Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Shahbaz Shamim"'
Autor:
Akinsola Adegboye Akande, Uzma Salar, Khalid Mohammed Khan, Shazia Syed, Sherifat Adeyinka Aboaba, Sridevi Chigurupati, Abdul Wadood, Muhammad Riaz, Muhammad Taha, Saurabh Bhatia, Kanwal, Shahbaz Shamim, Shahnaz Perveen
Publikováno v:
ACS Omega, Vol 6, Iss 35, Pp 22726-22739 (2021)
Externí odkaz:
https://doaj.org/article/9e311ed964a64ad8bb39b38e86115a25
Autor:
Fayaz Ali, Shahbaz Shamim, Mehreen Lateef, Khalid Mohammed Khan, Muhammad Taha, Uzma Salar, Abdul Wadood, Ashfaq Ur Rehman, Noor Ul Ain Nawaz, Shahnaz Perveen
Publikováno v:
ACS Omega, Vol 6, Iss 24, Pp 15794-15803 (2021)
Externí odkaz:
https://doaj.org/article/9532eedd41a04444994d1262fbd11469
Publikováno v:
Life, Vol 13, Iss 3, p 736 (2023)
Flavonoids, isoflavonoids, neoflavonoids, and their various subcategories are polyphenolics–an extensive class of natural products. These compounds are bioactive and display multiple activities, including anticancer, antibacterial, antiviral, antio
Externí odkaz:
https://doaj.org/article/1b82d0eb2d5f4f7fad9e4908f0ed174f
Autor:
Eboh Monday Odin, Abdul Hameed, Uchechukwu C. Okoro, Khalid Mohammed Khan, Shahbaz Shamim, Shafia Iftekhar, Efeturi A. Onoabedje, Irfan Ali, Samuel A. Egu
Publikováno v:
Mini-Reviews in Organic Chemistry. 19:591-607
Abstract: Quinoline-5,8-dione and naphthoquinone nuclei are very important substructures in industrial chemicals and pharmaceuticals. These compounds exhibit a wide variety of activities, including antifungal, antibacterial, antimalarial, antineoplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37baf2c52f72fc4e2b6b16ec085cdfc6
https://doi.org/10.2174/1570193x18666211007120708
https://doi.org/10.2174/1570193x18666211007120708
2‐Mercapto Benzoxazole Derivatives as Novel Leads: Urease Inhibition, In Vitro and In Silico Studies
Autor:
Ashfaq Ur Rehman, Uzma Salar, Shahnaz Perveen, Mehreen Lateef, Shahbaz Shamim, Dorcas Olufunke Moronkola, Muhammad Taha, Fazal Rahim, I. A. Oladosu, Abdul Wadood, Modinat M. Balogun, Khalid Mohammed Khan
Publikováno v:
ChemistrySelect. 6:8490-8498
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfcf9a16fbae19b992072abf95ebde07
https://doi.org/10.1002/slct.202102362
https://doi.org/10.1002/slct.202102362
Autor:
Kanwal, Saurabh Bhatia, Shahnaz Perveen, Akinsola Akande, Sherifat A. Aboaba, Muhammad Taha, Sridevi Chigurupati, Uzma Salar, Shahbaz Shamim, Khalid Mohammed Khan, Muhammad Riaz, Abdul Wadood, Shazia Syed
Publikováno v:
ACS Omega, Vol 6, Iss 35, Pp 22726-22739 (2021)
ACS Omega
ACS Omega
Benzimidazole scaffolds are known to have a diverse range of biological activities and found to be antidiabetic and antioxidant. In this study, a variety of arylated benzimidazoles 1–31 were synthesized. Except for compounds 1, 6, 7, and 8, all are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f556cbd4d8f05b3de7a40783a4e5f1
https://doi.org/10.1021/acsomega.1c03056
https://doi.org/10.1021/acsomega.1c03056
Autor:
Noor Ul Ain Nawaz, Mehreen Lateef, Shahbaz Shamim, Fayaz Ali, Khalid Mohammed Khan, Abdul Wadood, Muhammad Taha, Uzma Salar, Ashfaq Ur Rehman, Shahnaz Perveen
Publikováno v:
ACS Omega, Vol 6, Iss 24, Pp 15794-15803 (2021)
ACS Omega
ACS Omega
N-Aryl-3,4-dihydroisoquinoline carbothioamide analogues 1-22 were synthesized by a simple one-step reaction protocol and subjected to in vitro urease inhibition studies for the first time. All compounds 1-22 were found active and showed significant t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21f54b06393d06a4519138d1282cffd
https://doaj.org/article/9532eedd41a04444994d1262fbd11469
https://doaj.org/article/9532eedd41a04444994d1262fbd11469
Autor:
Shahbaz Shamim, Mohammad Mahdavi, Mohammad Ali Faramarzi, Bagher Larijani, Hayat Wali, Muhammad Taha, Uzma Salar, Ayaz Anwar, Shahnaz Perveen, Khalid Mohammed Khan
Publikováno v:
Journal of the Iranian Chemical Society. 18:2017-2034
Functionalized quinazolinone derivatives 1–30 were synthesized by two-step reaction. First, anthranilic acid was treated with substituted phenyl isothiocyanate to synthesize 3-aryl-2-thioxo-2,3-dihydroquinazolinone derivatives 1–8 which in turn r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e79f2f01bf411f9fc51939a9cd04c8c
https://doi.org/10.1007/s13738-021-02159-2
https://doi.org/10.1007/s13738-021-02159-2
Autor:
Sahib Gul Afridi, Farman Ali Khan, Khalid Mohammed Khan, Shahnaz Perveen, Shahbaz Shamim, Kanwal, Ajmal Khan, Farman Ali, Muhammad Arif Lodhi, Nisar Ullah
Publikováno v:
Medicinal Chemistry Research. 30:120-132
Scaffold varied dihydropyrimidone derivatives 1–20 were evaluated for their selective urease inhibitory kinetics potential. Compounds 1, 2, 3, 4, 5, 6, and 12 were found to be the most promising urease inhibitors and showed the inhibition (Ki value
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f247eb9e3fb6a759083c120a9ca981e
https://doi.org/10.1007/s00044-020-02643-z
https://doi.org/10.1007/s00044-020-02643-z
Autor:
Ashfaq Ur Rehman, Muhammad Taha, Muhammad Ali, Khalid Mohammed Khan, Shahbaz Shamim, Shahnaz Perveen, Ahmad Alhowail, Sridevi Chigurupati, Uzma Salar, Abdul Wadood, Nisar Ullah
Publikováno v:
Bioorganic chemistry. 101
(E)-3-(2-Benzylidenehydrazinyl)-5,6-diphenyl-1,2,4-triazines analogs 1–27 were synthesized by multi-step reaction scheme and subjected to in vitro inhibitory screening against α-amylase and α-glucosidase enzymes. Out of these twenty-seven synthet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25233d9d9c7e8f2e38cbf851c07d3561
https://pubmed.ncbi.nlm.nih.gov/32544738
https://pubmed.ncbi.nlm.nih.gov/32544738