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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3955 |
AR7
|
Retinoid Receptor | Metabolism |
AR7 是一种非典型的 RARA/RARα(视黄酸受体 α) 拮抗剂,能够特异性激活伴侣介导的自噬活性,对自噬无影响。 | |||
T7894 |
Tazarotenic acid
6-[2-(3,4-二氢-4,4-二甲基-2H-1-苯并噻喃-6-基)乙炔基]-3-吡啶甲酸,AGN-190299 |
Others | Others |
Tazarotenic acid (AGN-190299) 是 Tazarotene 的代谢物。它与视黄酸受体 (RAR) 的结合位点是类视黄醇作用的可能的分子靶点。它对疣状角化不良具有潜在的研究价值。 | |||
T14912 |
CD3254
|
Retinoid Receptor | Metabolism |
CD3254 是一种具有选择性和强效性的类视黄醇 X 受体 (RXR) 激动剂,可抑制伴有OGD/再氧合的神经元细胞死亡。 | |||
T7388 |
GSK805
|
ROR | Metabolism |
GSK805 是能够生物利用的、具有 CNS 穿透性的 RORγt 抑制剂。 | |||
T23383 |
SR11237
SR 11237 |
Others; RAR/RXR | Metabolism; Others |
SR11237 是一种泛视黄醇 X 受体 (RXR) 激动剂。 SR11237 导致 RXR/RXR 同源二聚体形成并反式激活包含 RXR 反应元件的报告基因。 | |||
T17209 |
UVI 3003
|
Retinoid Receptor; Autophagy | Autophagy; Metabolism |
UVI 3003 是一种高度选择性的类视黄醇 X 受体拮抗剂。在 Cos7 细胞中,它抑制非洲爪蟾蜍和人RXRα的活性,IC50值分别为 0.22 和 0.24 μM。 | |||
T9635 |
Cedirogant
ABBV-157 |
ROR | Metabolism |
Cedirogant (ABBV-157) 是一种口服有活性的 RORγt 反向激动剂,可用于研究银屑病。 | |||
T11844 |
LG-100064
4-[(5,6,7,8-四氢-3,5,5,8,8-五甲基-2-萘基)羰基]苯甲酸 |
Retinoid Receptor; Autophagy | Autophagy; Metabolism |
LG-100064 是一种类视黄醇 X 受体激动剂,对 RXRα、RXRβ 和 RXRγ 的 EC50值分别为 330、200 和 260 nM,可用于癌症研究。 | |||
T11303 |
Fluorobexarotene
|
Retinoid Receptor | Metabolism |
Fluorobexarotene 是一种有效的 类视黄醇 X 受体 (RXR) 激动剂。Fluorobexarotene 对 RXRα 受体的 Ki 值为 12 nM,EC50 值为 43 nM。Fluorobexarotene 具有明显的 RXR 结合亲和力,比 Bexarotene 高75%。 | |||
T22843 |
HX 531
|
Retinoid Receptor | Metabolism |
HX 531 是的RXR 拮抗剂 (IC50:18 nM) 。它能减少高脂饮食小鼠的骨骼肌、白色脂肪组织和肝脏中的甘油三酯含量。 | |||
TP1313L |
Cecropin B acetate
Cecropin B acetate(80451-05-4 Free base) |
P450; Retinoid Receptor; Parasite | Metabolism; Microbiology/Virology |
Cecropin B acetate 通过破坏 PXR/类视黄醇 X 受体 α (RXR-α) 复合物与 DNA 序列的结合来诱导 NF-κB 活化并抑制 CYP3A29。 Cecropin B acetate 具有很强的抗菌活性。 | |||
T77499 |
MSU-42011
|
NOS; Retinoid Receptor; NO Synthase; PERK; Lipid | Apoptosis; Immunology/Inflammation; Metabolism |
MSU-42011 是一种具有口服活性的类视黄醇 X 受体 (RXR) 激动剂。MSU-42011 有效抑制iNOS,低SREBP 诱导和激活RXR 以及 p-ERK 蛋白水平的表达。MSU-42011在kras 驱动的肺癌小鼠模型中表现出抗肿瘤活性。MSU-42011可有效治疗临床前Krasdriven 肺癌且具有免疫调节活性。 | |||
T23665 |
AGN 191701
AGN-191701,AGN191701 |
||
AGN 191701 is an agonist of the Retinoid X receptor. | |||
T69695 | Izumerogant | ||
Izumerogant is an inverse agonist of the retinoid-related orphan receptor-gamma (RORγ). | |||
T24727 |
ROR Modulator I
ROR-Modulator-I,RORModulatorI |
||
ROR Modulator I is the first potent inverse agonist of the retinoid-related orphan receptor. It also has dual selectivity for RORβ and RORγt. | |||
