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For: Islam MS, Ghawas HM, El-Senduny FF, Al-Majid AM, Elshaier YAMM, Badria FA, Barakat A. Synthesis of new thiazolo-pyrrolidine-(spirooxindole) tethered to 3-acylindole as anticancer agents. Bioorg Chem 2019;82:423-30. [PMID: 30508794 DOI: 10.1016/j.bioorg.2018.10.036] [Cited by in Crossref: 33] [Cited by in F6Publishing: 26] [Article Influence: 8.3] [Reference Citation Analysis]
Number Citing Articles
1 Al-majid AM, Ghawas HM, Islam MS, Soliman SM, El-senduny FF, Badria FA, Ali M, Shaik MR, Ghabbour HA, Barakat A. Synthesis of spiroindolone analogue via three components reaction of olefin with isatin and sarcosine: Anti-proliferative activity and computational studies. Journal of Molecular Structure 2020;1204:127500. [DOI: 10.1016/j.molstruc.2019.127500] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
2 Farooq S, Mazhar A, Ghouri A, Ihsan-Ul-Haq, Ullah N. One-Pot Multicomponent Synthesis and Bioevaluation of Tetrahydroquinoline Derivatives as Potential Antioxidants, α-Amylase Enzyme Inhibitors, Anti-Cancerous and Anti-Inflammatory Agents. Molecules 2020;25:E2710. [PMID: 32545290 DOI: 10.3390/molecules25112710] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
3 Insuasty D, Castillo J, Becerra D, Rojas H, Abonia R. Synthesis of Biologically Active Molecules through Multicomponent Reactions. Molecules 2020;25:E505. [PMID: 31991635 DOI: 10.3390/molecules25030505] [Cited by in Crossref: 35] [Cited by in F6Publishing: 11] [Article Influence: 17.5] [Reference Citation Analysis]
4 Barakat A, Alshahrani S, Al-Majid AM, Ali M, Altowyan MS, Islam MS, Alamary AS, Ashraf S, Ul-Haq Z. Synthesis of a New Class of Spirooxindole-Benzo[b]Thiophene-Based Molecules as Acetylcholinesterase Inhibitors. Molecules 2020;25:E4671. [PMID: 33066293 DOI: 10.3390/molecules25204671] [Cited by in Crossref: 4] [Article Influence: 2.0] [Reference Citation Analysis]
5 Khalili M, Esmaeili AA, Khojastehnezhad A. Catalyst-free Facile Synthesis of Novel Fused Spiro[benzo[4,5]thiazolo[3,2- a ]pyrano[2,3- d ]pyrimidine-4,3'-indoline]-3-carbonitrile Derivatives via One-pot Three-Component Reaction. Organic Preparations and Procedures International. [DOI: 10.1080/00304948.2021.2011577] [Reference Citation Analysis]
6 Altowyan MS, Barakat A, Al-Majid AM, Al-Ghulikah HA. Spiroindolone Analogues as Potential Hypoglycemic with Dual Inhibitory Activity on α-Amylase and α-Glucosidase. Molecules 2019;24:E2342. [PMID: 31242688 DOI: 10.3390/molecules24122342] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
7 Espadinha M, Lopes EA, Marques V, Amaral JD, dos Santos DJ, Mori M, Daniele S, Piccarducci R, Zappelli E, Martini C, Rodrigues CM, Santos MM. Discovery of MDM2-p53 and MDM4-p53 protein-protein interactions small molecule dual inhibitors. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114637] [Reference Citation Analysis]
8 Barakat A, Islam MS, Ali M, Al-majid AM, Alshahrani S, Alamary AS, Yousuf S, Choudhary MI. Regio- and Stereoselective Synthesis of a New Series of Spirooxindole Pyrrolidine Grafted Thiochromene Scaffolds as Potential Anticancer Agents. Symmetry 2021;13:1426. [DOI: 10.3390/sym13081426] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 8.0] [Reference Citation Analysis]
