140 related articles for article (PubMed ID: 38571594)
1. Design, synthesis, and molecular docking of new phenothiazine incorporated
Abdula AM; Qarah AF; Alatawi K; Qurban J; Abualnaja MM; Katuah HA; El-Metwaly NM
Heliyon; 2024 Apr; 10(7):e28573. PubMed ID: 38571594
[TBL] [Abstract][Full Text] [Related]
2. New Route to the Synthesis of Novel Pyrazolo[1,5-a]pyrimidines and Evaluation of their Antimicrobial Activity as RNA Polymerase Inhibitors.
Abdallah AEM; Elgemeie GH
Med Chem; 2022; 18(9):926-948. PubMed ID: 35236270
[TBL] [Abstract][Full Text] [Related]
3. Synthesis, molecular docking, antimycobacterial and antimicrobial evaluation of new pyrrolo[3,2-c]pyridine Mannich bases.
Jose G; Suresha Kumara TH; Sowmya HBV; Sriram D; Guru Row TN; Hosamani AA; More SS; Janardhan B; Harish BG; Telkar S; Ravikumar YS
Eur J Med Chem; 2017 May; 131():275-288. PubMed ID: 28340368
[TBL] [Abstract][Full Text] [Related]
4. Antimicrobial activity of novel 5-benzylidene-3-(3-phenylallylideneamino)imidazolidine-2,4-dione derivatives causing clinical pathogens: Synthesis and molecular docking studies.
Ali D; Alarifi S; Chidambaram SK; Radhakrishnan SK; Akbar I
J Infect Public Health; 2020 Dec; 13(12):1951-1960. PubMed ID: 33289644
[TBL] [Abstract][Full Text] [Related]
5. Novel Mannich bases of ciprofloxacin with improved physicochemical properties, antibacterial, anticancer activities and caspase-3 mediated apoptosis.
Abdel-Rahman IM; Mustafa M; Mohamed SA; Yahia R; Abdel-Aziz M; Abuo-Rahma GEA; Hayallah AM
Bioorg Chem; 2021 Feb; 107():104629. PubMed ID: 33482607
[TBL] [Abstract][Full Text] [Related]
6. Design of new phenothiazine-thiadiazole hybrids via molecular hybridization approach for the development of potent antitubercular agents.
Ramprasad J; Nayak N; Dalimba U
Eur J Med Chem; 2015 Dec; 106():75-84. PubMed ID: 26520841
[TBL] [Abstract][Full Text] [Related]
7. Synthesis of BF₃ catalyzed Mannich derivatives with excellent ee from phenylpropanolamine, study of their antimicrobial activity and molecular docking.
Chennakesava Rao K; Easwaramoorthi K; Arun Y; Balachandran C; Muralidhara Rao KS; Govindhan M; Emi N; Prakasam T; Perumal PT
Bioorg Med Chem Lett; 2015 Oct; 25(19):4232-8. PubMed ID: 26296475
[TBL] [Abstract][Full Text] [Related]
8. 1,3,4-Oxadiazole
Al-Wahaibi LH; Mohamed AAB; Tawfik SS; Hassan HM; El-Emam AA
Molecules; 2021 Apr; 26(8):. PubMed ID: 33916955
[TBL] [Abstract][Full Text] [Related]
9. Benzothiazole Clubbed Imidazolone Derivatives: Synthesis, Molecular Docking, DFT Studies, and Antimicrobial Studies.
Desai N; Maheta A; Jethawa A; Ahmad I; Patel H; Dave B
Curr Comput Aided Drug Des; 2023; 19(2):123-136. PubMed ID: 36411562
[TBL] [Abstract][Full Text] [Related]
10. Design, Synthesis, Docking Study of Pyrazolohydrazinopyrimidin-4-one Derivatives and Their Application as Antimicrobials.
Alolayan RA; Ali Ahmed Elkanzi N; Hrichi H; Bakr RB
Chem Biodivers; 2023 May; 20(5):e202201209. PubMed ID: 36972046
[TBL] [Abstract][Full Text] [Related]
11. Cu (II)-catalyzed: synthesis of imidazole derivatives and evaluating their larvicidal, antimicrobial activities with DFT and molecular docking studies.