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. | |||
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). | |||
T25472 |
GW0791
GW 0791,GW-0791 |
||
GW0791 is a retinoid X receptor α (RXRα) agonist. | |||
T29720 |
Agn 190727
Agn-190727,Agn190727 |
||
Agn 190727 is a retonoic acid receptor that can induce retinoid-induced hypertriglyceridemia. | |||
T10246 |
Adapalene sodium salt
CD 271 sodium salt,阿达帕林钠 |
Others | Others |
Adapalene (CD 271; Differin) sodium salt is a synthetic retinoid and a Retinoic acid receptor agonist. | |||
T24857 |
TBTC
|
||
TBTC is a selective agonist of retinoid X receptor α that acts by improving behavioral deficit in Alzheimer's disease model mice. | |||
T70440 |
AGN-191659
|
||
AGN-191659 is a Retinoid X Receptor (RXR) pan-agonist. RXR pan-agonists have been shown to modulate endothelial cell proliferation. | |||
T63415 | RXR antagonist 1 | ||
RXR antagonist 1 是类视黄醇 X 受体 (Retinoid X Receptor (RXR)) 调节剂,表现出较高的 RXR 拮抗作用 (pA2: 8.06)。RXR antagonist 1 能够用于研究 2 型糖尿病。 | |||
T69921 |
BRF110
|
||
BRF110 is a brain penetrant, potent and selective agonist of nuclear receptor-related 1 (Nurr1):Retinoid X receptor α (RXRα) heterodimer. BRF110 is a neuroprotective agent that prevents dopaminergic neuron demise and striatal dopaminergic denervation in vivo against PD-causing toxins. It induced dopamine biosynthesis in vivo. BRF110 chronic dosing does not induce dyskinesia in mice model. | |||
T37414 |
CAY10771
|
||
CAY10771 is a dual agonist of farnesoid X receptor (FXR) and peroxisome proliferator-activated receptor δ (PPARδ).1It activates FXR and PPARδ in reporter assays using HEK293T cells (EC50s = 0.94 and 1.5 μM, respectively) and is selective for these receptors over retinoic acid receptor α (RARα), retinoid X receptor α (RXRα), PPARα, PPARγ, and liver X receptor α (LXRα) at 10 μM. 1.Schierle, S., Neumann, S., Heitel, P., et al.Design and structural optimization of dual FXR/PPARδ activatorsJ. Med. Ch... | |||
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. It increases transcriptional activity of PPARα and PPARγ in a cell-based luciferase reporter assay when used at a concentration of 10 μM. MD001 (10 μM) increases expression of PPARα, PPARγ, and retinoid X receptor (RXR), as well as PPARα and PPARγ target genes, in HepG2 cells. It... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN6735 |
Bigelovin
|
Apoptosis; Reactive Oxygen Species; Retinoid Receptor; Autophagy; RAR/RXR | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Bigelovin 是从海百合中分离得到的一种倍半萜内酯,是选择性视黄素 X 受体 α 激动剂。它通过抑制ROS 的生成来调节 mTOR 信号通路。它诱导凋亡和自噬,有抗肿瘤活性。 |