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Cat. No. Product name CAS No.
DCC4911 Sstr5a

Novel somatostatin receptor subtype 5 antagonist, stimulating glucoseinduced GLP-1 secretion, reducing blood glucose in a gut- and GLP-1R-dependent manner

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

5067-25-4
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

96-69-5
DCC4914 St056083

Novel inhibitor of the c-di-AMP synthetase DNA integrity scanning protein (DisA) in vitro

299419-24-2
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

1018143-39-9
DCC4916 st-1032

Novel histamine H3 receptor ligand

DCC4917 St1237

Potent, direct, non-cytotoxic Arachidonate_5-lipoxygenase>5-lipoxygenase (5-LO) inhibitor

1380593-17-8
DCC4918 St-161

Antiviral agent against LASV and a number of other viruses in the Arenaviridae family

DCC4919 St-1703

Novel histamine H3 receptor ligand

DCC4920 St-1892

Novel highly potent and soluble partial FXR agonist

1409411-32-0
DCC4921 St-198

Seletive dopamine D3 receptors

854924-64-4
DCC4922 St-1992

Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)

DCC4923 St-2001

Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)

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

DCC4925 St4070

Highly selective FAAH>fatty acid amide hydrolase (FAAH) inhibitor

1186236-75-8
DCC4926 St7710aa1

Novel PARP-1 inhibitor, showing significant in vitro target inhibition and capability to substantially bypass the multidrug resistance mediated by Pgp

1542067-20-8
DCC4927 Sta-9584

Novel tubulin-binding vascular disrupting agent (VDA)

906481-23-0
DCC4928 Stad-2

Cell permeable AKAP disruptor, selectively binding to PKA-RII and blocking the interaction of PKA-RI with AKAP

1542100-77-5
DCC4929 Stalobacin I

Novel Lipopeptide Antibiotic with Potent Antibacterial Activity against Multidrug-Resistant Bacteria

DCC4930 Stanozolol [10418-03-8]

Anabolic-androgenic steroid (AAS), acting as an agonist of the androgen receptor (AR)

10418-03-8
DCC4931 Stat3 -in-11

Novel STAT3 inhibitor, selectively inhibiting STAT3 phosphorylation and exhibiting potent antitumor activity

DCC4932 stat3 Inhibitor 6

Novel inhibitor of STAT3 signaling pathway

665014-97-1
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