Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Majid Nazir"'
Autor:
Muhammad Athar Abbasi, Zia Ur Rehman, Aziz Ur Rehman, Sabhat Zahra Siddiqui, Majid Nazir, Mubashir Hassan, Hussain Raza, Syed Adnan Ali Shah, sung-Yum Seo
Publikováno v:
Acta Chimica Slovenica, Vol 67, Iss 2, Pp 403-414 (2020)
The designed bi-heterocyclic sulfonamides were synthesized through a two-step protocol and their structures were ascertained by spectral techniques including IR, 1H NMR and 13C NMR along with CHN analysis. The in vitro inhibitory effects of these sul
Externí odkaz:
https://doaj.org/article/bf2ec3bb107843a59f213522901baa73
Autor:
S. Z. Siddiqui, Muhammad Athar Abbasi, Syed Afaq Ali Shah, Muhammad Shahid, Ayesha Zafar, Majid Nazir, Aziz-ur-Rehman, Hussain Raza
Publikováno v:
Russian Journal of Bioorganic Chemistry. 47:1086-1096
In the present research work, a new series of N-(substituted-phenyl)-3-(4-phenyl-1-piperazinyl)propanamides were synthesized. The synthesis was initiated by the coupling of different aromatic amines with 3-bromopropanoyl chloride in aqueous basic med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae41b70b72637e55f26802f052056554
https://doi.org/10.1134/s1068162021050186
https://doi.org/10.1134/s1068162021050186
Autor:
Syed Adnan Ali Shah, Wajiha Khan, Sung Y. Seo, Muhammad Athar Abbasi, Aziz-ur Rehman, Muhammad Shahid, Hussain Raza, Mubashir Hassan, Sabahat Zahra Siddiqui, Majid Nazir
Publikováno v:
Journal of Heterocyclic Chemistry. 57:2955-2968
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4137a247eb2e63079a5951954c04d29
https://doi.org/10.1002/jhet.4006
https://doi.org/10.1002/jhet.4006
Autor:
null Shakila, Muhammad A. Abbasi, null Aziz-ur-Rehman, Sabahat Z. Siddiqui, Majid Nazir, Hussain Raza, Ayesha Zafar, Syed A.A. Shah, Muhammad Shahid, Sung-Yum Seo
Publikováno v:
Journal of Molecular Structure. 1261:132953
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acadb171e087f81d0375c782e031a3ce
https://doi.org/10.1016/j.molstruc.2022.132953
https://doi.org/10.1016/j.molstruc.2022.132953
Autor:
Aziz Ur Rehman, S. Z. Siddiqui, Hussain Raza, Sung-Yum Seo, Majid Nazir, Mubashir Hassan, Muhammad Athar Abbasi, Syed Adnan Ali Shah, Zia Ur Rehman
Publikováno v:
Acta Chimica Slovenica, Vol 67, Iss 2, Pp 403-414 (2020)
The designed bi-heterocyclic sulfonamides were synthesized through a two-step protocol and their structures were ascertained by spectral techniques including IR, 1H NMR and 13C NMR along with CHN analysis. The in vitro inhibitory effects of these sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abdb60f8d62b1115151143d34315eaef
https://pubmed.ncbi.nlm.nih.gov/33855544
https://pubmed.ncbi.nlm.nih.gov/33855544
Autor:
Muhammad Athar, Abbasi, Misbah, Irshad, Aziz-Ur-Rehman, Sabahat Zahra, Siddiqui, Majid, Nazir, Syed Adnan, Ali Shah, Muhammad, Shahid
Publikováno v:
Pakistan journal of pharmaceutical sciences. 33(5)
In the presented work, 2,3-dihydro-1,4-benzodioxin-6-amine (1) was reacted with 4-chlorobenzenesulfonyl chloride (2) in presence of aqueous basic aqueous medium to obtain 4-chloro-N-(2,3-dihydro-1,4-benzodioxin-6-yl)benzenesulfonamide (3). In paralle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::016990bcdcffde331f4ea9ea770a1ba9
https://pubmed.ncbi.nlm.nih.gov/33824125
https://pubmed.ncbi.nlm.nih.gov/33824125
Autor:
Muhammad Shahid, Khalid Mohammed Khan, Farman Ali Khan, Sabahat Zahra Siddiqui, Kanwal, Majid Nazir, Aziz-ur-Rehman, Muhammad Athar Abbasi, Muhammad Arif Lodhi, Uzma Salar, Muhammad Ashraf
Publikováno v:
Bioorganic Chemistry. 81:253-263
Current study is based on the sequential conversion of indolyl butanoic acid (1) into ethyl indolyl butanoate (2), indolyl butanohydrazide (3), and 1,3,4-oxadiazole-2-thiol analogs (4) by adopting chemical transformations. In a parallel series of rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::043ab783a0854ce090d6b736e12479fa
https://doi.org/10.1016/j.bioorg.2018.08.010
https://doi.org/10.1016/j.bioorg.2018.08.010
Autor:
Aziz Ur Rehman, Muhammad Athar Abbasi, Mubashir Hassan, Sung-Yum Seo, Ayesha Mumtaz, Hussain Raza, Sahahat Zahra Siddiqui, Majid Nazir, Syed Adnan Ali Shah
Publikováno v:
Drug Research. 69:111-120
In this study, a new series of sulfonamides derivatives was synthesized and their inhibitory effects on DPPH and jack bean urease were evaluated. The in silico studies were also applied to ascertain the interactions of these molecules with active sit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::286f428073c4d2b7138ceaf1d417fff2
https://doi.org/10.1055/a-0654-5074
https://doi.org/10.1055/a-0654-5074
Autor:
Syed Adnan Ali Shah, Muhammad Shahid, Hussain Raza, Sabahat Zahra Siddiqui, Sung-Yum Seo, Majid Nazir, Aziz-ur-Rehman, Muhammad Athar Abbasi, Mubashir Hassan
Publikováno v:
RSC Advances. 8:25920-25931
In the study presented herein, 4-(1H-indol-3-yl)butanoic acid (1) was sequentially transformed in the first phase into ethyl 4-(1H-indol-3-yl)butanoate (2), 4-(1H-indol-3-yl)butanohydrazide (3) and 5-[3-(1H-indol-3-yl)propyl]-1,3,4-oxadiazole-2-thiol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f4ea3a2e08f3eabdfb70419b7b82958
https://doi.org/10.1039/c8ra04987d
https://doi.org/10.1039/c8ra04987d
Autor:
Majid, Nazir, Muhammad Athar, Abbasi, Aziz-Ur-Rehman, Sabahat Zahra, Siddiqui, Syed Adnan, Ali Shah, M, Shahid, H, Fatima, Sunniya, Iftikhar, Rahman Shah, Zaib Saleem
Publikováno v:
Pakistan journal of pharmaceutical sciences. 32(6)
In the study presented here, the nucleophilic substitution reaction of 5-[3-(1H-indol-3-yl)propyl]-1,3,4-oxadiazol-2-ylhydrosulfide was carried out with different alkyl/aralkyl halides (5a-r) to form its different S-substituted derivatives (6a-r), as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::caf36e6d0e32fcd3ce34e0c4e2cde310
https://pubmed.ncbi.nlm.nih.gov/31969290
https://pubmed.ncbi.nlm.nih.gov/31969290