
GW3965 hydrochloride
CAS No. 405911-17-3
GW3965 hydrochloride( GW 3965 hydrochloride | GW-3965 hydrochloride )
Catalog No. M14397 CAS No. 405911-17-3
A potent, selective, orally active LXR agonist that recruits the steroid receptor coactivator 1 to human LXRα in a cell-free ligand-sensing assay with an EC50 of 125 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 32 | In Stock |
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5MG | 51 | In Stock |
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10MG | 81 | In Stock |
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25MG | 178 | In Stock |
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50MG | 340 | In Stock |
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100MG | 506 | In Stock |
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500MG | 1107 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameGW3965 hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, selective, orally active LXR agonist that recruits the steroid receptor coactivator 1 to human LXRα in a cell-free ligand-sensing assay with an EC50 of 125 nM.
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DescriptionA potent, selective, orally active LXR agonist that recruits the steroid receptor coactivator 1 to human LXRα in a cell-free ligand-sensing assay with an EC50 of 125 nM; acts as a full agonist on hLXRα and hLXRβ in cell-based reporter gene assays with EC50 of 190 and 30 nM, respectively; increases expression of ABCA1 in the small intestine and peripheral macrophages in C57BL/6 mice at 10 mg/kg.Asthma Discontinued.
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In VitroGW3965 hydrochloride promotes GBM cell death?in vitro?with enhanced efficacy in EGFRvIII-expressing tumor cells. GW3965 hydrochloride up-regulates expression of the cholesterol transporter gene ABCA1 and the E3 ubiquitin ligase IDOL and reduces LDLR levels. LXR ligands inhibits platelet aggregation and calcium mobilization stimulated by collagen or CRP. GW3965 hydrochloride (1 or 5 μM) displays a minor inhibitory effect on fibrinogen binding and P-selectin exposure, when platelets are stimulated with 1 μg/mL CRP. But using higher concentrations of GW3965 hydrochloride (10 μM) or T0901317 (40 μM), the levels of fibrinogen and P-selectin on the platelet surface are reduced.
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In VivoGW3965 hydrochloride induces an increase of neuroactive steroids in the spinal cord, the cerebellum and the cerebral cortex of STZ-rats, but not in the CNS of non-pathological animals. GW3965 hydrochloride treatment induces an increase of dihydroprogesterone in the spinal cord of diabetic animals in association with an increase of myelin basic protein expression. GW3965 hydrochloride (40 mg/kg, p.o.) strongly induces ABCA1 expression and reduces LDLR expression, and this is accompanied by 59% inhibition of tumor growth, and a 25-fold increase in GBM cell apoptosis in vivo. GW3965 hydrochloride (2 mg/kg, i.v.) increases bleeding time and modulated platelet thrombus formation in vivo.
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SynonymsGW 3965 hydrochloride | GW-3965 hydrochloride
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PathwayNuclear Receptor/Transcription Factor
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TargetLXR
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RecptorhLXRα|hLXRβ|LXRα/SRC1?LiSA
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Research AreaInflammation/Immunology
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IndicationAsthma
Chemical Information
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CAS Number405911-17-3
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Formula Weight618.5133
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Molecular FormulaC33H32Cl2F3NO3
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCl.OC(=O)CC1=CC=CC(OCCCN(CC(C2=CC=CC=C2)C2=CC=CC=C2)CC2=CC=CC(=C2Cl)C(F)(F)F)=C1 |c:6,18,20,25,27,33,35,42,t:4,16,23,31|
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Chemical NameBenzeneacetic acid, 3-[3-[[[2-chloro-3-(trifluoromethyl)phenyl]methyl](2,2-diphenylethyl)amino]propoxy]-, hydrochloride (1:1)
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. Collins JL, et al. J Med Chem. 2002 May 9;45(10):1963-6.
2. Joseph SB, et al. Proc Natl Acad Sci U S A. 2002 May 28;99(11):7604-9.
3. Donkin JJ, et al. J Biol Chem. 2010 Oct 29;285(44):34144-54.
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