LP-922056
CAS No. 1365060-22-5
LP-922056( —— )
Catalog No. M28200 CAS No. 1365060-22-5
LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 40 | Get Quote |
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| 5MG | 63 | Get Quote |
|
| 10MG | 104 | Get Quote |
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| 25MG | 203 | Get Quote |
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| 50MG | 327 | Get Quote |
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| 100MG | 534 | Get Quote |
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| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameLP-922056
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NoteResearch use only, not for human use.
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Brief DescriptionLP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.
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DescriptionLP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.(In Vitro):LP-922056 can be used as a complementary chemical tool for exploring the role of Notum in Wnt signaling.(In Vivo):In mice, LP-922056 (3, 10, 30 mg/kg; gavage) significantly increases midshaft femur cortical bone thickness. LP-922056 (10 mg/kg) achieved high Cmax of 129 μM and AUC of 1533 μM h while volume of distribution is 0.13 L/kg and low clearance is 0.49 mL/min kg. LP-922056 (10 mg/kg; oral) increases cortical bone thickness and strength in the midshaft femur, bone mass in the femoral neck, and vertebral body cortical shell.
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In Vitro——
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In VivoAnimal Model:F1 male hybrid (129xC57) mice at 8.7 weeks of ageDosage:3, 10, 30 mg/kg Administration:Oral gavage; daily; for 25 days Result:Caused an increase in cortical bone thickness at all doses.Animal Model:Mouse Dosage:10 mg/kg (Pharmacokinetic Analysis) Administration:Orally Result:Achieved high Cmax (129 μM) and AUC (1533 μM?h) while has low clearance (0.49 mL/min?kg) and volume of distribution (0.13 L/kg).
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Synonyms——
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PathwayWnt/Notch/Hedgehog
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TargetWnt/beta/catenin
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RecptorsAHP
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Research Area——
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Indication——
Chemical Information
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CAS Number1365060-22-5
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Formula Weight300.78
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Molecular FormulaC11H9ClN2O2S2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (415.59 mM)
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SMILESO=C(O)CSC1=NC=NC2=C1SC(Cl)=C2C3CC3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Shah MM, et al. Enhancement of hippocampal pyramidal cell excitability by the novel selective slow-afterhyperpolarization channel blocker 3-(triphenylmethylaminomethyl)pyridine (UCL2077). Mol Pharmacol. 2006 Nov;70(5):1494-502.
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