About 30 results found for searched term "ROR" (0.034 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3931 | Aurora Kinase Inhibitor III | Aurora Kinase |
| Aurora Kinase Inhibitor 3 | ||
| Aurora Kinase Inhibitor III is a strong and selective Aurora A kinase inhibitor with an IC50 of 42 nM. | ||
| M4457 | Jatrorrhizine chloride | AChR/AChE |
| Jatrorrhizine chloride is a potent and orally active inhibitor of AChE (IC50=872 nM) over >115-fold selectivity for BuChE. | ||
| M5735 | Leuprolide Acetate | LHRH/GnRH |
| Leuprorelin acetate | ||
| Leuprolide acetate is a GnRH analog; leuprolide acetate acts as an agonist at pituitary GnRH receptors. | ||
| M6623 | CORM 2 | Others |
| Tricarbonyldichlororuthenium(II) dimer | ||
| CORM 2 is a carbon monoxide-releasing molecule. | ||
| M9028 | Nifuratel | Anti-infection |
| Macmiror; Magmilor; NF 113; SAP 113; Methylmercadone | ||
| Nifuratel is a local antiprotozoal and antifungal agent used in gynecology. | ||
| M9221 | GSK805 | ROR |
| ROR gamma-t-IN-1 | ||
| GSK805 is a potent, orally bioavailable RORγγ Inhibitor, with pIC50 of 8.4 and >8.2 for RORγ FRET assay and Th17 assay. | ||
| M9265 | Vimirogant | ROR |
| AGN-242428; VTP-43742; RORγ-IN-1 | ||
| Vimirogant (also known as AGN-242428 and VTP-43742) is a potent, selective and orally active RORγt inhibitor. | ||
| M10008 | Retrorsine | Alkaloids |
| Retrorsine is a naturally occurring pyrrolizidine alkaloid, which binds with DNA and inhibits the proliferative capacity of hepatocytes. | ||
| M13375 | Cetrorelix Acetate | LHRH/GnRH |
| Cetrorelix Acetate (SB-75 acetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. Sequence：Ac-D2Nal-D4Cpa-D3Pal-Ser-Tyr-DCit-Leu-Arg-Pro-DAla-NH2 | ||
| M13781 | Dihydrorhodamine 123 | Fluorescent Dye |
| DHR 123 | ||
| Dihydrorhodamine 123 (DHR 123) is a fluorescent probe (λex=488 nm, λem=525 nm). | ||
| M14531 | Cintirorgon | ROR |
| LYC-55716 | ||
| Cintirorgon (LYC-55716) is a first-in-class, selective and orally bioavailable RORγ agonist. | ||
| M16102 | Jatrorrhizine | TNIK |
| Jatrorrhizine, an isoquinoline alkaloid found in common medicinal plants, is also a TNIK inhibitor with antibacterial, anti-inflammatory and antitumor activities. | ||
| M16690 | Dihydrorobinetin | Flavonoids |
| Dihydrorobinetin | ||
| M17098 | Dihydroresveratrol 3-O-glucoside | Phenols |
| Dihydroresveratrol 3-O-glucoside | ||
| M17196 | Dihydroresveratrol | Phenols |
| Dihydroresveratrol | ||
| M18177 | Jatrorrhizine hydrochloride | Others |
| Jatrorrhizine hydrochloride | ||
| M18311 | Tetrahydrojatrorrhizine | Antifungal |
| Tetrahydrojatrorrhizine | ||
| M18748 | Dehydrorotenone | Others |
| Dehydrorotenone | ||
| M21020 | Leuprorelin | LHRH/GnRH |
| Glp-His-Trp-Ser-Tyr-D-Leu-Leu-Arg-Pro-NHEt; Leuprolide | ||
| Leuprorelin is a natriuretic peptide analog of GnRH and a pituitary GnRH receptor agonist. It can be used in studies related to estrogen receptor (ER)-positive premenopausal breast cancer. | ||
| M22099 | Cintirorgon Sodium | Others |
| Cintirorgon Sodium | ||
| M22189 | Dextrorotation nimorazole phosphate ester | Others |
| Dextrorotation nimorazole phosphate ester | ||
| M22205 | Dextrorphan tartrate | Others |
| Dextrorphan tartrate | ||
| M22524 | Dihydrorotenone | Apoptosis |
| Dihydrorotenone is a potent mitochondrial inhibitor. Dihydrorotenone induces human plasma cell apoptosis by triggering endoplasmic reticulum stress and activating p38 signaling pathway. | ||
| M27931 | Cetrorelix | LHRH/GnRH |
| SB-75 | ||
| Cetrorelix is a potent gonadotrophin-releasing hormone (GnRH) antagonist. Cetrorelix inhibits the endogenous luteinizing hormone surge during ovarian stimulation. Cetrorelix reduces cyclophosphamide induced ovarian follicular destruction in mice. | ||
| M28137 | Cetrorelix diacetate | LHRH/GnRH |
| SB-75 diacetate | ||
| Cetrorelix diacetate (SB-075 diacetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. | ||
| M29259 | RORγt modulator 5 | ROR |
| RORγt modulator 5 is a RORγt modulator with a Ki value of <100 nM. RORγt modulator 5 has the potential for inflammatory, metabolic, autoimmune and other diseases mediated by RORy study (WO2017132432A1; compound 2). | ||
| M29284 | Aurora kinase inhibitor-8 | Aurora Kinase |
| Aurora kinase inhibitor-8 is a highly selective inhibitor of the Aurora kinases. | ||
| M29927 | Aurora kinase inhibitor-2 | Aurora Kinase |
| Aurora kinase inhibitor-2 is a selective and ATP-competitive Aurora kinase inhibitor with IC50s of 310 nM and 240 nM for Aurora A and Aurora B, respectively. | ||
| M39128 | Roridin L2 | Metabolite/Endogenous Metabolite |
| Roridin L2, a fungal metabolite, is a biosynthetic precursor of Satratoxin G. Roridin L2 possesses little in vitro or in vivo toxic activity. | ||
| M39598 | 4-Chlororesorcinol | Others |
| 4-Chlorobenzene-1,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||
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