
PPAR
170 produits trouvés pour "PPAR"
Licarin B
CAS :1.(-)-Licarin B (Licarine B) has anti-mycobacterial activity.Formule :C20H20O4Degré de pureté :99.82% - ≥95%Couleur et forme :SolidMasse moléculaire :324.37Norathyriol
CAS :Norathyriol is a potent PTP1B inhibitor with good cell permeability and oral availability.Formule :C13H8O6Degré de pureté :99.35% - 99.55%Couleur et forme :SolidMasse moléculaire :260.2Ref: TM-TN1990
1mg141,00€5mg335,00€10mg500,00€25mg807,00€50mg1.099,00€100mg1.485,00€200mg1.998,00€1mL*10mM (DMSO)447,00€Eupatilin
CAS :Eupatilin (NSC-122413), a flavone derived from Artemisia princepsPampanini, is a PPARα agonist, with pharmacological activity.Formule :C18H16O7Degré de pureté :98.53% - 99%Couleur et forme :SolidMasse moléculaire :344.32Troglitazone
CAS :Troglitazone (Romglizone) is a PPARγ agonist with anti-inflammatory and anti-tumor activity.Formule :C24H27NO5SDegré de pureté :98% - 99.8%Couleur et forme :Yellow SolidMasse moléculaire :441.54Ref: TM-T3170
2mg42,00€5mg62,00€10mg88,00€25mg172,00€50mg305,00€100mg558,00€500mg1.169,00€1mL*10mM (DMSO)85,00€DG172 dihydrochloride
CAS :DG172 dihydrochloride (DG-172 dihydrochloride) is an antagonist of PPARβ/δ(IC50 : 27 nM).
Formule :C20H22BrCl2N3Degré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :455.2Tetradecylthioacetic acid
CAS :Synthetic fatty acid TTA has β-sulfur, resists β-oxidation, and activates PPARs, especially PPARα.
Formule :C16H32O2SDegré de pureté :99.93%Couleur et forme :SolidMasse moléculaire :288.49T0070907
CAS :T0070907(IC50=1 nM) , an effective and specific PPARγ inhibitor, with the >800-fold selectivity over PPARα and PPARδ.
Formule :C12H8ClN3O3Degré de pureté :98.25% - 99.98%Couleur et forme :SolidMasse moléculaire :277.66Seladelpar
CAS :Seladelpar (MBX 8025) has been used in trials studying the treatment of Hyperlipidemia.Formule :C21H23F3O5SDegré de pureté :99.18% - 99.41%Couleur et forme :SolidMasse moléculaire :444.46Rosiglitazone
CAS :Rosiglitazone (BRL49653) is a PPARγ agonist, TRPC5 activator, and TRPM3 inhibitor with oral activity.Formule :C18H19N3O3SDegré de pureté :98.61% - 99.87%Couleur et forme :White To Off-White Crystalline PowderMasse moléculaire :357.43GW9662
CAS :GW9662 (TIMTEC-BB SBB006523) is a PPARγ antagonist (IC50=3.3 nM) with selectivity. GW9662 has anti-tumor effect. High-Quality, Low-Cost!Formule :C13H9ClN2O3Degré de pureté :98% - 99.98%Couleur et forme :Off-White SolidMasse moléculaire :276.68SR1664
CAS :SR1664 is a potent and selective PPARγ inhibitor with potential antidiabetic activity.Formule :C33H29N3O5Degré de pureté :98.02%Couleur et forme :SolidMasse moléculaire :547.6Ref: TM-T23389
1mg52,00€2mg74,00€5mg111,00€10mg144,00€25mg284,00€50mg411,00€100mg590,00€200mg833,00€1mL*10mM (DMSO)123,00€FH535
CAS :FH535, a Wnt/β-catenin signaling and PPAR inhibitor, exhibits anti-tumor activities.Formule :C13H10Cl2N2O4SDegré de pureté :98.25% - 99.5%Couleur et forme :SolidMasse moléculaire :361.2Ref: TM-T2413
5mg35,00€10mg54,00€25mg88,00€50mg156,00€100mg259,00€200mg383,00€500mg620,00€1mL*10mM (DMSO)60,00€Icariin
CAS :Icariin (Ieariline) is a flavonol glycoside that inhibits PDE5 and PDE4 activity and is a PPARα activator. Cost-effective and quality-assured.Formule :C33H40O15Degré de pureté :97.82% - 98.3%Couleur et forme :SolidMasse moléculaire :676.66GW6471
CAS :GW6471 is an antagonist of PPARα. GW6471 enhances the binding affinity of the PPAR α ligand-binding domain to the co-repressor proteins SMRT and NCoR.Formule :C35H36F3N3O4Degré de pureté :98.23% - 99.55%Couleur et forme :SolidMasse moléculaire :619.67Ref: TM-T8486
