl. 50 mg 100 mg susp. 50 mg 60 ml oral vial 100 mg as hydrochloride Trade Name s D Aknin Sanofi Winthrop Zacnan Lipha Santé J Minomycin Lederle- F Klinomycin Lederle 1972 generics Acneline Wyeth-Lederle Minolis Noviderm Mynocine Wyeth-Lederle GB I Aknemin Merck Sharp Dohme -comb. Dentomycin Wyeth Minocin Wyeth 1973 -comb. Minocin Cyanamid 1972 USA Takeda Dynacin Medicis Minocin Lederle 1971 Vectrin Warner Chilcott 1973 1973 Minoxidil ATC C02DC01 Dl 1AX01 Use antihypertensive RN 38304-91-5 MF C9HI5N5O MW EINECS 253-874-2 LD50 51 mg kg M . 1 g kg M . 49 mg kg R . 1321 mg kg R . CN 6- 1 -piperidinyl -2 4-pyrimidinediamine 3-oxide barbituric acid PÛCIj 2 4 6-trichloro-pyrimidine 6-chloro- 2 4-diamino-pyrimidine 2 4-diamino-6- 2 4-dichlorophenoxy -pyrimidine I .