Pharmaceutical Substances Syntheses, Patents, Applications - Part 215. 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. | Tuaminoheptane T 2141 Tyson L-Tryptophan . Tyson wfm Tuaminoheptane Heptylamine ATC R01AA11 R01AB08 Use sympathomimetic vasoconstrictor RN 123-82-0 MF C7H17N MW EINECS 204-655-5 LD50 60 mg kg M . 115 mg kg M . 130 mg kg R . CN 2-heptanamine sulfate 2 1 RN 6411-75-2 MF C7H17N 1 2H2O4S MW EINECS 229-113-5 LDS0 mg kg M . mg kg R . omyl methyl ketone nh2 Tuaminoheptane Reference s Norton . et al. J. Org. Chem. JOCEAH 19 1054 1954 . Formulation s nasal spray 50 mg 10 ml Trade Name s D Rinofluimucil-S Inpharzam -comb. F I Rhinofluimucil Zambon -comb. Otomicetina Deca -comb. Rinofluimucil Zambon Italia -comb. Tubocurarine chloride ATC M03AA02 Use muscle relaxant RN 6989-98-6 MF C37H41C1N2O6 HC1 5H2O MW LD 0 130 pg kg M . 150 mg kg M . CN 7 12 -dihydroxy-6 6 -dimethoxy-2 2 2 -trimethyltubocuraranium chloride hydrochloride pentahydrate anhydrous RN 57-94-3 MF C37H41C1N2O6 HC1 MW EINECS 200-356-9 LD50 97 pg kg M . 33 mg kg M . 66 pg kg R . 28 mg kg R . 2142 T Tuỉobuterol By extraction from Chondrodendron tomentosum Ampi Huasca and purification via the picrate. Reference s US 2 409 241 Squibb 1946 prior. 1944 . US 2 600 539 Parke Davis 1952 appl. 1947 . Everett A J. et al J. Chem. Soc. D CCJDAO 1970 1020. Codding . James . J. Chem. Soc. D CCJDAO 1972 1. Formulations amp. 3 mg ml Trade Name s D Curarin Asta ASTA wfm GB Jexin Duncan Flockhart Tubarine Wellcome wfm Curarin HAF Ethicon wfm J Amelizol Yoshitomi wfm Tubarine Calmic wfm USA Tubocurarine Chloride F D-Tubocurarine Abbott I. Curarin Schering wfm Lilly Abbott wfm Intocortrin T Squibb wfm IXiIobuterol ATC R03AC11 R03CC11 Use bronchodilator RN 41570-61-0 MF C 2H1SC1NO MW CN 2-chloro-a- l l-dimethylethyl amino methyl benzenemcthanol 2 -chloro- 2-chloro- acetophenone phenyl- glyoxol 1. H2hk H3 H3C CH3 2. NoBH4 1. tert-butylomine 2- sodium borohydride Reference s DOS 2 244 737 Hokuriku appl. J-prior. . .