Mullaivendhan J; Akbar I; Gatasheh MK; Hatamleh AA; Ahamed A; Abuthakir MHS; Gurusamy R
BMC Chem; 2023 Nov; 17(1):155. PubMed ID: 37980500
[TBL] [Abstract][Full Text] [Related]
12. Synthesis, design, and assessment of novel morpholine-derived Mannich bases as multifunctional agents for the potential enzyme inhibitory properties including docking study.
Boy S; Türkan F; Beytur M; Aras A; Akyıldırım O; Karaman HS; Yüksek H
Bioorg Chem; 2021 Feb; 107():104524. PubMed ID: 33317836
[TBL] [Abstract][Full Text] [Related]
13. Synthesis, biological evaluation and molecular dynamics studies of 1,2,4-triazole clubbed Mannich bases.
Patel VM; Patel NB; Chan-Bacab MJ; Rivera G
Comput Biol Chem; 2018 Oct; 76():264-274. PubMed ID: 30092449
[TBL] [Abstract][Full Text] [Related]
14. Design, synthesis, molecular docking of new lipophilic acetamide derivatives affording potential anticancer and antimicrobial agents.
Ahmed HEA; Ihmaid SK; Omar AM; Shehata AM; Rateb HS; Zayed MF; Ahmed S; Elaasser MM
Bioorg Chem; 2018 Feb; 76():332-342. PubMed ID: 29227917
[TBL] [Abstract][Full Text] [Related]
15. Synthesis, Physicochemical Properties and Molecular Docking of New Benzothiazole Derivatives as Antimicrobial Agents Targeting DHPS Enzyme.
Azzam RA; Elboshi HA; Elgemeie GH
Antibiotics (Basel); 2022 Dec; 11(12):. PubMed ID: 36551457
[TBL] [Abstract][Full Text] [Related]
16. Synthesis, Cytotoxic Analysis, and Molecular Docking Studies of Tetrazole Derivatives via N-Mannich Base Condensation as Potential Antimicrobials.
Atef Hatamleh A; Al Farraj D; Salah Al-Saif S; Chidambaram S; Radhakrishnan S; Akbar I
Drug Des Devel Ther; 2020; 14():4477-4492. PubMed ID: 33122891
[TBL] [Abstract][Full Text] [Related]
17. Molecular hybridization approach for phenothiazine incorporated 1,2,3-triazole hybrids as promising antimicrobial agents: Design, synthesis, molecular docking and in silico ADME studies.
Reddyrajula R; Dalimba U; Madan Kumar S
Eur J Med Chem; 2019 Apr; 168():263-282. PubMed ID: 30822714
[TBL] [Abstract][Full Text] [Related]
18. Synthesis, Docking Study, Cytotoxicity, Antioxidant, and Anti-microbial Activities of Novel 2,4-Disubstituted Thiazoles Based on Phenothiazine.
An TNM; Phuong PT; Quang NM; Son NV; Cuong NV; Tan LV; Tri MD; Alam M; Tat PV
Curr Org Synth; 2020; 17(2):151-159. PubMed ID: 32418517
[TBL] [Abstract][Full Text] [Related]
19. Designing, synthesis and characterization of 2-aminothiazole-4-carboxylate Schiff bases; antimicrobial evaluation against multidrug resistant strains and molecular docking.
Ejaz S; Nadeem H; Paracha RZ; Sarwar S; Ejaz S
BMC Chem; 2019 Dec; 13(1):115. PubMed ID: 31535091
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, in silico molecular docking analysis, pharmacokinetic properties and evaluation of antibacterial and antioxidant activities of fluoroquinolines.
Fekadu M; Zeleke D; Abdi B; Guttula A; Eswaramoorthy R; Melaku Y
BMC Chem; 2022 Jan; 16(1):1. PubMed ID: 35027086
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
