54 Results for "

LXR agonists

" in MedChemExpress (MCE) Product Catalog:
Products (54)

54 Results for "LXR agonists" in MCE Product Catalog:

  • Targets Recommended:
49
49 Publications Verification
Cat. No.: HY-10626
CAS No.: 293754-55-9
Purity:  99.93%
T0901317 is an orally active and highly selective LXR agonist with an EC50 of 20 nM for LXRα . T0901317 activates FXR with an EC50 of 5 μM . T0901317 is RORα and RORγ dual inverse agonist with Ki values of 132 nM and 51 nM, respectively . T0901317 induces apoptosis and inhibits the development of atherosclerosis in low-density lipoprotein (LDL) receptor-deficient mice .
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29
29 Cited Publications
Cat. No.: HY-10627A
CAS No.: 405911-17-3
Purity:  99.96%
Target:  

LXR

Research Areas:  

Cardiovascular Disease Cancer

GW3965 hydrochloride is a potent and selective liver X receptor (LXR) agonist with EC50s of 190 nM and 30 nM for hLXRα and hLXRβ, respectively .
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29
29 Cited Publications
Cat. No.: HY-10627
CAS No.: 405911-09-3
Target:  

LXR

Research Areas:  

Cardiovascular Disease

GW3965 is a potent, selective liver X receptor (LXR) agonist with EC50s of 190 nM and 30 nM for hLXRα and hLXRβ, respectively .
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14
14 Cited Publications
Cat. No.: HY-10629
CAS No.: 875787-07-8
Purity:  99.95%
Synonyms: WAY 252623
Target:  

LXR

Research Areas:  

Metabolic Disease Cancer

LXR-623 is a brain-penetrant partial LXRα and full LXRβ agonist, with IC50s of 24 nM and 179 nM, respectively.
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8
8 Cited Publications
Cat. No.: HY-16972
CAS No.: 1613028-81-1
Target:  

LXR

Research Areas:  

Cancer

SR9243 is a liver-X-receptor (LXR) inverse agonist that induces LXR-corepressor interaction.
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4
4 Cited Publications
Cat. No.: HY-112813
CAS No.: 2247372-59-2
Purity:  99.42%
Research Areas:  

Metabolic Disease

TUG-1375 is an agonist of free fatty acid receptor 2 (FFA2/GPR43), with a pKi of 6.69. TUG-1375 is inactive on FFA3, FFA4, PPARα, PPARγ, PPARδ, LXRα or LXRβ .
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3
3 Cited Publications
Cat. No.: HY-111498A
CAS No.: 610318-54-2
Purity:  99.76%
Synonyms: Abequolixron
Target:  

LXR

Research Areas:  

Inflammation/Immunology Cancer

RGX-104 is an orally bioavailable and potent liver-X nuclear hormone receptor (LXR) agonist that modulates innate immunity via transcriptional activation of the ApoE gene.
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3
3 Cited Publications
Cat. No.: HY-111498
CAS No.: 610318-03-1
Purity:  99.88%
Synonyms: Abequolixron hydrochloride
Target:  

LXR

Research Areas:  

Inflammation/Immunology Cancer

RGX-104 hydrochloride is a small-molecule LXR agonist that modulates innate immunity via transcriptional activation of the ApoE gene.
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2
2 Cited Publications
Cat. No.: HY-101442
CAS No.: 1416153-62-2
Purity:  99.89%
Target:  

LXR

Research Areas:  

Metabolic Disease

SR9238 is a synthetic liver X receptor (LXR) inverse agonist with IC50s of 214 nM and 43 nM for LXRα and LXRβ, respectively.
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2
2 Cited Publications
Cat. No.: HY-123402
CAS No.: 264206-85-1
Purity:  99.19%
Target:  

LXR

Research Areas:  

