All ProductsDisplaying Products by Catalog Number (6500 - 6599)
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| Cat. No. | Product Name / Activity |
|---|---|
| 6500 | Janelia Fluor® 549, Maleimide |
| Yellow dye (Reactive group: maleimide). Application: flow cytometry, confocal microscopy, super resolution microscopy including dSTORM & STED. Suitable for live cell imaging | |
| 6502 | Janelia Fluor® 549, Tetrazine |
| Yellow dye (Reactive group: tetrazine). Application: confocal microscopy, super resolution microscopy including dSTORM & STED. Suitable for live cell imaging | |
| 6503 | Janelia Fluor® 549, free acid |
| Yellow dye (Reactive group: free acid). Application: flow cytometry, confocal microscopy, super resolution microscopy (SRM) including dSTORM & STED. Suitable for live cell imaging | |
| 6505 | Avasimibe |
| ACAT inhibitor | |
| 6506 | PF 06551600 malonate |
| Potent and selective JAK3 inhibitor | |
| 6507 | Saxagliptin hydrochloride |
| High affinity DPP-IV inhibitor; active in vivo | |
| 6508 | GSK 1702934A |
| Potent and selective TRPC3/6 activator | |
| 6510 | LNT 1 |
| Potent flap endonuclease 1 (FEN1) inhibitor; induces DNA damage response | |
| 6515 | (D)-PPA 1 |
| PD-1/PD-L1 interaction inhibitor | |
| 6516 | EPZ 015666 |
| Potent and selective PRMT5 inhibitor | |
| 6517 | Liraglutide |
| Highly potent, long-acting GLP-1 receptor agonist | |
| 6518 | BI 01383298 |
| Potent and selective SLC13A5 (Na+/citrate cotransporter) inhibitor | |
| 6520 | Abiraterone acetate |
| Potent CYP17A1 inhibitor | |
| 6521 | I-BET 762 |
| Potent and high affinity BET bromodomain inhibitor; anti-inflammatory; orally bioavailable. | |
| 6524 | TL 12-186 |
| Multikinase Degrader (PROTAC®) | |
| 6525 | TL 13-27 |
| Negative control for TL 12-186 (Cat. No. 6524) | |
| 6526 | Dynarrestin |
| Inhibitor of Hedgehog (Hh) signaling; inhibits cytoplasmic dynein | |
| 6528 | SGC AAK1 1 |
| AAK1 and BMP2K inhibitor; activates Wnt signaling | |
| 6529 | SGC AAK1 1N |
| Negative control for SGC AAK1 1 (Cat.No. 6528) | |
| 6530 | R 121919 hydrochloride |
| High affinity CRF1 antagonist; orally bioavailable | |
| 6531 | NLS-StAx-h |
| Wnt signaling inhibitor; inhibits β-catenin-transcription factor interactions | |
| 6532 | THAL SNS 032 |
| Potent and selective Cdk9 Degrader (PROTAC®) | |
| 6534 | TH 5427 hydrochloride |
| Potent NUDT5 inhibitor | |
| 6535 | NVP 2 |
| Potent and selective ATP-competitive CDK9 inhibitor | |
| 6537 | UNC 2881 |
| Potent Mer kinase inhibitor | |
| 6538 | PF 04449913 maleate |
| Potent Smo antagonist | |
| 6539 | Obatoclax mesylate |
| Inhibitor of Bcl-2 family members; antiapoptotic | |
| 6541 | AZD 2098 |
| Potent and selective CCR4 antagonist | |
| 6542 | Ivabradine hydrochloride |
| HCN channel blocker; inhibits If pacemaker current | |
| 6544 | CID 1375606 |
| GPR27 agonist | |
| 6545 | OB-1 |
| Stomatin-like protein-3 (STOML3) oligomerization inhibitor | |
| 6551 | PAMP-12 (human, porcine) |
| Potent MRGPRX2 agonist | |
| 6552 | PAMP-20 (human) |
| MRGPRX2 agonist; also non-competitive nAChR antagonist | |
| 6555 | TokeOni |
| NIR-emission luciferin analog; ideal for deep tissue applications; orally bioavailable and brain penetrant | |
| 6558 | CP 43 |
| Potent TAOK inhibitor | |
| 6559 | LY 450139 |
| γ-secretase pseudo-inhibitor | |
| 6561 | BAY 6035 |
| Potent and selective SMYD3 inhibitor | |
| 6562 | BAY 707 |
| Potent and selective MTH1 inhibitor | |
| 6564 | SGC GAK 1 |
| High affinity cyclin G associated kinase (GAK) inhibitor | |
| 6568 | Dooku 1 |
| Reversibly blocks Yoda1 activity; does not affect constitutive Piezo1 activity | |
| 6571 | Biotin-11-dUTP |
| Biotin-labeled dUTP | |
| 6572 | Biotin-LC-NAD+ |
| Biotinylated analog of β-NAD+; commonly used reagent in LSD1 and PARP1 assays | |
| 6573 | Biotin-NAD+ |
| Biotinylated-NAD+; substrate for ADP-ribosylation | |
| 6574 | Fluorescein-NAD+ |
| Fluorescent NAD+; substrate for ADP-ribosylation for use in PARP assays | |
| 6576 | ABT 594 hydrochloride |
| Selective α4β2 nAChR agonist | |
| 6577 | Pyridone 6 |
| Potent pan-JAK inhibitor; induces intermediate mesoderm; cell-permeable | |
| 6578 | GT 949 |
| Potent and selective positive allosteric modulator of EAAT2 | |
| 6579 | BAY 826 |
| Potent Tie2 inhibitor | |
| 6580 | PKUMDL WQ 2101 |
| Negative allosteric modulator of 3-phosphoglycerate dehydrogenase (PHGDH) | |
| 6581 | PKUMDL WQ 2201 |
| Negative allosteric modulator of 3-Phosphoglycerate dehydrogenase (PHGDH) | |
| 6583 | UCLA GP130 2 |
| gp130 agonist; brain penetrant and neuroprotectant | |
| 6584 | L-Azidohomoalanine hydrochloride |
| Unnatural amino acid for bio-orthogonal labeling of newly synthesized proteins | |
| 6585 | L-Azidonorleucine hydrochloride |
| Unnatural amino acid for bio-orthogonal or fluorescent labeling of newly synthesized proteins | |
| 6586 | Targapremir 210 |
| Inhibits formation of miR-210 | |
| 6587 | TAK 242 |
| TLR4 signaling inhibitor | |
| 6590 | Janelia Fluor® 646, Maleimide |
| Red dye (Reactive group: maleimide). Application: flow cytometry, confocal microscopy, super resolution microscopy including dSTORM & STED. Suitable for live cell imaging | |
| 6597 | SPRi 3 |
| Potent sepiapterin reductase (SPR) inhibitor; attenuates proliferation of CD4+ T cells | |
| 6599 | Yhhu 3792 |
| Notch signaling pathway activator; enhances the self-renewal capability of NSCs; active in vivo |