Details
Stereochemistry | ACHIRAL |
Molecular Formula | C19H28N4O3 |
Molecular Weight | 360.4506 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=C(OCCCCCC(C)(C)C2=NN=NN2)C=C(O)C(=C1)C(C)=O
InChI
InChIKey=WCGXJPFHTHQNJL-UHFFFAOYSA-N
InChI=1S/C19H28N4O3/c1-5-14-11-15(13(2)24)16(25)12-17(14)26-10-8-6-7-9-19(3,4)18-20-22-23-21-18/h11-12,25H,5-10H2,1-4H3,(H,20,21,22,23)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/29323699Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/20380377 | https://www.ncbi.nlm.nih.gov/pubmed/7902871 | https://www.ncbi.nlm.nih.gov/pubmed/24513188 | https://www.ncbi.nlm.nih.gov/pubmed/8393594
Sources: https://www.ncbi.nlm.nih.gov/pubmed/29323699
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/20380377 | https://www.ncbi.nlm.nih.gov/pubmed/7902871 | https://www.ncbi.nlm.nih.gov/pubmed/24513188 | https://www.ncbi.nlm.nih.gov/pubmed/8393594
LY-255283 is a tetrazole derivative that acts as the competitive antagonist of the Leukotriene B4 (LTB4) receptor 2 (BLT2). LY255283 shows potent inhibition of LTB4 binding to human neutrophils and of LTB4-induced aggregation of guinea-pig neutrophils. In guinea-pigs, this compound also suppressed both specific binding of LTB4 to lung membrane and LTB4-induced contraction of lung parenchyma. Intravenous and oral administration of LY255283 dose-dependently reduced airway obstruction in guinea-pigs induced by LTB4, but not by histamine and U- 46619. Antigen-induced lung eosinophilia in rats was inhibited by orally administered LY255283. LY255283 exhibited the ability to suppress the shock induced by endotoxin and splanchnic artery occlusion in rats. LY255283 (bolus i.v. and subsequent infusion) attenuated endotoxin-induced adult respira¬tory distress syndrome in the pig model. LY255283 is used in leukotriene receptor research along with other selective leukotriene receptor agonists and antagonist to identify and differentiate the physiological and cell signaling effects of the leukotriene B4 receptor on processes such as paclitaxel resistance in MCF-7/DOX breast cancer cells, monocyte-derived dendritic cell chemotaxis, and 5-lipoxygenase activity and interleukin-8 production in human neutrophils.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2095160 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7902871 |
85.1 nM [IC50] | ||
Target ID: CHEMBL2047 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24513188 |
35.2 µM [IC50] | ||
Target ID: CHEMBL3191 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11278893 |
950.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1659282
Guinea pigs were treated with LY-255283 at doses 3.0, 10.0 and 30 mg/kg
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27914516
PANC-1 cells were used for activity evaluation. The PANC-1 were maintained in DMEM supplemented with 10% (v/v) FBS and 1% penicillin-streptomycin at 37 °C in a 5% CO2 atmosphere. The cells were washed twice in serum-free DMEM and incubated in serum-free DMEM for 15 h before the experiment. To examine the involvement of LTB4 receptors in the effect of LTB4 on vimentin expression, PANC-1 cells were treated with the BLT1 antagonist and BLT2 antagonist for 48 h. the BLT2 antagonist LY255283 suppressed LTB4- induced vimentin expression in PANC-1 cells
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H037W1I5AL
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DTXSID30151872
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ACTIVE MOIETY