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  • ...RB, Herzenberg LA | title = High-dose oral N-acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosis | journal = [[PNAS]] | year = 20 ...79% in the placebo group developed symptoms.<ref>{{cite journal |author=S. De Flora, C. Grassi, L. Carati |title=Attenuation of influenza-like symptomato
    28 KB (3,682 words) - 16:42, 27 September 2010
  • --><ref>{{cite journal | author = Mulhall A, de Louvois J, Hurley R | title = Chloramphenicol toxicity in neonates: its inc ...This creates a problem: chloramphenicol succinate ester is an inactive [[prodrug]] and must first be hydrolysed to chloramphenicol; the hydrolysis process i
    29 KB (3,876 words) - 16:42, 27 September 2010
  • ...d it is today commonly known as EES (erythromycin ethylsuccinate, an ester prodrug that is commonly administered). [[de:Erythromycin]]
    19 KB (2,731 words) - 17:52, 18 September 2010
  • ...also been shown to be important in the action of another antimycobacterial prodrug [[PA-824]].<ref>{{Cite journal|author=Singh R, Manjunatha U, Boshoff HI, '' [[de:Isoniazid]]
    12 KB (1,566 words) - 16:43, 27 September 2010
  • Pyrazinamide is a [[prodrug]] that stops the growth of ''[[Mycobacterium tuberculosis]]''. [[de:Pyrazinamid]]
    12 KB (1,557 words) - 16:44, 27 September 2010
  • ...ef name="pmid11823459">{{cite journal |author=Vannelli TA, Dykman A, Ortiz de Montellano PR |title=The antituberculosis drug ethionamide is activated by [[de:Ethionamid]]
    2 KB (278 words) - 16:44, 27 September 2010
  • | last = de Clercq | first = Erik | last2 = Field | first2 = Hugh J | title = Antiviral prodrugs &mdash; the development of successful prodrug strategies for antiviral chemotherapy
    14 KB (1,878 words) - 16:44, 27 September 2010
  • Tenofovir disoproxil fumarate is a [[prodrug]] form of Tenofovir. Tenofovir is also available in a fixed-dose combinatio [[de:Tenofovir]]
    6 KB (871 words) - 16:45, 27 September 2010
  • | metabolism = Metabolized to 5'phosphates, de-riboside, and deriboside carboxylic acid ...or [[peginterferon alfa-2a]]) and other viral infections. Ribavirin is a [[prodrug]], which when metabolised resembles [[purine]] [[RNA]] [[nucleotide]]s. In
    23 KB (3,222 words) - 16:45, 27 September 2010
  • ...opium was used in diverse preparations known as [[laudanum]] (see [[Thomas de Quincey]]'s "[[Confessions of an English Opium-Eater]]", 1821) and [[parego Codeine is considered a [[prodrug]], since it is metabolised ''[[in vivo]]'' to the primary active compounds
    40 KB (5,581 words) - 16:45, 27 September 2010
  • ...j.1365-2036.2000.00788.x}}</ref> [[Clopidogrel]] (Plavix) is an inactive [[prodrug]] that partially depends on CYP2C19 for conversion to its active form; inhi [[de:Omeprazol]]
    17 KB (2,299 words) - 09:15, 5 September 2010
  • As a [[prodrug]], enalapril is metabolised ''in vivo'' to the active form enalaprilat by v Enalapril is a prodrug that is converted by deesterification to converting enzyme inhibitor, enala
    5 KB (725 words) - 16:48, 27 September 2010
  • --><ref>{{cite journal | author=De Clercq E | title=HIV resistance to reverse transcriptase inhibitors. | jour ...bolism of CycloSaligenyl 3'-azido-2', 3'-dideoxythymidine monophosphate, a prodrug of 3'-azido-2', 3'-dideoxythymidine (zidovudine). | journal=Mol Pharmacol |
    21 KB (3,049 words) - 16:51, 27 September 2010
  • ...nalog of [[enalapril]]. Unlike other ACE inhibitors, lisinopril is not a [[prodrug]] and is excreted unchanged in the urine. In cases of [[Effective dose|over [[de:Lisinopril]]
    10 KB (1,316 words) - 09:44, 20 September 2010
  • ...tential to participate in the carbon cycle via microbiologically catalyzed de-esterification and decomposition of the resulting cellulose and organic aci ...urizing properties. Using chitin and chitosan as carriers, a water-soluble prodrug has been synthesized. Modified chitosans have been prepared with various ch
    68 KB (9,959 words) - 10:10, 20 September 2010
  • ...anafax DM |title=Clinical pharmacokinetics of XP13512, a novel transported prodrug of gabapentin |journal=Journal of Clinical Pharmacology |volume=48 |issue=1
    5 KB (682 words) - 22:07, 21 September 2010
  • ...]). This is the same route that is used to convert many different opiate [[prodrug]]s into the active form. The proportion of drug that is converted into the * [[Hydrocodone]] - a hepatic prodrug of hydromorphone
    38 KB (5,300 words) - 22:13, 21 September 2010
  • ...ame="pmid19238739">{{cite journal | author = Schwartz AR, Pizon AF, Brooks DE | title = Dextromethorphan-induced serotonin syndrome | journal = Clinical ...he NMDA receptor itself, it is likely that dextromethorphan functions as a prodrug to its nearly 10-fold more potent metabolite dextrorphan, and this is the t
    26 KB (3,444 words) - 22:15, 21 September 2010
  • A water-soluble [[prodrug]] form, [[fospropofol]], has recently been developed and tested with positi [[de:Propofol]]
    21 KB (2,875 words) - 21:03, 24 September 2010
  • ...nt l’etude experimentale de l’emploi clinique du gamma hydroxybutyrate de Na | journal = Aggressologie | volume = 1 | page =407 | language = French| ...h as [[baclofen]] and [[phenibut]].<ref>{{cite journal |author=Smolders I, De Klippel N, Sarre S, Ebinger G, Michotte Y |title=Tonic GABA-ergic modulatio
    55 KB (7,839 words) - 21:04, 24 September 2010