Synthesis, Molecular Docking Studies And Biological Evaluation Of Some Unsaturated Carbonyl Derivatives / (Record no. 172302)

MARC details
000 -LEADER
fixed length control field 04563namaa22004451i 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - أخر تعامل مع التسجيلة
control field 20250702123547.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250522s2024 ua a|||fr|m|| 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloguing agency EG-GICUC
Language of cataloging eng
Transcribing agency EG-GICUC
Modifying agency EG-GICUC
Description conventions rda
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract eng
-- ara
049 ## - Acquisition Source
Acquisition Source Deposit
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 572
092 ## - LOCALLY ASSIGNED DEWEY CALL NUMBER (OCLC)
Classification number 572
Edition number 21
097 ## - Degree
Degree M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Local Call Number Cai01.12.02.M.Sc.2024.Ha.S.
100 0# - MAIN ENTRY--PERSONAL NAME
Authority record control number or standard number Hager Ahmed Sayed Ali,
Preparation preparation.
245 10 - TITLE STATEMENT
Title Synthesis, Molecular Docking Studies And Biological Evaluation Of Some Unsaturated Carbonyl Derivatives /
Statement of responsibility, etc. By Hager Ahmed Sayed; Supervisor Prof. Dr. Ismail Abdelshafy Abdelhamid, Dr .Nada Sabry Ibraheem Abd Elhady, Dr.Marwa Mohamed Mohamed Ahmed Sharaky.
246 15 - VARYING FORM OF TITLE
Title proper/short title التحضير ودراسات الالتحام الجزيئي والتقييم البيولوجي لبعض مشتقات الكربونيل غير المشبعة الجديدة /
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 2024.
300 ## - PHYSICAL DESCRIPTION
Extent 80 pages :
Other physical details illustrations ;
Dimensions 25 cm. +
Accompanying material CD.
336 ## - CONTENT TYPE
Content type term text
Source rda content
337 ## - MEDIA TYPE
Media type term Unmediated
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term volume
Source rdacarrier
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) -Cairo University, 2024.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Bibliography: pages 71-80.
520 ## - SUMMARY, ETC.
Summary, etc. Eight Novel chalcones were synthesized and their structures were confirmed by different spectral tools. All the prepared compounds were subjected to SRB cytotoxic screening against several cancer cell lines. Compound 5c exerted the most promising effect against MCF7 and HEP2 cells with IC50 values of 9.5 and 12 µg/mL, respectively. Real-time PCR demonstrated the inhibitory effect of compound 5c on the expression level of Antigen kiel 67 (KI-67), Survivin, Interleukin-1beta (IL-1B), Interleukin-6 (IL-6), Cyclooxygenase-2 (COX-2) and Protein kinase B (AKT1) genes. Flow-cytometric analysis of the cell cycle indicated that compound 5c stopped the cell cycle at the G0/G1 phase in MCF7 treated cells. ELISA assay showed that Caspase 8, Caspase 9, P53, BAX, and Glutathione (GSH) were extremely activated and Matrix metalloproteinase 2 (MMP2), Matrix metalloproteinase 9 (MMP9), BCL2, Malondialdehyde (MDA), and IL-6 were deactivated in 5c treated MCF7 and HEP2 cells. Wound healing revealed that chalcone 5c reduced the ability to close the scrape wound and decreased the number of migrating MCF7 and HEP2 cells compared to the untreated cells after 48 h. Theoretical molecular modeling against P53 cancer mutant Y220C and Bcl2 showed binding energies of -22.8 and -24.2 Kcal/mole, respectively which confirmed our ELISA results.
520 ## - SUMMARY, ETC.
Summary, etc. لقد تم تحضير ثمانية من مركبات الشالكون وتم التاكد منهم باستخدام الوسائل الطيفية المختلفه,لقد تم عمل الدراسات النظريه مثل التصميم الجزيئي لتحديد ميكانزم عمل هذه المركبات ,نتائج التاثير السمي علي الخلايا اوضحت ان المركب 5c له تاثير قوي علي الخلايا MCF7و HEP2 وقد تم اختيارهم لعمل الدراسات الجزيئيه ,لقد اوضح تحلبل البي سي ار الكمي ان المركب تسبب في نقص التعبير الجيني لجينات ki67 and survivin، IL-1B، IL-6، COX-2، AKT1 ,التحليل الفلوسيتموتري اوضح ان توقف دورة الخليه لخلايا سرطان الثدي قد تم عند مرحلة G0/G1 , وقد اوضحت نتائج تحليل الاليزا زيادة نشاطCaspase 8،Caspase 9 ، P53، BAX و GSH,وتقليل نشاط MMP2,MMP9,BCL2,MDA and IL-6 واظهر فحص التئام الجروح ان مركب 5C قلل من عدد خلايا الثدي والحنجره السرطانيه المهاجره الي مكان الجرح.
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Issues CD Issued also as CD
546 ## - LANGUAGE NOTE
Text Language Text in English and abstract in Arabic & English.
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Biochemistry
Source of heading or term qrmak
653 #0 - INDEX TERM--UNCONTROLLED
Uncontrolled term Chalcones
-- Antioxidant
-- Anti-inflammatory
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Ismail Abdelshafy Abdelhamid
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Nada Sabry Ibraheem Abd Elhady
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Marwa Mohamed Mohamed Ahmed Sharaky
Relator term thesis advisor.
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Tayser Abdelkhalek
Relator term thesis advisor.
900 ## - Thesis Information
Grant date 01-01-2024
Supervisory body Ismail Abdelshafy Abdelhamid
-- Nada Sabry Ibraheem Abd Elhady
-- Marwa Mohamed Mohamed Ahmed Sharaky
-- Tayser Abdelkhalek
Universities Cairo University
Faculties Faculty of Science
Department Department of Chemistry
905 ## - Cataloger and Reviser Names
Cataloger Name Eman El gebaly
Reviser Names Eman Ghareb
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Edition 21
Suppress in OPAC No
Holdings
Source of classification or shelving scheme Home library Current library Date acquired Inventory number Full call number Barcode Date last seen Effective from Koha item type
Dewey Decimal Classification المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 25.05.2025 91166 Cai01.12.02.M.Sc.2024.Ha.S. 01010110091166000 22.05.2025 25.05.2025 Thesis
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