Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C27H32O4 |
| Molecular Weight | 420.5406 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 4 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(\C=C\C1=C(C)CCCC1(C)C)=C/C=C(/C(C)=C\C(O)=O)C2=CC=CC(=C2)C(O)=O
InChI
InChIKey=XKKDQOHDTASHCE-PAZAWXFKSA-N
InChI=1S/C27H32O4/c1-18(12-14-24-19(2)8-7-15-27(24,4)5)11-13-23(20(3)16-25(28)29)21-9-6-10-22(17-21)26(30)31/h6,9-14,16-17H,7-8,15H2,1-5H3,(H,28,29)(H,30,31)/b14-12+,18-11+,20-16-,23-13-
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Mechanism of inhibition of human nonpancreatic secreted phospholipase A2 by the anti-inflammatory agent BMS-181162. | 1995-01-06 |
|
| Inhibitor of phospholipase A2 blocks eicosanoid and platelet activating factor biosynthesis and has topical anti-inflammatory activity. | 1994-11 |
|
| Novel inhibitor of phospholipase A2 with topical anti-inflammatory activity. | 1992-11-30 |
Sample Use Guides
BMS-181162 reversibly inhibited phospholipase A2 purified from human synovial fluid with an IC50 of 8 microns. In A23187-stimulated human polymorphonuclear leukocytes, BMS-181162 blocked arachidonic acid release with an IC50 of 10 microns. Leukotriene B4 biosynthesis in these cells was also inhibited.
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6438744
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141948-79-0
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Y8U3B6ZM8D
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DB14097
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ACTIVE MOIETY
