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Design, synthesis and molecular modeling of novel pyridopyrazinone derivatives of expected antineoplastic activity / (Record no. 58007)

MARC details
000 -LEADER
fixed length control field 03130cam a2200325 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 161011s2016 ua dh f m 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EG-GiCUC
Language of cataloging eng
Transcribing agency EG-GiCUC
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
049 ## - LOCAL HOLDINGS (OCLC)
Holding library Deposite
097 ## - Thesis Degree
Thesis Level M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number Cai01.08.05.M.Sc.2016.Us.D
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Usama Mohamed Magdi Ammar
245 10 - TITLE STATEMENT
Title Design, synthesis and molecular modeling of novel pyridopyrazinone derivatives of expected antineoplastic activity /
Statement of responsibility, etc. Usama Mohamed Magdi Ammar ; Supervised Kamelia M. Amin , Ossama M. El-badry , Doaa E. Abdelrahman
246 15 - VARYING FORM OF TITLE
Title proper/short title تصمييم وتشييد ونمذجة جزيئية لبعض مشتقات البيريدوبيرازينون الجديدة و المتوقع لها فاعلية مضادة للأورام السرطانية
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Usama Mohamed Magdi Ammar ,
Date of publication, distribution, etc. 2016
300 ## - PHYSICAL DESCRIPTION
Extent 150 P. :
Other physical details charts , facsimiles ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. Cancer has proven to be one of the most intractable diseases to which humans are subjected. Cancer chemotherapy play an important role in the treatment of cancer. It has entered a new era of molecular targeted therapeutics, which is highly selective and not associated with the serious toxicities of conventional cytotoxic drugs. Unfortunately, targeted chemotherapy still has some limitations. The chief among them is the potential of cells to develp resistance. As a result, in most cases, it is advantageous to use them in combination, either with other targeted therapy or with traditional therapy. One of the most critical therapeutic target in the treatment of cancer is mutated BRAF kinase enzyme (V600EBRAF), which is involved in approximately 30% of human cancers.The present study was constructed to design and synthesize 42 pyridopyrazinone derivatives in order to investigate their activities against different cancer cell lines in addition, to study the possible interaction with the active site of mutated BRAF kinase enzyme. The 42 pyridopyrazinone derivatives were synthesized according to reported methods and their structures were elucidated using spectral analysis such as IR, 1HNMR and Mass spectroscopy in addition to elemental analysis. The in vitro antitumor screening was evaluated for the synthesized compounds against different cell lines such as melanoma, ovarian, thyroid and colon cancer using MTT assay method for 25 compounds and SRB assay method for 17 compound using sorafenib and doxorubicin as standards, respectivily. The results revealed that some of these compounds have a promising activity against thyroid and colon cancer
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Design, synthesis and molecular modeling
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Expected antineoplastic activity
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Novel pyridopyrazinone derivatives
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Doaa Ezzat Abdelrahman ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Kamelia Mahmoud Amin ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Ossama Metwally Elbadry ,
Relator term
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Enas
Reviser Cataloger
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Nazla
Reviser Revisor
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Holdings
Source of classification or shelving scheme Not for loan Home library Current library Date acquired Full call number Barcode Date last seen Koha item type Copy number
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 Cai01.08.05.M.Sc.2016.Us.D 01010110069784000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.08.05.M.Sc.2016.Us.D 01020110069784000 22.09.2023 CD - Rom 69784.CD