All ProductsDisplaying Products by Catalog Number (5700 - 5799)
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| Cat. No. | 产品名称/活性 |
|---|---|
| 5700 | ML 315 hydrochloride |
| Inhibitor of Clk and DYRK kinases | |
| 5702 | DiD perchlorate |
| Lipophilic fluorescent dye. Used for: membrane labeling. Application: fluorescent microscopy, flow cytometry. Suitable for live cell imaging | |
| 5706 | BAY 678 |
| Potent and selective cell-permeable human neutrophil elastase (HNE) inhibitor | |
| 5707 | RA 839 |
| Nrf2 activator; inhibits Nrf2/Keap1 interaction | |
| 5708 | BAY 41-8543 |
| Guanylyl cyclase (sGC) stimulator | |
| 5710 | NFAT inhibitor, Cell Permeable |
| Cell permeable NFAT inhibitor | |
| 5713 | MS 023 dihydrochloride |
| Potent and selective type I PRMT inhibitor | |
| 5714 | S 2101 |
| LSD1 inhibitor | |
| 5715 | (±)-ADX 71743 |
| Negative allosteric modulator of mGlu7 receptors; brain penetrant | |
| 5720 | AR-C 69931 tetrasodium salt |
| Highly potent P2Y12 antagonist | |
| 5722 | Ogerin |
| Selective positive allosteric modulator at GPR68 | |
| 5727 | MC 1742 |
| Potent class I and IIb HDAC inhibitor | |
| 5728 | EXP 3174 |
| Potent and selective AT1 antagonist | |
| 5729 | TASP 0390325 |
| Potent and selective V1B receptor antagonist; orally bioavailable | |
| 5736 | Aphidicolin |
| DNA polymerase α, δ and ε inhibitor | |
| 5737 | BAM 15 |
| Mitochondrial protonophore uncoupler | |
| 5738 | ML 382 |
| MRGPRX1 positive allosteric modulator | |
| 5741 | 25-Hydroxycholesterol |
| Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone | |
| 5742 | AZ PFKFB3 67 |
| Potent and selective PFKFB3 inhibitor | |
| 5744 | NVS-CECR2-1 |
| Potent and selective CECR2 inhibitor | |
| 5746 | NESS 0327 |
| Ultra-high affinity and selective CB1 antagonist | |
| 5747 | Apcin |
| Cdc20 inhibitor; inhibits Cdc20-substrate interaction | |
| 5748 | DAPI |
| Blue-fluorescent DNA stain / dye. Used for: nuclear counterstain, fixed and live-cell staining, assessing apoptosis. Application: flow cytometry, confocal microscopy, immunofluorescence (IHC, ICC), ISH | |
| 5751 | PF 3084014 hydrobromide |
| Potent γ-secretase inhibitor | |
| 5752 | PF 06260933 dihydrochloride |
| MAP4K4 (HGK) inhibitor; also inhibits MINK and TNIK | |
| 5756 | MLi-2 |
| Potent and selective LRRK2 inhibitor | |
| 5757 | Tariquidar dihydrochloride |
| Potent P-glycoprotein (P-gp) inhibitor | |
| 5758 | AGN 193109 |
| High affinity pan-RAR antagonist | |
| 5759 | SW 033291 |
| High affinity 15-PGDH inhibitor; promotes hematopoiesis and hepatocyte proliferation | |
| 5760 | P-3FAX-Neu5Ac |
| Sialic acid analog; sialyltransferase inhibitor | |
| 5763 | (R)-Citalopram oxalate |
| Enantiomer of escitalopram oxalate (Cat. No. 1427) | |
| 5764 | Deferoxamine mesylate |
| Iron chelator; also hypoxia mimetic and neuroprotectant | |
| 5766 | A 971432 |
| Potent and selective S1P5 agonist | |
| 5769 | TM 5275 sodium salt |
| Plasminogen activator inhibitor-1 (PAI-1) inhibitor; orally bioavailable | |
| 5770 | MONNA |
| Potent TMEM16A (Anoctamin-1) blocker | |
| 5772 | Sacubitril calcium |
| Membrane metallo-endopeptidase (neprilysin) inhibitor prodrug; orally bioavailable | |
| 5773 | Akti-1/2 |
| Potent and selective dual Akt1 and 2 inhibitor | |
| 5775 | AZ 6102 |
| Potent TNKS1/2 inhibitor | |
| 5778 | 2-Phospho-L-ascorbic acid trisodium salt |
| Ascorbic acid derivative; maintains differentiation potential in bone marrow-derived MSCs | |
| 5780 | MRT 68921 dihydrochloride |
| ULK inhibitor | |
| 5781 | A 425619 |
| Potent TRPV1 antagonist | |
| 5782 | Phalloidin-FITC |
| Green-fluorescent cytoskeleton stain. Binds and labels F-actin. Used for: F-actin staining. Application: fluorescent microscopy, immunofluorescence (IHC, ICC) | |
| 5783 | Phalloidin-TRITC |
| Red-orange fluorescent cytoskeleton stain. Binds and labels F-actin. Used for: F-actin staining. Application: fluorescent microscopy, immunofluorescence (IHC, ICC) | |
| 5790 | PF 05175157 |
| Potent acetyl-CoA carboxylase (ACC) 1 and 2 inhibitor | |
| 5791 | Bz 423 |
| ATP synthase inhibitor; proapoptotic | |
| 5795 | ATI 2341 |
| CXCR4 allosteric agonist | |
| 5798 | Irbesartan |
| Potent AT1 antagonist |