research use only
Cat.No.S7325
| Cell Lines | Assay Type | Concentration | Incubation Time | Formulation | Activity Description | PMID |
|---|---|---|---|---|---|---|
| 697 B-ALL cells | Function assay | 1 h | Inhibition of Mer kinase phosphorylation in human 697 B-ALL cells after 1 hr by Western blot analysis, IC50=0.022 μM | |||
| mouse 32D-EMC cells | Function assay | Inhibition of EGF-induced human intracellular domain of Mer/extracellular domain of EGFR phosphorylation expressed in mouse 32D-EMC cells after 1 hr by Western blot analysis | ||||
| Click to View More Cell Line Experimental Data | ||||||
| Molecular Weight | 463.58 | Formula | C25H33N7O2 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 1493764-08-1 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CCCCNC1=NC=C(C(=N1)NC2CCC(CC2)O)C(=O)NCC3=CC=C(C=C3)N4C=CN=C4 | ||
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In vitro |
DMSO
: 92 mg/mL
(198.45 mM)
Ethanol : 7 mg/mL Water : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
| Targets/IC50/Ki |
Mer
(Cell-free assay) 4.3 nM
Tyro3
(Cell-free assay) 250 nM
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|---|---|
| In vitro |
UNC2881 inhibits Mer kinase activity in 697 B-ALL cells with IC50 of 22 nM, and inhibits collagen-stimulated platelet aggregation.
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| In vivo |
UNC2881 have high systemic clearance (94.5 mL/min/kg) and 14% oral bioavailability in mice.
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References |
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