Structure | Cat No. | Product Name | CAS No. | Product description |
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V12525 | 沙可美林盐酸盐 | 159912-58-0 | Sabcomeline (BCI-224; BRL-55473; CEB-2424; SB-202026A) is a novel, potent and selective M1 receptor partial agonist that was under development for the treatment of Alzheimers disease. |
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V44690 | DOPE-mPEG | DOPE-mPEG, phospholipid polydisperse PEG (or DOPE liposome) | |
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V48037 | BIBF 1202-13C,d3 | BIBF 1202-13C,d3, 13C- and deuterium labeled BIBF 1202 | |
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V50812 | Y-08284 | 2688745-47-1 | Y08284 is a potent, selective, orally bioactive CBP bromodomain inhibitor (antagonist) with IC50 of 4.21 nM. |
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V21296 | 复格列汀) | 312954-58-7 | Fotagliptin is a novel and potent dipeptidyl peptidase IV inhibitor |
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V19728 | DHQZ-36 | 1542098-94-1 | DHQZ-36 is a novel and potent small moleculeretrograde trafficking inhibitor which is able to block infection by several human and monkey polyomaviruses. |
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V38994 | 联苯芦诺 | 350992-10-8 | Bifeprunox is a potent partial agonist of dopamine D2 and 5-HT1A receptors, with pKi of 7.19 and 8.83 for cortical 5-HT1A and striatal D2, respectively, and pEC50 of 6.37 for hippocampal 5-HT1A. |
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V46855 | 抗菌剂86 | 2807530-12-5 | anti-bacterial agent 86 (Compound A11) has the strongest activity and has anti-bacterial effect against methicillin-resistant Staphylococcus aureus. |
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V48529 | Kukoamine A-d8 diHCl | Kukoamine A-d8 diHCl, inhibitor of trypanothione reductase |