Strong evidence showed that many medicinal plants have the potential to reduce hyperlipidemia disease. The aim of this study was to determine the hypolipidemic activity of aqueous extracts of Fucus vesiculosus, Coleus forskohlii, Curcuma longa L., Rosmarinus officinalis L., Camellia sinensis L. and Melissa officinalis L. on lipid profile in serum taken from the blood of rats. Fifty-seven female albino rats were divided into 19 groups, each with three rats, that were treated orally with an aqueous plant extract in three different doses, except the control group which was treated with normal saline only. The chemical compositions of these extracts were analyzed using High Performance Liquid Chromatography (HPLC).The results showed that the dose of 5 mg/kg ofCurcuma longa was the powerful extract which reduced levels of cholesterol (CHO) and low-density lipoprotein (LDL) in serum rats' blood by 31 and 55%, respectively, compared with the control treatment. While, the effective extract to reduce triglycerides (TG) level was that ofFucus vesiculosus(50mg/kg) which reduced TG by 38% compared with the control. Also, Melissa officinalis(50 mg/kg ) extract reduced 30% of very low-density lipoprotein (VLDL) level as compared to the control treatment. In addition, Coleus forskohlii(100 mg/kg) extract increased high-density lipoprotein (HDL) level by 115% after being orally given to rats for four weeks. The results of the study indicated significant differences among the concentrationsof the secondary compoundswithin their extracts, which maybe responsible for the observed variations of hypolipidemic activity for each extract. Based on these results, further investigation should target understanding the mechanismsby which these plants can be used as food additives and as dietary supplement.

This study sheds light on various drugs of plant origin which have shown action on thyroid and its functioning as well as on the various factors associated with thyroid dysfunction. Therefore, the aim of this study is to determine the activity of the aqueous extracts of Fucus vesiculosus, Coleus forskohlii, Curcuma longa L., Rosmarinus officinalis L., Camellia sinensis L. and Melissa officinalis L. in regulation of thyroid hormones in serum taken from rats. Fifty-seven female albino rats were divided into 19 groups, each group with 3 rats, and treated orally with an aqueous plant extract in three different doses, except the control group which was treated with normal saline only. Also, a histological study was conducted on the thyroid gland after short-term treatment with different doses of these extracts. The results demonstrated that 5mg/kg of Curcuma longa was the most powerful extract which increased T3 level in a rats serum by 25% compared with the control treatment. Also, the most effective dose which increased T4 level was 1000mg/kg of Coleus forskohlii, which increased the hormone level by 7% compared with the control. Meanwhile, 1000mg/kg of Coleus forskohlii was the effective extract which reduced TSH level by 61% compared with the control. While, the extract of Rosmarinus officinalis 220mg/kg reduced T3 and T4 levels in the serum of rats by 56% and 17% respectively. However, oral administration with Camellia sinensis 1.25mg/kg increased TSH level by 10% compared with the control. The obtained data demonstrated that Curcuma longa and Coleus forskohlii, at low doses, can be very effective for completely treating hypothyroidism in rats.The findings of this study propose that the extracts may have the property to regulate thyroid levels in rats.

The therapeutic value of the phenolic component and pure thymol was well known; this study comprised the extraction of crude phenol from two plants (Thymus vulgaris and Artemisia annua) which contain thymol with pure thymol and evaluate their effect on hematological and histological by using three different concentrations of each plant extract and pure thymol to tested them on lab mice. All the mice were allowed free access to water and feed for 21 days in laboratory conditions; orally, pure water was administered to the control mice (group I), while groups II, III, and IV were given orally with T. vulgaris, A. annua, combination of last two crude phenol plant extract 50:50 and pure thymol respectively. The levels of CHO, TRI, and HDL were significantly reduced in A. annua and T. vulgaris crude phenolic extract at 20 mg/ml as compared to the control treatment, while pure Thymol at 10 mg/ml gave the best result in reducing the levels of CHO, TRI, and HDL. In comparison to the control group, serum levels of liver enzymes in groups treated with in A. annua, T. vulgaris extract, and pure Thymol were substantially reduced in concentration: 20, 10 and 30 mg/ml, respectively.

A series of 1,2,3-triazole, oxadiazole and aza-β-lactam derivatives were synthesized through consecutive reaction began from o-(N-propargyl) sulfonamido benzoic acid (1a). The reaction of (1a) with absolute ethanol in the presence of concentrated H2SO4 resulted in the formation of ester derivative (2a). The product of the previous reaction was reacted with 80% hydrazine hydrate to prepare benzohydrazide derivative (3a). 1,3,4-oxadiazole compound (4a) was obtained by condensation of compound (3a) with CS2 in presence KOH . Compound (3a) react with Phenyl isocyanates to give Carboxamide derivative (5a), that Condensation either with 2,4-dimethoxybenzaldhyde and p-hydroxybenzaldehyde to prepare the Schiff bases (6a-b). The cycloaddotion of Schiff-bases (6a-b) with phenyl isocyanate gave aza-β-lactams (7a-b). Benzamide derivatives (8a-c) were prepared via the reaction of compound (1a) with aniline derivatives, such as (p-toluidine, o-nitroaniline and m-nitroaniline). In a regioselective reaction 1,4-disubstituted-1,2,3-triazole derivative (9a-j) were synthesized via the click reaction of compounds 4a,5a and (8a-c) with benzyl azide and p-bromobenzyl azide. The compounds were identified using the spectral methods shown in the work. Cytotoxic effects of some final prepared compounds were studied in one cultured cellular models (MCF7 cell line) breast cancer (at various concentrations) by MTT assay, compound (9j) showed the better cytotoxic activity among the tested compounds.