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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC42737 | AMG-511 |
An orally bioavailable, highly potent and selective pan-class I phosphatidylinositol-3 kinase (PI3K) inhibitor
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| DC42732 | L312 |
Novel selective PPARγ modulator (sPPARγM), potently inhibiting CDK5-mediated PPARγ phosphorylation and displaying a selective gene expression profile in epididymal WAT
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| DC42730 | VA5 |
Novel irreversible transglutaminase 2 (TG2) inhibitor
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| DC42726 | GW450863X |
Novel potent and selective inhibitor of mitochondrial respiration supported by pyruvate
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| DC42725 | Symplostatin 4 |
Marine cyanobacterium-derived natural antimalarial agent; Potent Inhibitor of the Food Vacuole Falcipains
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| DC42719 | TDI007635 |
An isomeric anlog of G140 (AOB13353), acting as an inhibitor of h-cGAS (IC 50 = 0.0428µM)
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| DC42717 | DiaAlk |
Novel clickable, electrophilic diazene probe, enabling capture and site-centric proteomic analysis of oxidative post-translational modification (OxiPTM)
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| DC42716 | ABZI-2 |
Novel agonist of STING (stimulator of interferon genes) with enhanced binding to STING and cellular function
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| DC42711 | Quifenadine |
H1-histamine receptor blocker, antiarrhythmic
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| DC42707 | YKL-06-062 |
Novel second-generation SIK inhibitor, inducing not only synthesis of melanin but also melanosomal maturation, export, and localization features, even after import into keratinocytes
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| DC42706 | CP26 |
Novel inhibitor of ER-to-cytosol protein dislocation, exhibiting anti-dengue and anti-Zika virus activity
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| DC42704 | zr17-2 |
The first small molecule modulator of cold inducible RNA-binding protein (CIRBP) activity
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| DC42703 | zr17-2 HCl |
The first small molecule modulator of cold inducible RNA-binding protein (CIRBP) activity
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| DC42702 | SMS2-IN-Ly93 |
Novel potent and selective SMS2 inhibitor, showing more than 1400-fold selectivity over SMS1
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| DC42701 | VISTA modulator 6809-0223 |
Novel immune checkpoint VISTA (V-domain immunoglobulin suppressor of T-cell activation) modulator
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| DC42699 | ML152 |
Potent and selective inhibitor of Galactokinase (GALK)
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| DC42695 | ICI-199441 hydrochloride |
Highly potent κ agonist
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| DC42694 | JNJ-56022486 |
A novel potent and selective negative modulator of AMPA receptors containing TARP-gamma8
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| DC42692 | AZ13581837 |
Novel selective GPR120 agonist
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| DC42690 | JAY2-22-33 |
Novel neuroprotective agent, significantly reducing Aβ toxicity by delaying paralysis and improving cognitive performances in a transgenic mouse model of AD
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| DC42689 | MDL-801 |
Novel activator of SIRT6 deacetylation
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| DC42688 | AI-4-88 |
Inhibitor of CBFβ-RUNX protein-protein interaction
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| DC42687 | G-Glu-Ser |
Activator of calcium receptor; Flavor-enriching agent
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| DC42685 | Pentachloropseudilin |
Selective Myosin-1 (Myo1) inhibitor, suppressing transforming growth factor-β (TGF-β) activity by accelerating cell-surface type II TGF-β receptor turnover in target cells
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| DC42684 | DDD86481 |
Novel potent AfNMT inhibitor, potently inhibiting the NMT mutant and being fungicidal under repressed nmt expression
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| DC42683 | DDD86481 Tosylate |
Novel potent AfNMT inhibitor, potently inhibiting the NMT mutant and being fungicidal under repressed nmt expression
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| DC42682 | X2SS |
Fluorescent indicator for detecting the interaction between RNA and a ligand
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| DC42680 | SB-1317 |
A CDK, JAK and FLT inhibitor
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| DC42679 | AS115 |
Inhibitor of KIAA1363 (or AADACL1)
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| DC42677 | ML145 |
Selective GPR35 antagonist
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