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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC2362 | Gsk207040 |
Novel selective non-imidazole histamine H 3 receptor antagonist
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| DCC2361 | Gsk2008607 |
Novel competitive inhibitor of rTbIPMK with respect to Ins(1,4,5)P3
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| DCC2360 | Gsk1997132b |
Novel potent, metabolically stable and centrally penetrant PPARγ partial agonist
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| DCC2359 | Gsk1910364 |
Novel inhibitor of EPHX2 (epoxide hydrolase 2, alias soluble epoxide hydrolase or sEH), up-regulating cytoprotective genes and down-regulating proinflammatory cytokine production
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| DCC2358 | Gsk189254 |
Potent and selective H3 histamine receptor inverse agonist
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| DCC2357 | Gsk1829820a |
Potent non-cytotoxic inhinitor of Mycobacterium tuberculosis H37Rv
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| DCC2355 | Gsk1723980 |
Novel noncompetitive inhibitor of rTbIPMK
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