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Cat. No. Product Name Information
PC-20769

Bexarotene

RXR agonist

Bexarotene (LGD1069) is a highly potent and selective retinoid X receptors (RXR) agonist with EC50 of 33, 24, 25 nM for RXRα, RXRβ, and RXRγ respectively, with no affinity for RAR receptors.
PC-20433

Amsilarotene

RARα inhibitor

Amsilarotene (TAC-101) is a retinobenzoic acid with potential antineoplastic activity, shows selective affinity for RARα with binding Ki of 2.4 nM.
PC-20205

AGN194310

pan-RAR inhibitor

AGN194310 (VTP-194310) is a highly potent, pan-RAR antagonist with binding Kd value of 2-5 nM, inhibits prostate carcinoma lines LNCaP, PC3 and DU145 with IC50 of 16-34 nM.
PC-20204

MM11253

RARγ inhibitor

MM11253 is a selective antagonist of retinoic acid receptor γ (RARγ) with IC50 of 44 nM.
PC-20200

ER-50891

RARα inhibitor

ER-50891 (ER50891) is a potent, selective antagonist of RARα receptor with IC50 of 31.2 nM, displays >300-fold selectivity over RARγ and RARβ.
PC-20199

LE135

RARβ inhibitor

LE135 is a retinoic acid receptor (RAR) antagonist that displays moderate selectivity for RARβ over RARα (Ki values=0.22 and 1.4 μM, respectively), highly selective over RARγ and RXRα.
PC-20198

BMS-195614

RARα antagonist

BMS-195614 (BMS614) is a selective antagonist of neutral retinoic acid receptor RARα with Ki of 2.5 nM.
PC-49025

Ro41-5253

RARα antagonist

Ro 41-5253 is a potent and selective retinoic acid receptor-α (RARα) antagonist with IC50 of 16 nM.
PC-35992

Fenretinide

RAR agonist

Fenretinide (NSC 374551, 4-HPR, 4-Hydroxyphenyl retinamide) is a synthetic retinoid derivative with potential antineoplastic and chemopreventive activities, binds to and activates RARs, thereby inducing cell differentiation and apoptosis in some tumor cell types..
PC-35622

UAB30

RXR agonist

UAB30 (9cUAB30) is a novel synthetic rexinoid that binds selectively to the retinoid X receptor (RXR) leading to activation of genes involved in induction of differentiation and apoptosis.
PC-35535

HX600

NURR1 (NR4A2) agonist

HX600 (HX-600) is a synthetic agonist of RXR-Nurr1 heterodimer complex, also selectively activate NGFI-B/RXR heterodimers.
PC-35516

AC261066

RARβ2 agonist

AC261066 (AC-261066, AC261) is a potent, selective, orally available RARβ2 agonist with pEC50 of 8.1, displays selectivity over RARβ1, RARα and RARγ (pEC50=6.4, 6.2 and 6.3).

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