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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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
More description
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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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| DC43242 | Arteannuin L |
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| DC43241 | Norlichexanthone |
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| DC43240 | Cannabichromene |
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| DC43239 | Coniferaldehyde |
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| DC43238 | Encecalin |
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| DC43237 | CL-214828 |
Strong neuroleptic agent, showing no cataleptic effect and antagonism against apomorphine
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| DC43236 | Faradiol |
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| DC43235 | Lansiumarin C |
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| DC43233 | Curzerenone |
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