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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC43017 | Retro-2 |
Inhibitor of Ribosome-Inactivating Proteins (RIPs); Blocker of Leishmania parasitophorous vacuoles (LPV) development
More description
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| DC43015 | YH16899 |
Novel inhibitor of the KRS-67LR interaction by directly blocking the association between KRS and 67LR, suppressing the dynamic movement of the N-terminal extension of KRS and reducing membrane localization of KRS
More description
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| DC43014 | YM-01 Tosylate |
Potent antitumor agent, selectively targeting cancer cells and overcoming tamoxifen resistance
More description
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| DC43013 | 6-Hydroxykaempferol 3,6-diglucoside |
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| DC43012 | ML243 |
Selective Small-Molecule Inhibitor of Breast Cancer Stem Cells
More description
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| DC43011 | Calanolide E |
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| DC43010 | Cimidahurinine |
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| DC43009 | Glyasperin A |
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| DC43008 | Lobetyolinin |
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| DC43007 | Shizukaol C |
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| DC43006 | KPT-330, (E)-RN |
An orally bioavailable selective CRM1 inhibitor
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| DC43004 | Isosalvianolic acid C |
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| DC43003 | Ivangustin |
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| DC42999 | Ergosterol peroxide glucoside |
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| DC42998 | AS1940477 Hydrobromide |
Novel and potent p38 mitogen-activated protein kinase (MAPK) inhibitor
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| DC42997 | Pterisolic acid B |
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| DC42996 | Palbinone |
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| DC42994 | Isodunnianol |
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| DC42993 | Cannabidiol |
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| DC42992 | Buddlejasaponin IV |
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| DC42990 | ML252 |
Potent, Brain Penetrant K(v)7.2 Channel Inhibitor
More description
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| DC42989 | GN6958 |
Non-peptidic selective SUMO-sentrin specific protease (SENP)1 protease inhibitor
More description
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| DC42988 | Tripterifordin |
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| DC42987 | Tristin |
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| DC42986 | Oplodiol |
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| DC42985 | Isocoronarin D |
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| DC42983 | Tormentic acid |
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| DC42982 | Pomolic acid |
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| DC42980 | Atroscine |
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| DC42977 | 6-O-Feruloylglucose |
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