• Salts
  • In salts, the mesylate is present as the CH3SO3− anion. (wikipedia.org)
  • The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: ##STR00001## which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). (patentsencyclopedia.com)
  • Farmotidine Flavoxate Hydrochloride Flufenamic acid, its salts, its esters, their salts Flunarizine Hydrochloride Flupenthixol Fluphenazine Enanthate and Decanoate Flurazepam Flurbiprofen Flutamide Fluoxetine Hydrochloride Garabpin Galanthamine Hydrobromide Gallamine, its salts, its quaternary compound Gemfibrozil Genodeoxycholic Acid Gliclazide Glucagon Glycopyrrolate GlydiazinamideGuanethidine Gugulipid Halogenated Hydroxyquinolines Haloperidol Heparin Hepatitis B. Vaccine Hyaluronidase Hydrocortisone 17-Butyrate Hydrotalcite Hydroxyzine, its salts Ibuprofen Imipramine, its salts Indapamide Indomethacin, its salts Insulin Human Interferon Alpha Inj. (wikipedia.org)
  • ethyl
  • Bromine is introduced in 8 by an allylic bromination with NBS and the amide group is cleaved with ethanol and caesium carbonate accompanied by elimination of bromide to the diene ethyl ester 9. (wikipedia.org)
  • ethers
  • After protection of the hydroxyl groups as tert-butyldimethylsilyl ethers, reduction of the ester with lithium aluminium hydride and selective deprotection of the secondary hydroxyl group gave lactone diol 1.11. (wikipedia.org)
  • Minor components are the polyethyelene glycol esters of ricinoleic acid, polyethyelene glycols and polyethyelene glycol ethers of glycerol. (wikipedia.org)
  • amide
  • The ester 3 is converted into an amide in 4 by reaction with ammonia and the next step to lactam 5 is an iodolactamization with iodine initiated by trimethylsilyltriflate. (wikipedia.org)
  • salt
  • When modifying the International Nonproprietary Name of a pharmaceutical substance containing the group or anion, the correct spelling is mesilate (as in imatinib mesilate, the mesylate salt of imatinib). (wikipedia.org)
  • bond
  • As illustrated in Retrosynthetic Scheme I, Taxol was derived from diol 7.2 by an ester bond formation, according to the Ojima-Holton method. (wikipedia.org)
  • conditions
  • Reductive opening of the ketal under modified Hunter conditions in dichloromethane yields an inseparable mixture of isomeric mesylates. (wikipedia.org)