Zobrazeno 1 - 10
of 32
pro vyhledávání: '"AFZAL BASHA SHAIK"'
Autor:
Menavath Tulasi Naik Ram, Sai Kushal Gunturu, Afzal Basha Shaik, Yadlapalli Jaya Prasanth Babu, Sardena Siyonu Kumari
Publikováno v:
Journal of Pharmaceutical Research, Vol 21, Iss 4, Pp 123-127 (2022)
Crude Flavonoids extracted from crushed seeds of dried ripe fruits of Solanum surattense Burm F. were screened for antimicrobial activity against two bacteria – Streptococcus mutans and Aggregatibacter actinomycetemcomitans – which were found to
Externí odkaz:
https://doaj.org/article/015a317ec83f48d295b8962c8ec1622d
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 2, Pp 103581- (2022)
A series of chalcone analogues (1–15) were synthesized by Claisen-Schmidt condensation in good yields (70–95%) and characterized by FT-IR, 1H NMR and mass spectral methods. Additionally, compounds 3 and 7 were characterized by 13C NMR. Antituberc
Externí odkaz:
https://doaj.org/article/33fe2407f34c41bcb172add7a8cacff7
Autor:
Surendra Babu Lagu, Rajendra Prasad Yejella, Srinath Nissankararao, Richie R. Bhandare, Venu Sampath Golla, Bontha Venkata Subrahmanya Lokesh, M. Mukhlesur Rahman, Afzal Basha Shaik
Publikováno v:
PLoS ONE, Vol 17, Iss 6 (2022)
A series of newer previously synthesized fluorinated chalcones and their 2-amino-pyridine-3-carbonitrile and 2-amino-4H-pyran-3-carbonitrile derivatives were screened for their in vitro antitubercular activity and in silico methods. Compound 40 (MIC~
Externí odkaz:
https://doaj.org/article/b48d8a259f454e2fa4b4da7727a6a5cc
Autor:
Richie R. Bhandare, Afzal Basha Shaik
Publikováno v:
Applied Sciences, Vol 11, Iss 22, p 10734 (2021)
Molecular hybridization (MH) of heterocyclic rings has enabled scientists to design and develop novel drugs and drug-like candidates. In our previous work, considering the importance of MH, we synthesized different kinds of chloropyrazine-tethered py
Externí odkaz:
https://doaj.org/article/fe0dd6beffe444b68eab5c30c39fe01a
Autor:
Afzal Basha Shaik, Mukhlesur Rahman
Publikováno v:
Medicinal Chemistry of Chemotherapeutic Agents ISBN: 9780323905756
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2470e42d346d8ffcbec82ab0463db6c3
https://doi.org/10.1016/b978-0-323-90575-6.00016-8
https://doi.org/10.1016/b978-0-323-90575-6.00016-8
Publikováno v:
Arabian Journal of Chemistry, Vol 15, Iss 2, Pp 103581-(2022)
A series of chalcone analogues (1–15) were synthesized by Claisen-Schmidt condensation in good yields (70–95%) and characterized by FT-IR, 1H NMR and mass spectral methods. Additionally, compounds 3 and 7 were characterized by 13C NMR. Antituberc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b748d0b06e34c79ae23c188775d27fd9
http://www.sciencedirect.com/science/article/pii/S1878535221005967
http://www.sciencedirect.com/science/article/pii/S1878535221005967
Publikováno v:
Revue Roumaine de Chimie. 65:771-776
In an effort to study the effect of 1,3,4-thidiazole based molecules on bacteria, fungal and tuberculosis species, we synthesized a series of Schiff bases (2a-2m) by reacting a variety of carbonyl compounds with 5-amino-1,3,4- thiadiazole-2-thiol. Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b96909457118184a54c02e49b4f9b4
https://doi.org/10.33224/rrch.2020.65.9.01
https://doi.org/10.33224/rrch.2020.65.9.01
Publikováno v:
Asian Journal of Chemistry. 31:1212-1220
Twenty novel pyrimidine derivatives were synthesized from 2,5-dichloro-3-acetylthienyl chalcones by reacting with guanidine HCl in presence of KOH and ethanol under reflux for 6 h. Their structural characterizations were evaluated by ATR-FTIR, 1H NMR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c29f97cc905ed755309f77a52d6b6add
https://doi.org/10.14233/ajchem.2019.21747
https://doi.org/10.14233/ajchem.2019.21747
Publikováno v:
Journal of Research in Pharmacy. 23:156-163
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::808500c45ef50d25bd7b45d85b9b8d04
https://doi.org/10.12991/jrp.2019.120
https://doi.org/10.12991/jrp.2019.120
Autor:
Surendra Babu Lagu, Rajendra Prasad Yejella, Srinath Nissankararao, Richie R. Bhandare, Venu Sampath Golla, Bontha Venkata Subrahmanya Lokesh, M. Mukhlesur Rahman, Afzal Basha Shaik
Publikováno v:
PloS one. 17(6)
A series of newer previously synthesized fluorinated chalcones and their 2-amino-pyridine-3-carbonitrile and 2-amino-4H-pyran-3-carbonitrile derivatives were screened for their in vitro antitubercular activity and in silico methods. Compound 40 (MIC~
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c55a206687a76f087ba47f994ea3ee9
https://pubmed.ncbi.nlm.nih.gov/35709194
https://pubmed.ncbi.nlm.nih.gov/35709194