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For: Bennani FE, Doudach L, Cherrah Y, Ramli Y, Karrouchi K, Ansar M, Faouzi MEA. Overview of recent developments of pyrazole derivatives as an anticancer agent in different cell line. Bioorg Chem 2020;97:103470. [PMID: 32120072 DOI: 10.1016/j.bioorg.2019.103470] [Cited by in Crossref: 31] [Cited by in F6Publishing: 18] [Article Influence: 10.3] [Reference Citation Analysis]
Number Citing Articles
1 Gulia N, Małecki M, Szafert S. Direct Preparation of N-Substituted Pyrazoles from Primary Aliphatic or Aromatic Amines. J Org Chem 2021;86:9353-9. [PMID: 34197110 DOI: 10.1021/acs.joc.1c00606] [Reference Citation Analysis]
2 Kumar G, Saroha B, Kumar R, Kumari M, Dalal S, Kumar S. Design, synthesis, biological evaluation, and molecular docking studies of some novel N , N ‐dimethylaminopropoxy‐substituted aurones. Journal of Heterocyclic Chem 2022;59:297-308. [DOI: 10.1002/jhet.4384] [Reference Citation Analysis]
3 Chaudhry F, Shahid W, Al-Rashida M, Ashraf M, Ali Munawar M, Ain Khan M. Synthesis of imidazole-pyrazole conjugates bearing aryl spacer and exploring their enzyme inhibition potentials. Bioorg Chem 2021;108:104686. [PMID: 33581666 DOI: 10.1016/j.bioorg.2021.104686] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Benarjee V, Saritha B, Hari Gangadhar K, Sailaja B. Synthesis of some new 1,4-benzoxazine-pyrazoles in water as EGFR targeting anticancer agents. Journal of Molecular Structure 2022;1265:133188. [DOI: 10.1016/j.molstruc.2022.133188] [Reference Citation Analysis]
5 Nguyen HT, Le TV, Tran PH. AC-SO3H/[CholineCl][Urea]2 as a green catalytic system for the synthesis of pyrano[2,3-c]pyrazole scaffolds. Journal of Environmental Chemical Engineering 2021;9:105228. [DOI: 10.1016/j.jece.2021.105228] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
6 Abbas AA, Abdellattif MH, Dawood KM. Inhibitory activities of bipyrazoles: a patent review. Expert Opin Ther Pat 2021;:1-25. [PMID: 34232805 DOI: 10.1080/13543776.2021.1953474] [Reference Citation Analysis]
7 Becerra D, Rojas H, Castillo J. 3-(tert-Butyl)-N-(4-methoxybenzyl)-1-methyl-1H-pyrazol-5-amine. Molbank 2021;2021:M1196. [DOI: 10.3390/m1196] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Al-otaibi JS, Mary Y, Mary Y, Soman S, Acharjee N, B.narayana. Theoretical and experimental investigation of a pyrazole derivative- solvation effects, reactivity analysis and MD simulations. Chemical Physics Letters 2022;793:139469. [DOI: 10.1016/j.cplett.2022.139469] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Fabitha K, Chandrakanth M, Pramod RN, Arya CG, Li Y, Banothu J. Recent Developments in the Synthesis of Indole‐Pyrazole Hybrids. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201064] [Reference Citation Analysis]
10 Zhang XH, Guo Q, Wang HY, Li YH, Khamis MY, Ma LY, Wang B, Liu HM. Gramine-based structure optimization to enhance anti-gastric cancer activity. Bioorg Chem 2021;107:104549. [PMID: 33383324 DOI: 10.1016/j.bioorg.2020.104549] [Reference Citation Analysis]
