Weight | 296.153 g/mol |
---|---|
Formula | C14H11Cl2NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
meclofenamic acid (644-62-2)
Meclofenamate · Meclomen · Meclofenamate Sodium
Score:
#7 in Physiology
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#888 in Biochemistry
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#2367 in Biology
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#2933 in Chemistry
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- Exacerbation of psoriasis with meclofenamate. (The New England Journal of Medicine, 1983)
- Biomarkers of oxidative stress study III. Effects of the nonsteroidal anti-inflammatory agents indomethacin and meclofenamic acid on measurements of oxidative products of lipids in CCl4 poisoning. (Free Radical Biology and Medicine, 2005)
- Meclofenamic acid and diclofenac, novel templates of KCNQ2/Q3 potassium channel openers, depress cortical neuron activity and exhibit anticonvulsant properties. (Molecular Pharmacology, 2005)
- Double blind randomized controlled trial of sodium meclofenamate (Meclomen) and diclofenac sodium (Voltaren): post validation reapplication of the WOMAC Osteoarthritis Index. (The Journal of Rheumatology, 1992)
- Salicylate, mefenamate, meclofenamate, and quinine on cochlear potentials (Otolaryngology-Head and Neck Surgery, 1990)
- Effects of topical applications of meclofenamic acid and ibuprofen on bone loss, subgingival microbiota and gingival PMN response in the primate Macaca fascicularis. (Journal of Periodontal Research, 1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Meclofenamate
- Meclomen
- Meclofenamate Sodium
- Sodium Meclofenamate
- Parke Davis Brand of Sodium Meclofenamate
- Meclofenamate Sodium Monohydrate
-
SMILESCC1=C(C(=C(C=C1)Cl)NC2=CC=CC=C2C(=O)O)Cl
-
InChIKeySBDNJUWAMKYJOX-UHFFFAOYSA-N
- Pubchem - meclofenamic acid
- Wikipedia - meclofenamic acid
Meclofenamic acid (meclofenamate sodium, brand Meclomen) is a drug used for joint, muscular pain, arthritis and dysmenorrhea. It is a member of the anthranilic acid derivatives (or fenamate) class of NSAID drugs and was approved by the FDA in 1980. Like other members of the class, it is a COX inhibitor and prevents formation of prostaglandins.
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