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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC0146 | 11ß-hsd1 Inhibitor 544 | 
                               Potent inhibitor of both mouse and human 11β-HSD1 
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| DCC0145 | 11-oxo-ete | 
                               Cellular antiproliferative agent, inhibiting BrdU incorporation acrossing multiple cell lines with varying potency 
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| DCC0144 | 11-deoxy-pgf2a | 
                               Selective activator of TREK-2 channels, stimulating DRG c-fiber nociceptor K2P currents and limiting calcium influx 
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| DCC0143 | 10-fthf | 
                               Donor of formyl groups in anabolism used as a substrate in formyltransferase reactions, which is important in purine biosynthesis 
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| DCC0142 | 10074-a4 | 
                               Novel Myc-Max-specific inhibitor 
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| DCC0141 | 1.16-hexadecanedithiol | 
                               Long chain dithiol for self-assembled monolayers (SAMs) in sensors 
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| DCC0140 | 1,4-nhq | 
                               Inhibitor of the Cdc42-PBD interaction, blocking the association of Cdc42 with the PBD 
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| DCC0139 | 1,3,6-trihydroxyxanthone | 
                               Anti-androgenic, Antimicrobial, and anticancer agent 
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| DCC0138 | 1(r)-(trifluoromethyl)oleyl Alcohol | 
                               Novel potent ferroptosis inhibitor 
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| DCC0137 | 0026-59-kk | 
                               Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent 
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| DCC0136 | 002-04-kk | 
                               Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent 
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| DCC0135 | [n9a]lvia | 
                               Novel α-Conotoxin LvIA Analogue, highly selectively trgeting α3β2 nicotinic acetylcholine receptors with >2000-fold higher selectivity than LvIA 
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| DCC0134 | [d-trp]cj-15208 | 
                               Short-duration κ opioid receptor antagonist with weak KOR agonist activity 
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| DCC0133 | [dmt1,5]n/ofq(1-13)-nh2 | 
                               Novel highly potent dual NOP/mu receptor peptide agonist, exerting antitussive effects in an in vivo model of cough 
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| DCC0132 | (z)-5-tetradecen-1-ol | 
                               Novel ligand of the mouse orphan odorant receptor Olfr288 
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| DCC0131 | (wrk)5 | 
                               Novel Antimicrobial Peptide with Repeating Unit against Multidrug-Resistant Bacteria 
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| DCC0130 | (wrk)4 | 
                               Novel Antimicrobial Peptide with Repeating Unit against Multidrug-Resistant Bacteria 
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| DCC0129 | (s)-syaf080 | 
                               Novel Potent Antagonist of the Human A 2B Adenosine Receptor 
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| DCC0128 | (s)-syaf030 | 
                               Novel Potent Antagonist of the Human A 2B Adenosine Receptor 
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| DCC0127 | (s)-retro-1.1 | 
                               Novel potent inhibitor of Shiga toxin (STX) cytotoxicity 
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| DCC0126 | (s)-pomalidomide | 
                               Inhibitor of angiogenesis and growth of B-cell neoplasias, inducing complete regressions of Burkitt's lymphoma cell tumors 
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| DCC0125 | (s)-ncc122 | 
                               Potent D1 dopamine ligand 
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| DCC0124 | (s)-nbp | 
                               More active enantiomer of NBP; Neuroprotective agent used clinically in the acute phase of ischemic stroke, improving functional recovery and promoting angiogenesis and collateral vessel circulation 
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| DCC0123 | (s)-gyramide A | 
                               Novel bacterial DNA gyrase inhibitor, exhibiting antimicrobial activity and inhibiting bacterial cell division 
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| DCC0122 | (s)-fty720 Vinylphosphonate | 
                               Novel allosteric Sphingosine kinase 1 (SK1) inhibitor 
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| DCC0121 | (s)-ftopm | 
                               mGlu5 PAM, displaying intrinsic agonist activity 
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| DCC0120 | (s)-fpopm | 
                               Selective mGlu5 positive allosteric modulator (PAM) 
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| DCC0119 | (s)-folcisteine | 
                               S-Enantiomer of folcisteine, a plant growth regulator 
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| DCC0118 | (s)-esba Hydrochloride | 
                               Selective kynurenine aminotransferase 2 (KAT2) inhibitor 
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| DCC0117 | (s)-desmethyl-nnc112 | 
                               PET precursor for NNC112 
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