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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| 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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