11 Bayrakdar A, Mert S, Kasımoğulları R, Bangaru S, Manivannan P. Synthesis, spectroscopic (FT-IR and NMR), DFT and molecular docking studies of ethyl 1-(3-nitrophenyl)-5-phenyl-3-((4-(trifluoromethyl)phenyl)carbamoyl)-1H-pyrazole-4-carboxylate. Res Chem Intermed. [DOI: 10.1007/s11164-022-04681-1] [Reference Citation Analysis]
12 Sokov SA, Odin IS, Zlotski SS, Denisova AG, Golovanov AA. Reactions of Activated Enynes with Diazomethane. Russ J Org Chem 2021;57:1575-83. [DOI: 10.1134/s107042802110002x] [Reference Citation Analysis]
13 Malik MS, Asghar BH, Syed R, Alsantali RI, Morad M, Altass HM, Moussa Z, Althagafi II, Jassas RS, Ahmed SA. Novel Pyran-Linked Phthalazinone-Pyrazole Hybrids: Synthesis, Cytotoxicity Evaluation, Molecular Modeling, and Descriptor Studies. Front Chem 2021;9:666573. [PMID: 34109154 DOI: 10.3389/fchem.2021.666573] [Reference Citation Analysis]
14 Brullo C, Rapetti F, Bruno O. Pyrazolyl-Ureas as Interesting Scaffold in Medicinal Chemistry. Molecules 2020;25:E3457. [PMID: 32751358 DOI: 10.3390/molecules25153457] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
15 Azimi F, Ghasemi JB, Azizian H, Najafi M, Faramarzi MA, Saghaei L, Sadeghi-Aliabadi H, Larijani B, Hassanzadeh F, Mahdavi M. Design and synthesis of novel pyrazole-phenyl semicarbazone derivatives as potential α-glucosidase inhibitor: Kinetics and molecular dynamics simulation study. Int J Biol Macromol 2021;166:1082-95. [PMID: 33157144 DOI: 10.1016/j.ijbiomac.2020.10.263] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
16 Bennani FE, Doudach L, Karrouchi K, Tarib A, Rudd CE, Ansar M, Faouzi MEA. Targeting EGFR, RSK1, RAF1, PARP2 and LIN28B for several cancer type therapies with newly synthesized pyrazole derivatives via a computational study. J Biomol Struct Dyn 2022;:1-25. [PMID: 35442150 DOI: 10.1080/07391102.2022.2064915] [Reference Citation Analysis]
17 Ahmed MF, Santali EY, El-Haggar R. Novel piperazine-chalcone hybrids and related pyrazoline analogues targeting VEGFR-2 kinase; design, synthesis, molecular docking studies, and anticancer evaluation. J Enzyme Inhib Med Chem 2021;36:307-18. [PMID: 33349069 DOI: 10.1080/14756366.2020.1861606] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Deng Y, Dong Z, Gao F, Guo Y, Sun M, Li Y, Wang Y, Chen Q, Wang K, Yan W. The Regiocontrollable Enantioselective Synthesis of Chiral Trifluoromethyl-Containing Spiro-Pyrrolidine-Pyrazolone Compounds via Amino-Regulated 1,3-Proton Migration Reaction. J Org Chem 2021;86:13011-24. [PMID: 34494838 DOI: 10.1021/acs.joc.1c01705] [Reference Citation Analysis]
19 Golovanov AA, Odin IS, Gusev DM, Vologzhanina AV, Sosnin IM, Grabovskiy SA. Reactivity of Cross-Conjugated Enynones in Cyclocondensations with Hydrazines: Synthesis of Pyrazoles and Pyrazolines. J Org Chem 2021;86:7229-41. [PMID: 33955756 DOI: 10.1021/acs.joc.1c00569] [Reference Citation Analysis]
20 Wang G, Sun S, Guo H. Current status of carbazole hybrids as anticancer agents. Eur J Med Chem 2021;:113999. [PMID: 34838335 DOI: 10.1016/j.ejmech.2021.113999] [Reference Citation Analysis]
21 Guo H, Diao Q. 1,3,5-Triazine-azole Hybrids and their Anticancer Activity. CTMC 2020;20:1481-92. [DOI: 10.2174/1568026620666200310122741] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