2mg35,00€5mg52,00€10mg88,00€25mg177,00€50mg311,00€100mg533,00€200mg802,00€1mL*10mM (DMSO)87,00€Palmitelaidic Acid
CAS :Palmitelaidic Acid (trans-Palmitoleic acid) is one of the most abundant fatty acids in serum and tissue.Formule :C16H30O2Degré de pureté :99.76%Couleur et forme :SolidMasse moléculaire :254.41NSC-87877 disodium
CAS :NSC-87877 disodium (NSC87877) is a cell-permeable inhibitor of both SHP-1 and SHP-2. NSC-87877 also inhibits EGF-induced Erk1/2 activation in HEK293 cells.Formule :C19H13N3O7S2·2NaDegré de pureté :97.89%Couleur et forme :SolidMasse moléculaire :503.42Glabrone
CAS :Glabrone shows antiviral activity against influenza virus.Formule :C20H16O5Degré de pureté :99.08% - 99.55%Couleur et forme :SolidMasse moléculaire :336.34Tesaglitazar
CAS :Tesaglitazar is a potent and selective peroxide PPARα / γ receptor dual agonist with a more potent affinity for PPARγ than PPARα, The EC50 values for rat PPARαFormule :C20H24O7SDegré de pureté :99.95%Couleur et forme :SolidMasse moléculaire :408.47Ref: TM-T17044
1mg46,00€5mg87,00€10mg137,00€25mg255,00€50mg427,00€100mg667,00€200mg924,00€1mL*10mM (DMSO)97,00€THR-0921
CAS :THR-0921 (CLX-0921) is a peroxisome proliferator-activated receptor (PPAR) agonist that can be used to study cardiovascular and metabolic diseases.Formule :C28H25NO7SDegré de pureté :100% - 99.83%Couleur et forme :SolidMasse moléculaire :519.5713-Oxo-9E,11E-octadecadienoic acid
CAS :13-Oxo-9E,11E-octadecadienoic acid from tomato juice, an isomer of 9-oxo-ODA, activates PPARα and lowers triglycerides in diabetic mice.Formule :C18H30O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :294.43AVE-8134
CAS :AVE-8134 is an agonist of PPARα. For human and rodent PPARα receptor, the EC50 values are 100 and 3000 nM, respectively.Formule :C22H23NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :381.42GW 9578
CAS :GW 9578 is a PPARα agonist with potent lipid-lowering activity for the study of psoriasis, arthritis, alopecia, asthma and type I diabetes.Formule :C26H34F2N2O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :492.62Peliglitazar racemate
CAS :Peliglitazar racemate(BMS 426707-01 racemate) is the racemate of Peliglitazar.Peliglitazar racemate may be used as a potential antidiabetic and anti-obesityFormule :C30H30N2O7Degré de pureté :97.75%Couleur et forme :SolidMasse moléculaire :530.57BVT.13
CAS :BVT.13 is an orally active selective PPARγ agonist with antidiabetic activity comparable to rosiglitazone, supporting research in metabolic regulation.Formule :C18H11Cl2N3O4Degré de pureté :98.59%Couleur et forme :SolidMasse moléculaire :404.2FTX-6746
CAS :FTX-6746 is an orally active and selective PPARG reverse inhibitor with anticancer activity. It can be used in research on urothelial carcinoma.Formule :C16H7ClF2N2ODegré de pureté :98.68%Couleur et forme :SolidMasse moléculaire :316.69GSK376501A
CAS :GSK376501A is a selective and effective modulator of peroxisome proliferator-activated receptor γ (PPARγ) for the study of type 2 diabetes.Formule :C32H37NO6Degré de pureté :97.71% - >99.99%Couleur et forme :SolidMasse moléculaire :531.64Pparδ agonist 2
CAS :Pparδ agonist 2 is an agonist of PPARδ.Formule :C20H18F3N3O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :437.44Daltroban
CAS :Daltroban (SKF 96148) is a specific thromboxane A2 (TXA2) receptor antagonist.Formule :C16H16ClNO4SDegré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :353.82Ref: TM-T15049
1mg55,00€5mg122,00€10mg177,00€25mg295,00€50mg420,00€100mg572,00€200mg772,00€1mL*10mM (DMSO)111,00€Saroglitazar
