All ProductsDisplaying Products by Catalog Number (7400 - 7499)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7401 | tri-GalNAc COOH |
| Asialoglycoprotein receptor ligand with PEG linker and carboxylic acid group for onward chemistry | |
| 7402 | TAT-Gap19(I130A) |
| Control peptide for TAT-Gap19 | |
| 7403 | Thalidomide 4'-ether-alkylC8-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7404 | VH 032 amide-alkylC9-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7405 | TWS 119 |
| Potent GSK3 inhibitor; induces neuronal and CD8(+) T cell differentiation | |
| 7406 | Rf470DL |
| Blue rotor-fluorogenic fluorescent D-amino acid for labeling peptidoglycans in live bacteria | |
| 7407 | LEI 401 |
| High affinity N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) inhibitor | |
| 7408 | OGDA |
| Green fluorescent D-amino acid; compatible with STED microscopy | |
| 7410 | PARPYnD |
| PARP inhibitor; photoaffinity probe | |
| 7414 | DSRM-3716 |
| Potent and reversible SARM1 NAD hydrolase inhibitor | |
| 7417 | MitoBrilliant™ Live 646 |
| Red fluorescent mitochondrial stain for live cells, Δψm dependent | |
| 7420 | LC 2 |
| Selective KRAS Degrader (PROTAC®) | |
| 7421 | LC 2 Epimer |
| Negative control for LC 2 (Cat. No. 7420) | |
| 7422 | TH 1760 |
| Potent and selective NUDT15 hydrolase inhibitor | |
| 7423 | INT 131 |
| PPARγ partial agonist | |
| 7425 | CG 428 |
| Potent tropomyosin receptor kinase (TRK) Degrader | |
| 7426 | CG 428-Neg |
| Negative control for CG 428 (Cat. No. 7425) | |
| 7427 | CG 858 |
| Selective BRAF-V600E protein Degrader (uSMITE™) | |
| 7428 | CG 858-Neg |
| Negative control for CG 858 (Cat. No. 7427) | |
| 7432 | SIM1 |
| Potent and selective trivalent BET Bromodomain Degrader (PROTAC®) | |
| 7433 | cis-SIM1 |
| Negative control for SIM1 (Cat. No. 7432) | |
| 7434 | Pomalidomide 4'-PEG1-azide |
| Cereblon ligand with PEG linker and terminal azide for onward chemistry | |
| 7435 | Pomalidomide 4'-PEG3-azide |
| Cereblon ligand with PEG linker and terminal azide for onward chemistry | |
| 7436 | Pomalidomide 4'-PEG4-azide |
| Cereblon ligand with PEG linker and terminal azide for onward chemistry | |
| 7437 | Pomalidomide 4'-PEG5-azide |
| Cereblon ligand with PEG linker and terminal azide for onward chemistry | |
| 7439 | Pomalidomide 4'-alkylC2-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7440 | Pomalidomide 4'-alkylC3-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7441 | Pomalidomide 4'-alkylC4-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7442 | Pomalidomide 4'-alkylC5-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7443 | Pomalidomide 4'-alkylC6-azide |
| Cereblon ligand with alkyl linker and terminal azide for onward chemistry | |
| 7444 | DA ZP1 |
| Fluorogenic Zn(II) sensor for isolation of stem cell derived β cells | |
| 7445 | GPR52 Comp-43 |
| GPR52 receptor antagonist | |
| 7446 | SCOTfluor 510, fluoro |
| Amine-reactive fluorescent probe precursor | |
| 7447 | SCOTfluor glucose probe 510 |
| Fluorescent glucose probe | |
