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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC2687 Imp-1700
Novel cell-active and potent inhibitor of bacterial DNA repair, potentiating quinolone antibiotic activity in methicillin-resistant Staphylococcus aureus
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DCC2686 Imp-1002
Novel resistance breaking antimalarial N-myristoyltransferase (NMT) inhibitor, binding to NMT peptide binding pocket
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DCC2685 Imm-h004
Novel potent inhibitor of BV2 microglia activation, protecting PC12 cells and primary neurons against indirect toxicity mediated by exposure to conditioned medium (CM) from LPS-treated BV2 cells
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DCC2684 Imidacloprid
Insect neurotoxin, blocking nicotinic acetylcholine receptors and preventing acetylcholine from transmitting impulses between nerves
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DCC2683 Imc-76
BCL2 i-motif-interactive compound, destabilizing or unfolding the i-motif
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DCC2682 Imc-48
BCL2 i-motif-interactive compound, stabilizing or facilitating the folding of the i-motif
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DCC2681 Imb-yh-8
Novel inhibitor of protein kinase B (PknB), inhibiting PknB auto-phosphorylation and the phosphorylation of GarA by PknB in a dose-dependent manner
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DCC2680 Imb-xma0038
Novel anti-tuberculosis agent, targeting Mycobacterial tuberculosis (Mtb) aspartate semialdehyde dehydrogenase
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DCC2679 Imarikiren Dihydrochloride
Novel orally effective direct renin inhibitor for treating diabetic nephropathy and hypertension
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DCC2678 Iloperidone Hydrochloride
Dual D 2 /5-HT 2 antagonist as an antipsychotic agent
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DCC2677 Ilmofosine
Antineoplastic phospholipid, being effective against many tumor types, including ovary, non-small cell lung, kidney, and melanoma, exhibiting competitive inhibition of protein kinase C (PKC) activity
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DCC2676 Ikkß-in-124
Novel allosteric inhibitor of IκBα phosphorylation and NF-κB transcriptional activity through selective capture of the inactive conformation and hence blockade of IKKβ S177/S181 phosphorylation
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DCC2675 Ikarugamycin
Natural Inhibitor of Clathrin-Mediated Endocytosis
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DCC2674 Ihr-saha
Novel dual SMO-HDAC antagonist, retaining similar specificity for SAHA-targeted HDACs, disabling deviant Hedgehog signaling and preventing GLI binding to DNA
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DCC2673 Iglu-antagonist-21a
Highly potent fluorescent iGlu receptor antagonist
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DCC2672 Igf2bp2/imp2 Inhibitor 9
Novel Inhibitor of RNA-Binding Protein IGF2BP2/IMP2 for Cancer Therapy
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DCC2671 Igf2bp2/imp2 Inhibitor 6
Novel Inhibitor of RNA-Binding Protein IGF2BP2/IMP2 for Cancer Therapy
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DCC2670 Igf2bp2/imp2 Inhibitor 4
First Small-Molecule Inhibitor of RNA-Binding Protein IGF2BP2/IMP2 for Cancer Therapy
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DCC2669 Ifn-1 Inducer L56
Novel Type I Interferon Inducer; Intercalator of DNA; Inhibitor of the retrovirus replications including HIV
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DCC2668 Ifn-1 Inducer E51
Novel Type I Interferon Inducer
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DCC2667 Ifn-1 Inducer C3
Novel Type I Interferon Inducer
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DCC2666 Iferanserin
Selective serotonin 5-HT2A receptor antagonist
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DCC2665 Idrapril
Angiotensin converting enzyme (ACE) inhibitor
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DCC2664 Idr-1018 Tfa Salt
Novel immunomodulatory and antibiofilm innate defense regulator peptide
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DCC2663 Idr-1002
Innate Defence Regulator Peptide, Enhancing Monocyte Migration and Adhesion on Fibronectin
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DCC2662 Idr-0099118
Novel concentration dependent bactericidal agent against M. tuberculosis, being markedly more efficient at killing M. tuberculosis under acidic conditions
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DCC2661 Idr-0081053
Novel bactericidal agent against M. tuberculosis under acidic conditions, being effective at sterilizing cultures in a concentration-dependent fashion at the highest concentrations
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DCC2660 idoxifene
Selective ER modulator (SERM)
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DCC2659 Ido1/2 Inhibitor 4t
The first inhibitor targeting both IDO1/2 that has excellent in vitro inhibitory activity (IDO1 IC50 = 28 nM and IDO2 IC50 = 144 nM)
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DCC2658 Idi-3783
Novel mutant-selective Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) inhibitor
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