22 Lei ZC, Li N, Yu NR, Ju W, Sun XN, Zhang XL, Dong HJ, Sun JB, Chen L. Design and Synthesis of Novel Celastrol Derivatives as Potential Anticancer Agents against Gastric Cancer Cells. J Nat Prod 2022. [PMID: 35536757 DOI: 10.1021/acs.jnatprod.1c01236] [Reference Citation Analysis]
23 Liu X, Nie Y, Tang Q, Tian A, Hu Z, Yan J, Zhang S. Pyrazole-based trinuclear and mononuclear complexes: synthesis, characterization, DNA interactions and cytotoxicity studies. Transit Met Chem 2021;46:481-94. [DOI: 10.1007/s11243-021-00466-4] [Reference Citation Analysis]
24 Khwaza V, Mlala S, Oyedeji OO, Aderibigbe BA. Pentacyclic Triterpenoids with Nitrogen-Containing Heterocyclic Moiety, Privileged Hybrids in Anticancer Drug Discovery. Molecules 2021;26:2401. [PMID: 33918996 DOI: 10.3390/molecules26092401] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
25 Vishnu WK, Abeesh P, Guruvayoorappan C. Pyrazole (1, 2-diazole) induce apoptosis in lymphoma cells by targeting BCL-2 and BCL-XL genes and mitigate murine solid tumour development by regulating cyclin-D1 and Ki-67 expression. Toxicol Appl Pharmacol 2021;418:115491. [PMID: 33737021 DOI: 10.1016/j.taap.2021.115491] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Song F, Li Z, Bian Y, Huo X, Fang J, Shao L, Zhou M. Indole/isatin-containing hybrids as potential antibacterial agents. Arch Pharm (Weinheim) 2020;353:e2000143. [PMID: 32667714 DOI: 10.1002/ardp.202000143] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
27 Costa RF, Turones LC, Cavalcante KVN, Rosa Júnior IA, Xavier CH, Rosseto LP, Napolitano HB, Castro PFDS, Neto MLF, Galvão GM, Menegatti R, Pedrino GR, Costa EA, Martins JLR, Fajemiroye JO. Heterocyclic Compounds: Pharmacology of Pyrazole Analogs From Rational Structural Considerations. Front Pharmacol 2021;12:666725. [PMID: 34040529 DOI: 10.3389/fphar.2021.666725] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Hou Y, Shang C, Meng T, Lou W. Anticancer potential of cardiac glycosides and steroid-azole hybrids. Steroids 2021;171:108852. [PMID: 33887267 DOI: 10.1016/j.steroids.2021.108852] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
29 Al-Otaibi JS, Sheena Mary Y, Fazil S, Mary YS, Sarala S. Modeling the structure and reactivity landscapes of a pyrazole-ammonium ionic derivative using wavefunction-dependent characteristics and screening for potential anti-inflammatory activity. J Biomol Struct Dyn 2021;:1-13. [PMID: 34328395 DOI: 10.1080/07391102.2021.1957020] [Reference Citation Analysis]
30 Farhat J, Alzyoud L, Alwahsh M, Al-Omari B. Structure-Activity Relationship of Benzofuran Derivatives with Potential Anticancer Activity. Cancers (Basel) 2022;14:2196. [PMID: 35565325 DOI: 10.3390/cancers14092196] [Reference Citation Analysis]
31 Allaka BS, Basavoju S, Gamidi RK. Transition Metal‐ and Oxidant‐Free Regioselective Synthesis of 3,4,5‐Trisubstituted Pyrazoles by Means of [3+2] Cycloaddition Reactions. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200605] [Reference Citation Analysis]
32 Luo B, Ning Y. Comprehensive Overview of Carboxamide Derivatives as Succinate Dehydrogenase Inhibitors. J Agric Food Chem 2022. [PMID: 35041423 DOI: 10.1021/acs.jafc.1c06654] [Reference Citation Analysis]
