ROR
Retinoic Acid-Related Orphan Receptors (RORs) are nuclear receptors that regulate various physiological processes, including circadian rhythm, immune response, and metabolism. ROR inhibitors are of interest in the study of autoimmune diseases, metabolic disorders, and cancer, as they can modulate gene expression and influence cellular functions. At CymitQuimica, we offer ROR inhibitors to support your research in immunology, endocrinology, and oncology.
Found 42 products of "ROR"
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ROR1 ligand-1
<p>ROR1ligand-1 (9-1) serves as the ligand for PROTAC ROR1 degrader-1. By linking with ligands of either the VHL type or CRBN, the first selective and efficient ROR1 PROTAC molecule was designed and synthesized.</p>Formula:C23H30BrN7Color and Shape:SolidMolecular weight:484.44RORγt inverse agonist 33
<p>RORγt inverse agonist 33 (compound (R)-D4) is an orally bioavailable RORγt inverse agonist with an IC50 of 21 nM, playing a significant role in rheumatoid arthritis research.</p>Formula:C27H37NO5SColor and Shape:SolidMolecular weight:487.651Bevurogant
CAS:<p>Bevurogant is an antagonist of RORγt receptor and can be used in studies about the treatment of chronic inflammatory diseases.</p>Formula:C26H28N8O3SPurity:99.32%Color and Shape:SolidMolecular weight:532.62TMP-778
CAS:<p>TMP-778 is a selective inverse agonist of RORγt.</p>Formula:C31H30N2O4Purity:99.68%Color and Shape:SolidMolecular weight:494.58RORγt inverse agonist 31
<p>RORγt inverse agonist 31 (14g) is a potent antagonist of the retinoic acid receptor-related orphan receptor γt (RORγt), exhibiting an inhibitory concentration (</p>Formula:C23H15Cl2F3N4O3SPurity:98%Color and Shape:SolidMolecular weight:555.36ROR1-IN-2
<p>ROR1-IN-2 (compound 9I) is a potent and selective inhibitor of ROR1. It exhibits antiproliferative activity in various cancer cell lines and significantly inhibits tumor growth in vivo.</p>Formula:C30H27N3O4Color and Shape:SolidMolecular weight:493.20016RORγ antagonist 1
<p>RORγ antagonist 1 (compound 22), a potent derivative of betulinic acid, acts as an antagonist to RORγ with a dissociation constant (K D) of 0.18 μM.</p>Formula:C35H60N2O2Purity:98%Color and Shape:SolidMolecular weight:540.86TMP920
CAS:<p>TMP920 inhibits RORγt binding to the SRC1 peptide (IC50: 0.03 μM). TMP920 is a highly potent and selective RORγt antagonist.</p>Formula:C29H30N2O3Purity:98%Color and Shape:SolidMolecular weight:454.56XY018
CAS:<p>XY018 is a ROR-γ antagonist with anti-tumor activity, inhibits ROR-γ activity, and can be used to study drug-resistant prostate cancer.</p>Formula:C23H15F7N2O4Purity:99.95% - 99.96%Color and Shape:SolidMolecular weight:516.37Nobiletin
CAS:<p>Nobiletin: a citrus-derived flavone with anti-inflammatory and anti-cancer properties; water-insoluble, very weak acid.</p>Formula:C21H22O8Purity:98.65% - 99.76%Color and Shape:SolidMolecular weight:402.39Cedirogant
CAS:<p>Cedirogant (ABBV-157) is an orally active retinoid-related orphan receptor-γt(RORγt) inverse agonist that is used for psoriasis study.</p>Formula:C24H20Cl3F3N2O3Purity:99.20%Color and Shape:SolidMolecular weight:547.78Cintirorgon
CAS:<p>Cintirorgon (LYC-55716) is a selective, oral agonist of RORγ. Cintirorgon modulates gene expression of RORγ expressing T lymphocyte immune cells.</p>Formula:C27H23F6NO6SPurity:99.92%Color and Shape:SolidMolecular weight:603.53SR1001
CAS:<p>SR 1001 is an inverse agonist for RORα/RORγ (Kis: 172/111 nM).</p>Formula:C15H13F6N3O4S2Purity:98.93%Color and Shape:SolidMolecular weight:477.4GSK2981278
CAS:<p>GSK2981278 (ROR gama modulator 1) is a highly potent and selective inverse agonist of retinoic acid receptor-related orphan receptor gamma (ROR gamma).</p>Formula:C25H35NO5SPurity:99.31% - 99.67%Color and Shape:SolidMolecular weight:461.61SR1078
CAS:<p>SR1078 is an agonist of retinoic acid receptor-related orphan receptor (ROR)α/γ.</p>Formula:C17H10F9NO2Purity:99.58%Color and Shape:SolidMolecular weight:431.25SR0987
CAS:<p>SR0987 is a RORγt agonist,</p>Formula:C16H10ClF6NO2Purity:99.43%Color and Shape:SolidMolecular weight:397.7Neoruscogenin
CAS:<p>1. Neoruscogenin represents a universal pharmacological tool for RORα research due to its specific selectivity profile versus other nuclear receptors.</p>Formula:C27H40O4Purity:99.5% - 99.92%Color and Shape:SolidMolecular weight:428.6S18-000003
CAS:<p>S18-000003: Oral retinoic acid receptor gamma-t inhibitor, IC50 29 nM, reduces IL-17 production.</p>Formula:C26H25F3N2O4SPurity:99.24% - 99.31%Color and Shape:SolidMolecular weight:518.55RORγt inverse agonist 13
CAS:<p>RORγt inverse agonist 13 (Compound 3i) is a potent, orally active and selective RORγt inverse agonist (IC50=63.8 nM), with improved drug-like properties[1].</p>Formula:C23H17Cl2F3N2O4Purity:99.04%Color and Shape:SolidMolecular weight:513.29GSK805
CAS:<p>GSK805 is a potent, orally bioavailable and CNS-penetrant RORγt inhibitor.Cost-effective and quality-assured.</p>Formula:C23H18Cl2F3NO4SPurity:98% - ≥95%Color and Shape:SolidMolecular weight:532.36
