All ProductsDisplaying Products by Catalog Number (7800 - 7899)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7800 | CPS2 |
| Potent and selective CDK2 Degrader (PROTAC®) | |
| 7801 | CST 967 |
| Potent and selective USP7 Degrader (PROTAC®) | |
| 7804 | preQ1-biotin |
| PreQ1 with biotin handle for RNA labeling and purification | |
| 7806 | preQ1-alkyne |
| preQ1 with alkyne handle for click chemistry | |
| 7807 | Hh-Ag1.5 |
| Potent and high affinity Smo receptor agonist | |
| 7808 | NDT 30805 |
| Potent NLRP3 inflammasome inhibitor | |
| 7809 | TEPP 46 |
| Potent and selective pyruvate kinase M2 (PKM2) allosteric activator | |
| 7810 | eIF4A i28 |
| eIF4A inhibitor | |
| 7811 | CITFA |
| Potent G protein-coupled estrogen receptor (GPER) agonist | |
| 7812 | CIMBA hydrochloride |
| Potent and selective G protein-coupled estrogen receptor (GPER) antagonist | |
| 7813 | LL-K9-3 |
| Selective HyT-based degrader of the CDK9-cyclin T1 complex | |
| 7814 | Tricyclic cytosine tC |
| Fluorescent tricyclic cytosine analog for RNA imaging | |
| 7816 | UNC 6852 |
| Polycomb repressive complex 2 (PRC2) Degrader (PROTAC®) | |
| 7818 | GSK 215 |
| Potent and selective focal adhesion kinase (FAK) Degrader (PROTAC®) | |
| 7820 | CU-76 |
| Selective inhibitor of cyclic GMP-AMP synthase (cGAS) | |
| 7821 | ML 162 |
| Inhibits glutathione peroxidase (GPX4); induces ferroptosis | |
| 7823 | AZD 4547 |
| Potent and selective FGFR inhibitor | |
| 7825 | AZD 7648 |
| Potent and selective DNA-PK inhibitor; enhances CRISPR-mediated HDR efficiency | |
| 7826 | Sonidegib |
| Potent Smoothened receptor antagonist | |
| 7828 | HHP 9 |
| BET bromodomain Degrader (PROTAC®); also potent Hedgehog pathway inhibitor | |
| 7829 | Thalidomide 4'-ether-alkylC6-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7830 | Klotho-derived peptide 1 |
| TGF-β receptor 2 (TβR2) binding peptide; disrupts the TGF-β/TβR2 interaction | |
| 7831 | AUNP 12 |
| Peptide inhibitor of the PD-1 signaling pathway | |
| 7832 | TAT-PDHPS1 |
| YAP inhibitor | |
| 7833 | preQ1-azide |
| preQ1 with azide handle for click chemistry | |
| 7834 | sCy5DA |
| FDAA for super-resolution microscopy of bacteria | |
| 7835 | sCy5DL-amide |
| FDAA for super-resolution microscopy of bacteria | |
| 7837 | JB 300 |
| Aurora A Degrader (PROTAC®) | |
| 7840 | AZD 8055 |
| Highly potent and selective mTOR inhibitor | |
| 7841 | Imipramine hydrochloride |
| Potent inhibitor of 5-HT and noradrenalin transporters; promotes immunostimulatory tumor microenvironment | |
| 7842 | NAMPT PROTAC® A7 |
| Potent and selective nicotinamide phosphoribosyl transferase (NAMPT) Degrader (PROTAC®) | |
| 7844 | Tocriscreen Kinase Inhibitor 3.0 |
| A bioactive compound library of 210 kinase inhibitors (100 μL 10 mM DMSO solutions) for high-throughput screening, high-content screening, target validation and assay development | |
| 7845 | AZ1 USP25/28 inhibitor |
| Selective USP25 and USP28 inhibitor | |
| 7847 | Klotho-derived peptide 6 |
| Wnt/β-catenin signaling inhibitor | |
| 7850 | MK 2206 dihydrochloride |
