| 1 |
Ghorbani-Choghamarani A, Aghavandi H, Talebi SM. A new copper-supported zinc ferrite as a heterogeneous magnetic nanocatalyst for the synthesis of bis(pyrazolyl)methanes and oxidation of sulfides. Sci Rep 2022;12:20775. [PMID: 36456752 DOI: 10.1038/s41598-022-25170-w] [Reference Citation Analysis]
|
| 2 |
Damena T, Alem MB, Zeleke D, Desalegn T, Eswaramoorthy R, Demissie TB. Synthesis, characterization, and biological activities of zinc(II), copper(II) and nickel(II) complexes of an aminoquinoline derivative. Front Chem 2022;10. [DOI: 10.3389/fchem.2022.1053532] [Reference Citation Analysis]
|
| 3 |
Vchislo NV, Verochkina EA. Syntheses of quinolines and their derivatives from α,β-unsaturated aldehydes. Chem Heterocycl Comp. [DOI: 10.1007/s10593-022-03102-w] [Reference Citation Analysis]
|
| 4 |
Albayrak F, Çiçek M, Alkaya D, Kulu I. Design, synthesis and biological evaluation of 8-aminoquinoline-1,2,3-triazole hybrid derivatives as potential antimicrobial agents. Med Chem Res. [DOI: 10.1007/s00044-022-02866-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 5 |
Damena T, Zeleke D, Desalegn T, Demissie TB, Eswaramoorthy R. Synthesis, Characterization, and Biological Activities of Novel Vanadium(IV) and Cobalt(II) Complexes. ACS Omega 2022;7:4389-404. [PMID: 35155932 DOI: 10.1021/acsomega.1c06205] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
|
| 6 |
Ajani OO, Iyaye KT, Ademosun OT. Recent advances in chemistry and therapeutic potential of functionalized quinoline motifs – a review. RSC Adv 2022;12:18594-614. [DOI: 10.1039/d2ra02896d] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
| 7 |
Andac CA, Çakmak O, Ökten S, Çağlar-andac S, Işıldak İ. In-silico Pharmacokinetic and Affinity Studies of Piperazine/Morpholine Substituted Quinolines in Complex with GAK as Promising Anti-HCV Agent. J Comput Biophys Chem 2021;20:869-79. [DOI: 10.1142/s273741652150054x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
|
| 8 |
Patil SK, Vibhute BT. Synthesis, characterization, anticancer and DNA photocleavage study of novel quinoline Schiff base and its metal complexes. Arabian Journal of Chemistry 2021;14:103285. [DOI: 10.1016/j.arabjc.2021.103285] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 9 |
da Costa Rodrigues K, Bortolatto CF, de Oliveira RL, Paltian JJ, Larroza A, Soares MP, Alves D, Wilhelm EA, Luchese C. 4-Phenylselanyl-7-chloroquinoline attenuates hepatic injury triggered by neonatal exposure to monosodium glutamate in rats. Life Sci 2021;280:119751. [PMID: 34174321 DOI: 10.1016/j.lfs.2021.119751] [Reference Citation Analysis]
|
| 10 |
Antoci V, Oniciuc L, Amariucai-Mantu D, Moldoveanu C, Mangalagiu V, Amarandei AM, Lungu CN, Dunca S, Mangalagiu II, Zbancioc G. Benzoquinoline Derivatives: A Straightforward and Efficient Route to Antibacterial and Antifungal Agents. Pharmaceuticals (Basel) 2021;14:335. [PMID: 33917439 DOI: 10.3390/ph14040335] [Cited by in Crossref: 10] [Cited by in F6Publishing: 13] [Article Influence: 5.0] [Reference Citation Analysis]
|
| 11 |
Karkhah MK, Kefayati H, Shariati S. Synthesis of benzo[ h ]quinolone and benzo[ c ]acridinone derivatives by Fe 3 O 4 @ PS‐Arginine [ HSO 4 ] as an efficient magnetic nanocatalyst. J Heterocyclic Chem 2020;57:4181-91. [DOI: 10.1002/jhet.4125] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
|
| 12 |
Özcan E, Ökten S, Eren T. Decision making for promising quinoline‐based anticancer agents through combined methodology. J Biochem Mol Toxicol 2020;34. [DOI: 10.1002/jbt.22522] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
|
| 13 |
