Cat. No. | Product Name | Field of Application | Chemical Structure |
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DC43274 | Horminone |
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DC43273 | Calcium Fusarate |
A picolinic acid derivative isolated from various Fusarium species.
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DC43272 | 1-Hydroxy-2-oxopomolic acid |
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DC43271 | Procurcumenol |
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DC43270 | Shoreic acid |
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DC43268 | ICT5040 |
Novel CXCR4 antagonist
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DC43267 | 23-deoxojessic acid |
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DC43266 | 7,3',4'-Trihydroxyflavone |
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DC43265 | Agrimonolide |
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DC43264 | Rosamultic acid |
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DC43263 | 1-Decarboxy-3-oxo-ceanothic acid |
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DC43262 | Taxiphyllin |
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DC43261 | WRR139 |
Novel inhibitor of the cytosolic enzyme N-glycanase 1 (NGLY1, the human PNGase), inactivating the transcription factor Nrf1 and potentiating proteasome inhibitor cytotoxicity
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DC43260 | Gestonorone |
Long acting potent steroidal progestin
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DC43259 | 18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one |
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DC43258 | Ceanothic acid |
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DC43257 | 9,17-Octadecadiene-12,14-diyne-1,11,16-triol |
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DC43256 | BMY7378 |
Potent and selective antagonist of the 5-HT1A receptor
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DC43255 | Spiradine F |
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DC43253 | GSK690 |
Novel potent and selective reversible KDM1A inhibitor and Lysine-specific demethylase 1 (LSD1)-specific inhibitor
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DC43252 | Jatrophane 4 |
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DC43251 | Jatrophane 3 |
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DC43250 | Jatrophane 2 |
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DC43249 | Platycoside A |
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DC43248 | Beta-mangostin |
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DC43247 | FIIN-4 |
A potent, irreversible, type II inhibitor against FGFR (IC50 = 2.6, 2.6, 5.6, 9.2 nM, respectively, against FGFR1-4) whose 4-acrylamidebenzyl moiety covalently modifies FGFR P-loop cysteine in its DFG-out conformation with good target selectivity based on
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DC43246 | Stigmastane-3,5,6-triol |
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DC43245 | BB-78485 |
Potent inhibitor of LpxC and lipid A biosynthesis
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DC43244 | Arteannuin N |
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DC43243 | Arteannuin M |
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