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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| DCC1976 | Ephb1-in-10 |
Potent and selective covalent inhibitor of receptor tyrosine kinase EphB1
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| DCC1975 | Epha2-agonist-27 |
Novel agonist of EphA2 receptor tyrosine kinase
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| DCC1974 | Epetraborole R-mandelate |
Novel potent and selective leucyl-tRNA synthetase inhibitor
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| DCC1973 | Epc-k1 |
Vitamin E derivative, suppressing inflammation during hepatic ischemia-reperfusion injury and exerting hepatoprotective effects
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| DCC1972 | Ep-7041 |
Novel, potent, and selective Factor XIa inhibitor
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| DCC1971 | Ent-verticilide |
Unnatural verticilide enantiomer, inhibiting type 2 ryanodine receptor-mediated calcium leak and being antiarrhythmic.
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| DCC1970 | Entpd5-in-2f |
Novel inhibitor of Ectonucleoside Triphosphate Diphosphohydrolase 5 (ENTPD5)
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| DCC1969 | Entpd5-in-1a |
Novel inhibitor of Ectonucleoside Triphosphate Diphosphohydrolase 5 (ENTPD5)
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| DCC1967 | Ent Naxagolide Hydrochloride |
Dopamine D2-receptor agonist for the treatment of extrapyramidal disorders, also being an antiparkinson agent
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| DCC1966 | Enprostil |
PGE2 analog, inhibiting gastric acid secretion
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| DCC1965 | Enpp1 Inhibitor 43 |
Novel potent inhibitor of ecto-nucleotide pyrophosphatase/phosphodiesterases 1 (ENPP1 or NPP1), showing good in vitro potency, stability in SGF/SIF/PBS, selectivity, ADME properties and pharmacokinetic profile and finally potent anti-tumor response in viv
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| DCC1964 | Enmd-2076 Tartrate |
Novel oral inhibitor of angiogenic and proliferation kinases, having activity in recurrent, platinum resistant ovarian cancer
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| DCC1963 | Enl-in-7 |
Novel potent inhibitor of eleven-nineteen leukemia (ENL) protein, selectively targeting the ENL YEATS domain
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| DCC1962 | Eniporide Hydrochloride |
Sodium/hydrogen exchange inhibitor
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| DCC1961 | Endosidin8.1 |
Novel modulator of the PIN1 accumulation, selectively modifying PIN1 basal plasma membrane targeting in Arabidopsis with minimal effects on apical plasma membrane proteins
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