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Titlebook: Antiepileptic Drugs; Pharmacology and The Mervyn J. Eadie,Frank J. E. Vajda Book 1999 Springer-Verlag Berlin Heidelberg 1999 catecholamines

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發(fā)表于 2025-3-30 09:52:01 | 只看該作者
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53#
發(fā)表于 2025-3-30 17:14:47 | 只看該作者
54#
發(fā)表于 2025-3-30 22:20:35 | 只看該作者
https://doi.org/10.1007/978-3-662-31601-6 predicted from its chemistry; rather they were discovered by routine screening of various 1,2-benzisoxazole derivatives. Its formula is C.H.N.O.S, and its molecular weight is 212. It has a p.. of 9.66, so that its water solubility is dependent on the pH. Below a pH of 8, it has a solubility of only
55#
發(fā)表于 2025-3-31 04:12:06 | 只看該作者
Antiepileptic Drugs978-3-642-60072-2Series ISSN 0171-2004 Series E-ISSN 1865-0325
56#
發(fā)表于 2025-3-31 06:12:52 | 只看該作者
Grundlagen der Eisenwerkstoffe,atment for partial seizures, whether or not they became secondarily generalized, and for primary generalized tonic-clonic seizures. The estimated patient exposure to the drug currently exceeds 50,000 patient years. Oxcarbazepine is under active investigation in the United States.
57#
發(fā)表于 2025-3-31 12:13:09 | 只看該作者
https://doi.org/10.1007/3-540-29793-6c, sedative and antiepileptic activity and received marketing approval in 1960 (. et al. 1960). Although effective, the drug was noted to have significant toxicity and chemists then turned to synthesizing structural analogues in the hope of finding compounds with enhanced pharmacological activity and reduced toxicity.
58#
發(fā)表于 2025-3-31 16:04:53 | 只看該作者
https://doi.org/10.1007/978-3-642-60072-2catecholamines; chemistry; clinical trial; cortex; drug; drug development; epilepsy; kinetics; neuropeptides
59#
發(fā)表于 2025-3-31 21:07:10 | 只看該作者
978-3-642-64244-9Springer-Verlag Berlin Heidelberg 1999
60#
發(fā)表于 2025-4-1 00:15:32 | 只看該作者
Mervyn J. Eadie,Frank J. E. VajdaIncludes supplementary material:
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