33 Das T, Mohapatra S, Priyadarsini Mishra N, Nayak S. Catalyst and base free aza-Michael addition reaction: Synthesis of poly-substituted 4-pyrazole based benzopyrans. Tetrahedron Letters 2022;96:153762. [DOI: 10.1016/j.tetlet.2022.153762] [Reference Citation Analysis]
34 Patel G, Maurya RK, Tyagi S, Kant R, Yadav PP. PIDA‐Mediated Intramolecular N‐N Bond Formation to Access 2‐Aminoindazoles and 2,2′‐Biindazoles**. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201112] [Reference Citation Analysis]
35 Devi P, Singh K, Dabas P. Synthesis of Co +2 , Ni +2 , Cu +2 , and Zn +2 complexes of Schiff base 5-methyl-3-((3,5-dichlorosalicylidene) amino)-pyrazole, spectral, and biological studies. Journal of Coordination Chemistry. [DOI: 10.1080/00958972.2022.2035726] [Reference Citation Analysis]
36 Alsayari A, Asiri YI, Muhsinah AB, Hassan MZ. Anticolon Cancer Properties of Pyrazole Derivatives Acting through Xanthine Oxidase Inhibition. J Oncol 2021;2021:5691982. [PMID: 34326873 DOI: 10.1155/2021/5691982] [Reference Citation Analysis]
37 Priya D, Gopinath P, Dhivya LS, Vijaybabu A, Haritha M, Palaniappan S, Kathiravan MK. Structural Insights into Pyrazoles as Agents against Anti‐inflammatory and Related Disorders. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202104429] [Reference Citation Analysis]
38 Luo G, Ma Y, Liang X, Xie G, Luo Y, Zha D, Wang S, Yu L, Zheng X, Wu W, Zhang C. Design, synthesis and antitumor evaluation of novel 5-methylpyrazolo[1,5-a]pyrimidine derivatives as potential c-Met inhibitors. Bioorg Chem 2020;104:104356. [PMID: 33142417 DOI: 10.1016/j.bioorg.2020.104356] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
39 Gangadhar KH, Benarjee V, Ratnamala A. Synthesis of Coumarin‐Thiazolidine‐2,4‐dione‐Pyrazole Hybrids as Epidermal Growth Factor Receptor (EGFR)‐Targeted Agents. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200270] [Reference Citation Analysis]
40 Becerra D, Cobo J, Castillo J. Ambient-Temperature Synthesis of (E)-N-(3-(tert-Butyl)-1-methyl-1H-pyrazol-5-yl)-1-(pyridin-2-yl)methanimine. Molbank 2021;2021:M1250. [DOI: 10.3390/m1250] [Reference Citation Analysis]
41 Alkhaibari I, Kc HR, Angappulige DH, Gilmore D, Alam MA. Novel pyrazoles as potent growth inhibitors of staphylococci, enterococci and Acinetobacter baumannii bacteria. Future Med Chem 2021. [PMID: 34877890 DOI: 10.4155/fmc-2021-0140] [Reference Citation Analysis]
42 Kamel MG, Sroor FM, Othman AM, Mahrous KF, Saleh FM, Hassaneen HM, Abdallah TA, Abdelhamid IA, Teleb MAM. Structure-based design of novel pyrazolyl–chalcones as anti-cancer and antimicrobial agents: synthesis and in vitro studies. Monatsh Chem. [DOI: 10.1007/s00706-021-02886-5] [Reference Citation Analysis]
43 Marandi A, Nasiri E, Koukabi N, Seidi F. The Fe3O4@apple seed starch core-shell structure decorated In(III): A green biocatalyst for the one-pot multicomponent synthesis of pyrazole-fused isocoumarins derivatives under solvent-free conditions. Int J Biol Macromol 2021;190:61-71. [PMID: 34411618 DOI: 10.1016/j.ijbiomac.2021.08.085] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]