Metabolic Disease

GSK3987 is a pan LXRα/β agonist with EC50s of 50 nM, 40 nM for LXRα-SRC1 and LXRβ-SRC1, respectively. GSK3987 increases the expression of ABCA1 and SREBP-1c. GSK3987 induces cellular cholesterol efflux and triglyceride accumulation .
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1
1 Cited Publications
Cat. No.: HY-16940
CAS No.: 474-73-7
Synonyms: 24S-OHC; 24S-HC; Cerebrosterol
24(S)-Hydroxycholesterol (24S-OHC), the major brain cholesterol metabolite, plays an important role to maintain homeostasis of cholesterol in the brain. 24(S)-Hydroxycholesterol (24S-OHC) is one of the most efficient endogenous LXR agonist known and is present in the brain and in the circulation at relatively high levels. 24(S)-Hydroxycholesterol (24S-OHC) is a very potent, direct, and selective positive allosteric modulator of NMDARs with a mechanism that does not overlapthat of other allosteric modulators .
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1
1 Cited Publications
Cat. No.: HY-129098
CAS No.: 79066-03-8
Purity:  99.91%
Target:  

LXR

Research Areas:  

Metabolic Disease

DMHCA, a potent and selective LXR agonist, specifically activates the cholesterol efflux arm of the LXR pathway without stimulating triglyceride synthesis. DMHCA has anti-inflammatory effects?and can be used for the research of cholesterol homeostasis diabetes .
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1
1 Cited Publications
Cat. No.: HY-19919
CAS No.: 918348-67-1
Synonyms: EXEL04286652; XL-652; BMS-788
Target:  

LXR

Research Areas:  

Metabolic Disease

BMS-779788 is a LXR partial agonist with IC50 values of 68 nM for LXRα and 14 nM for LXRβ.
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1
1 Cited Publications
Cat. No.: HY-18282
CAS No.: 898800-26-5
Target:  

LXR

AZ876 is a selective, orally active agonist of liver X receptor (LXRα/β) (Ki=0.007 μM [LXRα, human], 0.011 μM [LXRβ, human]. AZ876 induces the expression of target genes such as ABCA1 and ABCG1, promotes reverse cholesterol transport (RCT) and regulates lipid metabolism and anti-inflammatory effects. AZ876 increases cardiac polyunsaturated fatty acid levels, reduces myocardial fibrosis, and reduces lesion area and monocyte adhesion in atherosclerosis models. AZ876 can be used in cardiovascular disease research, such as preventing and treating β-adrenergic-induced cardiac diastolic dysfunction and inhibiting the progression of atherosclerosis .
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Cat. No.: HY-W040150
CAS No.: 77058-74-3
Target:  

LXR

24S,25-Epoxycholesterol is an agonist for Liver X Receptor (LXR). 24S,25-Epoxycholesterol exhibits properties in regulating the cholesterol efflux , inhibiting tumor growth against gastric cancer and glioblastoma and inducing apoptosis in BMMC cells .
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Cat. No.: HY-N15574
CAS No.: 6901-60-6
Saringosterol is an orally active steroid found in Sargassum muticum. Saringosterol is a LXR agonist. Saringosterol can lower cholesterol levels and inhibit the mRNA and protein expression of peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT enhancer-binding protein α (C/EBPα). Saringosterol has anti-obesity, anti-atherosclerosis, anti-Mycobacterium tuberculosis and anti-depressant activities .
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Cat. No.: HY-144549
CAS No.: 1779524-90-1
Purity:  99.95%
Target:  

LXR

Research Areas:  

Cardiovascular Disease

LXR (Liver X receptor) agonist 1 is potent LXR agonist with AC50s of 1.5 nM and 12 nM for LXR-α and LXR-β, respectively. LXR agonist 1 has the potential for the research of atherosclerosis .
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Cat. No.: HY-101973
CAS No.: 1256918-39-4
Purity:  99.19%
Synonyms: BMS-852927
Target:  

LXR

Research Areas:  

Cardiovascular Disease

XL041 (BMS-852927) is an LXRβ-selective agonist.
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Cat. No.: HY-123148
CAS No.: 870768-70-0
Purity:  99.85%
Target:  

LXR

Research Areas:  

Inflammation/Immunology

IMB-808 is a potent LXRα/β dual agonist with EC50 values of 0.53 μM and 0.15 μM (0.15 μM, using GAL4-pGL4-luc reporter plasmid) for LXRβ and LXRα, respectively. IMB-808 promotes expression of genes related to reverse cholesterol transport (ABCA1 and ABCG1). IMB-808 can be used for the study of atherosclerosis research .
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Cat. No.: HY-W754708
CAS No.: 508-52-1
Ouabagenin is a naturally occurring LXR ligand with LXR selective agonist activity. Ouabagenin acts as an EC 3.6.3.9 (Na(+)/K(+)- transport ATPase) inhibitor .
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