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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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