All ProductsDisplaying Products by Catalog Number (5600 - 5699)
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Cat. No. | Product Name / Activity |
---|---|
5601 | DMXAA |
mSTING agonist; induces antitumor immunological responses | |
5602 | 6877002 |
CD40-TRAF6 interaction inhibitor | |
5603 | (-)-JQ1 |
Negative control for (+)-JQ1 | |
5604 | MI 14 |
Potent and selective PI 4-kinase IIIβ inhibitor | |
5607 | GNF 7 |
Ras signaling inhibitor; inhibits Ack1 and GCK | |
5608 | BS 181 dihydrochloride |
Selective cdk7 inhibitor | |
5609 | DFHBI |
GFP fluorophore mimic for imaging RNA in living cells; activated by binding Spinach2 and Broccoli aptamers | |
5610 | DFHBI 1T |
GFP fluorophore mimic for imaging RNA in living cells; activated by binding Spinach2 and Broccoli aptamers | |
5611 | Salvinorin B |
Activator of κ-opioid DREADD (KORD) | |
5613 | AZD 9272 |
Potent and selective mGlu5 antagonist; brain penetrant | |
5614 | AZD 2066 |
mGlu5 antagonist; orally bioavailable and brain penetrant | |
5617 | AZD 1480 |
Potent and selective JAK2 inhibitor; antiangiogenic | |
5619 | N-Acetylcysteine amide |
Glutathione (GSH) precursor; neuroprotective | |
5621 | GLPG 0974 |
Potent FFA2 (GPR43) antagonist | |
5622 | HTH 01-015 |
Potent and selective NUAK1 inhibitor | |
5625 | ML 334 |
Inhibitor of Keap1- Nrf2 interaction | |
5626 | SR 7826 |
Potent and selective LIMK inhibitor; antitumor | |
5631 | LDN 193188 |
Inhibitor of phosphatidylcholine transfer protein (PC-TP) | |
5632 | AZ Dyrk1B 33 |
Potent and selective Dyrk1B kinase inhibitor | |
5633 | MRS 2905 |
Potent and selective P2Y14 receptor agonist | |
5636 | GS 143 |
β-TrCP1 ligase inhibitor | |
5641 | MSC 2032964A |
Potent and selective ASK1 inhibitor; orally bioavailable | |
5642 | CMPD101 |
Potent and selective GRK2/3 inhibitor | |
5646 | EML 425 |
Reversible and non-competitive CBP/p300 inhibitor | |
5648 | Hydroxychloroquine sulfate |
Autophagy inhibitor; also TLR9 inhibitor | |
5651 | ONO 6818 |
High affinity and selective human neutrophil elastase 1 (HNE1) inhibitor; orally active | |
5653 | JW 74 |
Wnt pathway inhibitor | |
5654 | BMS 265246 |
Cdk inhibitor; potently inhibits cdk1 and cdk2 | |
5655 | GN 44028 |
Potent HIF-1α inhibitor | |
5656 | DY 268 |
Potent FXR antagonist | |
5658 | AR-C 141990 hydrochloride |
MCT1 inhibitor | |
5661 | 666-15 |
Potent and selective CREB inhibitor | |
5664 | O4I2 |
Oct3/4 inducer; induces expression of pluripotent-associated genes | |
5665 | IRAK1/4 Inhibitor I |
IRAK4 and IRAK1 inhibitor | |
5666 | JNJ 63533054 |
Potent and selective GPR139 agonist | |
5668 | VUF 11222 |
High affinity non-peptide CXCR3 agonist | |
5671 | SB 332235 |
Potent CXCR2 antagonist | |
5672 | GSK 319347A |
Potent and selective IKKε inhibitor | |
5673 | GW 2580 |
Selective cFMS kinase inhibitor; orally bioavailable | |
5674 | GW 501516 |
Potent and selective PPARδ agonist | |
5675 | AZ PFKFB3 26 |
Potent and selective PFKFB3 inhibitor | |
5676 | Guangxitoxin 1E |
Potent Kv2.1 and Kv2.2 channel blocker | |
5678 | RN 9893 hydrochloride |
Potent and selective TRPV4 antagonist | |
5679 | N-Acetylpuromycin |
Downregulates SnoN and Ski protein expression; promotes TGF-β signaling | |
5680 | Vatalanib succinate |
Potent VEGFR inhibitor; also aromatase inhibitor | |
5682 | OSU 03012 |
PDPK1 (PDK1) inhibitor; inhibits Akt signaling | |
5687 | Centrinone |
High affinity and selective PLK4 inhibitor | |
5690 | Centrinone B |
High affinity and selective PLK4 inhibitor | |
5692 | ITH 12575 |
Mitochondrial Na+/Ca2+ exchange (mNCX) inhibitor | |
5693 | VU 0409551 |
Selective positive allosteric modulator of mGlu5 receptors; brain penetrant and orally bioavailable | |
5694 | GSK 2033 |
Potent LXR antagonist | |
5697 | PMX 53c |
Negative control for PMX 53 (Cat. No. 5473) | |
5698 | 1-Methyl-D-tryptophan |
Indoleamine 2,3-dioxygenase (IDO) inhibitor | |
5699 | IP7e |
Potent Nurr1 activator |