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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1899 | Ebselen Oxide |
Novel dose-dependent inhibitor of HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9, inhibiting Pseudomonas aeruginosa alginate synthesis
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| DCC1898 | Ebov-in-c31 |
Novel PP1-targeting Ebola Virus (EBOV) inhibitor with improved pharmacological properties
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| DCC1897 | Ebopiprant |
Novel Oral and Selective Prostaglandin F 2α (PGF 2α ) Receptor Antagonist
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| DCC1896 | Ebmi-13b |
Highly potent and selective activator of isozymes CA-VA and CA-VII
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| DCC1895 | Ebi-13a |
Highly potent and selective activator of isozymes CA-VA and CA-VII
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| DCC1894 | Ea-b3a |
Novel degrader of GST-α and GST-α-EGFP fusion proteins as well as endogenous GST-π in cells and lysates
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| DCC1893 | E-5842 Citrate |
Sigma1 receptor ligand and potential atypical antipsychotic
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| DCC1892 | E3-ligase Degrader 10 |
Novel XIAP BIR2 domain-binding degrader of E3 ubiquitin ligases
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| DCC1891 | E235-1756 |
Potent Activator of P53-Independent Cellular Senescence
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| DCC1890 | e2012-bpyne |
γ-Secretase modulator (GSM) photoaffinity probe, revealing distinct allosteric binding sites on presenilin
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| DCC1889 | E09241 |
Novel OPG/RANKL upregulator, increasing OPG expression without affecting RANKL expression, promoting osteoblast differentiation while inhibiting osteoclast differentiation, regulating OPG expression through canonical Wnt/β-catenin signaling
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| DCC1888 | Dy428174 |
Novel potent Inhibitor of PI3Kalpha
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| DCC1887 | Dy3002 |
Novel Selective and Potent EGFR Inhibitor, Overcoming T790M-Mediated Resistance in Non-Small Cell Lung Cancer
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| DCC1886 | Dx-52-1 |
Antitumor antibiotic
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| DCC1885 | Dx2-hsp70 Inhibitor-1 |
Novel allosteric inhibitor of the tumor-promoting interaction between the oncogenic factor AIMP2-DX2 and HSP70
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| DCC1884 | Dwn-723-23 |
Novel Hsp70 agonist, showing no cellular toxicity and induced cellular stress response pathways
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| DCC1883 | Dw-1350 |
Novel and potent leukotriene B(4) receptor antagonist
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| DCC1882 | Dw10075 |
Novel potent and highly selective inhibitor of VEGFR, exhibiting antitumor activities both in vitro and in vivo.
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| DCC1881 | Dv-7028 Hydrochloride |
Potent and selective 5-HT 2A receptor antagonist
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| DCC1880 | Dv-7028 |
Selective 5-HT2A receptor antagonist
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| DCC1879 | Dutomycin |
Anthracycline antibiotic from Streptomyces
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| DCC1878 | Duocarmycin A |
Irreversible DNA minor groove binding alkylating agent, disrupting the nucleic acid architecture and leading to tumor cell death
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| DCC1877 | Du-34569 Maleate |
Antiviral agent against influenza A, parainfluenza Sendai, coxsackie A21, and rhinovirus
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| DCC1876 | Dtagv-1 |
Potent and selective degrader of mutant FKBP12F36V fusion proteins
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| DCC1875 | Dt2216nc |
Negative control for DT2216
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| DCC1874 | Dt-061 |
Novel potent and orally active activator of PP2A
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| DCC1873 | Ds-sg-44 |
Agonist of S1P receptors
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| DCC1872 | Dsr-98776 |
Novel selective mGlu5 receptor negative allosteric modulator (NAM) with potent antidepressant and antimanic activity
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| DCC1871 | Dsm705 |
Novel potent Dihydroorotate Dehydrogenase (DHODH) inhibitor
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| DCC1869 | Dsm-338 |
Novel Plasmodium falciparum Dihydroorotate Dehydrogenase (PfDHODH) Inhibitor (Pfalcip cells: 0.0018 μM)
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