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4-苯基-1,5-苯并二氮杂䓬-2-酮衍生物的合成与药理评价

Synthesis and Pharmacological Valorization of Derivatives of 4-Phenyl-1,5-Benzodiazepin-2-One.

作者信息

Nguema Ongone Terence, Achour Redouane, El Ghoul Mostafa, El Ouasif Latifa, Taghzouti Khalid, El Jemli Meryem, Cherrah Yahia, Alaoui Katim, Zellou Amina

机构信息

Laboratory of Heterocyclic Organic Chemistry, Drug Sciences Research Center, URAC 21, Pole of Competence Pharmacochemistry, Faculty of Sciences, Mohammed V University, Avenue Ibn Battouta, BP 1014, Rabat, Morocco.

PharmacodynamyResearch Team PRT, Laboratory of Pharmacology and Toxicology, Faculty of Medicine and Pharmacy, Mohammed V University, BP 6203, Rabat, Morocco.

出版信息

Adv Pharmacol Sci. 2018 Apr 1;2018:6042602. doi: 10.1155/2018/6042602. eCollection 2018.

Abstract

The objective of our work is to make a pharmacological study of molecules derived from 4-phenyl-1,5-benzodiazepin-2-one carrying long chains so that they have a structure similar to surfactants, with the benzodiazepine as a hydrophilic head and a carbon chain as a hydrophobic tail. First, we studied the acute toxicity of the above mentioned 4-phenyl-1,5-benzodiazepin-2-one derivatives. This study was conducted according to OECD 423 guidelines in female mice and revealed that these compounds are nontoxic. We then assessed the psychotropic effects of our products on the central nervous system (CNS). The results obtained show that 4-phenyl-1,5-benzodiazepin-2-one has no sedative effect at therapeutic doses of 100 and 200 mg/kg. On the other hand, its long-chain derivatives possess them. Moreover, all these products have no cataleptic and hypnotic effects at the doses studied. But at 100 mg/kg, these compounds all have the ability to significantly prolong the hypnotic effect of thiopental sodium.

摘要

我们工作的目标是对源自4-苯基-1,5-苯并二氮杂卓-2-酮且带有长链的分子进行药理学研究,以使它们具有类似于表面活性剂的结构,其中苯并二氮杂卓作为亲水头部,碳链作为疏水尾部。首先,我们研究了上述4-苯基-1,5-苯并二氮杂卓-2-酮衍生物的急性毒性。这项研究按照经合组织423指南在雌性小鼠中进行,结果表明这些化合物无毒。然后,我们评估了我们的产品对中枢神经系统(CNS)的精神作用。所得结果表明,4-苯基-1,5-苯并二氮杂卓-2-酮在100和200mg/kg的治疗剂量下没有镇静作用。另一方面,其长链衍生物具有镇静作用。此外,在研究的剂量下,所有这些产品都没有致僵和催眠作用。但在100mg/kg时,这些化合物都有能力显著延长硫喷妥钠的催眠作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4477/5902104/0db42622cbf0/APS2018-6042602.001.jpg

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