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Phytochemical and biological study of solanum indichum distichum : Family solaneaceae / Ala{u2019}a Youssef Hassanin Eid ; Supervised Hesham I. Elaskary , Shahira M. Ezzat

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Ala{u2019}a Youssef Hassanin Eid , 2018Description: 164 P. : charts , facsimiles ; 25cmOther title:
  • دراسة فيتوكميائي وحيوية لنبات السولانم انديكم دستيكم : العائلة الباذنجانية [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmacognosy Summary: Several Solanum species were found to be very important as natural sources of steroidal alkaloids. Based on the current literature, it was found that meager work was carried out on this species. Accordingly, it was necessary to carry out a phytochemical and pharmacological study of S. distichum fruits. The powdered S. distichum fruits were subjected to proximate and nutritional analysis including determination of moisture, ash, crude fibers, carbohydrate, protein, fat, macro- and micro elements as well as antioxidant vitamins A, C and E. Appropriate published analytical methods were applied. The fruits were rich in crude fibers, potassium, and vitamin A. The quantitative estimation of total phenolic, flavonoid and steroidal content of the total ethanol extract were estimated as 40.43 ± 0. 68 og of gallic acid equivalent/mg, 50.30 ± 0.42 og of quercetin equivalent /mg and 23.52 ± 0.57 og of ursolic acid equivalent /mg respectively. In vitro angiotensin-converting enzyme (ACE) and renin inhibitory activity showed that n-butanol and chloroform fractions are the most active two fractions among tested fractions. Ý-sitosterol and stigmasterol-O-glycoside were isolated from chloroform fraction, while khasianine, solamargine, indioside A and indioside F were isolated from n-butanol fraction.This is the first report on the ACE and renin inhibitory activity of Ý-sitosterol, stigmasterol-O-glycoside, khasianine, solamargine, indioside A, and indioside F
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.07.M.Sc.2018.Al.P (Browse shelf(Opens below)) Not for loan 01010110075975000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.07.M.Sc.2018.Al.P (Browse shelf(Opens below)) 75975.CD Not for loan 01020110075975000

Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmacognosy

Several Solanum species were found to be very important as natural sources of steroidal alkaloids. Based on the current literature, it was found that meager work was carried out on this species. Accordingly, it was necessary to carry out a phytochemical and pharmacological study of S. distichum fruits. The powdered S. distichum fruits were subjected to proximate and nutritional analysis including determination of moisture, ash, crude fibers, carbohydrate, protein, fat, macro- and micro elements as well as antioxidant vitamins A, C and E. Appropriate published analytical methods were applied. The fruits were rich in crude fibers, potassium, and vitamin A. The quantitative estimation of total phenolic, flavonoid and steroidal content of the total ethanol extract were estimated as 40.43 ± 0. 68 og of gallic acid equivalent/mg, 50.30 ± 0.42 og of quercetin equivalent /mg and 23.52 ± 0.57 og of ursolic acid equivalent /mg respectively. In vitro angiotensin-converting enzyme (ACE) and renin inhibitory activity showed that n-butanol and chloroform fractions are the most active two fractions among tested fractions. Ý-sitosterol and stigmasterol-O-glycoside were isolated from chloroform fraction, while khasianine, solamargine, indioside A and indioside F were isolated from n-butanol fraction.This is the first report on the ACE and renin inhibitory activity of Ý-sitosterol, stigmasterol-O-glycoside, khasianine, solamargine, indioside A, and indioside F

Issued also as CD

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