All ProductsDisplaying Products by Catalog Number (6400 - 6499)
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| Cat. No. | 产品名称/活性 |
|---|---|
| 6405 | PF 05180999 |
| Potent and selective PDE2A inhibitor | |
| 6407 | Fendiline Hydrochloride |
| Inhibits KRas localization to the plasma membrane; also L-type calcium channel blocker | |
| 6416 | CM 11 |
| Homo-PROTAC® for self-degradation of pVHL30 | |
| 6418 | Janelia Fluor® 585, NHS ester |
| Orange dye (Reactive group: NHS ester). Application: confocal microscopy, super resolution microscopy, and two-photon excitation fluorescence microscopy. Suitable for live cell imaging | |
| 6419 | Janelia Fluor® 635, NHS ester |
| Red dye (Reactive group: NHS ester). Application: flow cytometry, confocal microscopy, super resolution microscopy. Suitable for live cell imaging | |
| 6420 | Janelia Fluor® 669, NHS ester |
| Far red dye (Reactive group: NHS ester). Application: confocal miocrocopy, super resolution microscopy including dSTORM & STED. Suitable for live cell imaging | |
| 6422 | DREADD agonist 21 dihydrochloride |
| Potent hM3Dq and hM4Di DREADD agonist; water soluble version of DREADD agonist 21 (Cat. No. 5548) | |
| 6423 | Pep 2-8 |
| Potent PCSK9 inhibitor | |
| 6424 | Sodium Cromoglicate |
| Promotes ESCs/iPSCs differentiation into pancreatic endocrine islet cells | |
| 6425 | PSEM 308 hydrochloride |
| PSAML141F-GlyR and PSAML141F,Y115F-5-HT3 chimeric ion channel agonist | |
| 6426 | PSEM 89S |
| PSAML141F-GlyR and PSAML141F,Y115F-5-HT3 chimeric ion channel agonist | |
| 6429 | ML 210 |
| Selectively kills mutant HRAS-expressing cells; glutathione peroxidase inhibitor; induces ferroptosis | |
| 6430 | Takinib |
| Potent and selective TAK1/MAP3K7 kinase inhibitor | |
| 6431 | Phentolamine Mesylate |
| Adrenergic α receptor antagonist; antihypertensive | |
| 6433 | GSK 1016790A |
| Potent TRPV4 agonist; active in vivo | |
| 6434 | DFHO |
| RFP fluorophore mimic for imaging RNA in living cells; activated by binding Corn aptamers | |
| 6435 | ML 323 |
| Potent and selective USP1-UAF1 allosteric inhibitor | |
| 6436 | CY 09 |
| NLRP3 inhibitor; active in vivo | |
| 6438 | BRD 6989 |
| Cdk8 inhibitor; enhances IL-10 production | |
| 6439 | JNJ 0966 |
| Pro-MMP9 activation inhibitor | |
| 6442 | Gentamicin sulfate |
| Aminoglycoside antibiotic | |
| 6448 | ML 351 |
| Selective 12/15 LOX inhibitor; active in vivo | |
| 6451 | Pexacerfont |
| Potent and selective CRF1 antagonist; anxiolytic | |
| 6454 | LY 2603618 |
| Potent and selective Chk1 inhibitor | |
| 6456 | Fluorescein Tyramide |
| Green fluorescent reagent widely used for signal amplification in IHC and FISH | |
| 6457 | Cyanine 3 Tyramide |
| Orange fluorescent reagent widely used for signal amplification in IHC and FISH | |
| 6458 | Cyanine 5 Tyramide |
| Red fluorescent reagent widely used for signal amplification in IHC and FISH | |
| 6460 | ABX 464 |
| HIV RNA splicing modulator | |
| 6461 | PARPi-FL |
| Potent fluorescent PARP inhibitor; cell permeable | |
| 6462 | VH 032, amine |
| Functionalized VHL ligand for PROTACs | |
| 6463 | VH 032 amide-PEG3-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry | |
| 6464 | VH 032 amide-PEG4-amine |
| VHL ligand with PEG linker and terminal amine for onward chemistry | |
| 6465 | VH 032 amide-alkylC4-amine |
| VHL ligand with alkyl linker and terminal amine for onward chemistry | |
| 6466 | Thalidomide-4-hydroxyacetate |
| Carboxylic acid-functionalized Thalidomide; cereblon ligand for PROTACs | |
| 6467 | Thalidomide 4'-oxyacetamide-PEG3-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 6470 | A 410099.1 |
| High affinity XIAP antagonist; active in vivo | |
| 6471 | A 410099.1, amine |
| Functionalized IAP ligand for PROTACs | |
| 6472 | A 410099.1 amide-PEG3-amine |
| IAP ligand with PEG linker and terminal amine for onward chemistry | |
| 6473 | A 410099.1 amide-PEG2-amine |
| IAP ligand with PEG linker and terminal amine for onward chemistry | |
| 6474 | A 410099.1 amide-alkylC4-amine |
| IAP ligand with alkyl linker and terminal amine for onward chemistry | |
| 6475 | SU 6656 |
| Potent ATP-competitive Src family kinase inhibitor; also AMPK inhibitor; cell permeable | |
| 6476 | Compound E |
| γ-secretase inhibitor; induces neuronal differentiation | |
| 6477 | SAHM1 |
| Notch pathway inhibitor; prevents Notch complex assembly | |
| 6479 | CU CPT 9a |
| Highly potent TLR8 inhibitor | |
| 6480 | GSK 583 |
| Potent RIPK2 inhibitor; orally bioavailable and cell permeable | |
| 6481 | AP 14145 hydrochloride |
| Negative allosteric modulator of KCa2 (SK) channels | |
| 6482 | XMU MP 1 |
| Potent and selective MST1/2 inhibitor; orally bioavailable | |
| 6483 | Isoginkgetin |
| Pre-mRNA splicing inhibitor; cell permeable | |
| 6484 | Terbinafine hydrochloride |
| Selective K2P9.1 (TASK-3) activator; also inhibits fungal squalene epoxidase | |
| 6486 | Aprepitant |
| Potent long-acting hNK1 antagonist | |
| 6489 | Ocean Blue, SE |
| Blue fluorescent dye (Reactive group: NHS ester). Application: flow cytometry, fluorescence microscopy | |
| 6491 | YM 155 |
| Survivin suppressor | |
| 6492 | GSK'872 |
| Potent and selective RIP3 kinase inhibitor | |
| 6493 | A 317491 sodium salt |
| Selective, high affinity P2X3 and P2X2/3 antagonist; antinociceptive | |
| 6497 | GSK 2833503A |
| Potent and selective TRPC6 and TRPC3 antagonist | |
| 6498 | TASP 0277308 |
| Potent and selective S1P1 receptor antagonist; inhibits angiogenesis | |
| 6499 | MLN 4924 |
| Potent and selective NEDD8 activating enzyme (NAE) inhibitor; cell permeable |