The Hydrolysis of Bimatoprost in Corneal Tissue Generates a Potent Prostanoid FP Receptor Agonist
- 1 August 2002
- journal article
- Published by Elsevier BV in Survey of Ophthalmology
- Vol. 47, S34-S40
- https://doi.org/10.1016/s0039-6257(02)00323-5
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Bimatoprost: a member of a new class of agents, the prostamides, for glaucoma managementExpert Opinion on Investigational Drugs, 2001
- The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogsBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 2000
- Nepafenac, a Unique Nonsteroidal Prodrug with Potential Utility in the Treatment of Trauma-Induced Ocular Inflammation: II. In Vitro Bioactivation and Permeation of External Ocular BarriersInflammation, 2000
- Prostaglandin moieties that determine receptor binding specificity in the bovine corpus luteumReproduction, 1999
- 2‐Arachidonoylglycerol, an endogenous cannabinoid receptor agonist: identification as one of the major species of monoacylglycerols in various rat tissues, and evidence for its generation through Ca2+‐dependent and ‐independent mechanismsFEBS Letters, 1998
- Molecular characterization of human and mouse fatty acid amide hydrolasesProceedings of the National Academy of Sciences of the United States of America, 1997
- Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amidesNature, 1996
- Isolation and Structure of a Brain Constituent That Binds to the Cannabinoid ReceptorScience, 1992
- Comparison of the ocular hypotensive efficacy of eicosanoids and related compoundsExperimental Eye Research, 1984
- Synthesis and biological activity of prostaglandin lactonesJournal of Medicinal Chemistry, 1983