Ajani OO, Iyaye KT, Aderohunmu DV, Olanrewaju IO, Germann MW, Olorunshola SJ, Bello BL. Microwave-assisted synthesis and antibacterial propensity of N′-s-benzylidene-2-propylquinoline-4-carbohydrazide and N′-((s-1H-pyrrol-2-yl)methylene)-2-propylquinoline-4-carbohydrazide motifs. Arabian Journal of Chemistry 2020;13:1809-20. [DOI: 10.1016/j.arabjc.2018.01.015] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
|
| 14 |
Lopes EF, Penteado F, Thurow S, Pinz M, Reis AS, Wilhelm EA, Luchese C, Barcellos T, Dalberto B, Alves D, da Silva MS, Lenardão EJ. Synthesis of Isoxazolines by the Electrophilic Chalcogenation of β,γ-Unsaturated Oximes: Fishing Novel Anti-Inflammatory Agents. J Org Chem 2019;84:12452-62. [PMID: 31509698 DOI: 10.1021/acs.joc.9b01754] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 5.0] [Reference Citation Analysis]
|
| 15 |
de Freitas Couto S, Araujo SM, Bortolotto VC, Poetini MR, Pinheiro FC, Santos Musachio EA, Meichtry LB, do Sacramento M, Alves D, La Rosa Novo D, Mesko MF, Prigol M. 7-chloro-4-(phenylselanyl) quinoline prevents dopamine depletion in a Drosophila melanogaster model of Parkinson’s-like disease. Journal of Trace Elements in Medicine and Biology 2019;54:232-43. [DOI: 10.1016/j.jtemb.2018.10.015] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
|
| 16 |
Yao BR, Sun Y, Chen SL, Suo HD, Zhang YL, Wei H, Wang CH, Zhao F, Cong W, Xin WY, Hou GG. Dissymmetric pyridyl-substituted 3,5-bis(arylidene)-4-piperidones as anti-hepatoma agents by inhibiting NF-κB pathway activation. Eur J Med Chem 2019;167:187-99. [PMID: 30771605 DOI: 10.1016/j.ejmech.2019.02.020] [Cited by in Crossref: 31] [Cited by in F6Publishing: 35] [Article Influence: 7.8] [Reference Citation Analysis]
|
| 17 |
Nainwal LM, Tasneem S, Akhtar W, Verma G, Khan MF, Parvez S, Shaquiquzzaman M, Akhter M, Alam MM. Green recipes to quinoline: A review. Eur J Med Chem 2019;164:121-70. [PMID: 30594028 DOI: 10.1016/j.ejmech.2018.11.026] [Cited by in Crossref: 96] [Cited by in F6Publishing: 103] [Article Influence: 19.2] [Reference Citation Analysis]
|
| 18 |
Köprülü TK, Ökten S, Tekin Ş, Çakmak O. Biological evaluation of some quinoline derivatives with different functional groups as anticancer agents. J Biochem Mol Toxicol 2019;33:e22260. [PMID: 30431695 DOI: 10.1002/jbt.22260] [Cited by in Crossref: 30] [Cited by in F6Publishing: 31] [Article Influence: 6.0] [Reference Citation Analysis]
|
| 19 |
Liu L, Liu S, Hou G. Crystal structure of 4-(( E )-(( E )-5-(2-fluorobenzylidene)-1-((4-fluorophenyl)sulfonyl)-4-oxopiperidin-3-ylidene)methyl)benzonitrile, C 26 H 18 F 2 N 2 O 3 S. Zeitschrift für Kristallographie - New Crystal Structures 2018;233:1063-5. [DOI: 10.1515/ncrs-2018-0174] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
|
| 20 |
Li N, Xin W, Yao B, Cong W, Wang C, Hou G. N-phenylsulfonyl-3,5-bis(arylidene)-4-piperidone derivatives as activation NF-κB inhibitors in hepatic carcinoma cell lines. European Journal of Medicinal Chemistry 2018;155:531-44. [DOI: 10.1016/j.ejmech.2018.06.027] [Cited by in Crossref: 33] [Cited by in F6Publishing: 27] [Article Influence: 6.6] [Reference Citation Analysis]
|
| 21 |
Pinz MP, Dos Reis AS, Vogt AG, Krüger R, Alves D, Jesse CR, Roman SS, Soares MP, Wilhelm EA, Luchese C. Current advances of pharmacological properties of 7-chloro-4-(phenylselanyl) quinoline: Prevention of cognitive deficit and anxiety in Alzheimer's disease model. Biomed Pharmacother 2018;105:1006-14. [PMID: 30021335 DOI: 10.1016/j.biopha.2018.06.049] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 5.2] [Reference Citation Analysis]
|
| 22 |
Perin G, Araujo DR, Nobre PC, Lenardao EJ, Jacob RG, Silva MS, Roehrs JA. Ultrasound-promoted synthesis of 2-organoselanyl-naphthalenes using Oxone® in aqueous medium as an oxidizing agent. PeerJ 2018;6:e4706. [PMID: 29761042 DOI: 10.7717/peerj.4706] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 3.6] [Reference Citation Analysis]
|
