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