Nuclear Receptors

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  • TFM-4AS-1

    TFM-4AS-1 is a potent selective androgen receptor modulator (SARM) (IC50 = 30 nM), which exhibits limited effects on reproductive tissues and sebaceous glands; does not repress AP-1-sensitive MMP-1 reporter. Learn More

    Starting at: $140.00

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  • Cl-4AS-1

    Cl-4AS-1 is a potent steroidal androgen receptor agonist (IC50 = 12 nM), which inhibits 5α-reductase type I and II (IC50 values are 6 and 10 nM respectively). Learn More

    Starting at: $140.00

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  • PF 998425

    PF 998425 is a selective non-steroidal androgen receptor (AR) antagonist (IC50 values are 26 nM and 90 nM in AR binding assays and cellular assays respectively), which displays low affinity for progesterone receptor (IC50 > 10 μM). Learn More

    Starting at: $125.00

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  • GSK 3787

    GSK 3787 is a potent and selective peroxisome proliferator-activated receptor δ (PPARδ) antagonist (pIC50 = 6.6), which displays no measurable affinity for PPARα or PPARγ in vitro (pIC50< 5). Learn More

    Starting at: $69.00

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  • GW 0742

    GW 0742 is a potent and highly selective PPARδ agonist. EC50 values are 0.001, 1.1 and 2 μM for transactivation of human PPARδ, -α, and -γ receptors respectively. Learn More

    Starting at: $129.00

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  • DiMNF

    DiMNF is a selective aryl hydrocarbon receptor (AHR) modulator (SAhRM) which suppresses expression of CD55 and CD46 induced by IL-1β Learn More

    Starting at: $110.00

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  • L-Kynurenine

    Tryptophan catabolite; endogenous activator of the aryl hydrocarbon receptor (AhR). Learn More

    Starting at: $39.00

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  • CH 223191

    CH 223191 is a potent and specific aryl hydrocarbon receptor (AhR) antagonist, which displays no AhR agonist activity (at concentrations up to 100 μM) and blocks binding of 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) to the AhR in a dose-dependent manner. Learn More

    Starting at: $109.00

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  • Phortress

    Phortress is a prodrug of the antitumor agent 5F 203, which acts via binding to aryl hydrocarbon receptors. Learn More

    Starting at: $155.00

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  • 6,2',4'-Trimethoxyflavone

    6,2',4'-Trimethoxyflavone is an aryl hydrocarbon receptor antagonist with EC50 value of 0.9 μM. Learn More

    Starting at: $85.00

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  • ITE

    ITE is an endogenous agonist for the transcription factor aryl hydrocarbon receptor (AHR); Ki = 3 nM for binding to murine AHR. Learn More

    Starting at: $139.00

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  • CP 775146

    CP 775146 is a selective, high affinity PPARα agonist with Ki values of 24.5 nM for PPARα and >10 μM for PPARβ and PPARγ in vitro). Learn More

    Starting at: $169.00

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  • CITCO

    CITCO is a constitutive androstane receptor (CAR) agonist (EC50 = 49 nM), which displays > 100-fold selectivity over PXR receptors and no activity at LXR, ERα, ERβ, PPAR, RAR, FXR, VDR and THR. Learn More

    Starting at: $89.00

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  • TCPOBOP

    TCPOBOP is an agonist of the constitutive androstane receptor that induces activity of ER1 cytochrome P450 isozymes, NADPH-cytochrome c reductase, microsomal epoxide hydrolase and glutathione S transferase. Learn More

    Starting at: $79.00

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  • Pioglitazone hydrochloride

    Pioglitazone hydrochloride is a selective PPARγ agonist (EC50 = 0.69 μM). Learn More

    Starting at: $45.00

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  • GW 1929 hydrochloride

    GW 1929 hydrochloride is a highly selective orally active peroxisome proliferator-activated receptor (PPAR)γ agonist (pEC50 values are 8.05, < 4 and < 4 for human PPARγ, PPARα and PPARδ receptors respectively). Learn More

    Starting at: $135.00

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  • SR 202

    SR 202 is a selective PPARγ antagonist that inhibits PPARγ-dependent adipocyte differentiation and growth in vitro and in vivo. Learn More

    Starting at: $90.00

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  • Ciglitazone

    Ciglitazone is a selective agonist at PPAR&gamma with an EC50 value of 3 μM in vivo. Learn More

    Starting at: $139.00

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  • nTZDpa

    nTZDpa is a potent, selective non-thiazolidinedione PPARγ partial agonist (EC50 = 57 nM); produces ~25% maximum efficacy. Learn More

    Starting at: $100.00

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  • BADGE

    RS 39604 hydrochloride is a potent and selective 5-HT4 antagonist, with a pKi of 9.1 at 5-HT4 receptors in guinea pig striatal membranes and greater than 1000-fold selectivity over 5-HT1A, 2C, 3 and D1, D2, M1, M2, AT1, B1 and α1C receptors. Learn More

    Starting at: $80.00

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