Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Laxminarayana, Eppakayala"'
Publikováno v:
Results in Chemistry, Vol 10, Iss , Pp 101718- (2024)
A series of amide derivatives of 1,3,4-thiadiazole-benzimidazole (13a-j) has been designed, synthesized and screened for their anticancer activities against human breast cancer cell line (MCF-7), human lung cancer (A549), human colon cancer (Colo-205
Externí odkaz:
https://doaj.org/article/e62871eb9e554c1b9e1ce0d035118997
Autor:
Kishore Kumar Anantoju, Srinivasa Reddy Bireddy, Laxminarayana Eppakayala, Bhaskar Pittala, Thirumala Chary Maringanti, Janardhan Eppakayala
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101536- (2024)
A new series of 1,2,3-Triazole bearing Indole derivatives (6a–j, 8a & 9a) was developed and examined for their preliminary anticancer effects against five human cancer cell lines such as breast cancer cell line (MCF-7), human lung cancer cell line
Externí odkaz:
https://doaj.org/article/ec1238c285cc4faaad7dd4a47d67d9e2
Autor:
Veeranjaneyulu Pattabi, Madhu Raju Veeraboina, Laxminarayana Eppakayala, Srinivasu Navuluri, Naveen Mulakayala
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101442- (2024)
A library of aryl urea oxazole-pyrimidine derivatives (12a-j) have been synthesized and investigated for their anticancer activity profile against a panel of four human cancer cell lines including breast cancer (MCF-7), lung cancer (A549), colon canc
Externí odkaz:
https://doaj.org/article/4b52fb916ef1496fa61601a77723fbdf
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101403- (2024)
We have developed a new series of various aryl amide derivatives of thiazole-benzothaizole-pyrimidines (13a-j). Their chemical structures were characterized by 1HNMR, 13CNMR and mass spectral data. Further, in vitro anticancer properties of newly dev
Externí odkaz:
https://doaj.org/article/c5c9b7497a154102be6343354c3b12ef
Publikováno v:
Results in Chemistry, Vol 7, Iss , Pp 101303- (2024)
4-(5-(2-(4-(5-aryl-1,2,4-thiadiazol-3-yl)phenyl)-1H-imidazol-4-yl)-1,3,4-thiadiazol-2-yl) pyridines were synthesized from benzothioic O-acid and (E)-N'-hydroxy-4-(4-(5-(pyridin-4-yl)-1,3,4-thiadiazol-2-yl)-1H-imidazol-2-yl) benzamidine. New compounds
Externí odkaz:
https://doaj.org/article/8cb69f52bc73499bbd79a3730557c21d
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100977- (2023)
A new library of chalcone derivatives of oxazol-4-yl)-2-morpholinothiazole (10a-j) have been developed and synthesized. All these synthesized compounds were firmed by 1H NMR, 13C NMR and mass spectral data. Further, the in vitro anticancer effects of
Externí odkaz:
https://doaj.org/article/43f7e4b98f0a40c29e8a067958d78d7d
Autor:
Ravi Kumar Bommera, Shashikala Kethireddy, Rajeshwar Reddy Govindapur, Laxminarayana Eppakayala
Publikováno v:
BMC Chemistry, Vol 15, Iss 1, Pp 1-12 (2021)
Abstract Background 1,2,4-oxadiazole derivatives exhibited significant anti-cancer activity when they were evaluated, against human cancer cell lines. They also showed anti-inflammatory, analgesic, diabetic, immunosuppressive, α,β3-receptor antagon
Externí odkaz:
https://doaj.org/article/48d8f6d44b234650a5d9ff8b9004bb05
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100649- (2022)
A new series of 1,2,4-oxadiazole incorporated (2-(oxazol)-1H-imidazole derivatives 9a-j have been developed and synthesized. Further, the newly prepared compounds (9a-j) compounds were evaluated for their preliminary anticancer properties against fou
Externí odkaz:
https://doaj.org/article/079dc42c958c48a8a33d1357de615696
Autor:
Bhaskar Pittala, Srinivas Reddy Dachepally, Shashikala Kethireddy, Janardhan Eppakayala, Laxminarayana Eppakayala
Publikováno v:
Materials Today: Proceedings. 80:681-684
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b889aa054ef0d1c2fc68ec6dba578fc
https://doi.org/10.1016/j.matpr.2022.11.068
https://doi.org/10.1016/j.matpr.2022.11.068
Publikováno v:
Materials Today: Proceedings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33ec634b46b7a890d907935d8aea60f3
https://doi.org/10.1016/j.matpr.2023.03.598
https://doi.org/10.1016/j.matpr.2023.03.598