To enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC43678 | Esculentoside C |
|
|
| DC43677 | Thozalinone |
a psychostimulant
More description
|
|
| 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
More description
|
|
| DC43673 | Schisantherin C |
|
|
| DC43672 | Dulcoside A |
|
|
| DC43671 | HepIn-13 |
Novel Hepsin inhibitor, blocking prostate cancer bone metastasis
More description
|
|
| DC43669 | Torachrysone 8-O-glucoside |
|
|
| DC43668 | Oxotremorine M |
Muscarinic receptor agonist
More description
|
|
| DC43667 | beta-Amyrone |
|
|
| DC43666 | (S)-Baclofen hydrochloride |
Less active enantiomer of baclofen.
More description
|
|
| 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.
More description
|
|
| 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
More description
|
|
| DC43661 | A-412997 Dihydrochloride |
Selective agonist of dopamine D4 receptor
More description
|
|
| 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
More description
|
|
| DC43654 | Memoquin |
Multi-target-directed ligand for treatment of Alzheimer's disease
More description
|
|
| DC43653 | TNP-ATP sodium salt |
P2X receptor antagonist, selective for P2X1, P2X3 and heteromeric P2X2/3 receptors
More description
|
|
| DC43652 | Merck-22-6 |
A potent, allosteric dual Akt1, Akt2 inhibitor
More description
|
|
| DC43651 | Vitexilactone |
|
|
| DC43650 | ML175 |
Potent and Selective Inhibitor of Glutathione S-Transferase Omega 1 (GSTO1)
More description
|
|
| DC43649 | Esculentoside B |
|
|
| DC43648 | 2-Hydroxy-1,8-cineole |
|
|
| DC43647 | Canthin-6-one N-oxide |
|
|
| DC43646 | Homopterocarpin |
|
|
| DC43645 | Tirandamycin B |
|