CAS :Saroglitazar (Lipaglyn) is an agonist of PPAR with EC50 values of 0.65 pM and 3 nM for PPARα and PPARγ.Formule :C25H29NO4SDegré de pureté :98.51%Couleur et forme :SolidMasse moléculaire :439.57PPARα-MO-1
CAS :PPARα-MO-1 is a potent modulator of PPARα.Formule :C27H37NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :455.59LG100754
CAS :LG100754 (UVI 2112) is an insulin sensitizer and RXR modulator, antagonizing RXR homodimers while agonizing RXR:PPARα/γ heterodimers.Formule :C26H36O3Couleur et forme :SolidMasse moléculaire :396.56Chiglitazar
CAS :Chiglitazar is a PPAR α/γ/δ agonist and insulin sensitizer used in the treatment of type 2 diabetes mellitus , anti-inflammatory and anti-fibrotic.Formule :C36H29FN2O4Couleur et forme :SolidMasse moléculaire :572.63Inolitazone dihydrochloride
CAS :Inolitazone dihydrochloride is an effective, high-affinity PPARγ agonist; its biological activity is dependent on PPARγ (IC50:0.8 nM) to inhibit cell growth.Formule :C27H28Cl2N4O4SCouleur et forme :SolidMasse moléculaire :575.51ARH-049020
CAS :ARH-049020, a peroxisome proliferator-activated receptor (PPAR) agonist, is used potentially for the treatment of insulin resistance and type 2 diabetes.Formule :C24H31NO6Degré de pureté :97.19% - 99.82%Couleur et forme :SolidMasse moléculaire :429.51Reglitazar
CAS :Reglitazar, a dual PPARα/γ agonist, enhances insulin signaling, reduces insulin resistance, and lowers hypertriglyceridemia in obese rats.Formule :C22H20N2O5Degré de pureté :97.07% - 98.72%Couleur et forme :SolidMasse moléculaire :392.4BAY-0069
CAS :BAY-0069 is a potent and selective PPARγ transactivator that inhibits human PPARγ and murine PPARγ with IC50s of 6.3 nM and 24 nM, respectively.BAY-0069 can be
Formule :C22H16BrN3O4Degré de pureté :99.41%Couleur et forme :SoildMasse moléculaire :466.28Indeglitazar
CAS :Indeglitazar (PPM 204) is orally available pan-agonist of PPAR (PPAR subtypes alpha (α), delta (δ), and gamma (γ)).Formule :C19H19NO6SDegré de pureté :99.45%Couleur et forme :SolidMasse moléculaire :389.42Farglitazar
CAS :Farglitazar (GI-262570) is a PPAR-γ agonist and insulin sensitizer used in the study of diabetes.Formule :C34H30N2O5Degré de pureté :99.4% - 99.52%Couleur et forme :SolidMasse moléculaire :546.61Dazmegrel
CAS :Dazmegrel (UK 38,485) is a thromboxane A2 (TXA2) synthase inhibitor for the prevention of increased whole platelet aggregation in normal pregnancy.Formule :C16H17N3O2Degré de pureté :98.81%Couleur et forme :SolidMasse moléculaire :283.33Cevoglitazar
CAS :Cevoglitazar (LBM-642) is a PPARɑ agonist and PPARγ agonist. Cevoglitazar potently reduces food intake and body weight in obese mice and cynomolgus monkeys.Formule :C27H21F3N2O6SDegré de pureté :97%Couleur et forme :SolidMasse moléculaire :558.53K-111
CAS :K-111 is a PPAR alpha agonist. K-111 improves insulin resistance, reducing bodyweight, and ameliorating atherogenic dyslipidemia.Formule :C18H25Cl3O2Degré de pureté :99.64% - 99.88%Couleur et forme :SolidMasse moléculaire :379.75BAY-4931
CAS :BAY-4931 is a powerful, covalent, and selective inverse-agonist of PPARγ, exhibiting an IC50 value of 0.17 nM.Formule :C22H16ClN3O4Degré de pureté :99.73%Couleur et forme :SoildMasse moléculaire :421.83Ref: TM-T67933
1mg38,00€5mg84,00€10mg119,00€25mg260,00€50mg409,00€100mg605,00€500mg1.288,00€1mL*10mM (DMSO)93,00€Linotroban
CAS :Linotroban(CL-871502) is a potent selective thromboxane (TXA2) receptor antagonist with antithrombotic activity.Formule :C14H15NO5S2Degré de pureté :97.95% - >99.99%Couleur et forme :SolidMasse moléculaire :341.4Imiglitazar
