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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC2633 Ibl-302
First-in-class triple-acting PIM/PI3K/mTOR inhibitor, demonstrating single-agent, anti-tumour efficacy in suppression of pAKT, pmTOR and pBAD in the SKBR-3, BT-474 and HCC-1954 HER2+/PIK3CA-mutated cell lines
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DCC2632 Ibe-667
Novel activator of LFA-1-ICAM-1 binding
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DCC2631 Iaxo-101
Novel inhibitor of the cluster of differentiation 14 innate immunity pathway
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DCC2630 Iap-in-1
Novel antagonist of IAP (inhibitor of apoptosis protein)
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DCC2629 Ianthelliformisamine C Tfa Salt
Antibiotic enhancer against resistant Gram-negative bacteria
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DCC2628 Ianthelliformisamine B Tfa Salt
Antibiotic enhancer against resistant Gram-negative bacteria
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