| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC11523 | Landipirdine | A novel 5-HT receptor antagonist for the treatment of Parkinson's disease.. |
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| DC11895 | Foliglurax hydrochloride | A potent, selective, brain-penetrant and orally bioavailable mGluR4 positive allosteric modulator with EC50 of 79 nM. |
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| DC11894 | Foliglurax | A potent, selective, brain-penetrant and orally bioavailable mGluR4 positive allosteric modulator with EC50 of 79 nM. |
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| DC8883 | BP897 Featured | BP897 is a partially selective D3 dopamine receptor agonist. |
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| DC11103 | Tavapadon Featured | Tavapadon is a potent, orally-bioavailable, selective partial agonist of the dopamine D1 and D5 receptors. |
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| DC7014 | GPI-1046 | For the detailed information of GPI-1046, the solubility of GPI-1046 in water, the solubility of GPI-1046 in DMSO, the solubility of GPI-1046 in PBS buffer, the animal experiment (test) of GPI-1046, the cell expriment (test) of GPI-1046, the in vivo, in vitro and clinical trial test of GPI-1046, the EC50, IC50,and Affinity of GPI-1046, Please contact DC Chemicals.. |
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| DC7419 | GNE-7915 Featured | GNE-7915 is a highly potent, selective, and brain-penetrable LRRK2 small molecule inhibitor with IC50 of 9 nM in cellular LRRK2 assay; > 100 fold selectivity against a panel of 187 kianses(Ki). |
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| DC8379 | JH-II-127 Featured | JH-II-127 is a highly potent, selective, and brain penetrant LRRK2 inhibitor. |
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| DC8970 | Pramipexole Base | Pramipexole is a dopamine agonist of the non-ergoline class indicated for treating Parkinson's disease (PD) and restless legs syndrome (RLS). |
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| DC3151 | Pramipexole dihydrochloride | Pramipexole is a partial/full D2S, D2L, D3, D4, receptor agonist with a Ki of 3.9, 2.2, 0.5, 5.1 nM. |
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| DC5015 | Rotigotine Hydrochloride | Rotigotine is dopamine D2 and D3 receptor agonist. Ki values are 13 and 0.71 nM for D2 and D3 respectively. Rotigotine also has significant affinity for 5-HT1A and adrenergic α2B receptors. Rotigotine exhibits antiparkinsonian acitivity. |
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| DC4134 | Safinamide | Safinamide (EMD 1195686; FCE 26743) selectively and reversibly inhibits MAO-B with IC50 of 98 nM, exhibits 5918-fold selectivity against MAO-A. |
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| DC11485 | Tolcapone Featured | Tolcapone is an orally active catechol-O-methyltransferase (COMT) inhibitor. |
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| DC9332 | Tozadenant | Tozadenant (SYN-115) is an adenosine A2A receptor antagonist. |
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