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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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