CAS :Imiglitazar (TAK559) is a potent PPAR-β/δ receptor agonist with hypoglycemic effects.Formule :C28H26N2O5Degré de pureté :97.33%Couleur et forme :SolidMasse moléculaire :470.52Darglitazone
CAS :Darglitazone (CP-86325) is a potent, selective agonist of PPAR-γ with antidiabetic actions.Formule :C23H20N2O4SDegré de pureté :99.76%Couleur et forme :SolidMasse moléculaire :420.48LCB-2853
CAS :LCB-2853 is a potent thromboxane A2/prostaglandin H2 (TXA2/PGH2) receptor antagonist with antiplatelet aggregation, antivasospasm, and antithrombotic effects.Formule :C21H24ClNO4SDegré de pureté :97.15%Couleur et forme :SolidMasse moléculaire :421.94KD-3010
CAS :KD-3010 (Kalypsys) is an orally active potent and selective PPARδ agonist for the study of liver injury.Formule :C30H33F3N2O8S2Degré de pureté :99.61%Couleur et forme :SolidMasse moléculaire :670.72PPARγ agonist 8
CAS :PPARγ agonist 8, a compound that acts on the peroxisome proliferator-activated receptor gamma (PPARγ), has been shown to stimulate peroxisome proliferatorFormule :C19H12F4O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :380.36U-46619
CAS :U-46619 is an effective thromboxane A2 (TXA2) agonist and a thromboxane A2 analog (endoperoxide), capable of inducing contraction in the aortic smooth muscle (Formule :C21H34O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :350.49PPARδ agonist 9
CAS :PPARδ agonist 9 (compound 21), with an EC50 of 3.6 nM, is effective in vivo, decreasing serum MCP-1 concentrations in mice and markedly reducing atheroscleroticFormule :C26H28ClF3N4O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :569.04PPAR agonist 1
CAS :PPAR agonist 1 is an agonist of PPAR α/γ, used for reducing blood glucose, lipid levels, reducing body weight, and lowering cholesterol.Formule :C20H25NO6SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :407.48CRX000227
CAS :CRX000227 is a PPAR modulator suitable for researching metabolic and cell proliferative disorders [1].Formule :C25H24N4O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :444.55Edaglitazone
CAS :Edaglitazone (R-483) is a PPARγ agonist with antiplatelet activity that can be used in studies of diabetes and obesity.Formule :C24H20N2O4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :464.56Inolitazone
CAS :Inolitazone (RS5444) a high-affinity PPARγ agonist. Inolitazone exhibits IC50 for growth inhibition is ~0.8 nM in vitro.Formule :C27H26N4O4SDegré de pureté :99.41% - 99.53%Couleur et forme :SolidMasse moléculaire :502.58Ref: TM-T15581
1mg70,00€5mg149,00€10mg230,00€25mg374,00€50mg532,00€100mg713,00€500mgÀ demander1mL*10mM (DMSO)178,00€Ragaglitazar
CAS :Ragaglitazar(NNC-61-0029) is a potent dual activator of PPARγ and PPARα.Cost-effective and quality-assured.Formule :C25H25NO5Degré de pureté :97.46% - 98.56%Couleur et forme :SolidMasse moléculaire :419.47PPARγ phosphorylation inhibitor 1
CAS :PPARγ phosphorylation inhibitor 1, PPARγ agonist (IC50=24 nM), inhibits CDK5-mediated Ser273 phosphorylation, antidiabetic activity.Formule :C22H14Cl2N2O4Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :441.26SR 11023
CAS :SR 11023, an orally active PPAR γ antagonist, exhibits an IC 50 value of 109 nM and is significant in diabetes research [1].Formule :C33H36N2O3Couleur et forme :SolidMasse moléculaire :508.65Anti-NASH agent 2
CAS :Anti-NASH agent 2 (compound 21) is an inhibitor of neolipogenesis activity and α-SMA gene expression. It improves hepatic steatosis, edema, inflammatory infiltration, and liver fibrosis in NASH mouse models.
