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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC1195 | Cabdf1 Bd1 Inhibitor 1 | 
                               Novel selective CaBdf1 BD1 inhibitor 
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| DCC1194 | Caa0225 | 
                               Novel specific inhibitor of cathepsin L, effectively inhibiting degradation of LC3-II and GABARAP 
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| DCC1193 | Ca-074 | 
                               Potent and selective inhibitor of cathepsin B 
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| DCC1192 | Ca Ix/xii Inhibitor | 
                               Selective inhibitor of hCA IX and hCA XII 
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| DCC1191 | C5-chem-clip | 
                               Novel covalent cross-linker to the SARS-CoV-2 frameshifting element (FSE), directly targeting engagement of the SARS-CoV-2 FSE in cells, dose dependently reducing frameshifting in cells expressing the SARS-CoV-2 FSE, with no significant effect on frameshi 
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| DCC1190 | C562-1101 | 
                               Novel potent inhibitor of botulinum neurotoxin serotype E (BoNT/E) 
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| DCC1189 | C48/80 | 
                               Inducer of mast cell degranulation 
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| DCC1188 | C3b Inhibitor Cmp-5 | 
                               The first C3b-binding complement inhibitor, inhibiting the formation of the membrane attack complex (MAC) by preventing cleavage of C5 
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| DCC1187 | C3-005 | 
                               First-In-Class Inhibitor of the Interaction between Bacterial RNA Polymerase and Sigma Initiation Factor, Affecting the Viability and Toxin Release of Streptococcus pneumoniae 
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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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