MDL | MFCD00876422 |
---|---|
Molecular Weight | 360.45 |
Molecular Formula | C19H28N4O3 |
SMILES | CC(C1=CC(CC)=C(OCCCCCC(C2=NNN=N2)(C)C)C=C1O)=O |
LTB 4 ~100 nM (IC 50 , LTB 4 binds to guinea pig lung membranes) |
LY255283 competitively reduces conlractilc responses of lung parcnchyma to LTB, (pA
2
= 7.2)
[2]
.
LY255283 (10 μM, 7 days) significantly suppresses the invasiveness of highly aggressive 253 J-BV bladder cancer cells
[4]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay [4]
Cell Line: | 253 J-BV cells. |
Concentration: | 5 or 10 μM. |
Incubation Time: | 7 days. |
Result: | Inhibition of BLT2 signaling attenuates aggressive migration by 253 J-BV cells. |
LY255283 (3, 30 mg/kg) ameliorates lipopolysaccharide-induced ARDS in pigs, possibly by blocking the recruitment of activated PMNs into alveoli in a dose-dependent fashion
[3]
.
LY255283 (2.5 mg/kg, ip) inhibits transitional cell carcinoma metastasis in mice models. The result suggests that a BLT2–Nox–ROS–NF–κB cascade plays a critical role in bladder cancer invasion and metastasis
[4]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Mice (253 J-BV cells injected) [4] . |
Dosage: | 2.5 mg/kg. |
Administration: | IP injected 3 and 5 days after injection of cells. |
Result: | By 12 weeks after injection, in mice treated with LY255283 only 0-3 nodules formed per lung, and histological analysis confirmed that the number of micrometastatic lesions was markedly reduced. |
Solid
Room temperature in continental US; may vary elsewhere.
-20°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
DMSO : 100 mg/mL ( 277.43 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.7743 mL | 13.8715 mL | 27.7431 mL |
5 mM | 0.5549 mL | 2.7743 mL | 5.5486 mL |
10 mM | 0.2774 mL | 1.3872 mL | 2.7743 mL |