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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC1992 | Er-38925 |
Retinoic acid receptor (RAR) subtype α-selective agonist
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| DCC1991 | Er-119884 |
Selective squalene synthase (SQS) inhibitor
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| DCC1990 | Er Degrader 40 |
Novel Oral Selective Estrogen Receptor Degrader with Highly Improved Antitumor Effect and Favorable Druggability
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| DCC1989 | Epz033294 |
Novel SMYD2 inhibitor
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| DCC1988 | Epz032597 |
Novel selective SMYD2 inhibitor
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| DCC1986 | Epz005687n |
Inactive isomer of EPZ005687 and can be used as the negative control for EPZ005687
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| DCC1985 | Eptapirone Fumarate |
Potent, selective, high efficacy 5-HT1A receptor agonist
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| DCC1984 | Eps-in-1 |
Novel inhibitor of extracellular polymeric substances (EPS)
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| DCC1983 | Eprazinone |
Mucolytic and bronchospasm relieving agent
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| DCC1982 | Epi-nocardicin G |
The precursor of the nocardicins
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| DCC1981 | Epinastine Hydrobromide |
Second-generation antihistamine and mast cell stabilizer, being highly selective for the H1 receptor
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| DCC1980 | Epibestatin Hydrochloride |
Novel stabilizer of 14-3-3 PPIs, Diastereoepimer of aminopeptidase inhibitor bestatin
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| DCC1979 | Epi-0023 |
Novel selrctive SETD8 inhibitor without inhibiting G9a, SETD7, RmtA, and PRMT1
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| DCC1978 | Ephb3-in-9 |
The first potent and specific inhibitor of a single Eph isoform EphB3
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| DCC1977 | Ephb3-in-10 |
Novel clickable potent and specific inhibitor of EphB3
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