Alentemol, also known as U-66444B and alentamol, is a selective dopamine autoreceptor agonist described as an antipsychotic. Chromosomal breakage following treatment of CHO-K1 cells in vitro with U-68,553B is due to induction of undercondensation of heterochromatin.
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名称 | Alentemol HBr |
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Iupac 化学名称 | 2-(dipropylamino)-2,3-dihydro-1H-phenalen-5-ol hydrobromide |
同义词 | Alentemol HBr; Alentemol hydrobromide; Alentemol, alentamol, U-66444B; U 66444B; U66444B; |
英文同义词 | Alentemol HBr; Alentemol hydrobromide; Alentemol, alentamol, U-66444B; U 66444B; U66444B; |
分子式 | C19H26BrNO |
分子量 | 364.32 |
Smile | OC1=CC2=C3C(CC(N(CCC)CCC)C2)=CC=CC3=C1.[H]Br |
InChiKey | FWRWEZVGVJKNMU-UHFFFAOYSA-N |
InChi | InChI=1S/C19H25NO.BrH/c1-3-8-20(9-4-2)17-10-14-6-5-7-15-12-18(21)13-16(11-17)19(14)15;/h5-7,12-13,17,21H,3-4,8-11H2,1-2H3;1H |
Cas号 | 112892-51-0 |
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包装 | 价格 | 库存 | 纯度 | 备货期 |
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大货 | 询价 | 询价 | 询价 |
外观性状 | 固体粉末 |
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纯度 | 98% Min. |
存储 | 短期(几天到几周)为0-4摄氏度,长期(几个月)为-20摄氏度 |
可溶性 | 溶于DMSO |
处理方式 | |
运输条件 | 作为非危险化学品在环境温度下装运。这种产品在正常运输和海关工作期间可以稳定几周. |
海关编码 |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |
1: Yu RL, Aaron CS, Ulrich RG, Thilagar A, Kumaroo PV, Wang Y. Chromosomal breakage following treatment of CHO-K1 cells in vitro with U-68,553B is due to induction of undercondensation of heterochromatin. Environ Mol Mutagen. 1992;20(3):172-87. doi: 10.1002/em.2850200306. PMID: 1396608.
2: Althaus JS, Decker DE, Von Voigtlander PF, Buxser SE. Effects of dopamine agonists on dopamine secretion from PC12 cells: lack of functional autoreceptor activity. Res Commun Chem Pathol Pharmacol. 1991 May;72(2):131-42. PMID: 1678897.
3: Schwende FJ, Rykert UM. Determination of alentamol hydrobromide, a novel antipsychotic agent, in human blood plasma and urine by high-performance liquid chromatography with fluorescence detection and solid-phase extraction. J Chromatogr. 1991 Apr 19;565(1-2):488-96. doi: 10.1016/0378-4347(91)80415-9. PMID: 1874898.
4: Piercey MF, Broderick PA, Hoffmann WE, Vogelsang GD. U-66444B and U-68553B, potent autoreceptor agonists at dopaminergic cell bodies and terminals. J Pharmacol Exp Ther. 1990 Aug;254(2):369-74. PMID: 1974631.