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Cat. No. Product Name Field of Application Chemical Structure
DCC4938 Stat5b-in-6a
Highly Potent and Selective Inhibitor of the Transcription Factor STAT5b
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DCC4937 Stat5a-in-27
Novel cell-permeable selective STAT5a inhibitor prodrug, inhibiting tyrosine phosphorylation of STAT5a with selectivity over STAT5b in cultured human leukemia cells, and representing a valuable tool to define the non-redundant molecular functions of the t
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DCC4936 Stat3-in-b9
Novel inhibitor of signal transducer and activator of transcription 3 (STAT3), inhibiting the proliferation of tumor cells harboring abnormal activation of STAT3, such as, MDA-MB-468, MDA-MB-231 and DU145
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DCC4935 Stat3-in-a69
Novel inhibitor targeting the DNA-binding domain of STAT3, suppressing tumor growth, metastasis and STAT3 target gene expression in vivo
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DCC4934 Stat3-in-3
Novel potent and selective inhibitor of STAT3
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DCC4933 Stat3-in-13r
Novel inhibitor of STAT3, targeting SH2 domain
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DCC4932 stat3 Inhibitor 6
Novel inhibitor of STAT3 signaling pathway
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DCC4931 Stat3 -in-11
Novel STAT3 inhibitor, selectively inhibiting STAT3 phosphorylation and exhibiting potent antitumor activity
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DCC4930 Stanozolol [10418-03-8]
Anabolic-androgenic steroid (AAS), acting as an agonist of the androgen receptor (AR)
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DCC4929 Stalobacin I
Novel Lipopeptide Antibiotic with Potent Antibacterial Activity against Multidrug-Resistant Bacteria
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DCC4928 Stad-2
Cell permeable AKAP disruptor, selectively binding to PKA-RII and blocking the interaction of PKA-RI with AKAP
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DCC4927 Sta-9584
Novel tubulin-binding vascular disrupting agent (VDA)
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DCC4926 St7710aa1
Novel PARP-1 inhibitor, showing significant in vitro target inhibition and capability to substantially bypass the multidrug resistance mediated by Pgp
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DCC4925 St4070
Highly selective FAAH>fatty acid amide hydrolase (FAAH) inhibitor
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DCC4924 St-2262
Novel selective NaV1.7 inhibitor, blocking the extracellular vestibule of the channel with an IC50 of 72 nM and greater than 200-fold selectivity over off-target sodium channel isoforms, NaV1.1-1.6 and NaV1.8
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DCC4923 St-2001
Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)
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DCC4922 St-1992
Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)
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DCC4921 St-198
Seletive dopamine D3 receptors
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DCC4920 St-1892
Novel highly potent and soluble partial FXR agonist
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DCC4919 St-1703
Novel histamine H3 receptor ligand
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DCC4918 St-161
Antiviral agent against LASV and a number of other viruses in the Arenaviridae family
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DCC4917 St1237
Potent, direct, non-cytotoxic Arachidonate_5-lipoxygenase>5-lipoxygenase (5-LO) inhibitor
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DCC4916 st-1032
Novel histamine H3 receptor ligand
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DCC4915 St101036
Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs
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DCC4914 St056083
Novel inhibitor of the c-di-AMP synthetase DNA integrity scanning protein (DisA) in vitro
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DCC4913 St029248
Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs
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DCC4912 St026567
Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs
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DCC4911 Sstr5a
Novel somatostatin receptor subtype 5 antagonist, stimulating glucoseinduced GLP-1 secretion, reducing blood glucose in a gut- and GLP-1R-dependent manner
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DCC4910 Sstr3-antagonist-3a
Novel potent sstr3 antagonist, showing to reduce glucose excursion in a mouse oGTT assay
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DCC4909 Sstr3-agonist-5c
Novel non-peptidic highly potent somatostatin receptor 3 (SSTR3) agonist
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