Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ammar A. Razzak Mahmood Kubba"'
Publikováno v:
Indonesian Journal of Pharmacy, Pp 17-34 (2021)
A new series of flurbiprofen derivatives containing thiosemicarbazide moiety (3-7) was synthesized from flurbiprofen as parent nucleus by esterification, hydrazide formation, and heating with different aryl isothiocyanate substituents, respectively.
Externí odkaz:
https://doaj.org/article/4626fbc3c69f418ca266989d595e3495
Autor:
Ali Azeez Ali Al-Jumaili, Sahar B. Aljuboori, Ammar A. Razzak Mahmood Kubba, Rawaa Fathel, Haneen Talab
Publikováno v:
INNOVATIONS in Pharmacy, Vol 10, Iss 3 (2019)
Objective: This study goal was to screen participants from different settings in Baghdad for depression using Beck Depression Inventory (BDI) scale and identify factors influencing the levels of depression. Methods: This cross-sectional study incl
Externí odkaz:
https://doaj.org/article/0380b32f03f04ef0860401a8d713a253
Publikováno v:
Indonesian Journal of Pharmacy.
A new series of flurbiprofen derivatives containing thiosemicarbazide moiety (3-7) was synthesized from flurbiprofen as parent nucleus by esterification, hydrazide formation, and heating with different aryl isothiocyanate substituents, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd9d9634474381464abce84595d2b0a9
https://doi.org/10.22146/ijp.730
https://doi.org/10.22146/ijp.730
Publikováno v:
Iraqi Journal of Pharmaceutical Sciences, Vol 27, Iss 1 (2018)
Two compounds,[2-amino-4-(4-nitro phenyl) 1,3-thiazole],(4) and [2-amino-4-(4-bromo phenyl) 1,3-thiazole],(5), were synthesized by refluxing thiourea (1) with each of para-ntiro and para-bomophanacyl bromides(2) and (3) respectively, in absolute meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bf04858e12c452cdc9bd2cfdca6f3bc
https://doi.org/10.31351/vol27iss1pp69-78
https://doi.org/10.31351/vol27iss1pp69-78
Autor:
Sahar B. Al-Juboori, Rawaa Fathel, Ali Azeez Al-Jumaili, Haneen Talab, Ammar A. Razzak Mahmood Kubba
Publikováno v:
INNOVATIONS in Pharmacy, Vol 10, Iss 3 (2019)
Innovations in Pharmacy
Innovations in Pharmacy
Objective: This study goal was to screen participants from different settings in Baghdad for depression using Beck Depression Inventory (BDI) scale and identify factors influencing the levels of depression. Methods: This cross-sectional study include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::476869b97685a0e7c36b3eb7c563c1e6
https://pubs.lib.umn.edu/index.php/innovations/article/view/2036
https://pubs.lib.umn.edu/index.php/innovations/article/view/2036
Publikováno v:
Indonesian Journal of Pharmacy. 31:92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c20d119beb1312b37bb43f2112bdcb8
https://doi.org/10.14499/indonesianjpharm31iss2pp92
https://doi.org/10.14499/indonesianjpharm31iss2pp92
Publikováno v:
Research Journal of Pharmacy and Technology. 13:3329
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b40bdd2816e221c90607ccfda2904f47
https://doi.org/10.5958/0974-360x.2020.00591.0
https://doi.org/10.5958/0974-360x.2020.00591.0
Publikováno v:
Iraqi Journal of Pharmaceutical Sciences, Vol 27, Iss 1 (2018)
2-amino-4-(4-chloro phenyl)-1,3-thiazole (1) was synthesized by refluxing thiourea with para-chloro phenacyl bromide in absolute methanol. The condensation of amine compound (1) with phenylisothiocyanate in the presence of pyridine will produce 1-(4-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4d3726aaffaac1e56c0a75c52bb9f7
https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/776
https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/776
Autor:
Michel Koch, François Tillequin, Brigitte Deguin, Ammar A. Razzak Mahmood Kubba, Marc Litaudon
Publikováno v:
Biochemical Systematics and Ecology. 33:305-307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7b328c2da08a7700d8219f22d4b9e6e
https://doi.org/10.1016/j.bse.2004.06.008
https://doi.org/10.1016/j.bse.2004.06.008