All ProductsDisplaying Products by Catalog Number (7200 - 7299)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7200 | Tocriscreen FDA-Approved Drugs Library |
| Drug repurposing library; a library of 190 compounds equivalent to active components of drug formulations approved by the FDA (100 μL 10 mM DMSO solutions) | |
| 7201 | Phalloidin-Janelia Fluor® 646 |
| Red-fluorescent F-actin probe. Binds and labels F-actin. Used for: F-actin labelling. Application: confocal microscopy, super resolution microscopy (SRM) including dSTORM & STED, flow cytometry | |
| 7203 | Pomalidomide 4'-PEG1-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7204 | Pomalidomide 4'-PEG3-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7205 | Pomalidomide 4'-alkylC3-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7206 | 5-Ethynyluridine |
| Uridine analog, used for labeling RNA synthesis | |
| 7207 | 5-Ethynyl-2'-deoxyuridine |
| Thymidine analog for labeling DNA; can be linked to a fluorophore by click chemistry | |
| 7208 | Pomalidomide 4'-alkylC7-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7209 | Pomalidomide 4'-alkylC4-acid |
| Cereblon ligand with alkyl linker and terminal acid for onward chemistry | |
| 7210 | Pomalidomide 4'-alkylC6-acid |
| Cereblon ligand with alkyl linker and terminal acid for onward chemistry | |
| 7211 | Pomalidomide 4'-alkylC8-acid |
| Cereblon ligand with alkyl linker and terminal acid for onward chemistry | |
| 7212 | Pomalidomide 4'-PEG2-acid |
| Cereblon ligand with PEG linker and terminal acid for onward chemistry | |
| 7213 | Pomalidomide 4'-PEG4-acid |
| Cereblon ligand with PEG linker and terminal acid for onward chemistry | |
| 7214 | VH 032 amide-PEG2-acid |
| VHL ligand with PEG linker and terminal acid for onward chemistry | |
| 7215 | VH 032 amide-PEG4-acid |
| VHL ligand with PEG linker and terminal acid for onward chemistry | |
| 7216 | VH 032 amide-alkylC3-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7217 | VH 032 amide-alkylC5-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7218 | PZM21 |
| Selective μ receptor agonist | |
| 7219 | CRBN PROTAC® 14a |
| Cereblon Degrader (PROTAC®) | |
| 7220 | A 410099.1 amide-PEG4-amine |
| IAP ligand with PEG linker and terminal amine for onward chemistry | |
| 7221 | A 410099.1 amide-PEG5-amine |
| IAP ligand with PEG linker and terminal amine for onward chemistry | |
| 7222 | Baricitinib |
| Highly potent JAK1 and JAK2 inhibitor; also inhibits JAK3 and Tyk2 | |
| 7223 | Dabrafenib mesylate |
| Potent and selective B-Raf, CDK16 and NEK9 inhibitor; anticancer; also targets human proteins in the SARS-CoV-2 interactome | |
| 7224 | Oseltamivir phosphate |
| Influenza virus neuraminidase inhibitor; antiviral prodrug | |
| 7225 | Favipiravir |
| Viral RNA polymerase inhibitor | |
| 7226 | Remdesivir |
| Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide prodrug | |
| 7227 | GS 441524 |
| Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleotide | |
| 7228 | Mpro 13b-K |
| Coronavirus Mpro inhibitor | |
| 7229 | Galidesivir dihydrochloride |
| Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral | |
| 7230 | MPro N3 |
| Coronavirus Mpro inhibitor | |
| 7231 | EIDD 1931 |
| Viral RNA-dependent RNA polymerase (RdRP) inhibitor; broad spectrum antiviral nucleoside | |
