Robenacoxib-d5

Product Name Robenacoxib-d5
Alternate Names Robenacoxib Stable Isotopes, Stable Isotopes of Robenacoxib
CAT No. CS-O-35332
CAS No. 220991-32-2 (unlabeled)
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 332.30 g/mol
Mol. For. C₁₆H₈D₅F₄NO₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Robenacoxib
Smileys O=C(O)CC1=CC(C([2H])([2H])C([2H])([2H])[2H])=CC=C1NC2=C(F)C(F)=CC(F)=C2F
Canonical Smiles CCC1=CC(=C(C=C1)NC2=C(C(=CC(=C2F)F)F)F)CC(=O)O
InchIKey ZEXGDYFACFXQPF-UHFFFAOYSA-N
Inchl InChI=1S/C16H13F4NO2/c1-2-8-3-4-12(9(5-8)6-13(22)23)21-16-14(19)10(17)7-11(18)15(16)20/h3-5,7,21H,2,6H2,1H3,(H,22,23)
IUPAC 2-[5-ethyl-2-(2,3,5,6-tetrafluoroanilino)phenyl]acetic acid
Controlled No
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Robenacoxib-d5 is a deuterated form of the nonsteroidal anti-inflammatory drug (NSAID), robenacoxib. It is commonly used in veterinary medicine for the treatment of pain and inflammation associated with osteoarthritis and postoperative pain in dogs and cats. Chemically, robenacoxib-d5 is a selective inhibitor of cyclooxygenase-2 (COX-2), an enzyme involved in the production of prostaglandins that cause pain and inflammation. By inhibiting COX-2, robenacoxib-d5 reduces pain and inflammation without affecting the production of prostaglandins involved in normal physiological processes. Robenacoxib-d5 is administered orally in tablet form and is rapidly absorbed into the bloodstream, with peak plasma concentrations reached within 1-2 hours. It has a half-life of approximately 4 hours in dogs and 2.5 hours in cats. As with all NSAIDs, robenacoxib-d5 carries a risk of adverse effects, particularly gastrointestinal ulceration and bleeding, as well as renal and hepatic toxicity. It should not be used in animals with a history of sensitivity to NSAIDs, or those with pre-existing renal or hepatic disease. Careful monitoring is recommended during treatment with robenacoxib-d5, and it should only be used under the guidance of a licensed veterinarian.

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