Aryl Hydrocarbon Receptor
Aryl Hydrocarbon Receptor(芳烃受体)
Aryl Hydrocarbon Receptor (AhR or AHR or ahr or ahR) is a protein that in humans is encoded by the AHR gene. The aryl hydrocarbon receptor is a ligand-activated transcription factor involved in the regulation of biological responses to planar aromatic (aryl) hydrocarbons, and regulates xenobiotic-metabolizing enzymes such as cytochrome P450s, most notably cyp 1A1.
Aryl Hydrocarbon Receptor is a member of the family of basic helix-loop-helix transcription factors. AhR binds several exogenous ligands including natural plant flavonoids, polyphenolics and indoles, as well as synthetic polycyclic aromatic hydrocarbons and dioxin-like compounds. AhR is a cytosolic transcription factor that is normally inactive, binding to several co-chaperones. Upon ligand binding to chemicals such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), the chaperones dissociate resulting in AhR translocating into the nucleus and dimerizing with ARNT (AhR nuclear translocator), leading to changes in gene transcription.
Aryl Hydrocarbon Receptor 相关产品(35)
- GC64275AHR antagonist 5CAS: 2247953-39-3
AHR antagonist 5 是有效的,具有口服活性的芳香烃受体 (AHR) 拮抗剂,IC50 为 < 0.5 μM。AHR antagonist 5 联合检测点抑制剂 anti-PD-1 对肿瘤生长有抑制作用,详细信息请参见专利 WO2018195397,example 39。
- GC64898L-Kynurenine-d4-1CAS: 194546-33-3
L-Kynurenine-d4-1 是 L-Kynurenine 氘代物。L-Kynurenine是L-色氨酸的代谢物。它是一种芳香烃受体 (aryl hydrocarbon receptor) 激动剂。
- GC68631AhR agonist 2纯度: >99.50%
AhR agonist 2 (Compound 12a) 是一种有效的芳烃受体 (AhR) 激动剂,EC50 为 0.03 nM。AhR agonist 2 诱导 AhR 的快速核富集,触发下游基因的转录并促进皮肤屏障修复。AhR agonist 2 具有研究银屑病的潜力。
- GC69908Skatole-d3CAS: 111399-60-1纯度: >98.00%
Skatole-d3 是 Skatole 的氘代物。Skatole 是肠道菌群产生的物质,通过激活芳基烃受体 (aryl hydrocarbon receptors) 和 p38 调节肠上皮细胞功能。
- GC70236L-Kynurenine-13C10 sulfate hemihydrate纯度: >99.00%
L-Kynurenine-13C10 sulfate hemihydrate是13C标记的l -犬尿氨酸硫酸盐。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC64275 | AHR antagonist 5 | 2247953-39-3 | - | |
AHR antagonist 5 是有效的,具有口服活性的芳香烃受体 (AHR) 拮抗剂,IC50 为 < 0.5 μM。AHR antagonist 5 联合检测点抑制剂 anti-PD-1 对肿瘤生长有抑制作用,详细信息请参见专利 WO2018195397,example 39。 | ||||
| GC64898 | L-Kynurenine-d4-1 | 194546-33-3 | - | |
L-Kynurenine-d4-1 是 L-Kynurenine 氘代物。L-Kynurenine是L-色氨酸的代谢物。它是一种芳香烃受体 (aryl hydrocarbon receptor) 激动剂。 | ||||
| GC67892 | CHD-5 | 289494-16-2 | - | |
CHD-5 是一种有效的 AhR (芳香烃受体)拮抗剂。 | ||||
| GC68631 | AhR agonist 2 | - | >99.50% | |
AhR agonist 2 (Compound 12a) 是一种有效的芳烃受体 (AhR) 激动剂,EC50 为 0.03 nM。AhR agonist 2 诱导 AhR 的快速核富集,触发下游基因的转录并促进皮肤屏障修复。AhR agonist 2 具有研究银屑病的潜力。 | ||||
| GC69347 | KYN-101 | 2247950-73-6 | >98.00% | |
KYN-101 是一种有效的、选择性的和具有口服活性的 AHR 抑制剂。KYN-101 降低 CYP1A1 mRNA 表达。KYN-101 具有抗癌活性。 | ||||
| GC69908 | Skatole-d3 | 111399-60-1 | >98.00% | |
Skatole-d3 是 Skatole 的氘代物。Skatole 是肠道菌群产生的物质,通过激活芳基烃受体 (aryl hydrocarbon receptors) 和 p38 调节肠上皮细胞功能。 | ||||
| GC70236 | L-Kynurenine-13C10 sulfate hemihydrate | - | >99.00% | |
L-Kynurenine-13C10 sulfate hemihydrate是13C标记的l -犬尿氨酸硫酸盐。 | ||||
| GC72826 | CB7993113 | 819827-50-4 | >98.00% | |
CB7993113是一种强效的AHR拮抗剂,IC50为0.33μM。 | ||||
| GC72948 | Dibenzo(a,i)pyrene | 189-55-9 | >98.00% | |
Dibenzo(a,i)pyrene是2,3,7,8-四氯二苯并-对二恶英TCDD受体配体。 | ||||
| GC74164 | 25-Hydroxytachysterol3 | 39932-44-0 | >98.00% | |
25-Hydroxytachysterol3是维生素D3的代谢物 | ||||
| GN10706 | Diosimin | 520-27-4 | >98.00% | |
A citrus-derived flavonoid | ||||