9 Bora D, Kaushal A, Shankaraiah N. Anticancer potential of spirocompounds in medicinal chemistry: A pentennial expedition. Eur J Med Chem 2021;215:113263. [PMID: 33601313 DOI: 10.1016/j.ejmech.2021.113263] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Islam MS, Al-Majid AM, Azam M, Verma VP, Barakat A, Haukka M, Elgazar AA, Mira A, Badria FA. Construction of Spirooxindole Analogues Engrafted with Indole and Pyrazole Scaffolds as Acetylcholinesterase Inhibitors. ACS Omega 2021;6:31539-56. [PMID: 34869980 DOI: 10.1021/acsomega.1c03978] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
11 Beloglazkina A, Zyk N, Majouga A, Beloglazkina E. Recent Small-Molecule Inhibitors of the p53-MDM2 Protein-Protein Interaction. Molecules 2020;25:E1211. [PMID: 32156064 DOI: 10.3390/molecules25051211] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
12 Zhang W, Chen S, Liu X, Feng T, Yang W, Zhou Y. Design, synthesis and evaluation of structurally diverse chrysin-chromene-spirooxindole hybrids as anticancer agents. Bioorganic & Medicinal Chemistry 2019;27:115109. [DOI: 10.1016/j.bmc.2019.115109] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 2.3] [Reference Citation Analysis]
13 Islam MS, Al-majid AM, El-senduny FF, Badria FA, Rahman AFMM, Barakat A, Elshaier YAMM. Synthesis, Anticancer Activity, and Molecular Modeling of New Halogenated Spiro[pyrrolidine-thiazolo-oxindoles] Derivatives. Applied Sciences 2020;10:2170. [DOI: 10.3390/app10062170] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
14 Zhou LM, Qu RY, Yang GF. An overview of spirooxindole as a promising scaffold for novel drug discovery. Expert Opin Drug Discov 2020;15:603-25. [PMID: 32106717 DOI: 10.1080/17460441.2020.1733526] [Cited by in Crossref: 41] [Cited by in F6Publishing: 17] [Article Influence: 20.5] [Reference Citation Analysis]
15 Altowyan MS, Barakat A, Al-Majid AM, Al-Ghulikah HA. Spiroindolone analogues bearing benzofuran moiety as a selective cyclooxygenase COX-1 with TNF-α and IL-6 inhibitors. Saudi J Biol Sci 2020;27:1208-16. [PMID: 32346326 DOI: 10.1016/j.sjbs.2020.02.010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
16 Shahidul Islam M, Al‐majid AM, Azam M, Prakash Verma V, Barakat A, Haukka M, Domingo LR, Elgazar AA, Mira A, Badria FA. Synthesis of Spirooxindole Analogs Tethered Pyrazole Scaffold as Acetylcholinesterase Inhibitors. ChemistrySelect 2021;6:14039-53. [DOI: 10.1002/slct.202103255] [Reference Citation Analysis]
17 Al-majid AM, Soliman SM, Haukka M, Ali M, Islam MS, Shaik MR, Barakat A. Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphone Function. Symmetry 2020;12:1337. [DOI: 10.3390/sym12081337] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
18 Chowdhary S, Shalini, Arora A, Kumar V. A Mini Review on Isatin, an Anticancer Scaffold with Potential Activities against Neglected Tropical Diseases (NTDs). Pharmaceuticals 2022;15:536. [DOI: 10.3390/ph15050536] [Reference Citation Analysis]
19 Lotfy G, Aziz YMA, Said MM, El Ashry ESH, El Tamany ESH, Barakat A, Ghabbour HA, Yousuf S, Ul‐haq Z, Choudhary MI. Synthesis of Oxindole Analogues, Biological Activity, and In Silico Studies. ChemistrySelect 2019;4:10510-6. [DOI: 10.1002/slct.201901228] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
20 Wang K, Li Y, Chen R, Sun A, Wang Z, Zhao Y, Wang M, Sheng S. Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives. Adv Synth Catal 2022;364:2047-52. [DOI: 10.1002/adsc.202200269] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Badria FA, Atef S, Al-Majid AM, Ali M, Elshaier YAMM, Ghabbour HA, Islam MS, Barakat A. Synthesis and Inhibitory Effect of Some Indole-Pyrimidine Based Hybrid Heterocycles on α-Glucosidase and α-Amylase as Potential Hypoglycemic Agents. ChemistryOpen 2019;8:1288-97. [PMID: 31649838 DOI: 10.1002/open.201900240] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
