Pub. Date : 1993 Mar 17
PMID : 8461333
4 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | A novel active-site directed specific inhibitor of phospholipase A2 (PLA2), 1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol (MJ33), administered endotracheally co-dispersed in liposomes, significantly reduced the formation of thiobarbituric acid reactive substances (TBARS) in isolated rat lungs subjected to ischemia-reperfusion. | Thiobarbituric Acid Reactive Substances | phospholipase A2 group IB | Rattus norvegicus |
2 | A novel active-site directed specific inhibitor of phospholipase A2 (PLA2), 1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol (MJ33), administered endotracheally co-dispersed in liposomes, significantly reduced the formation of thiobarbituric acid reactive substances (TBARS) in isolated rat lungs subjected to ischemia-reperfusion. | Thiobarbituric Acid Reactive Substances | phospholipase A2 group IB | Rattus norvegicus |
3 | A novel active-site directed specific inhibitor of phospholipase A2 (PLA2), 1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol (MJ33), administered endotracheally co-dispersed in liposomes, significantly reduced the formation of thiobarbituric acid reactive substances (TBARS) in isolated rat lungs subjected to ischemia-reperfusion. | Thiobarbituric Acid Reactive Substances | phospholipase A2 group IB | Rattus norvegicus |
4 | A novel active-site directed specific inhibitor of phospholipase A2 (PLA2), 1-hexadecyl-3-trifluoroethylglycero-sn-2-phosphomethanol (MJ33), administered endotracheally co-dispersed in liposomes, significantly reduced the formation of thiobarbituric acid reactive substances (TBARS) in isolated rat lungs subjected to ischemia-reperfusion. | Thiobarbituric Acid Reactive Substances | phospholipase A2 group IB | Rattus norvegicus |