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- Vitamin D Related/Nuclear Receptor
- Orphan Nuclear Receptor
Orphan Nuclear Receptor
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Orphan Nuclear Receptor Related Products (43)
Related Products (43)
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SS-RJW100
0 ImagesCat. No.: HY-131445APurity: 99.91%SS-RJW100 is a enantiomer of RJW100, which is a racemic agonist of nuclear receptor liver receptor homolog 1 (LRH-1) and steroidogenic factor 1 (SF-1). SS-RJW100 promotes recruitment of coregulator protein fragments in vitro, recruits the transcriptional intermediary factor 2 (Tif2) coactivator to LRH-1. SS-RJW100 diminishes LRH-1 allosteric activation networks, shows poor thermal stability. -
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- SID7970631
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(+)-LRH-1 agonist-2
0 ImagesCat. No.: HY-147105APurity: 99.38%(+)-LRH-1 modulator-1 is a stereoisomer of LRH-1 modulator-1. LRH-1 modulator-1 (compound 6N) is a potent LRH-1 (liver receptor homolog-1) modulator/agonist. LRH-1 modulator-1 has anti-inflammatory effects in intestinal organoids. LRH-1 modulator-1 induces the anti-inflammatory cytokine IL-10 and reduces the inflammatory cytokines IL-1b and TNFa. -
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LysoPalloT-NH-amide-C3-ph-m-O-C11
0 ImagesCat. No.: HY-148608CAS No.: 1778686-61-5LysoPalloT-NH-amide-C3-ph-m-O-C11 is an agonist for GPR174 with an EC50 of 34 nM. -
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NR2F2-IN-1
0 ImagesCat. No.: HY-156190CAS No.: 1049691-47-5NR2F2-IN-1 is a COUP-TFII (orphan nuclear receptor NR2F2) inhibitor with antitumor activity against prostate cancer. NR2F2-IN-1 directly binds to the COUP-TFII ligand-binding domain and disrupts COUP-TFII interaction with transcription regulators including FOXA1. NR2F2-IN-1 can be used for the research of prostate cancer. -
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PSB-22269
0 ImagesCat. No.: HY-159920PSB-22269 is a GPR17 antagonist with a Ki value of 8.91 nM. PSB-22269 further demonstrated significant inhibitory effects in cAMP and G protein activation assays. Molecular docking studies revealed that the binding site of PSB-22269 contains positively charged arginine residues and a hydrophobic pocket. PSB-22269 provides a strategy to promote remyelination and holds promise for research in the field of multiple sclerosis. -
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Photoregulin1
0 ImagesCat. No.: HY-109869CAS No.: 1003736-23-9Photoregulin1 is a compound with the potential to inhibit retinitis pigmentosa that modulates gene expression in retinal cells and slows the degeneration of photoreceptors in a mouse model. -
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TLX agonist 3
0 ImagesCat. No.: HY-180403CAS No.: 3032232-47-3TLX agonist 3 is a potent and selective tailless homolog (TLX, NR2E1) agonist with an EC50 of 0.25 μM and a Kd of 1.6 μM). TLX agonist 3 shows high selectivity over related nuclear receptors, and promotes TLX oligomerization with an EC50 of 5.0 μM. TLX agonist 3 can be used for the research of neurodegenerative diseases. -
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LRH-1 antagonist-1
0 ImagesCat. No.: HY-128453CAS No.: 1185486-16-1LRH-1 antagonist-1 (Compound 3d2) is a LRH-1 antagonist with a Kd of 1.8 μM. LRH-1 antagonist-1 inhibits the transcriptional activity of LRH-1 and reduces the expression of G0S2. LRH-1 antagonist-1 inhibits the proliferation of LRH-1-positive cancer cells. LRH-1 antagonist-1 can be used for research on pancreatic cancer, colon cancer and breast cancer. -
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BMH-9
0 ImagesCat. No.: HY-118912CAS No.: 457937-39-2BMH-9 (Compound Z54) is a modulator for nuclear receptor subfamily 2, group F, member 6 (NR2F6) (also known as nuclear orphan receptor Ear2). BMH-9 is an activator for p53 signaling pathway through interaction with DNA. BMH-9 inhibits proliferation of human cancer cells, exhibits antitumor efficacy in NOD-SCID mouse models. -
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SF-1 antagonist-1
0 ImagesCat. No.: HY-148259CAS No.: 2842079-86-9SF-1 antagonist-1 (compound 11) is a antagonist of steroidogenic factor 1 (SF-1). SF-1 antagonist-1 affects SF-1 transcriptional activity with an EC50 value of <200 nM. SF-1 antagonist-1 inhibits the proliferation of Rat Leydig tumor cells. SF-1 antagonist-1 can be used for the research of cancer. -
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GPR27 agonist-1
0 ImagesGPR27 Agonist-1 (compound I) is a selective GPR27 agonist with pEC50 of 6.34. -
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XY25028
0 ImagesCat. No.: HY-181971XY25028 is an orally active LRH-1 inhibitor with an IC50 of 0.30 μM. XY25028 inhibits the proliferation of androgen receptor (AR)-positive prostate cancer cells and suppresses the expression of AR target genes KLK2 and KLK3. XY25028 can be used in the research of castration-resistant prostate cancer. -
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XY25026
0 ImagesCat. No.: HY-181970XY25026 is an orally active LRH-1 inhibitor with an IC50 of 0.28 μM. XY25026 inhibits the proliferation of androgen receptor (AR)-positive prostate cancer cells, suppresses the expression of AR target genes KLK2 and KLK3, and inhibits tumor growth in xenograft models. XY25026 is applicable to the research of castration-resistant prostate cancer. -
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- TLX agonist 2
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LRH-1 antagonist-1 dihydrochloride
0 ImagesCat. No.: HY-128453ACAS No.: 2932459-63-5LRH-1 antagonist-1 (Compound 3d2) dihydrochloride is a LRH-1 antagonist with a Kd of 1.8 μM. LRH-1 antagonist-1 dihydrochloride inhibits the transcriptional activity of LRH-1 and reduces the expression of G0S2. LRH-1 antagonist-1 dihydrochloride inhibits the proliferation of LRH-1-positive cancer cells. LRH-1 antagonist-1 dihydrochloride can be used for research on pancreatic cancer, colon cancer and breast cancer. -
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- LRH-1 agonist-1
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Iso-RJW100
0 ImagesCat. No.: HY-155168CAS No.: 1276664-61-9Iso-RJW100 (compound 24-endo) is a dual-liver receptor homologue-1 (LRH-1) and steroidogenic factor-1 (SF-1) agonist with pEC50 of 6.4 and 7.2, respectively. -
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Benfluorex
0 ImagesCat. No.: HY-B1058ACAS No.: 23602-78-0Synonyms: JP-992Benfluorex (JP-992) is a hepatic nuclear factor 4 alpha (HNF4α) activator. -
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TLX activator-1
0 ImagesCat. No.: HY-184491CAS No.: 3108130-51-1TLX activator-1 is a highly selective TLX activator with an EC50 of 0.010 μM. TLX activator-1 regulates gene expression, upregulates genes related to ATP production and lysosomal function, and inhibits genes associated with inflammatory signaling pathways and Apoptotic signaling pathways. TLX activator-1 exhibits anti-neurodegenerative activity. TLX activator-1 can be used for the research of neurodegenerative diseases. -
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