目录号 | 产品详情 | 靶点 | |
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T40302 | |||
FXR/TGR5 agonist 1 has agonist action on FXR and TGR5 , and can be used for the treatment of fatty liver disease. | |||
T6053 | FXR Autophagy | ||
Turofexorate Isopropyl (XL335) 是一种口服有效的,选择性 FXR 激动剂,EC50为 4 nM。 | |||
T2015 | FXR Autophagy | ||
Fexaramine 是小分子法尼醇 X 受体 (FXR) 激动剂,EC50为 25 nM,与天然化合物相比,亲和力提高了 100 倍。 | |||
T7886 | FXR Autophagy | ||
Nidufexor 是一种可口服的法尼醇 X 受体激动剂,可研究非酒精性脂肪性肝炎。 | |||
T15806 | FXR Autophagy | ||
LY2562175 是一种有效的选择性 FXR 激动剂,其EC50值为 193 nM。 | |||
T6344 | FXR Autophagy | ||
Sevelamer hydrochloride (Sevelamer HCl) 是一种磷酸盐结合药物,用于通过与膳食磷酸盐结合并阻止其吸收来治疗高磷血症。 | |||
T2233 | FXR Autophagy | ||
GW 4064 是一种有效的法尼醇 X 受体 (FXR) 激动剂,EC50为 65 nM。 | |||
T13092 | FXR | ||
Tauro-Obeticholic acid 是一种牛磺酸的特性代谢物。Obeticholic Acid 是口服具有活性的法尼样 X 受体激动剂。 | |||
T4379 | FXR Autophagy | ||
Tropifexor (LJN452) 是一种新型的高效 FXR 激动剂,EC50 为 0.2 nM。 | |||
T31587 | FXR | ||
DY268 是一种法尼样X 受体 (FXR)的拮抗剂(在 time-resolved FRET 分析中,IC50=7.5 nM)。在细胞分析中,它能够抑制 FXR 反式激活,IC50=468 nM。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPY-06768 | NR1H4 Protein, Human, Recombinant (His) | Human | E. coli | ||
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TMPY-06756 | NR1H4 Protein, Mouse, Recombinant (His) | Mouse | E. coli | ||
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TMPH-01355 | FXR1 Protein, Human, Recombinant (His) | Human | E. coli | ||
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TMPY-02987 | Vitamin D Receptor/VDR Protein, Mouse, Recombinant (His) | Mouse | Baculovirus-Insect Cells | ||
VDR (vitamin D (1,25- dihydroxyvitamin D3) receptor), also known as NR1I1, belongs to the NR1I family, NR1 subfamily. It is composed of three domains: a modulating N-terminal domain, a DNA-binding domain and a C-terminal ligand-binding domain. Vitamin D receptors (VDRs) are members of the NR1I family, which also includes pregnane X (PXR) and constitutive androstane (CAR) receptors, that form heterodimers with members of the retinoid X receptor family. VDRs repress expression of 1alpha-hydroxylase (the proximal activator of 1,25(OH)2D3) and induce expression of the 1,25(OH)2D3 inactivating enzyme CYP24. Also, it has recently been identified as an additional bile acid receptor alongside FXR and may function to protect gut against the toxic and carcinogenic effects of these endobiotics. VDR is expressed in the intestine, thyroid and kidney and has a vital role in calcium homeostasis. It is the nuclear hormone receptor, also called transcription factor that mediates the action of vitamin D3. Inherited mutations in the VDR gene leads to rickets.
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TMPY-02706 | Vitamin D Receptor/VDR Protein, Human, Recombinant (His) | Human | Baculovirus-Insect Cells | ||
VDR (vitamin D (1,25- dihydroxyvitamin D3) receptor), also known as NR1I1, belongs to the NR1I family, NR1 subfamily. It is composed of three domains: a modulating N-terminal domain, a DNA-binding domain and a C-terminal ligand-binding domain. Vitamin D receptors (VDRs) are members of the NR1I family, which also includes pregnane X (PXR) and constitutive androstane (CAR) receptors, that form heterodimers with members of the retinoid X receptor family. VDRs repress expression of 1alpha-hydroxylase (the proximal activator of 1,25(OH)2D3) and induce expression of the 1,25(OH)2D3 inactivating enzyme CYP24. Also, it has recently been identified as an additional bile acid receptor alongside FXR and may function to protect gut against the toxic and carcinogenic effects of these endobiotics. VDR is expressed in the intestine, thyroid and kidney and has a vital role in calcium homeostasis. It is the nuclear hormone receptor, also called transcription factor that mediates the action of vitamin D3. Inherited mutations in the VDR gene leads to rickets.
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