| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5311 | Ugm-in-1 | Novel inhibitor of UGM, impeding C. glutamicum growth |
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| DCC5312 | Ugm-in-2 | Novel inhibitor of UGM, impeding C. glutamicum growth |
|
| DCC5313 | Uic-94003 | Novel potent human immunodeficiency virus type 1 (HIV-1) protease inhibito |
|
| DCC5314 | Uk-447841 | Selective NEP inhibitor for treatment of the symptoms of Female sexual arousal disorder (FSAD) |
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| DCC5315 | Uk-505749 | Selective NEP inhibitor for treatment of the symptoms of Female sexual arousal disorder (FSAD) |
|
| DCC5316 | Ukcp-110 | Potent VMAT2 inhibitor |
|
| DCC5317 | Ul-766 | Novel chemically stable fluorescent marker of the ureter |
|
| DCC5318 | Um1024 | Novel Vaccine Adjuvant for Mycobacterium tuberculosis |
|
| DCC5319 | Umb103 | Novel potent and selective dual PLK1 and BRD4 inhibitor, inducing apoptosis in pediatric tumor cell lines, leading to significant tumor regression |
|
| DCC5320 | Umb298 | Novel, Potent, and Selective CBP/P300 Inhibitor |
|
| DCC5321 | Umc160 | Novel Potent and Selective Dual Bromodomain 4 (BRD4)/Polo-like Kinase 1 (PLK1) Inhibitor |
|
| 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 |
|
| 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 |
|
| 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 |
|
| DCC5325 | Unc0737 Featured | UNC0737 is a negative control of UNC0638 and the N-methyl analog of UNC0638. UNC0737 was designed to eliminate the hydrogen bond interaction seen in the G9a-UNC0224 cocrystal structure between Asp1083 of G9a and the secondary amino group at the 4-position of UNC0224's quinazoline ring3. UNC0737 was >300-fold less potent than UNC0638 in G9a and GLP biochemical assays. As expected, UNC0737 was a poor inhibitor of G9a (IC50 = 5,000 ± 200 nM (n = 2)) and GLP (IC50 > 10,000 nM (n = 2)) in the SAHH-coupled assays. |
|
| DCC5326 | Unc0965 | Biotinylated UNC0638, enabling chemiprecipitation of G9a from whole cell lysates |
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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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| DCC5328 | Unc10112749a | Novel inhibitor of ROP18, inhibiting ROP18 within cells, and abrogating its effects on the host IRG pathway |
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| DCC5329 | Unc10245092 | Novel Peptide Inhibitor for Calcium and Integrin Binding Protein 1 (CIB1) |
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| DCC5330 | Unc1653 | Negative control for UNC1666 which is a dual Mer and Flt-3 tyrosine kinase inhibitor |
|
| DCC5331 | Unc32a | Orally Active Adenosine A 1 Receptor Agonist |
|
| DCC5332 | Unc4859 | Novel Ligand of EEDm acting as an allosteric inhibitor of PRC2 |
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| DCC5333 | Unc5114 | Novel allosteric inhibitor of PRC2 catalytic activity |
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| DCC5334 | Unc5115 | Novel allosteric inhibitor of PRC2 catalytic activity |
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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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| DCC5336 | Unc5636 | Novel selective activator of PRC2-EED-I363M, showing minimal effects on the activity of PRC2-WT |
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| DCC5337 | Unc6212 | Novel inhibitor for histone methyllysine reader proteins (KmeRP), targeting CBX5 chromodomain |
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| DCC5338 | Unc6349 | Novel inhibitor for histone methyllysine reader proteins (KmeRP), targeting CBX5 chromodomain |
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| DCC5339 | Unc6641 | Novel peptidomimetic antagonist of the PHF1 Tudor domain, binding both PHF1 Tudor domain and the related protein PHF19 |
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| DCC5340 | Unc6864 | Novel inhibitor for histone methyllysine reader proteins (KmeRP), targeting CBX5 chromodomain |
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