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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC2627 Ianthelliformisamine A Tfa Salt
Antibiotic enhancer against resistant Gram-negative bacteria
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DCC2626 Ianthellamide A
Selective kynurenine-3-hydroxylase inhibitor
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DCC2625 Iag-10
Novel potent and selective inhibitor of human DNA polymerase kappa (hpol κ)
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DCC2624 Hz-ma Hybrid 11b
Novel potent and selective inhibitor of fat mass obesity-associated protein (FTO), being selectively over alkylation repair homologue 5 (ALKBH5), another DNA/RNA demethylase
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DCC2623 Hys-32
Novel analogue of combretastatin A-4, enhancing connexin43 expression
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DCC2622 Hymenidin
Natural antagonist of serotonergic receptors and inhibitor of CDK5/p25 and GSK-3ß
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DCC2621 Hydroxytriolein
Novel anticancer agent, inhibiting lung cancer cell proliferation via a PKCa and ERK1/2 dependent mechanism
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DCC2620 Hydroxymatairesinol
Natural antioxidant and anti-cancer agent, blocking the MAPK/NF-κB and activating Nrf2/HO-1
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DCC2619 Hydroxyellipticine-1a
Novel selective r(CGG)exp probe, improving pre-mRNA splicing defects, inhibiting formation of nuclear inclusions and RANT in a FXTAS cellular model
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DCC2618 Hydrolapachol
Novel potent and selective inhibitor of Schistosoma mansoni dihydroorotate dehydrogenase (SmDHODH)
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DCC2617 Hydrocaffeoyl-fasudil 1d
Novel multitarget Fasudil derivative, inducing the NRF2 signature, promoting the expression of the antioxidant response enzymes HO-1 and NQO1, via a KEAP1-dependent mechanism
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DCC2616 Hydro-1080
Activable Probe for Noninvasive Hydroxyl Radical Imaging, emitted in 1000-1400 nm after responding to ·OH
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DCC2615 Hycanthone Mesylate
Inhibitor of apurinic endonuclease-1 (APE1) by direct protein binding
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DCC2614 Hy1-pt
Novel CK2-Specific Pt(II) Compound, Reversing Cisplatin-Induced Resistance by Inhibiting Cancer Cell Stemness and Suppressing DNA Damage Repair in Non-small Cell Lung Cancer Treatments
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DCC2613 Hur-ligand-4
Novel human antigen R (HuR) ligand, acting as a HuR-RNA interferer
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DCC2612 Human Vitronectin (351-359)
Adhesive peptide (sequence 351-359 mapped on the Human Vitronectin Protein), covalent and selective functionalizing on glass and titanium surfaces, increasng osteoblast attachment and adhesion strength and to promoting osseointegration
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DCC2611 Huhs029
Novel analgesic agent, activating TRPA1 and subsequently desensitizing the channel, exhibiting higher inhibitory activity than resveratrol
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DCC2610 hts05737
Novel activator of PC2
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DCC2609 Htl6641
Novel, potent, selective, and orally efficacious dual antagonist of the orexin receptors
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DCC2608 Htl26119
Novel allosteric antagonist of the glucagon-like peptide-1 receptor (GLP-1R)
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DCC2607 Htl0028125
Novel macrocyclic calcitonin gene-related peptide (CGRP) receptor antagonist
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DCC2606 Htl0028016
Novel macrocyclic calcitonin gene-related peptide (CGRP) receptor antagonist
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DCC2605 Hsp90-in-s89
Novel heat shock protein 90 (Hsp90), more potent enantiomer
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DCC2604 Hsp90-in-89
Novel heat shock protein 90 (Hsp90) inhibitor
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DCC2603 Hsp90-in-30f
Novel potent inhibitor of heat shock protein 90 (Hsp90), effectively reducing the expression levels of Hsp90 client proteins including Her2, EGFR, Met, Akt, and c-Raf
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DCC2602 Hsp90-aha1 Inhibitor A16
Novel Hsp90-Aha1 chaperone complex formation inhibitor, enhancing F508del-CFTR channel activity
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DCC2601 Hsp27-in-i
Novel inhibitor of heat shock 27 kDa protein (HSP27), significantly inducing AR degradation in GBM cells via the proteasomal pathway, selectively inhibiting AR-overexpressed GBM cell growth with IC 50 values around 5 nM
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DCC2600 Hsk21542
Novel Peripherally-Restricted Kappa Opioid Receptor (KOR) Agonist with Antinociceptive and Antipruritic Effects
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DCC2599 Hsgn-94
Novel inhibitor of lipoteichoic acid (LTA) biosynthesis, potently inhibiting S. aureus and E. faecalis growth and biofilm formation
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DCC2598 Hsd1237
Novel potent inhibitor of the recombinant FLT3 kinase and its mutant forms, blocking the proliferation of AML cell lines, harboring oncogenic FLT3-ITD mutations with remarkable IC50 values, which were comparable to the approved FLT3 inhibitor quizartinib,
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