Formule :C32H51N3O2Couleur et forme :SolidMasse moléculaire :509.766PPARγ agonist 17
CAS :PPARγ agonist17 (Compound C1) is an orally active PPARγ agonist. It enhances PPARγ activity, arrests the cell cycle of HT-29 cells at the G2/M phase, inhibits cell migration, and induces apoptosis. PPARγ agonist17 exhibits broad-spectrum antiproliferative activity against cancer cells with relatively low toxicity to normal cells and does not cross the blood-brain barrier.Formule :C48H63NO7Couleur et forme :SolidMasse moléculaire :766.016PPARγ modulator-2
CAS :PPARγmodulator-2 (Compound (R)-2n) is a reversible modulator of PPARγ, inhibiting the PPARγ ligand-binding domain (LBD) with an IC50 of 41 nM. It helps lower blood glucose levels, improves glucose tolerance and insulin sensitivity, and demonstrates antidiabetic activity in db/db mouse models.Formule :C26H21NO7S3SeCouleur et forme :SolidMasse moléculaire :634.6Amezalpat
CAS :Amezalpat is a PPARα antagonist with an IC50 of 58 nM [nanomolar]. Amezalpat also exhibits antitumor activity.Formule :C34H41N3O4Couleur et forme :SolidMasse moléculaire :555.707PPARγ-IN-5
CAS :PPARγ-IN-5 (Compound A3) is an inhibitor of PPARγ. In liver cells, it reduces lipid accumulation and shows no significant cytotoxicity in HepG2 cells at a concentration of 400 µM. PPARγ-IN-5 is applicable for research on non-alcoholic fatty liver disease.Formule :C22H23ClO7Couleur et forme :SolidMasse moléculaire :434.867PPARα/δ agonist 3
CAS :PPARα/δ agonist 3 (Compound 8) is an orally active PPAR agonist capable of activating PPARα, PPARδ, and PPARγ, with EC50 values of 5.6 nM, 3.4 nM, and 1278 nM, respectively. It exhibits anti-cholestatic activity in mouse models of cholestatic liver disease induced by ANIT or CDCA.Formule :C23H25F3N2O4Couleur et forme :SolidMasse moléculaire :450.451PPARδ agonist 11
CAS :Compound 11, a selective PPARδ agonist, demonstrates an EC50 of 20 nM, indicating its high affinity for PPARδ receptors. This compound efficiently reduces levels of nitric oxide (NO), as well as the pro-inflammatory cytokines TNFα and IL-6 in LPS-stimulated RAW264.7 cells via the NF-κB pathway, showcasing its anti-inflammatory properties. Additionally, Compound 11 exhibits remarkable stability in human liver microsomes and plasma. It significantly ameliorates foot edema induced by Carrageenan, displaying favorable pharmacokinetic properties with a bioavailability of approximately 100%.Formule :C19H15F3N2O3S2Couleur et forme :SolidMasse moléculaire :440.46Fonadelpar
CAS :Fonadelpar is an agonist of PPARδ. It also is used in the research of neuroparalytic keratopathy.Formule :C25H23F3N2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :504.52PPARγ agonist 10
CAS :PPARγ agonist 10 (compound 33g) serves as a PPARγ agonist, enhancing insulin secretion, glucose uptake, and insulin sensitivity in βTC6 cells [1].Formule :C17H14N4O3S2Couleur et forme :SolidMasse moléculaire :386.45Aleglitazar
CAS :Aleglitazar (R1439) (R1439) is a potent dual PPARα/γ agonist, with IC50s of 38 nM and 19 nM for human PPARa and PPARγ, respectively.Formule :C24H23NO5SDegré de pureté :99.03%Couleur et forme :SolidMasse moléculaire :437.51Ref: TM-T14176
1mg233,00€5mg532,00€10mg718,00€25mg1.099,00€50mg1.485,00€100mg1.998,00€1mL*10mM (DMSO)538,00€PPARγ-IN-2
CAS :"PPARγ-IN-2 (Compound 5a), a PPARγ inhibitor, exhibits an EC50 of 0.106 μM in inhibiting TG accumulation in 3T3-L1 preadipocytes.
Formule :C19H21N5ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :335.4Mavodelpar free base
CAS :Mavodelpar free acid (REN001 free acid) is an selective agonist of PPARδ.
Formule :C31H30FNO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :515.57Anti-NASH agent 1
CAS :Anti-NASH Agent 1 (Compound 3d), derived from Elafibranor, serves as a strong PPAR-α/δ agonist aimed at treating nonalcoholic steatohepatitis (NASH).
Formule :C26H33NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :423.54

