| Vedaprofen |
![]() Last updated: 16/09/2025 |
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(Also known as: CERM-10202; PM-150) |
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A non-steroidal anti-inflammatory (NSAID) and analgesic veterinary drug which is structurally related to ketoprofen and carprofen | |
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Used to control pain, especially that associated with musculo-skeletal disorders and traumas | |
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Horses; Dogs |
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Approved - usually supplied as a prescription only medicine to be authorised by a veterinarian (POM-V) | |
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Approved |
| Chemical structure |
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None | |
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C₁₉H₂₂O₂ | |
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CC(C1=CC=C(C2=CC=CC=C21)C3CCCCC3)C(=O)O | |
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No data | |
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VZUGVMQFWFVFBX-UHFFFAOYSA-N | |
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InChI=1S/C19H22O2/c1-13(19(20)21)15-11-12-16(14-7-3-2-4-8-14)18-10-6-5-9-17(15)18/h5-6,9-14H,2-4,7-8H2,1H3,(H,20,21) | |
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Yes |
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| Common Name | Relationship | Link |
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| vedaprofen | - | ![]() |
| General status |
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Anti-inflammatory, Analgesic, Medicinal drug | ||||||||||||||
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Arylpropionic acid | ||||||||||||||
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Inhibits phospholipase A2 blocking the formation of chemical mediators leading to peripheral sensitisation and hyperalgesia | ||||||||||||||
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[Leukocyte migration, Inhibitor], [Cyclooxygenase, Inhibitor] | ||||||||||||||
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71109-09-6 | ||||||||||||||
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275-196-6 | ||||||||||||||
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Musculo-Skeletal system: Anti-inflammatory and antirheumatic products | ||||||||||||||
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QM01AE90 | ||||||||||||||
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Allowed susbstance (Table 1: Equidae) | ||||||||||||||
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282.38 | ||||||||||||||
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2-(4-cyclohexylnaphthalen-1-yl)propanoic acid | ||||||||||||||
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4-cyclohexyl-α-methylnaphthalene-1-acetic acid | ||||||||||||||
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Beige coloured solid | ||||||||||||||
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Current | |||
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1980s-1990s, synthesis & characterisation; 1997, first EU approvals | |||
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Usually supplied in gel and in injectable formulations | |||
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Vedaprofen is synthesised through a multi-step chemical process starting with 1-cyclohexylnaphthalene as the core structure. The initial step involves chloromethylation of the naphthalene ring to introduce a reactive side chain. This intermediate then undergoes functional group interconversion to form an ester derivative. The final key transformation is alkylation with methyl iodide, which introduces the propionic acid moiety, yielding vedaprofen as the active compound. | |||
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Published GHG data is not available for most pharmaceuticals. However, according to industry, global averages suggest producing 1 kg of a typical active pharmaceutical ingredient can range from 10 to 100 kg CO₂e for small molecule drugs and potentially up to 1000 kg CO₂e for complex biologicals such as vaccines, depending on the drug type, its formulation, complexity of synthesis, solvent recovery, and energy sources used. |
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150 | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. | ||||||||||
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| Known metabolites |
None
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| Terrestrial ecotoxicology |
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222 | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) Rat5 = Verified data used for regulatory purposes |
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| General |
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High (class III) | - | - | ||||||||
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222 | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) Rat5 = Verified data used for regulatory purposes |
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Largely metabolisd and around 70% excreted in the urine with up to 14% in the faeces. | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) 5 = Verified data used for regulatory purposes |
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| Health issues |
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May cause gastrointestinal problems May be ulcerogenic Possible kidney, liver, spleen and thymus toxicant |
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| Handling issues |
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No information available | |||
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Not listed (Not listed) | |||
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vedaprofen | ||
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| Record last updated: | 16/09/2025 |
| Contact: | aeru@herts.ac.uk |
| Please cite as: | Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |
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