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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC43689 | Methylenetanshinquinone |
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| DC43688 | Dehydrotumulosic acid |
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| DC43687 | Spathulenol |
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| DC43686 | Arnidiol |
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| DC43685 | 1,3,5-Trihydroxyxanthone |
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| DC43684 | 3-O-(2'E ,4'Z-decadienoyl)-20-deoxyingenol |
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| DC43683 | Moronic acid |
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| DC43681 | Galangin 3-methyl ether |
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| DC43680 | Dihydroguaiaretic acid |
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| DC43679 | Proglumide |
CCK antagonist; selectively blocks CNS effects
More description
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| DC43678 | Esculentoside C |
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| DC43677 | Thozalinone |
a psychostimulant
More description
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| DC43676 | Cucurbitacin B 2-O-beta-D-glucoside |
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| DC43675 | Dehydrocrenatidine |
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| DC43674 | Dexoxadrol |
An dissociative anaesthetic drug which has been found to be an NMDA antagonist and produces similar effects to PCP in animals
More description
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| DC43673 | Schisantherin C |
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| DC43672 | Dulcoside A |
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| DC43671 | HepIn-13 |
Novel Hepsin inhibitor, blocking prostate cancer bone metastasis
More description
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| DC43669 | Torachrysone 8-O-glucoside |
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| DC43668 | Oxotremorine M |
Muscarinic receptor agonist
More description
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| DC43667 | beta-Amyrone |
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| DC43666 | (S)-Baclofen hydrochloride |
Less active enantiomer of baclofen.
More description
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| DC43665 | 1,5-Bis(4-hydroxy-3-methoxyphenyl)penta-1,4-diene |
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| DC43664 | TUG-1387 |
A close structural analog of AH-7614 that lacks activity at FFA4 that can serve as negative control.
More description
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| DC43662 | AI-4-57 Hydrochloride |
Ligand to the CBFß portion of the CBFß-SMMHC fusion protein, inhibiting its binding to the Runt domain of RUNX proteins, also being a modest potency inhibitor of the binding of wildtype CBFß to the RUNX1 Runt domain
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| DC43661 | A-412997 Dihydrochloride |
Selective agonist of dopamine D4 receptor
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| DC43660 | Neoprzewaquinone A |
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| DC43659 | Morusinol |
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| DC43658 | Jolkinol A |
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| DC43656 | (-)-Syringaresinol |
A lignan found in Castela emoryi, in Prunus mume or in Magnolia thailandica. This compound inhibits Helicobacter pylori motility in vitro
More description
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