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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| 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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