Cat. No. | Product Name | Field of Application | Chemical Structure |
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DCC4790 | Smac127 |
Proapoptotic and anti-inflammatory agent, inducing apoptosis by inhibiting apoptosis proteins (IAPs)
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DCC4789 | Sma-12b |
Novel inhibitor of IL-1
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DCC4788 | Sm4487 |
Novel potent and selective inhibitor of galactokinase (GALK1)
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DCC4787 | Sm-337 |
Non-peptidic Smac mimetic, binding to XIAP, cIAP-1 and cIAP-2 proteins with higher affinities in cell growth inhibition in the MDA-MB-231 cell line
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DCC4786 | Sm-131 |
Novel Potent, Cell-Permeable, Conformationally Constrained Second Mitochondria Derived Activator of Caspase (Smac) Mimetic
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DCC4785 | Sm-130686 |
Potent, orally-active agonist of the ghrelin/growth hormone secretagogue receptor (GHSR) and growth hormone secretagogue
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DCC4784 | Slupp-417 |
Novel efflux pump inhibitor (EPI)
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DCC4783 | Slupp-225 |
Novel efflux pump inhibitor (EPI)
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DCC4782 | Slr080811 |
Novel SphK2-selective inhibitor
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DCC4781 | Slp7111228 |
Novel selective SphK1 inhibitor
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DCC4780 | Slp120701 |
Novel SphK2-selective inhibitor with improved half-life to 8 h in mice
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DCC4779 | Slm6071469 |
Novel potent SphK2-selective inhibitor (Ki = 89 nM, 73-fold SphK2-selective) with validated in vivo activity
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DCC4778 | Sll-039 |
Novel highly selective and potent κ opioid agonist (κ, Ki = 0.47 nM, κ/μ = 682, κ/δ = 283)
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DCC4777 | Slk/stk10-in-31 |
Novel Potent Dual inhibitor of SLK (STE20-like kinase) and STK10 (serine/threonine kinase 10)
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DCC4776 | Slec-8 |
Potential synthetic lethal lead, targeting E-cadherin-deficient cells
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DCC4775 | Sl910102 |
Novel nonpeptide AT1 receptor antagonist, acting as a modulator on RAAS and KKS activation during COVID-19
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DCC4774 | Sl-651498 |
Full agonist of GABAA receptors containing α2 and α3 subunits, and partial agonist of α1 and α5 subunits.
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DCC4773 | Sl-3-19 |
Novel microtubule-destabilizing agent, exerting potent antitumor activity against esophageal squamous cell carcinoma
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DCC4772 | Sl-1-73 |
Novel microtubule-destabilizing agent, exerting potent antitumor activity against esophageal squamous cell carcinoma
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DCC4771 | Skp2 Inhibitor C2 |
First-in-class Specific Inhibitor of Skp2-Mediated p27 Degradation
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DCC4770 | skp Inhibitor C20 |
Specific Inhibitor of Skp2-Mediated p27 Degradation
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DCC4769 | skp Inhibitor C16 |
Specific Inhibitor of Skp2-Mediated p27 Degradation
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DCC4768 | Skog102 |
Novel inhibitor of OLIG2 in glioblastoma
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DCC4767 | Sklb70326 |
Novel inhibitor of cell-cycle progression, inducing G0/G1 phase arrest and apoptosis in human hepatic carcinoma cells
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DCC4766 | Sklb-677 |
Novel FLT3 and Wnt/β-catenin signaling inhibitor, displaying potent activity in models of FLT3-driven AML
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DCC4765 | Sklb-329 |
Novel multikinase inhibitor, potently inhibiting angiogenesis-related kinases including VEGFR1/2/3, and FGFR2, and the Src kinase
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DCC4764 | Sklb-163 |
Potent anticancer agent, downregulating RhoGDI, activating JNK-1 signaling pathway and caspase-3, and reducing phosphorylated Akt and p44/42 MAPK
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DCC4763 | Sklb050 |
Biological Active Reagents
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DCC4762 | Sklb028 |
Millepachine analog, inhibiting tubulin polymerization by irreversibly binding to the colchicine-binding site in β-tubulin
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DCC4761 | sklb023 |
Novel inhibitor of NF
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