All ProductsDisplaying Products by Catalog Number (7700 - 7799)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7700 | MitoBrilliant™ 646 |
| Universal red fluorescent mitochondrial stain for both live and fixed cells | |
| 7701 | RAGE 229 |
| ctRAGE-DIAPH1 interaction antagonist; reduces inflammatory signaling in diabetic mice | |
| 7705 | Masitinib |
| Potent colony-stimulating factor 1 receptor (CSF-1R) tyroine kinase inhibitor | |
| 7706 | ADU-S100 disodium salt |
| STING agonist | |
| 7709 | Trametinib |
| Potent and selective MEK inhibitor; orally bioavailable | |
| 7710 | Vismodegib |
| Potent hedgehog pathway inhibitor | |
| 7711 | Polybrene |
| Viral transduction enhancer | |
| 7713 | AMG 510 |
| Potent and selective KRASG12C inhibitor | |
| 7714 | EDA-DA |
| Unnatural dipeptide building block with alkyne group for functionalizing peptidoglycan | |
| 7715 | C25-140 |
| TRAF6-Ubc13 interaction inhibitor | |
| 7716 | N-methylated pomalidomide |
| Functionalized cereblon ligand for generating Degrader negative controls; also used as Pomalidomide negative control | |
| 7718 | 3',2'-cGAMP sodium salt |
| Induces expression of STING and STING-related genes; antiviral | |
| 7719 | TH 9619 disodium salt |
| MTHFD2 inhibitor | |
| 7720 | SJ 6986 |
| Molecular glue; induces degradation of GSPT1/2 | |
| 7721 | SJ 11646 |
| Potent and selective LCK Degrader (PROTAC®) | |
| 7722 | JQ1-FITC |
| Fluorescent BET bromodomain probe; suitable for use in TR-FRET | |
| 7723 | RGD peptide |
| Minimal recognition sequence for integrin binding; potent integrin inhibitor | |
| 7725 | GLP-2 (3-33) |
| Peptide antagonist of glucagon-like peptide-2 (GLP-2) receptor | |
| 7726 | DMSO, Cell Cryopreserve Grade |
| Intracellular cryoprotective agent | |
| 7727 | SJ 10542 |
| Potent and selective JAK2/3 Degrader (PROTAC®) | |
| 7728 | VU 6015929 |
| Potent and selective discoidin domain receptor 1/2 inhibitor | |
| 7729 | Phenyl-glutarimide 4'-piperazine |
| Piperazine-functionalized cereblon ligand for PROTAC development | |
| 7730 | AS2717638 |
| Selective, brain penetrant LPA5 antagonist | |
| 7732 | Pomalidomide 4'-alkylC10-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7733 | Thalidomide 5'-amine-alkylC10-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7734 | proTAME |
| Cell-permeable APC/C inhibitor | |
| 7735 | Thalidomide 5'-amine-PEG1-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7736 | Thalidomide 5'-amine-PEG2-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7737 | Thalidomide 5'-amine-PEG3-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7739 | Polyamine Supplement x1000 (lyophilized) |
| Media supplement to boost cell growth; used as component of CEPT cocktail to enhance stem cell viability | |
| 7741 | STING agonist C53 |
| Pan-polymorph STING agonist | |
| 7742 | TFRGAP-NH2 |
| PAR3 peptide agonist | |
| 7743 | Linifanib |
| Potent inhibitor of PDGFRβ, KDR, FLT3 and CSF-1R | |
| 7745 | CST 905 |
| Potent and selective BRAFV600E Degrader (PROTAC®) | |
| 7749 | ICG-d7 |
| Near-infrared (NIR) fluorescent dye; partially deuterated form of Indocyanine Green (Cat. No. 7510), suitable for in vivo imaging. | |
| 7750 | Ac4GlcNAlk |
| Metabolic chemical reporter for studying glycosylation and glycoproteins | |
| 7751 | 1-Hex-GlcNAlk |
| Metabolic chemical reporter for studying glycosylation and glycoproteins | |
| 7753 | BL660-NO |
| Nitric oxide activity-based sensing NIR bioluminescent probe | |
| 7754 | M4K2163 dihydrochloride |
| Potent and selective ALK2 inhibitor | |
| 7755 | Asunaprevir |
| Potent hepatitis C virus (HCV) NS3 protease inihibitor | |
| 7756 | DAF FM diacetate |
| Cell permeable photostable nitric oxide (NO) fluorescent indicator | |
| 7757 | AZ 13824374 |
| Potent and selective ATAD2 bromodomain inhibitor | |
| 7758 | VH 101, acid |
| VHL ligand, carboxylic acid functionalized at the benzylic position | |
| 7759 | UNC 1215, acid |
| Functionalized L3MBTL3 ligand for PROTACs | |
| 7760 | Selinexor |
| Selective exportin 1 (XPO1/CRM1) inhibitor | |
| 7761 | Ivosidenib |
| Potent inhibitor of mutant isocitrate dehydrogenase (mIDH1) | |
| 7762 | EED 226 |
| Potent and selective EED inhibitor | |
| 7764 | DMHBO+ |
| Fluorescent upon binding to Chili aptamer; for imaging RNA in cells | |
| 7768 | Disulfide biotin azide |
| Azide-activated biotinylation reagent; labels alkyne moieties via copper-catalyzed click chemistry | |
| 7769 | Chem-CLIP control probe |
| Control probe for Chem-CLIP experiments | |
| 7771 | TP-040 |
| Potent and selective O-GlcNAcase (OGA) inhibitor | |
| 7773 | tDHU, acid |
| Functionalized cereblon ligand for PROTAC development | |
| 7774 | VH 032 |
| Inhibitor of VHL; blocks interaction of VHL and HIF-α | |
| 7778 | TH 10785 |
| OGG1 activator | |
| 7780 | β-GalNAc-PEG4-Azide |
| Asialoglycoprotein receptor ligand with PEG4 linker and azide group for onward chemistry | |
| 7781 | tri-GalNAc-C5-amine |
| Asialoglycoprotein receptor ligand with alkylC5 linker and amine group for onward chemistry | |
| 7783 | Upadacitinib |
| JAK1-selective inhibitor | |
| 7786 | GSK 2256098 |
| Potent focal adhesion kinase (FAK) inhibitor | |
| 7787 | Ortho AP 1867 |
| Selective binding ligand for FKBP12F36V; precursor for dTAG compounds | |
| 7788 | TBIA |
| Bivalent SHAPE cross-linking reagent | |
| 7789 | IA |
| SHAPE-JuMP monoadduct control for TBIA (Cat. No. 7788) | |
| 7791 | WS 6 |
| Induces growth and proliferation of pancreatic islet cells, murine totipotent stem cells, GABAergic neurons and hippocampal neurons | |
| 7794 | CTPI 2 |
| Selective mitochondrial citrate transporter (SLC25A1) inhibitor | |
| 7799 | CCT 369260 |
| Molecular glue; induces degradation of BCL6 |