All ProductsDisplaying Products by Catalog Number (6800 - 6899)
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| Cat. No. | Product Name / Activity |
|---|---|
| 6802 | 6 TMR Tre |
| Fluorescent trehalose; selectively labels mycobacterial cell envelope | |
| 6804 | Hoechst Janelia Fluor® 646 |
| Fluorogenic, red-emitting DNA probe. Used for: fixed and live-cell imaging. Application: confocal microscopy, super resolution microscopy (SRM) (PALM, PAINT), lattice light sheet microscopy | |
| 6807 | NNC 0640 |
| Negative allosteric modulator of glucagon and GLP-1 receptors | |
| 6811 | Lapatinib |
| Potent and selective dual ErbB2 (HER-2) and EGFR inhibitor | |
| 6812 | Afatinib dimaleate |
| Potent dual specificity EGFR/HER2 inhibitor; active in vivo | |
| 6813 | Ibrutinib |
| Potent and selective BTK inhibitor | |
| 6814 | Sorafenib |
| Potent Raf-1 inhibitor; also inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and cKIT | |
| 6816 | Sitagliptin phosphate |
| Potent and selective DPP IV inhibitor | |
| 6818 | Artemether |
| Antimalarial; also inhibits neuroinflammation | |
| 6819 | Mefloquine hydrochloride |
| Cx36 and Cx50 gap channel blocker; also antimalarial and antischistosomal | |
| 6821 | ZAP 180013 |
| Zap70 inhibitor; inhibits interaction with ITAMs | |
| 6825 | SGC 3027 |
| Potent and selective PRMT7 inhibitor | |
| 6826 | AZ 1729 |
| FFA2 allosteric agonist; displays bias for the Gi signaling pathway | |
| 6827 | Artesunate |
| Suppresses ROS-induced activation of the NLRP3 inflammasome; antimalarial | |
| 6830 | Conivaptan hydrochloride |
| Very high affinity vasopressin V1A and V2 antagonist; orally bioavailable | |
| 6831 | TRPV3 74a |
| Selective TRPV3 antagonist; brain penetrant | |
| 6832 | Ec2la |
| Positive allosteric modulator of CB2 receptors; active in vivo | |
| 6833 | RO 5263397 hydrochloride |
| Potent TA1 receptor agonist | |
| 6834 | Auxin |
| Chemical dimerizer used in auxin-inducible degron (AID) system; phytohormone | |
| 6835 | ABT 737 |
| Bcl-2 family inhibitor; mimics BH3 and induces apoptosis in cancer cell lines | |
| 6838 | SGC 3027N |
| Negative control for SGC 3027 (Cat. No. 6825) | |
| 6848 | GSK 2795039 |
| NADPH oxidase 2 (NOX2) inhibitor | |
| 6850 | Thalidomide 4'-ether-alkylC2-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 6851 | Pomalidomide 4'-alkylC2-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 6852 | VH 032 amide-alkylC2-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 6853 | VH 032 amide-alkylC6-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 6856 | α-Mangostin |
| Inhibits proliferation and induces apoptosis selectively in pancreatic CSCs and cancer cell lines | |
| 6858 | MMG 11 |
| TLR2 antagonist | |
| 6859 | FITM |
| Potent and selective negative allosteric modulator of mGlu1 receptors | |
| 6860 | SB 290157 trifluoroacetate |
| Potent C3a receptor antagonist | |
| 6861 | Anle138b |
| Oligomeric aggregation inhibitor; inhibits prion protein and α-synuclein aggregate formation | |
| 6862 | Psoralen-triethylene glycol azide |
| RNA conformation probe; reagent for COMRADES RNA platform | |
| 6865 | uPSEM 792 hydrochloride |
| Highly potent PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | |
| 6866 | uPSEM 817 tartrate |
| Highly potent and selective PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | |
| 6868 | 8-Azaadenosine |
| ADAR1 (adenosine deaminases acting on double-stranded RNA) inhibitor; inhibits leukemia stem cell self-renewal | |
| 6870 | AZ 12799734 |
| Potent TGF-βRI inhibitor | |
| 6871 | MO-I-500 |
| FTO inhibitor; anticonvulsant | |
| 6873 | DC 271 |
| Fluorescent retinoic acid analog; solvochromatic probe | |
| 6874 | AMG 333 |
| Potent and selective TRPM8 antagonist; active in vivo | |
| 6875 | TRPC6-PAM-C20 |
| Selective positive allosteric modulator (PAM) of TRPC6 | |
| 6877 | VU 0134992 |
| Kir4.1 blocker | |
| 6878 | BMS 466442 |
| Potent and selective inhibitor of asc-1 | |
| 6879 | VH 032 amide-PEG1-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry | |
| 6880 | VH 032 amide-alkylC10-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 6881 | SB 4 |
| Potent BMP4 agonist | |
| 6882 | DiFMUP |
| Fluorescent phosphatase substrate | |
| 6884 | TC SL C5 |
| Metastasis-associated lung adenocarcinoma transcript 1 (Malat1) RNA inhibitor | |
| 6886 | ML 67-33 |
| K2P2.1 (TREK-1), K2P10.1 (TREK-2) and K2P4.1 (TRAAK) channel activator | |
| 6887 | ML 335 |
| Selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2) activator | |
| 6889 | ML 418 |
| Kir 7.1 inhibitor; also inhibits Kir 6.2 | |
| 6890 | VH 032 amide-alkylC8-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 6891 | PND 1186 |
| Potent FAK inhibitor; orally bioavailable | |
| 6892 | RIPGBM |
| RIPK2 modulator; pro-drug of cRIPGM; orally bioavailable and brain penetrant | |
| 6893 | VU 6005649 |
| Positive allosteric modulator of mGlu7 and mGlu8 receptors; also NK1 antagonist; brain penetrant | |
| 6896 | Dynapyrazole A |
| Hedgehog signaling inhibitor; dynein inhibitor | |
| 6897 | P110 |
| Dynamin-related protein 1 (Drp1) inhibitor; cell-permeable |