| 7448 | SCOTfluor lactic acid probe 510 |
| Fluorescent lactic acid probe | |
| 7449 | Se-NADA |
| Orange fluorescent benzoselenadiazole D-amino acid (FDAA) for imaging bacteria; also photosensitizer | |
| 7450 | SGC CK2-1 |
| Potent CK2A2 and CK2A1 inhibitor; also inhibits DYRK2 | |
| 7454 | Cediranib |
| Potent inhibitor of VEGFR, PDGFR and FGFR | |
| 7456 | Thalidomide, 5'-fluoro |
| Fluoro functionalized Thalidomide; cereblon ligand for PROTACs | |
| 7457 | CAM 833 |
| Selective orthosteric inhibitor of the BRCA2-RAD51 interaction | |
| 7458 | iBET-BD2 |
| Potent and selective pan-BD2 inhibitor; orally bioavailable | |
| 7460 | SGC SMARCA-BRDVIII |
| Potent and selective SMARCA2/4 and PB1(bromo 5)-selective SWI/SNF bromodomain inhibitor | |
| 7462 | ET 18-OCH3 |
| Selective PI-PLC inhibitor, also PAF receptor agonist | |
| 7463 | SJF 0628 |
| Potent BRAF Degrader (PROTAC® | |
| 7464 | SJF 0661 |
| Negative control for SJF 0628 (Cat. No. 7463) | |
| 7466 | BI dihydrochloride |
| DFHBI derivative for imaging of RNA in living cells that bind Broccoli aptamers | |
| 7468 | Pomalidomide 5'-piperazine |
| Cereblon ligand with terminal piperazine for onward chemistry | |
| 7469 | Pomalidomide 5'-piperazine-4-methylpiperidine |
| Cereblon ligand with terminal piperidine for onward chemistry | |
| 7470 | Pomalidomide 5'-fluoro-6'-piperazine |
| Cereblon ligand with terminal piperazine for onward chemistry | |
| 7471 | Pomalidomide 5'-fluoro-6'-piperazine-4-methylpiperidine |
| Cereblon ligand with terminal piperidine for onward chemistry | |
| 7472 | Lenalidomide 5'-piperazine |
| Cereblon ligand with terminal piperazine for onward chemistry | |
| 7473 | Lenalidomide 5'-piperazine-4-methylpiperidine |
| Cereblon ligand with terminal piperidine for onward chemistry | |
| 7474 | EN6 |
| H+-ATPase activator; activates autophagy; inactivates mTORC1 signaling | |
| 7476 | EN 219 |
| Covalent RNF114 ligand | |
| 7479 | Ac4ManNAz |
| Azide-containing monosaccharide building block; used as glycoprotein, glycolipid and glycoRNA probe | |
| 7481 | BCI |
| DUSP6 and DUSP1 inhibitor | |
| 7482 | NVS MLLT-1 |
| Selective MLLT1/3 inhibitor | |
| 7483 | BDY FL VH032 |
| High-affinity VHL fluorescent probe for TR-FRET and FP assays | |
| 7485 | Covidcil-19 |
| Binds to SARS-CoV-2 frameshifting element and reduces frameshifting efficiency | |
| 7486 | Roxadustat |
| HIF-PH inhibitor; erythropoietic | |
| 7488 | MRTX 849 |
| Mutation-selective inhibitor of KRASG12C | |
| 7489 | TCH-165 |
| Enhancer of 20S proteasome assembly and 20S-mediated protein degradation | |
| 7492 | Lomitapide mesylate |
| Potent microsomal triglyceride transfer protein (MTP) inhibitor | |
| 7493 | Tasimelteon |
| Selective dual melatonin receptor (MT1/MT2) agonist | |
| 7494 | CIA 1 |
| COUP-TFII inhibitor | |
| 7496 | FMK 9a |
| Potent ATG4B/autophagin-1 inhibitor; also inhibits calpain and cathepsin B | |
| 7497 | Vandetanib |
| Potent VEGFR-2 inhibitor, also inhibits EGFR and RET oncoproteins activity | |
| 7498 | SPOP-i-6lc |
| SPOP E3 ubiquitin ligase inhibitor |