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カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
T23383 | SR11237 | SR 11237 | Others , RAR/RXR |
SR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element. | |||
T63597 | RXR antagonist 2 | ||
RXR antagonist 2 is a potent antagonist of RXR (Ki: 0.391 μM, Kd: 0.281 μM). RXR antagonist 2 has shown research potential for RXR-related diseases. | |||
T63415 | RXR antagonist 1 | ||
RXR antagonist 1 is a Retinoid X Receptor (RXR) modulator that exhibits high RXR antagonism (pA2: 8.06). RXR antagonist 1 can be used to study type 2 diabetes. | |||
T22843 | HX 531 | Retinoid Receptor | |
RXR antagonist | |||
T6410 | Bexarotene | Ro 26-4455,Targretin,LGD1069 | Retinoid Receptor , Autophagy |
Bexarotene (LGD1069) is a retinoid analogue that is used to treat the skin manifestations of cutaneous T cell lymphoma (CTCL). | |||
TQ0097 | AGN 193109 | Retinoid Receptor , Autophagy | |
AGN 193109, a retinoid analog, is a potent and specific antagonist of RARs (Kds: 2 nM, 2 nM, and 3 nM for RARα, RARβ, and RARγ). | |||
T17209 | UVI 3003 | Retinoid Receptor , Autophagy | |
UVI 3003 is a highly selective antagonist of the retinoid X receptor. UVI 3003 inhibits Xenopus and human RXRα in Cos7 cells (IC50s: 0.22 and 0.24 μM, respectively). | |||
T3955 | AR7 | Retinoid Receptor | |
AR7 is a retinoic acid receptor α (RARα) antagonist. | |||
T5341 | WYC-209 | WYC209 | Apoptosis , Retinoid Receptor , Autophagy |
WYC-209 inhibits proliferation of malignant murine melanoma tumor-repopulating cells (TRCs, IC50: 0.19 uM). It targets the retinoic acid receptor (RAR). | |||
T7586 | Trifarotene | CD5789 | Retinoid Receptor , Autophagy |
Trifarotene (CD5789) is a potent and selective RARγ agonist with 65-fold and 16-fold selectivitiy for the RARγ (EC50=7.7 nM) over RARα (EC50=500 nM) and RARβ (EC50=125 nM). | |||
TQ0064 | Peretinoin | NIK333 | HCV Protease , Retinoid Receptor , S1P Receptor , Autophagy |
Peretinoin (NIK333) is an oral acyclic retinoid with a vitamin A-like structure that targets retinoid nuclear receptors such as RXR and RAR. | |||
T7370 | Talarozole | R115866 | Others , P450 , Retinoid Receptor , Autophagy |
Talarozole (R115866) is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.Talarozole for the treatment of... | |||
T6696 | Tazarotene | Tazorac,AGN 190168,Zorac | Retinoid Receptor , Autophagy |
Tazarotene (Zorac) is a synthetic, topical retinoid. Tazarotene induces the expression of tazarotene-induced gene 3 (TIG3), a tumor suppressor gene. In psoriasis, tazarotene normalizes abnormal keratinocyte differentiati... | |||
T1093 | Adapalene | CD271 | Apoptosis , Retinoid Receptor , Autophagy |
Adapalene (CD271) is a dual RAR and RXR agonist, utilized in the treatment of skin conditions. | |||
T11844 | LG-100064 | Retinoid Receptor , Autophagy | |
LG-100064 is an agonist of retinoid-X-receptor (RXR)(EC50s of 330 nM, 200 nM, and 260 nM for RXRα, RXRβ and RXRγ) | |||
T4538 | Palovarotene | Ro 3300074,R 667 | Retinoid Receptor , Autophagy |
Palovarotene (Ro 3300074) is an agonist of nuclear retinoic acid receptor γ (RAR-γ). | |||
T6694 | Tamibarotene | NSC 608000,Am 80,Amnolake | Apoptosis , Retinoid Receptor , Autophagy |
Tamibarotene (Amnolake) is an orally active, synthetic retinoid, developed to overcome all-trans retinoic acid (ATRA) resistance, with potential antineoplastic activity. | |||
T21314 | Amsilarotene | TAC-101,TAC 101,TAC101 | CDK |
Amsilarotene (TAC101) inhibits the phosphorylation of retinoblastoma gene product (RB) and increases the presence of 2 cyclin-dependent kinases (CDK) inhibitors resulting in cell cycle arrest. This agent also causes a cy... | |||
T5843 | Tarenflurbil | MPC7869,(R)-Flurbiprofen,R-flurbiprofen | Retinoid Receptor , Autophagy |
Tarenflurbil ((R)-Flurbiprofen) is the non-cyclooxygenase inhibiting R-enantiomer of the non-steroidal anti-inflammatory drug flurbiprofen, which was assessed as a remedy for Alzheimer's disease. | |||
