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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2393 | Gsk4028 |
Negative control for GSK4027
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| DCC2392 | Gsk-3ß/hdac Inhibitor C11 |
First-in-Class GSK-3β/HDAC Dual Inhibitor as a Disease-Modifying Agent To Combat Alzheimer’s Disease
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| DCC2391 | Gsk3-in-40 |
Potent and irreversible inhibitor of GSK3
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| DCC2389 | Gsk3i Xv |
Novel highly potent cell-permeable, reversible, ATP-competitive inhibitor of GSK-3 (IC50 = 0.4 and 0.6 nM for GSK-3α and GSK-3β, respectively)
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| DCC2388 | Gsk3830052 |
Novel DNMT1-selective inhibitor (IC 50 = 0.11 ± 0.02 µM)
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| DCC2387 | Gsk366a |
Novel anti-TB agent against Mycobacterium tuberculosis and Mycobacterium bovis BCG, targeting MmpL3 and inhibiting EchA6
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| DCC2386 | Gsk360a |
Novel inhibitor of prolyl hydroxylase (PHD) domain-containing enzyme
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| DCC2385 | Gsk-354 |
Novel lysine specific histone demethylase 1 (LSD1) inhibitor, exhibiting high selectivity to LSD1 over MAOs
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| DCC2384 | Gsk334429 |
Novel selective non-imidazole histamine H 3 receptor antagonist
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| DCC2383 | Gsk3277329 |
Novel agonist of toll-like receptor 2 (TLR2), stimulating the release of G-CSF in activated THP-1 cells, peripheral blood mononuclear cells, and human umbilical vein endothelial cells
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| DCC2382 | Gsk3182571 |
Promiscuous kinase inhibitor, a close analog of CTx-0294885
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| DCC2381 | Gsk317354a |
Novel selective inhibitor of G protein-coupled receptor kinase 2 (GRK2)
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| DCC2380 | gsk314181a |
Potent and selective antagonist of P2X7 receptor
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| DCC2379 | Gsk3038548a |
Novel potent RORγ inverse agonist
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| DCC2378 | Gsk-3008348-n1-methyl |
Novel quaternized GSK-3008348 derivative, acting as a highly selective αvβ6 Integrin Inhibitor
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| DCC2377 | Gsk299115a |
Novel inhbitor of protein kinase GRK1/2/5 and PKA
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| DCC2376 | Gsk2838232 |
Novel human immune virus (HIV) maturation inhibitor
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| DCC2375 | Gsk-2807 |
Novel potent and selective, SAM-competitive inhibitor of SMYD3
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| DCC2374 | Gsk270822a |
Novel selective inhibitor of G protein-coupled receptor kinase 2 (GRK2)
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| DCC2373 | Gsk2565363c |
Betulin derivative as antitumor agent
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| DCC2372 | Gsk246053 |
Specific ATPase competitive kinesin-5 inhibitor
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| DCC2371 | Gsk-239512 |
Novel selective histamine H3 receptor antagonist
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| DCC2370 | Gsk237701a |
Novel I-kappa-B kinase-3 (IKK3) inhibitor
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| DCC2369 | Gsk2263167 |
Novel S1P1 receptor agonist
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| DCC2368 | Gsk2256294a |
Novel highly potent, reversible soluble epoxide hydrolase (sEH) inhibitor, exhibiting potent cell-based activity, a concentration-dependent inhibition of the conversion of 14,15-EET to 14,15-DHET, attenuating cigarette smoke-induced inflammation by both i
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| DCC2367 | Gsk223 |
Selective inhibitor of iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway
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| DCC2366 | Gsk2220400a |
Inhibitor of insulin receptor, also tageting IGF-1R and ALK
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| DCC2365 | Gsk2188764 |
Novel inhibitor of T. brucei IPMK, partially inhibiting rTbIPMK activity
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| DCC2364 | Gsk2163632a |
Novel insulin-like growth factor 1 receptor inhibitor, binding to a novel region of the GRK active site cleft that could likely be exploited to achieve more selectivity
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| DCC2363 | Gsk2141795 Hydrochloride |
Novel AKT Inhibitor, Enhancing Anti-Tumor Effects in Combination with the MEK Inhibitor
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