| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4769 | skp Inhibitor C16 | Specific Inhibitor of Skp2-Mediated p27 Degradation |
|
| DCC4770 | skp Inhibitor C20 | Specific Inhibitor of Skp2-Mediated p27 Degradation |
|
| DCC4771 | Skp2 Inhibitor C2 | First-in-class Specific Inhibitor of Skp2-Mediated p27 Degradation |
|
| DCC4772 | Sl-1-73 | Novel microtubule-destabilizing agent, exerting potent antitumor activity against esophageal squamous cell carcinoma |
|
| DCC4773 | Sl-3-19 | Novel microtubule-destabilizing agent, exerting potent antitumor activity against esophageal squamous cell carcinoma |
|
| DCC4774 | Sl-651498 | Full agonist of GABAA receptors containing α2 and α3 subunits, and partial agonist of α1 and α5 subunits. |
|
| DCC4775 | Sl910102 | Novel nonpeptide AT1 receptor antagonist, acting as a modulator on RAAS and KKS activation during COVID-19 |
|
| DCC4776 | Slec-8 | Potential synthetic lethal lead, targeting E-cadherin-deficient cells |
|
| DCC4777 | Slk/stk10-in-31 | Novel Potent Dual inhibitor of SLK (STE20-like kinase) and STK10 (serine/threonine kinase 10) |
|
| DCC4778 | Sll-039 | Novel highly selective and potent κ opioid agonist (κ, Ki = 0.47 nM, κ/μ = 682, κ/δ = 283) |
|
| DCC4779 | Slm6071469 | Novel potent SphK2-selective inhibitor (Ki = 89 nM, 73-fold SphK2-selective) with validated in vivo activity |
|
| DCC4780 | Slp120701 | Novel SphK2-selective inhibitor with improved half-life to 8 h in mice |
|
| DCC4781 | Slp7111228 | Novel selective SphK1 inhibitor |
|
| DCC4782 | Slr080811 | Novel SphK2-selective inhibitor |
|
| DCC4783 | Slupp-225 | Novel efflux pump inhibitor (EPI) |
|
| DCC4784 | Slupp-417 | Novel efflux pump inhibitor (EPI) |
|
| DCC4785 | Sm-130686 | Potent, orally-active agonist of the ghrelin/growth hormone secretagogue receptor (GHSR) and growth hormone secretagogue |
|
| DCC4786 | Sm-131 | Novel Potent, Cell-Permeable, Conformationally Constrained Second Mitochondria Derived Activator of Caspase (Smac) Mimetic |
|
| 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 |
|
| DCC4788 | Sm4487 | Novel potent and selective inhibitor of galactokinase (GALK1) |
|
| DCC4789 | Sma-12b | Novel inhibitor of IL-1 |
|
| DCC4790 | Smac127 | Proapoptotic and anti-inflammatory agent, inducing apoptosis by inhibiting apoptosis proteins (IAPs) |
|
| DCC4791 | Smapp1 | Novel activator of PP1, inducing HIV-1 transcription, reactivation of latent HIV-1 in chronically infected cells, and CDK9 phosphorylation |
|
| DCC4792 | Smart-h | Potent inhibitor of microtubule polymerization |
|
| DCC4793 | Smart-oh | Potent inhibitor of microtubule polymerization |
|
| DCC4794 | Smases D Inhibitor-1 | Novel inhibitor of Loxosceles sphingomyelinases D (SMases D) |
|
| DCC4795 | Smases D Inhibitor-5 | Novel inhibitor of Loxosceles sphingomyelinases D (SMases D) |
|
| DCC4796 | Smcy 5.5 | Fluorogenic fluorescent probe for imaging lipid droplets; suitable for use with two-photon microscopy |
|
| DCC4797 | Smdc818909 | Novel Allosteric Inhibitor of p97 |
|
| DCC4798 | Smer10 | Novel enhancer of the clearance of mutant aggregate-prone proteins by autophagy in mammalian cell models of Huntington's and Parkinson's disease, independent of rapamycin |
|
