| 1 |
De S, Aamna B, Sahu R, Parida S, Behera SK, Dan AK. Seeking heterocyclic scaffolds as antivirals against dengue virus. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114576] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
|
| 2 |
Velidandi A, Kannuri R, Thupurani MK. Synthesis, In Silico Studies, and Larvicidal Activity of Novel Hydrazinyl 1,3-Thiazine Derivatives. Russ J Org Chem 2022;58:814-9. [DOI: 10.1134/s1070428022060094] [Reference Citation Analysis]
|
| 3 |
de Jesus Santos A, Macêdo NA, de Holanda Cavalcanti SC, Sarmento VHV, Moreira Lira AA, Dos Santos CP, La Corte Santos R, Souza Nunes R. Larvicidal formulation containing N-tosylindole: A viable alternative to chemical control of Aedes aegypti. Colloids Surf B Biointerfaces 2022;213:112380. [PMID: 35151995 DOI: 10.1016/j.colsurfb.2022.112380] [Reference Citation Analysis]
|
| 4 |
Seen SB, Gong Y, Ashton M. The application of the Fischer indole synthesis in medicinal chemistry. Advances in Heterocyclic Chemistry 2022. [DOI: 10.1016/bs.aihch.2022.11.001] [Reference Citation Analysis]
|
| 5 |
Mara Silva de Pádua G, Maria De Souza J, Celia Moura Sales M, Gomes de Vasconcelos L, Luiz Dall'Oglio E, Faraggi TM, Moreira Sampaio O, Campos Curcino Vieira L. Evaluation of Chalcone Derivatives as Photosynthesis and Plant Growth Inhibitors. Chem Biodivers 2021;18:e2100226. [PMID: 33998137 DOI: 10.1002/cbdv.202100226] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
|
| 6 |
Jacinto MJ, Souto RS, Silva VCP, Prescilio IC, Kauffmann AC, Soares MA, de Souza JR, Bakuzis AF, Fontana LC. Biosynthesis of Cube-Shaped Fe3O4 Nanoparticles for Removal of Dyes Using Fenton Process. Water Air Soil Pollut 2021;232. [DOI: 10.1007/s11270-021-05233-w] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
|
| 7 |
Kumar P, Lee JH, Lee J. Diverse roles of microbial indole compounds in eukaryotic systems. Biol Rev Camb Philos Soc 2021;96:2522-45. [PMID: 34137156 DOI: 10.1111/brv.12765] [Cited by in Crossref: 12] [Cited by in F6Publishing: 15] [Article Influence: 6.0] [Reference Citation Analysis]
|
| 8 |
Makhanya TR, Gengan RM. Zeolite‐catalyzed synthesis of nicotinyl‐fused indolo‐pyrazoles and evaluation of their activities against Anopheles arabiensis and Lipoxygenase. J Heterocyclic Chem 2021;58:706-715. [DOI: 10.1002/jhet.4190] [Reference Citation Analysis]
|
| 9 |
Falqueto SA, Pitaluga BF, de Sousa JR, Targanski SK, Campos MG, de Oliveira Mendes TA, da Silva GF, Silva DHS, Soares MA. Bacillus spp. metabolites are effective in eradicating Aedes aegypti (Diptera: Culicidae) larvae with low toxicity to non-target species. J Invertebr Pathol 2021;179:107525. [PMID: 33383067 DOI: 10.1016/j.jip.2020.107525] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 10 |
Targanski SK, Sousa JR, Pádua GM, Sousa JM, Vieira LC, Soares MA. Larvicidal activity of substituted chalcones against Aedes aegypti (Diptera: Culicidae) and non‐target organisms. Pest Manag Sci 2021;77:325-34. [DOI: 10.1002/ps.6021] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
|
