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 | |
7419 | Kyoto Probe-1 |
Fluorescent probe that selectively identifies undifferentiated iPS/ES cells | |
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 | |
7424 | EMI 48 |
Inhibitor of EGFR mutants | |
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 | |
7480 | DBCO PEG4 Biotin |
Biotinylation reagent for labeling azide-containing biomolecules via Cu(I)-free click chemistry | |
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 New |
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 |