Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H14ClNO2 |
| Molecular Weight | 263.719 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(CC(O)=O)=C(C)N1C2=CC=C(Cl)C=C2
InChI
InChIKey=SJCRQMUYEQHNTC-UHFFFAOYSA-N
InChI=1S/C14H14ClNO2/c1-9-7-11(8-14(17)18)10(2)16(9)13-5-3-12(15)4-6-13/h3-7H,8H2,1-2H3,(H,17,18)
Clopirac is a non-steroidal anti-inflammatory drug. It is a weak inhibitor of prostaglandin synthetase and has standard anti-inflammatory and analgesic activity. It effectivity inhibits prostaglandin synthesis in vitro. The metabolites of clopirac in humans and monkeys include the glucuronide of clopirac and the pyrrole carboxylic acid. Efficacy of clopirac in rheumatoid arthritis, trauma conditions, osteoarthritis and pain was evaluated in many clinical trials.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Prostaglandin synthetase |
230.0 µM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1228193 https://www.ncbi.nlm.nih.gov/pubmed/1228200 https://www.ncbi.nlm.nih.gov/pubmed/777001 https://www.ncbi.nlm.nih.gov/pubmed/776999 https://www.ncbi.nlm.nih.gov/pubmed/776987 https://www.ncbi.nlm.nih.gov/pubmed/776986 https://www.ncbi.nlm.nih.gov/pubmed/776985 |
Palliative | Unknown Approved UseUnknown |
||
| Palliative | Unknown Approved UseUnknown |
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| Palliative | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Pharmacological study of clopirac, a new anti-inflammatory agent (author's transl)]. | 1975 |
|
| [Clopirac in the treatment of posttraumatic inflammation (author's transl)]. | 1975 |
|
| [Double-blind study of indomethacin and CP 172 AP (clopirac) in lombarthrosis (author's transl)]. | 1975 |
|
| [Studies of the therapeutic effectiveness of clopirac in osteoarthritis (author's transl)]. | 1975 |
|
| [Open trial for the evaluation of the therapeutic effectiveness of i-p chlorophenyl-2,5-dimethyl-3-pyrrole acetic acid (clopirac) in rheumatoid arthritis (author's transl)]. | 1975 |
|
| Double-blind cross-over study of clopirac and naproxen in rheumatoid arthritis. | 1975 |
|
| [Open study of clopirac in the treatment of non articular rheumatism (author's transl)]. | 1975 |
|
| [Clopirac effectiveness in traumatology and non articular rheumatisms (author's transl)]. | 1975 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12259
Rat: 150 mg/kg
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12259
The ability of clopirac to inhibit the conversion of [3H]arachidonic acid into PGE, was measured in a microsomal enzyme preparation isolated from bovine seminal vesicles. The defined IC50 value was about 45 uM.
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C257
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ACTIVE MOIETY