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Synthesis of cinnoline derivatives as anticancer agents / (Record no. 61344)

MARC details
000 -LEADER
fixed length control field 03519cam a2200325 a 4500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GiCUC
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170619s2016 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 Cai01.08.04.M.Sc.2016.Ma.S
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Marwa Sobhy Ahmed Hassan
245 10 - TITLE STATEMENT
Title Synthesis of cinnoline derivatives as anticancer agents /
Statement of responsibility, etc. Marwa Sobhy Ahmed Hassan ; Supervisied Manal Mostafa Kandeel , Aliaa Mohamed Kamal , Bassem Heshmat Naguib
246 15 - VARYING FORM OF TITLE
Title proper/short title تشيييد مشتقات الينولين كمضادات للاورام
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Marwa Sobhy Ahmed Hassan ,
Date of publication, distribution, etc. 2016
300 ## - PHYSICAL DESCRIPTION
Extent 123 P. :
Other physical details charts , facsimiles ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University -Faculty of Pharmacy - Department of Organic Chemistry
520 ## - SUMMARY, ETC.
Summary, etc. The present thesis comprises four chapters. The first chapter is an introduction which is composed of two parts. The first part is a brief literature survey on the synthesis of cinnoline, pyrimidocinnoline and triazepinocinnoline derivatives. The second part is a survey covering topoisomerase I inhibitors as one of the recent fields of research, some reported cinnoline derivatives with anticancer activity and mechanisms of anticancer activity of some reported cinnoline derivatives. The second chapter demonstrates the aim of the work, along with the Schemes that had been carried out to obtain new cinnoline derivatives. The third chapter explains the theoretical discussion of the experimental work used for the preparation of the newly synthesized compounds, together with explanation of their spectroscopic data. Scheme of starting materials, reveals the preparation of the root compounds viz. 4-amino-6-substituted cinnoline-3-carboxamides (IIa,b), 4- amino-6-substituted cinnoline-3-carbohydrazides (Va,b) and their corresponding acids IIIa,b and esters IVa,b are presented. Scheme 1, compounds IIa,b were refluxed with acetic anhydride to yield pyrimidocinnoline derivatives VIa,b. However, the reaction of IIa,b with certain phenacyl bromides gave 4-(2-aryl-2-oxoethylamino)-6-substituted cinnoline-3- carboxamides (VIIa-g) rather than diazepinocinnolines A. Scheme 2, cyclization of the hydrazides Va,b with acetic acid gave triazepinocinnoline derivatives VIIIa,b. On the other hand, reacting Vb with different aromatic acids gave unexpectedly triazepinocinnoline derivatives IXa,b instead of the oxadiazolylcinnoline derivatives B. Moreover, heating Vb with the appropriate aromatic aldehyde yielded the corresponding arylidene derivatives Abstract vii Xa-d. Cyclization of the latter Xa with acetic anhydride gave unexpectedly pyrimidocinnoline derivative XI instead of oxadiazolylcinnoline derivative C. Scheme 3, cyclization of the hydrazide Vb with carbon disulphide yielded the triazepinocinnoline derivative XII instead of the expected pyrimidocinnoline derivative XIII. However, triazepinocinnoline derivative XII underwent thermal isomerization upon refluxing with xylene (high boiling point solvent) to give the more thermodynamically stable pyrimidocinnoline derivative XIII
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Cinnolines
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Pyrimidocinnolines
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Triazepinocinnolines
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Aliaa Mohamed Kama ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Bassem Heshmat Naguib ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Manal Mostafa Kandeel ,
Relator term
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 Cai01.08.04.M.Sc.2016.Ma.S 01010110072006000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.08.04.M.Sc.2016.Ma.S 01020110072006000 22.09.2023 CD - Rom 72006.CD