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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2023 | Etifoxine |
Activator of β2 and β3 subunit containing channels of the GABAA receptor complex, stimulating the production of GABA(A) active neurosteroids
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| DCC2022 | Ethylvanillin |
TRPA1 channel agonist
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| DCC2021 | Ethyl Lipotf |
Novel selective FTO inhibitor
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| DCC2020 | Ethyl 3-hydroxyhexanoate |
Natural potent antiviral agent, significantly inhibiting coxsackievirus group B (CVB) replication both in vivo and in vitro
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| DCC2019 | Etheofazine |
Novel anticancer agent
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| DCC2018 | Ethd-1 |
Cell-impermeant viability indicator, as high-affinity nucleic acid stain that is weakly fluorescent until bound to DNA and emits red fluorescence (excitation/emission maxima ~528/617).
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| DCC2017 | Etc-131 |
Novel inhibitor of PORCN, inhibiting ß-catenin reporter activity in a dose-dependent manner
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| DCC2016 | Etb067 |
H-89 analog as PKA and AKT1 inhibitor with specificity on no longer inhibiting CAMK2B and neither affecting viability of mice nor causing any detectable tissuedamage at the dose given
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| DCC2014 | Estetrol |
Selective estrogen receptor modulator (SERM), exhibiting estrogen agonism in certain tissues and estrogen antagonism in others
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| DCC2013 | Est64454 |
Novel Highly Soluble σ1 Receptor Antagonist for Pain Management
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| DCC2012 | escaline Hydrochloride |
Serotonin 5-HT2A Agonist
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| DCC2011 | Erythromycin Ethylsuccinate |
Broad-spectrum, topical macrolide antibiotic, diffusing through the bacterial cell membrane and reversibly binding to the 50S subunit of the bacterial ribosome
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| DCC2010 | Erythro-di-o-benzyl Droxidopa Hcl |
Precursor of adrenaline, suppressing the locomotor stimulation by MAO inhibitor
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| DCC2009 | Erythrocentaurin |
Anti-HBV agent, showing activities on HepG 2.2.15 cell line in vitro
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| DCC2008 | Erw1041e |
Novel potent inhibitor of recombinant human and mouse Transglutaminase enzyme activity, mainly TG2 and the close related enzyme TG1
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| DCC2007 | Er-thermo-yellow |
The First Fluorescent Probe for Targeted Visualization of Temperature at the Endoplasmic Reticulum #222222; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: 0.17px; text-align: start; text-in
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| DCC2006 | Erthermac |
Novel thermosensitive fluorescent dye, visualizing thermogenesis in stimulated single-cell brown adipocytes
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| DCC2005 | Ertapenem Disodium |
Carbapenem antibiotic, inhibiting cross-linking of the peptidoglycan layer of bacterial cell walls by blocking penicillin-binding proteins (PBPs)
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| DCC2004 | Erß Nir Probe P5 |
The first ERβ-targeted near-infrared (NIR) inherently fluorescent probe, showing the advantages of high ERβ selectivity, good optical properties, and excellent ERβ imaging capability in living cells
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| DCC2003 | Erso-dfp |
Novel Activator of the Anticipatory Unfolded Protein Response with Enhanced Selectivity for Estrogen Receptor Positive Breast Cancer
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| DCC2002 | Errα Degrader-1 |
Novel PROTAC Estrogen-related Receptor α (ERRα) Degrader
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| DCC2001 | Erk-cliptac |
Novel degrader of ERK1/2, eliciting downregulation of phospho-ERK1/2 signal.
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| DCC2000 | Erk Inhibitor Ii, Negative Control |
Negative control for ERK Inhibitor II AOB6420
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| DCC1999 | Eritoran |
Analogue of the lipid A portion of the endotoxin lipopolysaccharide (LPS) with potential immunomodulating activity, binding to the Toll-like receptor (TLR)/CD14/MD2 receptor complex, inhibiting the activation of the receptor complex by LPS
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| DCC1998 | Erioflorin |
Novel ATP-competitive Selective c-Jun N-terminal kinase (JNK) inhibitor
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| DCC1997 | Ergotamine |
Natural Nsp15 inhibitor against SARS-COV2
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| DCC1996 | Ercc1-xpf-in-4 |
Novel potent inhibitor of ERCC1-XPF activity, targeting DNA repair in tumor cells
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| DCC1995 | Erbb-in-1 |
Novel ErbB type I receptor tyrosine kinase inhibitor for the treatment of hyperproliferative diseases
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| DCC1994 | Erap1-in-2 |
Novel competitive inhibitor of ERAP1 aminopeptidase activity
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| DCC1993 | Erap1 -in-1 |
Novel Selective ERAP1 Inhibitor
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