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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC1186 C3001a
Novel selective activator for TREK, against other two-pore domain K (K2P) channels
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DCC1185 c1-resveratrol
Novel multi-functional resveratrol derivative for the treatment of atrial fibrillation
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DCC1184 C15alkopp
FPP analogue, bearing an alkyne group to allow for post-prenylation protein labeling
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DCC1183 C12-pr-spn
Novel broad-spectrum intracellular targeting antibacterial agent, interacting with the 70S ribosome of E. coli and inhibiting its protein synthesis, demonstrating superior clearance of bacteria from the spleen, liver, and kidneys of mice, infected with S.
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DCC1182 C10-pr-spn
Novel broad-spectrum intracellular targeting antibacterial agent, interacting with the 70S ribosome of E. coli and inhibiting its protein synthesis, demonstrating superior clearance of bacteria from the spleen, liver, and kidneys of mice, infected with S.
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DCC1181 C012 Dihydrochloride
Novel sensitizer of BRAF wild-type melanoma cells to vemurafenib, significantly reducing melanoma cell viability, with limited toxicity for normal human fibroblasts
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DCC1180 C000000956
Natural inhibitor of BACE1
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DCC1179 C[pro-arg-phe-phe-asn-ala-phe-dpro]
β-Hairpin Octapeptide, acting as a potent mouse melanocortin-4 receptor (mMC4R) antagonist
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DCC1178 Bzn-ejj-amide
Novel potent and selective PTP-1B inhibitor
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DCC1177 Bz(1,2,4,5)p4
Novel promising spectroscopic probe for inositol 5-phosphatase(s)
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DCC1176 Bxl0124
Novel Gemini vitamin D analog, targeting CD44-STAT3 signaling and inhibiting breast cancer invasion
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DCC1175 Bw284c51
Highly selective inhibitor of AChE
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DCC1174 Bw2258u89
Novel BB2 receptor antagonist. attenuating the feeding responses evoked by exogenous gastrin releasing peptide-29
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DCC1173 bvt-2733 Hydrochloride
Selective 11beta-hydroxysteroid dehydrogenase type 1 (11betaHSD1) inhibitor
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DCC1172 Bvt-116429
Novel 11β-HSD1 inhibitor
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DCC1171 Butylcycloheptyl Prodiginine
Natural inhibitor of microRNA-21, reducing growth of cancer cells
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DCC1170 Butafenacil
Potent inducer of anemia
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DCC1168 Budralazine
Direct-acting vasodilator with anti-tachycardiac effect
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DCC1167 Bucinnazine
Potent and selective agonist of μ-opioid receptor (MOR) with relatively low affinity for the δ-opioid receptor and the κ-opioid receptor
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DCC1165 Btzo-4
Negative control for BTZO-1
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DCC1164 Btz-n3
Novel effective reversible and noncovalent inhibitor of DprE1.
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DCC1163 Btx-yne
Novel unique Na V modulator, acting as a conspicuous outlier, eliminating fast but not slow inactivation
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DCC1162 Btt-3035
Novel inhibitor of alpha2beta1 integrin, decreasing average platelet adhesion in individuals with the C/T807T genotype but not in those harboring C807C
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DCC1161 B-tpmf
The first small-molecule inhibitor with significant selectivity among the KCa2 channel subtypes
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DCC1160 Btk-in-3
Novel potent inhibitor of Bruton’s tyrosine kinase (BTK)
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DCC1159 Btk-in-27
Novel potent and selective covalent inhibitor of Bruton’s tyrosine kinase (BTK), targeting a noncatalytic cysteine residue (Cys481) for covalent bond formation
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DCC1158 Bti-a-404
Novel selective and potent competitive inverse agonist of human GPR43
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DCC1157 Btgh84 Activator I
Novel activator of BtGH84, the first experimentally discovered small molecule activator of a glycoside hydrolase
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DCC1156 btb03195
Novel activator of PC1/3 and inhibitor of PC2
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DCC1155 btb03156
Novel cell-permeable modulator of cellular morphogenesis in yeast and mammalian cells
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