Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Shazia, Noreen"'
Autor:
Noreen Aslam, Jonathan M. White, Ansa M. Zafar, Mussarat Jabeen, Abdul Ghafoor, Naveed Sajjid, Shazia Noreen, Misbahul Ain Khan
Publikováno v:
ARKIVOC, Vol 2018, Iss 6, Pp 139-203 (2018)
Externí odkaz:
https://doaj.org/article/91f3ea69db9b42d9b475a132407d5a36
Autor:
Hamid Hussain, Masroor Hussain, Shazia Noreen, Sheikh Arslan Sehgal, Khayam Ul Haq, Sami Siraj, Rana Adnan Tahir, Awais Ihsan, Amjad Essa, Waheed Iqbal, Mahreen Ul Hassan
Publikováno v:
Combinatorial Chemistry & High Throughput Screening. 23:517-524
Background: Escherichia coli various strains can cause alarmingly serious infections. Countries like Pakistan harbour the class of bacteria with one of the highest rates of resistance, but very little has been done to explore their genetic pool. Obje
Autor:
Shazia Noreen, Misbahul Ain Khan, Abdul Ghafoor, Naveed Sajjid, Noreen Aslam, Mussarat Jabeen, Ansa Madiah Zafar, Jonathan M. White
Publikováno v:
ARKIVOC, Vol 2018, Iss 6, Pp 139-203 (2018)
This review summarizes the synthetic pathways to pyrano[2,3-c]pyrazoles which either have a hydrogen atom, aryl substituent or condensed spiro group at the 4-position. Synthesis focuses on two component or MCR’s including three, four and five compo
Autor:
Khayam Ul, Haq, Shazia, Noreen, Sheikh A, Sehgal, Rana A, Tahir, Amjad, Essa, Awais, Ihsan, Mahreen Ul, Hassan, Waheed, Iqbal, Masroor, Hussain, Hamid, Hussain, Sami, Siraj
Publikováno v:
Combinatorial chemistryhigh throughput screening. 23(6)
Escherichia coli various strains can cause alarmingly serious infections. Countries like Pakistan harbour the class of bacteria with one of the highest rates of resistance, but very little has been done to explore their genetic pool.This study was de
Autor:
Ansa Madeeha, Zafar, Ambar, Iqbal, Muhammad, Ashraf, Samina, Aslam, Sadia, Naureen, Noreen, Aslam, Mussarat, Jabeen, Naveed, Sajid, Abdul, Ghafoor, Shazia, Noreen, Mahrzadi Noureen, Shahi, Misbahul Ain, Khan
Publikováno v:
Pakistan journal of pharmaceutical sciences. 32(3 (Supplementary))
Twelve derivatives of dihydropyridine derivatives (6-17) were synthesized and evaluated for in-vitro cholinesterases (AChE, BChE) inhibitory activity. All compounds showed potent activity with IC50 values between 0.21±0.003 to 147.14±0.12μM for AC
Autor:
Noreen, Aslam, Jonathan M, White, Abdul, Ghafoor, Ajmal, Shafique, Faizul Hassan, Nasim, Bakht, Jahan, M, Ashraf, Mussarat, Jabeen, Ansa Madiah, Zafar, Shazia, Noreen, Naveed, Sajid, Misbahul Ain, Khan
Publikováno v:
Pakistan journal of pharmaceutical sciences. 32(2 (Supplementary))
In the present communication, synthesis of bis-pyrazolones containing aryl motifs (4-14) and their α-glucosidase inhibitory activity, hemolytic and antihemolytic activities were reported. The newly synthesized compounds were characterized by analyti
Autor:
Said, Umer, Usman Ismat, Butt, Asad Ali, Toor, Zeeshan, Razzaq, Muhammad Waris, Farooka, Shazia, Noreen, Abeeda, Butt, Henry Paul, Redmond
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 30(4)
Gall stone ileus associated with cholecysto-duodenal fistula is a rare pathology. It most commonly presents in elderly females in 72-90% of cases. In such a case, a patient typically presents with recurrent attacks of sub-acute intestinal obstruction
Autor:
Mussarat, Jabeen, Karamat, Mehmood, Misbah-Ul Ain, Khan, Noreen, Aslam, Ansa Madiha, Zafar, Naveed, Sajid, Shazia, Noreen, Samina, Aslam, Abdul, Ghafoor
Publikováno v:
Pakistan journal of pharmaceutical sciences. 31(3(Supplementary))
The transition metal complexes of Co(II), Ni(II), and Cu(II) derived from N'-((5-(2,5-dichlorophenyl)furan-2-yl)methylene)-2-hydroxybenzohydrazide (L24) and N'-((5-(2, 5-dichlorophenyl)furan-2-yl)methylene)benzohydrazide (L21) have been synthesized b
Autor:
Shazia Noreen, Muhammad Ashraf, Areesha Nazeer, Munawar Ali Munawar, Misbahul Ain Khan, Umber Alam, Sadia Naureen
Publikováno v:
Medicinal Chemistry Research. 24:1586-1595
A series of new trisubstituted imidazoles-3-(4,5-diaryl-1H-imidazol-2-yl)-2-phenyl-1H-indole derivatives (2a–2u) were synthesized and evaluated for their α-glucosidase inhibition. The new compounds showed significant α-glucosidase inhibitory acti