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  2. Ivermectin Drug Interactions in Cancer Treatment for Dogs - AOL

    www.aol.com/ivermectin-drug-interactions-cancer...

    Ivermectin may interact with cyclosporine, ketoconazole, erythromycin, and other medications used for dogs. ... Pharmacokinetic interaction of the antiparasitic agents ivermectin and spinosad in ...

  3. List of veterinary drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_veterinary_drugs

    This article lists veterinary pharmaceutical drugs alphabetically by name. Many veterinary drugs have more than one name and, therefore, the same drug may be listed more than once. Abbreviations are used in the list as follows: INN = International Nonproprietary Name; BAN = British Approved Name; USAN = United States Adopted Name

  4. Glycine receptor - Wikipedia

    en.wikipedia.org/wiki/Glycine_receptor

    The glycine receptor (abbreviated as GlyR or GLR) is the receptor of the amino acid neurotransmitter glycine. GlyR is an ionotropic receptor that produces its effects ...

  5. Oclacitinib - Wikipedia

    en.wikipedia.org/wiki/Oclacitinib

    Oclacitinib, sold under the brand name Apoquel among others, is a veterinary medication used in the control of atopic dermatitis and pruritus from allergic dermatitis in dogs at least 12 months of age. [1] [4] Chemically, it is a synthetic cyclohexylamino pyrrolopyrimidine janus kinase inhibitor that is relatively selective for JAK1. [5]

  6. Morphine-3-glucuronide - Wikipedia

    en.wikipedia.org/wiki/Morphine-3-glucuronide

    Morphine-3-glucuronide is a metabolite of morphine produced by UGT2B7. [1] It is not active as an opioid agonist, [2] but does have some action as a convulsant, which does not appear to be mediated through opioid receptors, [3] but rather through interaction with glycine and/or GABA receptors.

  7. N-Phenylacetyl-L-prolylglycine ethyl ester - Wikipedia

    en.wikipedia.org/wiki/N-Phenylacetyl-L...

    N-Phenylacetyl-l-prolylglycine ethyl ester is promoted as a nootropic and is a prodrug of cyclic glycine-proline. [a] [2] Other names include the brand name Noopept (Russian: Ноопепт), developmental code GVS-111, and proposed INN omberacetam. [2] [3] [4] Its synthesis was first reported in 1996. [2] It is orally available.

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