| 7234 | Nitazoxanide |
| Pyruvate flavodoxin/ferredoxin oxidoreductase inhibitor; also inhibits Wnt signaling; broad spectrum anti-infective | |
| 7235 | Arbidol |
| Inhibits replication of SARS-CoV-2 in vitro; broad spectrum antiviral | |
| 7236 | Digoxigenin Tyramide |
| Reagent used for Tyramide Signal Amplification in IHC, ICC and ISH | |
| 7240 | ZNL 02-096 |
| Potent and selective Wee1 Degrader (PROTAC®) | |
| 7242 | Ac-FLTD-CMK |
| Potent and selective inhibitor of caspases 1, 5 and 4 | |
| 7254 | ARCC 4 |
| Potent and selective androgen receptor Degrader (PROTAC®) | |
| 7255 | ARCC 4 negative control |
| Negative control for ARCC 4 (Cat. No. 7254) | |
| 7256 | ARV 771 |
| Potent BET bromodomain PROTAC®; also degrades BRD-tagged chimeric antigen receptors (CAR) in T cells | |
| 7258 | Gefitinib-based PROTAC® 3 |
| Potent EGFR PROTAC® Degrader | |
| 7259 | TBK1 PROTAC® 3i |
| Potent TANK-binding kinase 1 (TBK1) PROTAC® | |
| 7260 | TBK1 control PROTAC® 4 |
| Negative control for TBK1 PROTAC® 3i (Cat. No. 7259) | |
| 7261 | SJF 1521 |
| Selective EGFR PROTAC® Degrader | |
| 7262 | SJF 1528 |
| Potent EGFR PROTAC® Degrader; also degrades HER2 | |
| 7265 | GMB 475 |
| BCR-ABL1 kinase PROTAC® Degrader | |
| 7266 | SJF 8240 |
| c-MET PROTAC®; also degrades exon-14-deleted c-MET | |
| 7267 | SJFδ |
| Potent and selective p38δ PROTAC® | |
| 7268 | SJFα |
| Potent and selective p38α PROTAC® | |
| 7270 | iP300w |
| Potent p300/CBP inhibitor | |
| 7271 | Brivaracetam |
| SV2A ligand; antiepileptic | |
| 7273 | C-Laurdan |
| Two-photon polarity-sensitive lipid membrane probe. Used for: cell membrane imaging. Application: One and Two-photon microscopy for membrane Polarity | |
| 7275 | Laurdan |
| Polarity sensitive lipid membrane fluorescent probe. Used for: imaging lipid rafts. Application: fluorescent microscopy | |
| 7277 | HBC 530 |
| GFP fluorophore mimic for imaging RNA in live cells; activated by binding to Pepper aptamers; suitable for confocal and two-photon microscopy | |
| 7278 | α1A-AR Degrader 9c |
| Selective α1A adrenergic receptor Degrader (PROTAC®) | |
| 7279 | Janelia Fluor® 646, Tetrazine |
| Red dye (Reactive group: tetrazine). Application: flow cytometry, confocal microscopy, super-resolution microscopy (SRM) including dSTORM & STED. Suitable for live cell imaging | |
| 7280 | GRL 0617 |
| Coronavirus PLpro inhibitor | |
| 7282 | Bortezomib |
| High affinity proteasome inhibitor | |
| 7283 | Apilimod dimesylate |
| Potent and selective PIKfyve inhibitor | |
| 7285 | DCLK1-IN-1 |
| Potent and selective doublecortin like kinase 1/2 (DCLK1/2) inhibitor; orally bioavailable | |
| 7287 | FAM-DEALA-Hyp-YIPD |
| Fluorescent HIF-1α peptide; can be used to evaluate the effect of VHL binding on degradation activity | |
| 7288 | Thalidomide-Cyanine 5 |
| High affinity cereblon fluorescent probe | |
| 7289 | Nimbolide |
| RNF114 inhibitor | |
| 7290 | Famotidine |
| Potent and high affinity H2 biased inverse agonist | |
| 7292 | I 432 |
| TMPRSS2 Inhibitor | |
| 7293 | VH 101 phenol-alkylC4-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 7294 | VH 101 phenol-alkylC6-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 7298 | xStAx-VHLL |
| Selective peptide-based β-catenin Degrader (PROTAC®) |