All ProductsDisplaying Products by Catalog Number (5400 - 5499)
0100020003000400050006000700080009001000110012001300140015001600170018001900200021002200230024002500260027002800290030003100320033003400350036003700380039004000410042004300440045004600470048004900500051005200530054005500560057005800590060006100620063006400650066006700680069007000710072007300740075007600770078007900800081008200830084008500860087008800
| Cat. No. | Product Name / Activity |
|---|---|
| 5400 | (S)-PFI 2 hydrochloride |
| Negative control of (R)-PFI 2 hydrochloride (Cat. No. 4892) | |
| 5401 | GSK 2250665A |
| Itk inhibitor | |
| 5402 | 6bK |
| Insulin degrading enzyme (IDE) inhibitor | |
| 5403 | TAK 960 hydrochloride |
| Potent and selective PLK1 inhibitor | |
| 5406 | ONO 8130 |
| EP1 receptor antagonist | |
| 5408 | Ispinesib |
| High affinity and selective allosteric KSP inhibitor | |
| 5410 | TC-I 2014 |
| Potent TRPM8 antagonist | |
| 5412 | TC AQP1 1 |
| Aquaporin 1 (AQP1) channel blocker | |
| 5413 | WH-4-023 |
| Potent and selective Lck and Src inhibitor; also inhibits SIK | |
| 5414 | CU-T12-9 |
| Potent TLR1/2 agonist | |
| 5417 | BMH 21 |
| RNA polymerase I inhibitor; also p53 pathway activator | |
| 5418 | CYM 5520 |
| Selective S1P2 allosteric agonist | |
| 5422 | XL 184 |
| Potent VEGFR inhibitor; also inhibits other RTKs | |
| 5424 | Deltarasin |
| High affinity PDEδ-KRas interaction inhibitor; binds to PDEδ | |
| 5425 | TGN 020 |
| Aquaporin 4 (AQP4) channel blocker | |
| 5427 | D-Luciferin sodium salt |
| Firefly luciferase substrate; cell permeable. | |
| 5429 | NG 25 |
| TGF-β-activated kinase (TAK1) inhibitor | |
| 5430 | AS 2444697 |
| Potent and selective IRAK4 inhibitor | |
| 5431 | SR 13800 |
| Potent MCT1 inhibitor | |
| 5432 | R 7050 |
| Inhibitor of TNF-α receptor 1 signaling | |
| 5433 | Heclin |
| HECT E3 ubiquitin ligase inhibitor | |
| 5436 | Cyanine 5, SE |
| Red fluorescent dye (Reactive group: NHS ester). Application: confocal microscopy, fluorescence microscopy, flow cytometry | |
| 5438 | NTRC 824 |
| Potent and selective non-peptide NTS2 antagonist | |
| 5440 | FITC |
| Green fluorescent dye | |
| 5443 | AM 6545 |
| High affinity and selective CB1 antagonist | |
| 5445 | SM 324405 |
| Potent TLR7 agonist | |
| 5446 | G 28UCM |
| FASN inhibitor | |
| 5449 | Erastin |
| Mitochondrial VDAC modulator; also Ferroptosis activator | |
| 5450 | XY1 |
| Negative control of SGC 707 (Cat. No. 5367) | |
| 5455 | W 54011 |
| High affinity C5a receptor antagonist | |
| 5456 | Zosuquidar trihydrochloride |
| High affinity P-gp inhibitor | |
| 5457 | SirReal 2 |
| Selective inhibitor of SIRT2 | |
| 5459 | Cytosporone B |
| High affinity Nur77 agonist | |
| 5460 | 968 |
| Allosteric inhibitor of glutaminase | |
| 5461 | Foxy 5 |
| Wnt5a peptide mimetic | |
| 5462 | AAQ chloride |
| Photoswitchable Kv channel blocker | |
| 5465 | BDY FL, SE |
| Green BDY (BODIPY® or boron-dipyrromethene) fluorescent dye supplied with an NHS ester for the labeling of primary amines | |
| 5470 | QAQ dichloride |
| Photoswitchable Nav, Kv and Cav channel blocker | |
| 5471 | CGP 60474 |
| Potent cdk inhibitor | |
| 5472 | CGP 74514 dihydrochloride |
| Potent CDK1 inhibitor | |
| 5473 | PMX 53 |
| Potent C5a receptor antagonist | |
| 5474 | Cytochalasin B |
| Inhibitor of actin polymerization | |
| 5476 | Cell Activation Cocktail 500X |
| Cell activation cocktail | |
| 5479 | CRID3 sodium salt |
| Potent NLRP3 inflammasome inhibitor; inhibits IL-1β production | |
| 5480 | KRIBB11 |
| HSF1 inhibitor | |
| 5485 | GlyH 101 |
| Reversible, voltage-dependent CFTR chloride channel blocker | |
| 5488 | BML 111 |
| FPR2 (lipoxin A4 receptor) agonist | |
| 5490 | 5J 4 |
| CRAC channel blocker; anti-inflammatory | |
| 5491 | Aliskiren hemifumarate |
| Potent renin inhibitor; antihypertensive | |
| 5492 | BMS 566419 |
| Inosine monophosphatase dehydrogenase (IMPDH) inhibitor | |
| 5493 | XL 413 hydrochloride |
| Potent and selective Cdc7 inhibitor | |
| 5494 | R 547 |
| Potent and selective cdk inhibitor; orally bioavailable | |
| 5495 | CW 008 |
| PKA signaling activator; promotes osteogenesis from hMSCs | |
| 5496 | LP 99 |
| Selective BRD7 and BRD9 inhibitor | |
| 5497 | ent-LP 99 |
| Negative Control for LP 99 | |
| 5498 | AP 811 |
| High affinity, selective NPR3 antagonist |