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Cat. No. Product Name Field of Application Chemical Structure
DCC4952 Stock1n-65837
Potent natural modulator of human Toll-like receptor 7 (TLR7)
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DCC4951 Stk683963
Novel activator of cellular ATG4B activity
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DCC4950 Stk630921
Novel blocker of IL-17A binding to the IL-17A receptor (IL-17RA)
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DCC4949 Stk508411
Novel inhibitor of the heterogeneous ribonuclear protein A18 (hnRNP A18)
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DCC4948 Stk295900
Dual inhibitor of topoisomerase 1 and 2, inducing G(2) arrest in the absence of DNA damage. Inhibitor of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay
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DCC4947 Stk-22
Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor
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DCC4946 Stk-15
Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor
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DCC4945 Sting Inhibitor C-171
Novel covalent antagonist of hsSTING
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DCC4944 Sting Agonist 11
Novel non-nucleotide STING agonist, demonstrating antitumor activity when dosed intratumorally in a syngeneic mouse model
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DCC4943 Stictic Acid
Natural anti-feline infectious peritonitis virus (FIPV) agent, specifically targeting the 3CLpro of FIPV and inhibiting its replication
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DCC4942 Stg -001
Novel RBP4 antagonist for treatment of Stargardt disease
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DCC4941 Stf-038533
Novel inhibitor of expression from canonical CREB response element-containing promoters
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DCC4940 Sterigmatocystin
Natural inducer of G1 arrest in primary human esophageal epithelial cells but G2 arrest in immortalized cells
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DCC4939 Stemazole
Novel human stem/progenitor cells proliferation activator, promoting survival and preserving stemness in human embryonic stem cells
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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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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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