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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC42614 | UNC7938 |
Novel destabilizer of the endosome membrane, enhancing the endosome-leakage activity of cell-penetrating peptides and facilitating the endosomal escape of macromolecules initially internalized by mammalian cells via endocytosis
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| DC42612 | Glybenclamide Potassium Salt |
Water soluble glyburide, inhibitor of the sulfonylurea receptor 1 (SUR1), regulating subunit of the ATP-sensitive potassium channels (KATP) in pancreatic beta cells
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| DC42610 | Z-VAD-FMK |
Cell-permeable, Irreversible, Non-cytotoxic Pan Caspase Inhibitor
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| DC42608 | IN04 |
Novel inhibitor of LRRK1, suppressing osteoclast function, but not osteoclast differentiation
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| DC42605 | cjoc42 |
Novel inhibitor of the oncoprotein gankyrin, preventing the decrease in p53 protein levels associated with high amounts of gankyrin, restoring p53-dependent transcription and sensitivity to DNA damage
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| DC42603 | GSK205 |
Selective Transient receptor potential vanilloid 4 (TRPV4) antagonist
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| DC42602 | DB-310 |
Novel LMP2 inhibitor as a potential treatment for Alzheimer's disease
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| DC42601 | NC03 |
Novel PI4K2A inhibitor, decreasing the PI4P pools in Golgi and endosomes
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| DC42599 | Quinabactin |
Aba-mimicking agonist, preferentially activating dimeric ABA receptors and possesses ABA-like potency in vivo
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| DC42598 | DC_Y134 |
Novel Selective, Cell Active Inhibitor of Protein Arginine Methyltransferase 5 (PRMT5)
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| DC42597 | PLX4032 |
A selective inhibitor of B-RAF protein kinase carrying V600E mutation
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| DC42595 | LGH447-(1S,3R,5R) |
Less active enantiomer of LGH447 (AOB37522)
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| DC42594 | MLS8969 |
Novel Inhibitor of Human Cytomegalovirus
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| DC42590 | ML075 (SF-11) |
Selective NPY-Y2 Receptor Antagonist
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| DC42589 | CB-83 |
Novel G6PD inhibitor
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| DC42588 | UNC10112785 |
Novel potent inhibitor of CDK8, CDK19, and CDK9 with IC50 at 1.05, 2.67, and 19.9 nM, respectively, causing MYC loss through both transcriptional and posttranslational mechanisms, and suppressing PDAC anchorage-dependent and anchorage-independent growth,
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| DC42585 | RHI002 |
HIV inhibitor, showing selective activity against human RNaseH2
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| DC42584 | CAP-53194 |
Novel potent and selective Plk1 inhibitor
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| DC42582 | ML036 |
Novel potent inhibitor of human cathepsin L
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| DC42581 | EtDO-P4 |
A potent and specific inhibitor of the cerebroside synthase
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| DC42579 | ML206 |
Modulator of Lipid Storage
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| DC42578 | (-)-ML206 |
Less active enantiomer of ML206 (AOB1395), acting as a modulator of lipid storage
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| DC42575 | HyT36(-Cl) (Deschloro-HyT36) |
Control molecule for HyT36 (AOB4848) which is a hydrophobic inducer of the degradation of stabilized proteins
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| DC42569 | HJ-PI01 |
Novel Pim-2 inhibitor, inducing apoptosis and autophagic cell death in triple-negative human breast cancer
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| DC42567 | SC-10 |
PKC activator, stimulating PKC mediated myosin light chain phosphorylation without activating MLC kinase
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| DC42566 | Fluzinamide |
Antiepileptic anticonvulsant, significantly attenuating after discharge durations and the severity of the accompanying convulsive responses
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| DC42564 | Pemafibrate sodium |
Novel selective PPARalpha modulator (SPPARMalpha), improving dyslipidemia, enhancing reverse cholesterol transport and decreasing inflammation and atherosclerosis
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| DC42563 | Varespladib Sodium |
Selective Phospholipase A2 Inhibitor
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| DC42562 | Autogramin-2 |
Novel autophagy inhibitor, selectively targeting cholesterol transfer protein GRAM domain-containing protein 1A (GRAMD1A), and directly competing with cholesterol binding to the GRAMD1A StART domain
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| DC42565 | PF-562271 HCl |
Novel focal adhesion kinase (FAK) inhibitor
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