| Potent and selective allosteric Akt1, Akt2 and Akt3 inhibitor | |
| 7851 | EM 12-FS |
| Molecular glue; induces degradation of NQAT1 | |
| 7852 | EM12-SO2F |
| Potent covalent inhibitor of Cereblon | |
| 7853 | Mpro 13b-H |
| Negative control for Mpro 13b-K (Cat. No. 7228) | |
| 7854 | PEI STAR™ transfection reagent |
| Polyethylenimine (PEI) transfection reagent, chemically-defined | |
| 7855 | Mag-Fura-2 AM |
| Magnesium (Mg2+) indicator, membrane permeable | |
| 7856 | MQAE |
| Fluorescent Cl- indicator; membrane permeable | |
| 7857 | BDY FL Lenalidomide |
| Fluorescent cereblon ligand | |
| 7858 | PD 4'-oxyacetic acid |
| Functionalized cereblon ligand for PROTAC development | |
| 7859 | PD 4'-piperazine |
| Stable cereblon ligand, for PROTAC synthesis | |
| 7860 | sBADA |
| Green fluorescent D-amino acid for labeling peptidoglycans in bacteria | |
| 7861 | VH 032, thiol |
| Functionalized VHL ligand for PROTAC® development | |
| 7862 | TBTA |
| Click chemistry auxiliary reagent; stabilizing ligand for copper-catalyzed azide-alkyne cycloaddition reaction | |
| 7863 | THPTA |
| Click chemistry auxiliary reagent; accelerating ligand for copper-catalyzed azide-alkyne cycloaddition reaction | |
| 7864 | LY 2109761 |
| Selective TGF-β kinase inhibitor | |
| 7865 | AMG 900 |
| Potent pan-Aurora kinase inhibitor | |
| 7866 | IDR 1002 |
| Innate defence regulator peptide | |
| 7867 | VH 032 amide-alkylC5-azide |
| VHL ligand with alkylC5 linker and terminal azide for onward chemistry | |
| 7868 | PE 22-28 |
| Potent inhibitor of TREK-1 channels | |
| 7870 | ING-2 AM |
| Fluorescent sodium ion (Na+) indicator, membrane permeable | |
| 7871 | IPG-4 AM |
| Fluorescent potassium ion (K+) indicator, membrane permeable | |
| 7873 | Phen Green SK diacetate |
| Heavy metal ion indicator, membrane permeable | |
| 7874 | N-Acetylcysteine |
| Glutathione (GSH) precursor; maintains stem cell function in culture. | |
| 7876 | PZ 3022 |
| PanK Activator | |
| 7878 | XIE62-1004 |
| Inducer of autophagy via interaction of p62 and LC3 | |
| 7879 | CHDI 00484077 |
| Potent and selective HDAC class IIa inhibitor | |
| 7882 | HDAC4 CHDI Degrader 11 |
| Potent and selective HDAC4 Degrader (PROTAC®) | |
| 7883 | dTAG-Biotin |
| Affinity probe for mutant FKBP12F36V proteins | |
| 7884 | VH 101, thiol |
| Thiol functionalized VHL ligand | |
| 7886 | HER2 PROTAC® CH7C4 |
| Potent and selective HER2 targeting Degrader (PROTAC®) | |
| 7887 | Ivacaftor |
| Potent and selective CFTR potentiator | |
| 7890 | CBMR 0083 |
| Potent allosteric FFA1 (GPR40) and 4 (GPR120) agonist | |
| 7891 | Gilteritinib |
| Potent FLT3 inhibitor; also potently inhibits AXL | |
| 7892 | dTAG-Fluorescein |
| Fluorescent probe for labeling mutant FKBP12 (F36V) proteins | |
| 7893 | 5-Ph-IAA-AM |
| Selective and potent TAG Degrader for auxin-inducible degron 2 system; 5-Ph-IAA analog | |
| 7894 | Auxinole |
| Auxin antagonist of TIR1/AFB receptors; also OsTIR1 inhibitor in auxin-inducible degron (AID) system | |
| 7898 | ZZL 7 |
| Inhibitor of SERT and nNOS interaction |