T1872 | Fenretinide | 4-HPR,MK-4016,4-hydroxy(phenyl)retinamide | Retinoid Receptor , Autophagy |
Fenretinide (4-HPR) is an orally-active synthetic retinoid derivative with potential antineoplastic and chemopreventive activities. | |||
T21714 | BMS453 | BMS 453,BMS-189453 | Retinoid Receptor |
BMS453 (BMS-189453), a synthetic retinoid, is a potent and selective agonist of RARβ and a potent testicular toxin. BMS453 inhibits breast cell growth predominantly through the induction of active TGFβ. | |||
T11847L | Liarozole | R75251 dihydrochloride | P450 , Retinoid Receptor |
Liarozole (R75251 dihydrochloride) is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 1... | |||
T5854 | AM580 | NSC608001,CD336,Ro 40-6055 | Retinoid Receptor , Autophagy |
AM580 (CD336) is a retinoic acid receptor agonist that is selective for RARα( IC50 : 8 nM ) | |||
T4371 | CD437 | AHPN,O-Desmethyl Adapalene,Apoptosis Activator VI | Retinoid Receptor , Autophagy |
CD437 (AHPN) is a specifc Retinoic Acid Receptor γ (RARγ) agonist. | |||
T0499 | Oxybenzone | KAHSCREEN BZ-3,Benzophenone 3,Eusolex 4360,Escalol 567 | Apoptosis , Retinoid Receptor , Autophagy |
Oxybenzone (Eusolex 4360) is an organic compound used in sunscreens. It is a derivative of benzophenone. | |||
T1288 | TTNPB | AGN191183,Arotinoid acid,Ro 13-7410,AGN-191183,Ro 13-7410 | Apoptosis , Retinoid Receptor , Autophagy |
TTNPB (Ro 13-7410,AGN-191183), a potent RAR agonist, inhibits binding of [3H]tRA of human RARα (IC50: 5.1 nM), β (IC50: 4.5 nM), and γ (IC50: 9.3 nM), respectively. | |||
T15811 | LY2955303 | Others , Retinoid Receptor | |
LY2955303 is an effective and selective retinoic acid receptor gamma (RARγ) antagonist (Ki: 1.09 nM). | |||
T14912 | CD3254 | Retinoid Receptor | |
CD3254 is a selective and potent retinoid X receptor-like (RXR) agonist that inhibits neuronal cell death with OGD/reoxygenation. | |||
T11303 | Fluorobexarotene | Retinoid Receptor | |
Fluorobexarotene possesses an apparent RXR binding affinity that is 75% greater than Bexarotene. Fluorobexarotene is a potent retinoid-X-receptor (RXR) agonist, with a Ki value of 12 nM and an EC50 value of 43 nM for RX... | |||
T77499 | MSU-42011 | NOS , Retinoid Receptor , NO Synthase , PERK , Lipid | |
MSU-42011 is an orally active retinoid X receptor-like (RXR) agonist.MSU-42011 potently inhibits the expression of iNOS, low SREBP-induced and activated RXR, and p-ERK at the protein level.MSU-42011 has demonstrated anti... | |||
T63042 | NDB | FXR | |
NDB is a selective and potent hFXRα antagonist that inhibits GW4064-stimulated FXR/RXR interactions and FXRα target gene expression in primary mouse hepatocytes.NDB is used in the study of diabetes. | |||
T16425 | PA452 | Retinoid Receptor , RAR/RXR | |
PA452 is a selective antagonist of retinoic X receptor (RXR) and suppresses the effect of Retinoic acid on Th1/Th2 development. | |||
TP1313L | Cecropin B acetate | Cecropin B acetate(80451-05-4 Free base) | P450 , Retinoid Receptor , Parasite |
Cecropin B acetate induces NF-κB activation and suppresses CYP3A29 by disrupting the association of the PXR/retinoid X receptor alpha (RXR-α) complex with DNA sequences. Cecropin B acetate exhibits strong antimicrobial a... | |||
T21497 | 9-cis-Retinoic Acid | Alitretinoin | Apoptosis |
9-cis-Retinoic Acid (Alitretinoin) is a derivative of vitamin A. It is a RAR/RXR agonist with anticancer, antitumor, anti-inflammatory, and neuroprotective activities, induces apoptosis, regulates the cell cycle, and can... | |||
T22924 | LG 101506 | Others | |
RXR modulator | |||
T32107 | HX-603 | HX 603 | |
HX-603 is a selectivity agonist of RXR that inhibits the activation of RAR-RXR heterodimers as well as RXR homodimers. | |||
T70440 | AGN-191659 | ||
AGN-191659 is a Retinoid X Receptor (RXR) pan-agonist. RXR pan-agonists have been shown to modulate endothelial cell proliferation. | |||
T22844 | HX 630 | Others | |
RXR agonist | |||
T15748 | LG100754 | UVI 2112 | PPAR |
