LA1011
LA1011 is a heat shock protein (Hsps) co-inducer that selectively enhances heat shock-induced Hsp70, Hsp40, and Hsp27 expression. LA1011 exhibits neuroprotective effects in APPxPS1 transgenic Alzheimer's disease mice, preventing hippocampal neuronal loss, reducing tau pathology and neurofibrillary tangle accumulation in the hippocampus, decreasing amyloid plaque formation in the hippocampus, and increasing dendritic spine density in hippocampal CA1. LA1011 can be used for research on Alzheimer's disease.
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- CAS. Nr.: 1439268-65-1
- Formel: C25H36Cl2F3N3O4
- Molecular Weight:570.47
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
HSP70 |
HSP40 |
In Vitro
LA1011 (5-10 µM) does not alter yeast Hsp90 ATPase activity[1].
LA1011 (5 µM; 30 min-17 h) co-induced Hsp70 promoter-driven YFP expression in SH-SY5Y-pHsp70-YFP cells under 42°C heat shock conditions[1].
LA1011 (5 µM; 1-16 h) selectively co-induces Hsp27, Hsp40, and Hsp70 in heat-shocked SH-SY5Y cells without altering Hsp levels under non-stressed conditions[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:SH-SY5Y cells
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Concentration:5 µM
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Incubation Time:1 h (42°C heat shock); 16 h (37°C recovery)
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Result:Increased Hsp27, Hsp40, and Hsp70 levels under heat shock.
Did not alter Hsp27, Hsp40, Hsp70, Hsp60, or Hsp90 levels without heat shock.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:B6C3-Tg (APPswe/PS1dE9)85Dbo/Mmjax (C57BL/6 genetic background; male; 3 months old at start)[1]
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Dosage:3 mg/kg
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Administration:i.p.; once daily; 6 months
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Result:Improved spatial learning and memory in the Morris water maze.
Required less time to find the platform than transgenic saline controls.
Prevented loss of hippocampal neurons.
Decreased the number of abnormally accumulated neurofibrillary tangles in the hippocampus to the level found in wild-type mice.
Increased dendritic spine number in hippocampal CA1 compared with transgenic saline controls.
Decreased amyloid plaque formation in the hippocampus.
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Animal Model:wild-type C57BL/6 (male; 3 months old at start)[1]
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Dosage:3 mg/kg
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Administration:i.p.; once daily; 6 months
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Result:Improved memory performance in the Morris water maze.
Required less time to complete the task than wild-type saline controls.
Did not affect dendritic spine number in wild-type mice.
Chemical Information
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CAS. Nr. 1439268-65-1
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Molecular Weight 570.47
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Formel C25H36Cl2F3N3O4
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SMILES
O=C(C1=C(CCN(C)C)N(C)C(CCN(C)C)=C(C1C2=CC=C(C(F)(F)F)C=C2)C(OC)=O)OC.Cl.Cl
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Protokoll
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Protocol for Hematoxylin-Eosin (H&E) Staining
Hematoxylin-eosin staining is a routine histological method that stains nuclei mainly blue-purple with hemalum and stains cytoplasm, extracellular matrix, and many stromal components pink with eosin, allowing tissue architecture, cell morphology, necrosis, inflammation, fibrosis, tumor growth pattern, and treatment-associated injury to be evaluated by light microscopy. In cancer cells, primary neurons, mouse tumor models, intestinal organoids, inflammatory macrophage preparations, and drug-screening tissues, H&E is a morphology assay rather than a molecular assay; it should be interpreted with complementary molecular or immunostaining assays when the biological question concerns specific proteins, RNA levels, ferroptosis, mitophagy, or immune phenotypes.
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Amyloid: Congo Red Amyloid Staining
Congo red amyloid staining is a histochemical method used to detect extracellular amyloid deposits in tissue sections based on the affinity of Congo red dye for β-pleated sheet-rich protein aggregates. When bound to amyloid, Congo red produces characteristic apple-green birefringence under polarized light microscopy, which is widely regarded as a diagnostic feature of amyloid deposition in histopathology. The diagnostic principle relies on the combination of dye binding (congophilia) and optical anisotropy under polarized illumination, which distinguishes amyloid from most non-amyloid eosinophilic extracellular deposits in routine histological evaluation. Amyloid identification by Congo red staining remains a cornerstone in diagnostic pathology despite the availability of adjunct methods such as immunohistochemistry and mass spectrometry, particularly because of its ability to localize deposits directly within tissue architecture. The specificity of Congo red-positive deposits is incre
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Alzheimer’s Disease Modeling
Alzheimer’s Disease (AD) is a neurodegenerative disorder characterized by a progressive decline in cognitive functions and loss of specific types of neurons and synapses. Alzheimer's symptoms can be simulated in mice by injecting drugs (such as Aβ) or genetically modified.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)