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Cat. No. Product Name Field of Application Chemical Structure
DCC5338 Unc6349
Novel inhibitor for histone methyllysine reader proteins (KmeRP), targeting CBX5 chromodomain
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DCC5337 Unc6212
Novel inhibitor for histone methyllysine reader proteins (KmeRP), targeting CBX5 chromodomain
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DCC5336 Unc5636
Novel selective activator of PRC2-EED-I363M, showing minimal effects on the activity of PRC2-WT
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DCC5335 Unc5635
Novel selective activator of PRC2-EED-I363M, showing minimal effects on the activity of PRC2-WT
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DCC5334 Unc5115
Novel allosteric inhibitor of PRC2 catalytic activity
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DCC5333 Unc5114
Novel allosteric inhibitor of PRC2 catalytic activity
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DCC5332 Unc4859
Novel Ligand of EEDm acting as an allosteric inhibitor of PRC2
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DCC5331 Unc32a
Orally Active Adenosine A 1 Receptor Agonist
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DCC5330 Unc1653
Negative control for UNC1666 which is a dual Mer and Flt-3 tyrosine kinase inhibitor
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DCC5329 Unc10245092
Novel Peptide Inhibitor for Calcium and Integrin Binding Protein 1 (CIB1)
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DCC5328 Unc10112749a
Novel inhibitor of ROP18, inhibiting ROP18 within cells, and abrogating its effects on the host IRG pathway
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DCC5327 Unc10112731
Novel MYC protein stablizer, increasing the abundance of endogenous MYC proteintargeting the receptor tyrosine kinases KIT and platelet-derived growth factor receptor α (PDGFRα)
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DCC5326 Unc0965
Biotinylated UNC0638, enabling chemiprecipitation of G9a from whole cell lysates
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DCC5324 Unbs3157
Novel nonhematotoxic DNA intercalating agent with potent antitumor activity, inducing apoptosis via inhibition of key proteins in the PI3K/Akt/mTOR signaling pathway
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DCC5323 Unag Ligand
Novel fluorescent UnaG ligand, binding UnaG with high affinity (Kd = 3 nM) to induce a 2.5-fold fluorescence intensity enhancement and a 10 nm red shift
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DCC5322 Um-c162
Novel anti-virulence agent, rescuing nematodes from a Staphylococcus aureus infection and preventing the formation of biofilm in a dose-dependent manner without interfering with bacterial viability
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DCC5321 Umc160
Novel Potent and Selective Dual Bromodomain 4 (BRD4)/Polo-like Kinase 1 (PLK1) Inhibitor
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DCC5320 Umb298
Novel, Potent, and Selective CBP/P300 Inhibitor
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DCC5319 Umb103
Novel potent and selective dual PLK1 and BRD4 inhibitor, inducing apoptosis in pediatric tumor cell lines, leading to significant tumor regression
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DCC5318 Um1024
Novel Vaccine Adjuvant for Mycobacterium tuberculosis
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DCC5317 Ul-766
Novel chemically stable fluorescent marker of the ureter
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DCC5316 Ukcp-110
Potent VMAT2 inhibitor
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DCC5315 Uk-505749
Selective NEP inhibitor for treatment of the symptoms of Female sexual arousal disorder (FSAD)
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DCC5314 Uk-447841
Selective NEP inhibitor for treatment of the symptoms of Female sexual arousal disorder (FSAD)
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DCC5313 Uic-94003
Novel potent human immunodeficiency virus type 1 (HIV-1) protease inhibito
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DCC5312 Ugm-in-2
Novel inhibitor of UGM, impeding C. glutamicum growth
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DCC5311 Ugm-in-1
Novel inhibitor of UGM, impeding C. glutamicum growth
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DCC5310 Ufr2709
Novel Nicotinic Acetylcholine Receptor Antagonist, Inhibiting Nicotine Reward and Decreases Anxiety and Decreasing Ethanol Intake in Alcohol-Preferring Rats
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DCC5309 Ufp512
Novel selective delta-opioid receptor agonist
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DCC5308 Ue2316
Potent and selective 11ß-HSD1 inhibitor, improving memory, including after intracerebroventricular drug administration to the central nervous system alone
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