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Cat. No. Product Name Field of Application Chemical Structure
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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DCC2657 Idh2 Inhibitor
Novel isocitrate dehydrogenase 2 (IDH2) mutants inhibitor for the treatment of cancer
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DCC2656 Ide-in-63 Tfa Salt
Novel highly potent substrate-selective inhibitor of insulin-degrading enzyme (IDE), blocking insulin binding while allowing glucagon cleavage, even at saturating inhibitor concentrations
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DCC2655 Ide-in-37 Tfa Salt
Novel highly potent substrate-selective inhibitor of insulin-degrading enzyme (IDE), blocking insulin binding while allowing glucagon cleavage, even at saturating inhibitor concentrations
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DCC2654 idaverine
M1 and M2 Antagonist
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DCC2653 Id110460003
Novel μ,δ-Opioid Receptor Dual-Biased Agonist, Overcoming the Limitation of Prior Biased Agonist
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DCC2652 Id110460002
Novel μ,δ-Opioid Receptor Dual-Biased Agonist, Overcoming the Limitation of Prior Biased Agonist
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DCC2651 Id110460001
Novel μ,δ-Opioid Receptor Dual-Biased Agonist, Overcoming the Limitation of Prior Biased Agonist
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DCC2650 Ict2700
Potent cytotoxin selectively by CYP1A1 as a tumor-selective treatment for human bladder cancers
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DCC2649 Icrf-193
DNA topoisomerase II inhibitor
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DCC2648 Icpd62
Novel inhibitor of heat shock protein 90 (Hsp90), demonstrating anticancer activity against colorectal, osteosarcoma and cervical cancer cell lines
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DCC2647 Icl-sirt078
Novel highly selective, substrate-competitive SIRT2 inhibitor, displaying a significant neuroprotective effect in a lactacystin-induced model of Parkinsonian neuronal cell death in the N27 cell line
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DCC2646 Icl-ccic-0019
Novel potent and selective inhibitor of choline kinase alpha (CHKA)
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DCC2645 Iclaprim
Novel selective bacterial dihydrofolate inhibitor, antibiotic, actively against Gram positive organisms
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DCC2644 Ici-56780
Antimalarial agent, displaying blood schizonticidal activity against P.berghei
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DCC2643 Ici-185282
Potent thromboxane receptor antagonist
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DCC2642 icec0943
Novel selective inhibitor of CDK7
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DCC2641 Ical-36
Novel inhibitor of CALP, exhibiting affinity of 22.6 ± 8.0 μM for CALP and no interaction with the NHERF PDZ domains
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DCC2640 Icagen-4
Inhibitor of voltage-gated K(+) (Kv) channels Kv1.3 and Kv1.5
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DCC2639 ica-27243
Neuronal Kv7 potassium channel activator
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DCC2638 Ic2418
MmpL3 inhibitor, being active against drug-resistant Mycobacterium tuberculosis
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DCC2637 Ibs399024
Novel HDAC6-selective inhibitor
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DCC2636 Ibrutinib-bfl
Novel fluorescent irreversible inhibitor of Bruton's tyrosine kinase (BTK)
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DCC2635 Ibpr002
Novel Aurora kinase inhibitor, revealing mechanisms of HURP in nucleation of centrosomal and kinetochore microtubules
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DCC2634 Ibpr001 Hydrochloride
Novel Aurora kinase inhibitor
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