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Others

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC4908 SS-thujaplicinol
Inhibitor of the replication of herpes simplex viruses 1 and 2 (HSV-1 and HSV-2)
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DCC4906 Ssr126768a
Novel Selective and Orally Active Oxytocin Receptor Antagonist for the Prevention of Preterm Labor
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DCC4905 SS-nicotinamide Adenine Dinucleotide, Reduced Disodium
Cofactor for mitochondrial deacetylase sirtuin-3 enzyme, regulating energy metabolism and immunity and modulating inflammasome assembly
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DCC4904 SS-nf-jq1
Novel chimeric degrader against bromodomain-containing (BRD) proteins, inducing the interaction of AhR and BRD proteins and displaying effective anticancer activity that correlated with protein knockdown activity
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DCC4903 SS-nf-atra
Novel chimeric degrader against cellular retinoic acid binding proteins (CRABPs), inducing the AhR-dependent degradation of CRABP-1 and CRABP-2 via the ubiquitin-proteasome pathway
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DCC4902 Ssm3 Tfa Salt
Potent furin inhibitor, blocking furin-dependent cell surface processing of anthrax protective antigen-83 in vitro.
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DCC4901 SS-lysine
Elongation factor P (EF-P) fuction modifier
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DCC4900 Ssj-183
Novel antimalarial agent
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DCC4899 SS-hydroxymethyl Chalcone
The first selective inhibitor of Histone Deacetylase 2 (HDAC2)
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DCC4898 SS-elemene
Novel inhibitor of Pak1 activation, anti-cancer ingredient isolated from the Chinese traditional herb Curcuma wenyujin
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DCC4897 SS-cit Tartrate
Non-selective potent dopamine reuptake inhibitor
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DCC4896 SS-cit
Non-selective potent dopamine reuptake inhibitor
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DCC4895 SS-carboline-1-carboxylic Acid
Potent competitive inhibitor of indoleamine 2,3-dioxygenase (IDO)
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DCC4894 SS-amyloid-in-7l
Potent ß-amyloid aggregation inhibitor; Antioxidant
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DCC4893 Ss1020
Novel antiestrogen, lacking estrogenic and genotoxic actions
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DCC4892 Srta-in-i
Novel potent inhibitor of Staphylococcus aureus sortase A (SrtA)
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DCC4891 Srt3190 (2s,3r)
Novel selective CXCR2 antagonist
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DCC4890 Srt3025 Hydrochloride
Novel potent SIRT1 activator
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