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