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Cat. No. Product Name Field of Application Chemical Structure
DCC4710 Sh-053-s-ch3-2'f
Potent and selective agonist of GABAA receptors α5 subunit
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DCC4709 Sh-053-r-ch3-2’f
Selective agonist of GABA A receptors α5 subunit
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DCC4708 Sgx393
Novel inhibitor of the CML mutant Bcr-AblT315I, preempting in vitro resistance when combined with nilotinib or dasatinib.
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DCC4707 Sglt1/2-in-8
Novel Potent SGLT1/2 Dual Inhibitor
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DCC4706 Sgk1 Inhibitor 17a
Novel highly selective SGK1 inhibitor with a highly optimized profile suitable for oral dosing as a potentially disease-modifying agent for osteoarthritis
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DCC4705 Sgi-9380
PKM2 activator, potently inhibiting proliferation of cancer cells in media lacking serine
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DCC4704 Sgi-10067
PKM2 activator, potently inhibiting proliferation of cancer cells in media lacking serine
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DCC4703 Sge201
Novel potent allosteric modulator of N-methyl-D-aspartate receptors (NMDAR)
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DCC4702 Sgc-gak-1n
Negative control for SGC-GAK-1 (GLXC-31266)
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DCC4701 Sgc-clk-1
Novel probe for CLK1, CLK2, and CLK4
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DCC4700 Sgc-camkk2-1
Novel probe for CAMKK2/CAMKK1
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DCC4699 Sfti-1
Highly Potent and Selective Plasmin Inhibitor, Attenuating Fibrinolysis in Plasma
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DCC4698 Sfrp-1 Inhibitor-1
Cell-permeable antagonist of secreted frizzled related protein-1(sFRP-1), inhibiting Wnt-3/frizzled interaction and restoring cellular response to Wnt-3 stimulation
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DCC4697 Sfom-0046
Novel anticancer agent, arresting cell cycle in S-phase and causes DNA replication stress leading to the phosphorylation of H2AX into gamma-H2AX
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DCC4696 Sf2535
Novel dual inhibitor of BRD4 and PI3K, inhibiting BRD4, PI3Kα, PI3Kδ, and PI3Kγ with IC 50 values of 277, 714, 27, and 1170 nM, respectively
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DCC4695 Sf-22 (npy Y2 Antagonist)
Potent, selective, and highly brain-penetrant NPY Y2 receptor antagonist
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DCC4694 Sf-1-087
Potent and selective STAT5 inhibitor
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DCC4693 Sew-05929
The First potent SecA inhibitor
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DCC4692 sew05920
Novel telomerase inhibitor
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DCC4691 Seviteronel
Novel potent CYP17 lyase inhibitor, inhibiting androgen production without mineralocorticoid excess or cortisol depletion
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DCC4690 Trichomonacid
Novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro
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DCC4689 Setin-1
The most potent inhibitor of Set7, inhibiting the KMTase G9a
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DCC4688 Sethrrs Inhibitor 36j
The first-in-class triple-site aaRS inhibitor, targeting Salmonella enterica threonyl-tRNA synthetase (SeThrRS) with IC 50 = 19 nM and K d = 35.4 nM
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DCC4687 Setastine
Highly selective H1 receptor antagonist
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DCC4686 Sertaconazole
Cytochrome P450 14α-demethylase inhibitor, also acting as a BuChE-IDO1 inhibitor
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DCC4685 Sert Inhibitor 69419
Novel serotonin reuptake inhibitor
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DCC4684 Ser@tpp@cur
Novel mitochondrial KIM-1 receptor modulator to be specifically internalized by renal tubular epithelial cells via KIM-1 receptor-mediated endocytosis and then actively distributed in mitochondria under the effect of TPP, effectively ameliorating injured
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DCC4683 Sephin1 Hydrochloride
Selective inhibitor of the phosphatase regulatory subunit PPP1R15A (R15A) that prolong the benefit of eIF2α phosphorylation, thereby protecting cells from proteostatic defects
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DCC4682 Se-nsaid-8
Novel selenium-nonsteroidal anti-inflammatory drug (Se-NSAID), inhibiting colorectal cancer (CRC) growth via the inhibition of the cell cycle in G1 and G2/M phases and reduces the cell cycle markers like cyclin E1 and B1 in a dose dependent manner
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DCC4681 Senp1-in-8e
Sentrin-specific protease 1 (SENP1) inhibitor
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