Cat. No. | Product Name | Field of Application | Chemical Structure |
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DC42765 | Soyasaponin Be |
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DC42764 | Soyasaponin Bd |
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DC42763 | Quassin |
Natural potent male antifertility agent
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DC42761 | JNJ-64619178 |
Novel potent and selective PRMT5 inhibitor, demonstrating tumor regression in a biomarker-driven human small cell lung cancer
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DC42760 | CPUY201112 |
Novel inhibitor of heat shock protein Hsp90, inducing p53-mediated apoptosis in MCF-7 cells
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DC42757 | Cipemastat (Ro 32-3555) |
Selective MMP-1 inhibitor
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DC42756 | Valbenazine Tosylate |
Novel inhibitor of the vesicular monoamine transporter 2 (VMAT2)
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DC42755 | UBP141 |
Novel NR2D-preferring antagonist inhibiting NMDA-EPSCs
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DC42753 | Annonacin |
Annonacin is a potent and lipophilic acetogenin from A. muricata that inhibits mitochondrial complex I (IC50 = 54.8 nM).1,2 Annonacin induces ATP depletion, tau pathologies, and dopaminergic cell death in rats (EC50s = 134, 44.1, and 60.8 nM, respectively
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DC42751 | CID-85469571 |
The first selective antagonist of orphan receptor GPR18
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DC42746 | BRD-K25923209 |
Novel inhibitor of BAF transcriptional repression
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DC42743 | NIM-7 |
The novel fluorescent probe, allowing lipid droplets and lysosomes to be labelled simultaneously and with high specificity, being visualized readily through yellow and red fluorescence, using different excitation and detection channels
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DC42742 | KNK423 |
Heat shock protein inhibitor, preventing the synthesis of inducible Hsps, such as Hsp105, Hsp72, and Hsp40, reducing thermotolerance of tumors in SCC VII tumor-containing mice
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DC42741 | F0911-7667 (HMS607P03) |
Novel activator of SIRT1, inducing autophagic cell death via the AMPK-mTOR-ULK complex and inducing mitophagy by the SIRT1-PINK1-Parkin pathway, downregulating 14-3-3γ, catalase, profilin-1, and HSP90α
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DC42740 | Psammaplysene A |
Naturally occurring inhibitor of FOXO1a nuclear export
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DC42739 | CPI-169 (R) |
Novel and potent EZH2 inhibitor
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DC42738 | A-331440 dihydrochloride |
Potent histamine H3 receptor antagonist
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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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