Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Samir Botros"'
Publikováno v:
Acta Chimica Slovenica, Vol 64, Iss 1, Pp 102-116 (2017)
A new series of 4-benzyl-6,7,8,9-tetrahydro[1]benzothieno[3,2-e][1,2,4]triazolo[4,3-a] pyrimidines was synthesized motivated by the widely reported anticancer activity of thieno[2,3-d]pyrimidines and triazolothienopyrimidines. The in vitro cytotoxic
Externí odkaz:
https://doaj.org/article/9460edad7d1f4f209be37966eda52240
Autor:
Sara Shamseldin, Liza Samir Botros, Salem Eid Salem, Sahar Abdel-Maksoud, Mohamed Zakaria Gad, Rasha Sayed Hanafi
Publikováno v:
Analytica, Vol 4, Iss 4, Pp 397-414 (2023)
The incidence of colorectal cancer (CRC) is increasing worldwide. It has variable signs and symptoms starting from changes in bowel habit to nausea and vomiting. Chemotherapeutic agents are often prescribed in CRC such as Capecitabine (CCB) and 5-Flu
Externí odkaz:
https://doaj.org/article/51b601229e714f02a2b1e50c9905ddd5
Publikováno v:
Acta Chimica Slovenica, Vol 64, Iss 1, Pp 102-116 (2017)
A new series of 4-benzyl-6,7,8,9-tetrahydro[1]benzothieno[3,2- e ][1,2,4]triazolo[4,3- a ] pyrimidines was synthesized motivated by the widely reported anticancer activity of thieno[2,3- d ]pyrimidines and triazolothienopyrimidines. The in vitro cyto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccbba2f36f3ddee76fc1cc392a2a1e7c
https://pubmed.ncbi.nlm.nih.gov/28380219
https://pubmed.ncbi.nlm.nih.gov/28380219
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02da5169a5cdc6a573b0f2cdf3a12664
https://doi.org/10.1080/03602559508017217
https://doi.org/10.1080/03602559508017217
Publikováno v:
Archives of pharmacal research. 35(12)
Synthesis, characterization and anticonvulsant properties of new bivalent ligands derived from phenytoin were described. Initial anticonvulsant screening was performed using maximal electroshock (MES) and pentylenetetrazole (PTZ) screens in mice. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c34116705e9ade3214c70095be267b1f
https://pubmed.ncbi.nlm.nih.gov/23263804
https://pubmed.ncbi.nlm.nih.gov/23263804
Publikováno v:
Archiv der Pharmazie. 318:318-327
5-Chlor-2-indolcarbohydrazid (1) kondensiert mit den Aldehyden 2a–k zu den Acylhydrazonen 3a–k. Behandelt man 3a–h kurz mit siedendem Acetanhydrid, so erhalt man die N-monoacetylierten 1,3,4-Oxadiazolylindole 4a–h. Die Cyclisierung von 3i–k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41eeac75722e184255fd2e3a3abba9bd
https://doi.org/10.1002/ardp.19853180407
https://doi.org/10.1002/ardp.19853180407
Autor:
S. F. Saad, Samir Botros
Publikováno v:
European Journal of Medicinal Chemistry. 24:585-590
The synthesis of seven 2-substituted 3-[4-[3-(4-aryl-1-piperazinyl)-isopropanoloxy]-phenyl]-4(3 H )quinazolones is described. Pharmacological tests showed that some of the synthesized compounds ( 3a–c and 3e ) possessed pronounced and sustained hyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::956cf34203dd19288720eaf9eca35f59
https://doi.org/10.1016/0223-5234(89)90025-1
https://doi.org/10.1016/0223-5234(89)90025-1
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f2491c4d45da5afbcd3f40532502e18
https://doi.org/10.1002/chin.198533228
https://doi.org/10.1002/chin.198533228
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2a3526cbc3b442d01b902664bd369d61
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034430394&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034430394&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3842432d7c15d3921182dc5a17df0952
http://www.scopus.com/inward/record.url?eid=2-s2.0-84994219788&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84994219788&partnerID=MN8TOARS