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Design, synthesis and anticancer activity evaluation of new heterocyclic derivatives as PARP inhibitors / (Record no. 74309)

MARC details
000 -LEADER
fixed length control field 02035cam a2200349 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032411.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 191007s2019 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 Ph.D
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number Cai01.08.05.Ph.D.2019.Gh.D
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Ghada Fathy Hussein Elmasry
245 10 - TITLE STATEMENT
Title Design, synthesis and anticancer activity evaluation of new heterocyclic derivatives as PARP inhibitors /
Statement of responsibility, etc. Ghada Fathy Hussein Elmasry ; Supervised Samir Mohamed Elmoghazy , Fadi Mohsen Awadallah , Enayat Ebrahim Aly
246 15 - VARYING FORM OF TITLE
Title proper/short title تصميم و تشييد بعض المشتقات الحلقية الغير متجانسة كمضادات للسرطان من خلال تثبيط انزيم بارب
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Ghada Fathy Hussein Elmasry ,
Date of publication, distribution, etc. 2019
300 ## - PHYSICAL DESCRIPTION
Extent 110 P. :
Other physical details charts , facsimiles ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Ph.D.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. This work deals with the design and synthesis of some novel pyrido[2,3-d]pyridazinone derivatives; VIIIa-g, IXa,b, Xa-d and XIa-g as PARP-1 inhibitors. Molecular modeling techniques were used to support the design. The twenty newly synthesized compounds were evaluated for their ability to inhibit PARP-1. The in vitro cytotoxic activity of the target compounds was also performed at National Cancer Institute, NCI, Maryland, USA against sixty cell lines. Computational ADME study was conducted to ensure that the most active compounds have proper pharmacokinetic and drug-likeness properties
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Olaparib
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term PARP-1 inhibitors
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyridopyridazinones
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Enayat Ebrahim Aly ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Fadi Mohsen Awadallah ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Samir Mohamed Elmoghazy ,
Relator term
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://172.23.153.220/th.pdf">http://172.23.153.220/th.pdf</a>
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Nazla
Reviser Revisor
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Shimaa
Reviser Cataloger
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.Ph.D.2019.Gh.D 01010110079512000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.08.05.Ph.D.2019.Gh.D 01020110079512000 22.09.2023 CD - Rom 79512.CD