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首页-小分子抑制剂&激动剂-Nuclear Receptor/Transcription Factor-RAR/RXR

Request The Product List ofRAR/RXR RAR/RXR

Cat. No. Product Name Information
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).
PC-35171

Trifarotene

RARγ agonist

Trifarotene (CD5789, CD-5789) is a potent and selective RARγ agonist with EC50 of 7.7 nM, 500- and 125-fold selectivity over RARα and RARβ.
PC-63510

WYC-209

RAR agonist

WYC-209 is a novel synthetic retinoid that inhibits proliferation of malignant murine melanoma tumor-repopulating cells (TRCs) with IC50 of 0.19 uM, targets retinoic acid receptor (RAR).
PC-62836

LY-2955303

RARγ antagonist

LY-2955303 is a potent and selective RARγ antagonist with binding Ki of 1.09 nM, displays >1000-fold selectivity against RARα and RARβ.
PC-62291

CD 437

RARγ agonist

CD437 (CD 437) is a retinoid-like small molecule that selectively induces apoptosis in cancer cells, but not in normal cells, directly inhibits DNA polymerase α with IC50 of 22 nM, also acts as an RARγ agonist.
PC-70298

UVI-3003

RXR antagonist

UVI-3003 (UVI 3003) is a full antagonist of RXR that demonstrates potent, nanomolar binding affinity, inhibits xenopus and human RXRα in Cos7 cells with IC50 of 0.22 and 0.24 uM, respectively.
PC-70297

SR-11237

RXR agonist

SR-11237 (BMS-649) is a selective pan retinoid X receptor (RXR) agonist with no retinoid A receptor (RAR) activity.
PC-70296

UVI 2008

RARβ/γ agonist, AKR1B10 inhibitor

UVI 2008 is a RARβ/γ agonist originated from TTNPB, is also a selective inhibitor of aldo-keto reductase family member 1B10 (AKR1B10) with IC50 of 6.1 uM.
PC-70295

BMS-948

RARβ agonist

A RARβ-selective agonist that exhibits a full transcriptional agonistic activity and activating RARβ as efficiently as the reference agonist TTNPB.
PC-70294

BMS-189453

RARβ agonist, RARα/RARγ antagonist

BMS-189453 (BMS189453, BMS453) is a synthetic retinoid that acts as an agonist of RARβ and an antagonist of RARα and RARγ.

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