Cat. No. | Product Name | Field of Application | Chemical Structure |
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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
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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
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DC43669 | Torachrysone 8-O-glucoside |
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DC43668 | Oxotremorine M |
Muscarinic receptor agonist
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DC43667 | beta-Amyrone |
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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 |
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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.
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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
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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 |
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DC43650 | ML175 |
Potent and Selective Inhibitor of Glutathione S-Transferase Omega 1 (GSTO1)
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DC43649 | Esculentoside B |
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DC43648 | 2-Hydroxy-1,8-cineole |
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DC43647 | Canthin-6-one N-oxide |
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DC43646 | Homopterocarpin |
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DC43645 | Tirandamycin B |
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DC43644 | Piketoprofen |
Topical Nonsteroidal Anti-inflammatory
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DC43643 | Tamarixetin |
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DC43642 | Ro 5-5453 |
Monoamine oxidase inhibitor
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