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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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
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| DCC4797 | Smdc818909 |
Novel Allosteric Inhibitor of p97
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| DCC4796 | Smcy 5.5 |
Fluorogenic fluorescent probe for imaging lipid droplets; suitable for use with two-photon microscopy
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| DCC4795 | Smases D Inhibitor-5 |
Novel inhibitor of Loxosceles sphingomyelinases D (SMases D)
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| DCC4794 | Smases D Inhibitor-1 |
Novel inhibitor of Loxosceles sphingomyelinases D (SMases D)
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| DCC4793 | Smart-oh |
Potent inhibitor of microtubule polymerization
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| DCC4792 | Smart-h |
Potent inhibitor of microtubule polymerization
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| DCC4791 | Smapp1 |
Novel activator of PP1, inducing HIV-1 transcription, reactivation of latent HIV-1 in chronically infected cells, and CDK9 phosphorylation
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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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