LG100754 (UVI 2112) is an insulin sensitizer that functions through RXR. LG100754 is an RXR dimer modulator. LG100754 acts as an RXR: RXR homodimer antagonist, but functions as an agonist towards RXR: PPARα and RXR: PPAR... | |||
T35159 | XCT0135908 | XCT 0135908,XCT-0135908 | |
XCT0135908 is a selectivity agonist of RXR -Nurr1 over a broad range of other RXR dimerization partners but with a rather low potency. | |||
T70237 | HX-600 | ||
HX-600 is a synthetic agonist for the RXR-Nurr1 heterodimer complex. HX-600 prevents ischemia-induced neuronal damage. | |||
T19703 | LG100268 | LG 100268,LG-100268 | |
LG100268 is an effective and selective rexinoid and retinoid-X receptor agonist. LG100268 binds to the α, β, and γ RXR receptors (IC50 = 3-4 nM). | |||
T10528 | Bexarotene D4 | LGD1069 D4 | Others |
Bexarotene D4 is a deuterium-labeled Bexarotene (LGD1069). Bexarotene is a selective RXR agonist used in the treatment of cutaneous T-cell lymphoma. | |||
T70976 | AGN-190121 | ||
AGN-190121 is a retinoic acid receptor (RAR) agonist. RAR and Retinoid X Receptor (RXR) ligands can act synergistically to induce hypertriglyceridemia through distinct mechanisms of action. | |||
T14145 | AGN194204 | IRX4204,NRX194204,VTP 194204 | Others |
AGN194204 (IRX4204) is inactive against RAR and is an orally active and selective RXR agonist with Kd values 0.4 nM, 3.6 nM and 3.8 nM and EC50s of 0.2 nM, 0.8 nM and 0.08 nM for RXRα, RXRβ and RXRγ, respectively. AGN194... | |||
T10262 | AGN 205327 | Others | |
AGN 205327 is a potent synthetic RARs agonist with EC50 of 3766/734/32 nM for RARα/β/γ respectively without inhibition of RXR. IC50 value: 3766/734/32 nM for RARα/β/γ Target: RAR agonist | |||
T69911 | CU-6PMN | ||
CU-6PM is a new fluorescent RXR agonist. CU-6PMN was designed based on the fact that umbelliferone emits strong fluorescence in a hydrophilic environment, but the fluorescence intensity decreases in hydrophobic environme... | |||
T35800 | MD001 | ||
MD001 is a dual agonist of peroxisome proliferator-activated receptor α (PPARα) and PPARγ.1 It binds to PPARα and PPARγ (Kds = 9.55 and 0.14 μM, respectively) but does not bind to PPARβ/δ at concentrations up to 500 μM. ... |
カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
TN6735 | Bigelovin | Apoptosis , Reactive Oxygen Species , Retinoid Receptor , Autophagy , RAR/RXR | |
Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a pote... | |||
T1330 | Acitretin | Ro 10-1670,Etretin | Apoptosis , Retinoid Receptor , Autophagy |
Acitretin (Ro 10-1670) is a second-generation, systemic retinoid that has been used in the treatment of psoriasis. | |||
T1611 | Isotretinoin | 13-cis-Retinoic acid | Retinoid Receptor , Endogenous Metabolite , Autophagy |
Isotretinoin (13-cis-Retinoic acid) binds to and activates nuclear retinoic acid receptors (RARs); activated RARs serve as transcription factors that promote cell differentiation and apoptosis. Isotretinoin is a naturall... | |||
T1051 | Retinoic acid | Vitamin A acid,ATRA,all-trans-Retinoic acid,Tretinoin | Retinoid Receptor , Endogenous Metabolite , PPAR , Autophagy |
Retinoic acid (Tretinoin), a metabolite of vitamin A, is a natural agonist of the retinoic acid receptor RAR and inhibits RARα/β/γ (IC50=14 nM). Retinoic acid induces cellular differentiation, reduces cellular proliferat... | |||
T3000 | Magnolol | NSC 293099,5,5'-Diallyl-2,2'-biphenyldiol | NF-κB , Retinoid Receptor , Antibacterial , PPAR , p53 , Autophagy |
Magnolol (5,5'-Diallyl-2,2'-biphenyldiol) is a dual agonist of RXRα( EC50=10.4 μM) and PPARγ(EC50=17.7 μM). It blocks TNF-α-induced NF-KB activation. |
カタログ番号 | 製品名 | Species | Expression System |
---|---|---|---|
TMPJ-01459 | FGF-21 Protein, Cynomolgus, Recombinant (His) | Cynomolgus | HEK293 Cells |
Fibroblast Growth Factor 21 (FGF21) is a growth factor that belongs to the FGF family. FGF family proteins play a central role during prenatal development and postnatal growth and regeneration of mamy tissues, by promoti... |