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Cat. No. Product Name Field of Application Chemical Structure
DC43678 Esculentoside C
DC43677 Thozalinone
a psychostimulant
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DC43676 Cucurbitacin B 2-O-beta-D-glucoside
DC43675 Dehydrocrenatidine
DC43674 Dexoxadrol
An dissociative anaesthetic drug which has been found to be an NMDA antagonist and produces similar effects to PCP in animals
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DC43673 Schisantherin C
DC43672 Dulcoside A
DC43671 HepIn-13
Novel Hepsin inhibitor, blocking prostate cancer bone metastasis
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DC43669 Torachrysone 8-O-glucoside
DC43668 Oxotremorine M
Muscarinic receptor agonist
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DC43667 beta-Amyrone
DC43666 (S)-Baclofen hydrochloride
Less active enantiomer of baclofen.
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DC43665 1,5-Bis(4-hydroxy-3-methoxyphenyl)penta-1,4-diene
DC43664 TUG-1387
A close structural analog of AH-7614 that lacks activity at FFA4 that can serve as negative control.
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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
DC43659 Morusinol
DC43658 Jolkinol A
DC43656 (-)-Syringaresinol
A lignan found in Castela emoryi, in Prunus mume or in Magnolia thailandica. This compound inhibits Helicobacter pylori motility in vitro
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DC43654 Memoquin
Multi-target-directed ligand for treatment of Alzheimer's disease
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DC43653 TNP-ATP sodium salt
P2X receptor antagonist, selective for P2X1, P2X3 and heteromeric P2X2/3 receptors
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DC43652 Merck-22-6
A potent, allosteric dual Akt1, Akt2 inhibitor
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DC43651 Vitexilactone
DC43650 ML175
Potent and Selective Inhibitor of Glutathione S-Transferase Omega 1 (GSTO1)
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DC43649 Esculentoside B
DC43648 2-Hydroxy-1,8-cineole
DC43647 Canthin-6-one N-oxide
DC43646 Homopterocarpin
DC43645 Tirandamycin B

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