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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1212 | Capreomycin |
Broad spectrum antibiotic used in the therapy of drug resistant tuberculosis as a second line agent
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| DCC1211 | Capravirine |
Reverse-transcriptase_inhibitor>Non-nucleoside reverse transcriptase inhibitor
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| DCC1210 | Cap Kl1 |
Novel self-assembling lysine-rich cationic amphipathic peptide (CAP)
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| DCC1209 | Cannabigerovarinic Acid |
Natural cannabinoid precursor
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| DCC1208 | Cannabigerolic Acid |
Natural cannabinoid precursor
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| DCC1207 | Cand1-cullin1 Destabilizer C60 |
Novel destabilizer of CAND1-Cullin1 interaction, inducing a p53-stress response pathway
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| DCC1206 | Camostat |
Transmembrane protease serine 2 (TMPRSS2) inhibitor for the treatment of chronic pancreatitis and postoperative gastric reflux, blocking SARS-CoV-2 replication in TMPRSS2-expressing human cells
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| DCC1205 | Calcium Ionophore A23187 |
Ionophore highly selective for Ca , potentiating responses to NMDA but not quisqualate
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| DCC1204 | Calcium Dibesilate |
Dual inhibitor of fibroblast growth factors (FGF) and vascular endothelial growth factor (VEGF) ; Anti-angiogenic
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| DCC1202 | cal-130 |
Novel inhibitor of p110
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| DCC1201 | Ca-in-5g |
Effective inhibitor of the carbonic anhydrase (CA) from Trypanosoma cruzi (TcCA)
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| DCC1200 | caged Gc-1 |
Potent agonist at thyroid hormone receptor (TR)
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| DCC1199 | Caged Az-13767370 |
Novel photocaged ERK1/2 inhibitor as a light-controlled anticancer agent
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| DCC1198 | Cacc(inh)-b01 |
Potent, selective class B inhibitor of calcium-activated chloride channels (CaCCs)
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| DCC1197 | Cabdf1 Bd2 Inhibitor-2 |
Novel selective CaBdf1 BD2 inhibitor
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| DCC1196 | Cabdf1 Bd1 Inhibitor 3 |
Novel inhibitor of CaBdf1 BD1 with low-micromolar affinity and three- to fivefold selectivity relative to human Brd4 BD1
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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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