Weight | 261.708 g/mol |
---|---|
Formula | C14H12ClNO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 3 |
tolfenamic acid (13710-19-5)
Rociclyn · Zambon brand of tolfenamic acid · Clotam
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#4170 in Chemistry
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- Sigma-Aldrich - tolfenamic acid61.20 - 168.00 USD
- Fisher Scientific - Search for tolfenamic acid
- TCI - tolfenamic acid78.00 USD
- Postoperative analgesia in the cat after ovariohysterectomy by use of carprofen, ketoprofen, meloxicam or tolfenamic acid (Journal of Small Animal Practice, 2000)
- Tolfenamic Acid and Pancreatic Cancer Growth, Angiogenesis, and Sp Protein Degradation (Journal of the National Cancer Institute, 2006)
- TOLFENAMIC ACID IS AS EFFECTIVE AS ERGOTAMINE DURING MIGRAINE ATTACKS (The Lancet, 1979)
- Directly Coupled 800 MHz HPLCNMR Spectroscopy of Urine and Its Application to the Identification of the Major Phase II Metabolites of Tolfenamic Acid (Analytical Chemistry, 1997)
- Tolfenamic Acid Rapid Release Versus Sumatriptan in the Acute Treatment of Migraine: Comparable Effect in a Double-Blind, Randomized, Controlled, Parallel-Group Study (Headache, 1998)
- Tolfenamic acid, metoclopramide, caffeine and their combinations in the treatment of migraine attacks (Cephalalgia, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rociclyn
- Zambon brand of tolfenamic acid
- Clotam
- N-(3-chloro-o-tolyl)anthranilic acid
- Bifenac
- GEA 6414
- Pharmacia brand of tolfenamic acid
- Provalis brand of tolfenamic acid
- N-(3-chloro-2-methylphenyl)anthranilic acid
-
SMILESCC1=C(C=CC=C1Cl)NC2=CC=CC=C2C(=O)O
-
InChIKeyYEZNLOUZAIOMLT-UHFFFAOYSA-N
- Pubchem - tolfenamic acid
- Wikipedia - tolfenamic acid
Tolfenamic acid (Clotam) is a member of the anthranilic acid derivatives (or fenamate) class of NSAID drugs discovered by scientists at Medica Pharmaceutical Company in Finland. Like other members of the class, it is a COX inhibitor and prevents formation of prostaglandins. It is used in the UK as a treatment for migraine.
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