Licofelone

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Licofelone
Licofelone structure.svg
Ball-and-stick model of the licofelone molecule
Names
IUPAC name
[6-(4-chlorophenyl)-2,2-dimethyl-7-phenyl-2,3-dihydro-1H-pyrrolizin-5-yl]acetic acid
Identifiers
156897-06-2 YesY
ChEMBL ChEMBL52854 N
ChemSpider 117391 N
Jmol 3D model Interactive image
PubChem 133021
UNII P5T6BYS22Y N
  • InChI=1S/C23H22ClNO2/c1-23(2)13-19-22(15-6-4-3-5-7-15)21(16-8-10-17(24)11-9-16)18(12-20(26)27)25(19)14-23/h3-11H,12-14H2,1-2H3,(H,26,27) N
    Key: UAWXGRJVZSAUSZ-UHFFFAOYSA-N N
  • InChI=1/C23H22ClNO2/c1-23(2)13-19-22(15-6-4-3-5-7-15)21(16-8-10-17(24)11-9-16)18(12-20(26)27)25(19)14-23/h3-11H,12-14H2,1-2H3,(H,26,27)
    Key: UAWXGRJVZSAUSZ-UHFFFAOYAP
  • CC1(CC2=C(C(=C(N2C1)CC(=O)O)C3=CC=C(C=C3)Cl)C4=CC=CC=C4)C
Properties
C23H22ClNO2
Molar mass 379.879 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Licofelone is a dual COX/LOX inhibitor[1][2] being considered as a treatment for osteoarthritis[3] and which is under development by Merckle GmbH with partners Alfa Wassermann and Lacer.

Licofelone is both an analgesic and an anti-inflammatory. Inhibition of 5-LOX may reduce the gastrointestinal toxicity associated with other non-steroidal anti-inflammatory drugs, which only inhibit COX (cyclooxygenase). Licofelone is the first drug to inhibit both. It has passed the phase III trials.[4]

References

  1. Lua error in package.lua at line 80: module 'strict' not found.
  2. Lua error in package.lua at line 80: module 'strict' not found.
  3. Lua error in package.lua at line 80: module 'strict' not found.
  4. http://www.drugdevelopment-technology.com/projects/licofelone/



<templatestyles src="Asbox/styles.css"></templatestyles>