22 Huang Y, Huang Y, Sun J, Yan C. A [3+2] cycloaddition reaction for the synthesis of spiro[indoline-3,3′-pyrrolidines] and evaluation of cytotoxicity towards cancer cells. New J Chem 2019;43:8903-10. [DOI: 10.1039/c9nj00994a] [Cited by in Crossref: 13] [Cited by in F6Publishing: 1] [Article Influence: 4.3] [Reference Citation Analysis]
23 Elyasi Z, Reza Najafi G, Safaei Ghomi J, Sharif MA. Design and fabrication of novel polymerized dual nature ionic liquid as highly effective catalyst for regioselective synthesis of monospiro derivatives. Journal of Molecular Liquids 2021;344:117800. [DOI: 10.1016/j.molliq.2021.117800] [Reference Citation Analysis]
24 Lotfy G, Abdel Aziz YM, Said MM, El Ashry ESH, El Tamany ESH, Abu-Serie MM, Teleb M, Dömling A, Barakat A. Molecular hybridization design and synthesis of novel spirooxindole-based MDM2 inhibitors endowed with BCL2 signaling attenuation; a step towards the next generation p53 activators. Bioorg Chem 2021;117:105427. [PMID: 34794098 DOI: 10.1016/j.bioorg.2021.105427] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
25 Ince T, Serttas R, Demir B, Atabey H, Seferoglu N, Erdogan S, Sahin E, Erat S, Nural Y. Polysubstituted pyrrolidines linked to 1,2,3-triazoles: Synthesis, crystal structure, DFT studies, acid dissociation constant, drug-likeness, and anti-proliferative activity. Journal of Molecular Structure 2020;1217:128400. [DOI: 10.1016/j.molstruc.2020.128400] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
26 Raposo LR, Silva A, Silva D, Roma-rodrigues C, Espadinha M, Baptista PV, Santos MM, Fernandes AR. Exploiting the antiproliferative potential of spiropyrazoline oxindoles in a human ovarian cancer cell line. Bioorganic & Medicinal Chemistry 2021;30:115880. [DOI: 10.1016/j.bmc.2020.115880] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Brandão P, Marques C, Burke AJ, Pineiro M. The application of isatin-based multicomponent-reactions in the quest for new bioactive and druglike molecules. Eur J Med Chem 2021;211:113102. [PMID: 33421712 DOI: 10.1016/j.ejmech.2020.113102] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
28 Al-Majid AM, Ali M, Islam MS, Alshahrani S, Alamary AS, Yousuf S, Choudhary MI, Barakat A. Stereoselective Synthesis of the Di-Spirooxindole Analogs Based Oxindole and Cyclohexanone Moieties as Potential Anticancer Agents. Molecules 2021;26:6305. [PMID: 34684885 DOI: 10.3390/molecules26206305] [Reference Citation Analysis]
29 Barakat A, Islam MS, Ghawas HM, Al-Majid AM, El-Senduny FF, Badria FA, Elshaier YAMM, Ghabbour HA. Design and synthesis of new substituted spirooxindoles as potential inhibitors of the MDM2-p53 interaction. Bioorg Chem 2019;86:598-608. [PMID: 30802707 DOI: 10.1016/j.bioorg.2019.01.053] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 6.3] [Reference Citation Analysis]
30 Brandão P, Marques CS, Carreiro EP, Pineiro M, Burke AJ. Engaging Isatins in Multicomponent Reactions (MCRs) - Easy Access to Structural Diversity. Chem Rec 2021;21:924-1037. [PMID: 33599390 DOI: 10.1002/tcr.202000167] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
31 Shah VR, Bhaliya JD, Patel GM. In silico approach: docking study of oxindole derivatives against the main protease of COVID-19 and its comparison with existing therapeutic agents. J Basic Clin Physiol Pharmacol 2021;32:197-214. [PMID: 33594850 DOI: 10.1515/jbcpp-2020-0262] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Pogaku V, Krishna VS, Balachandran C, Rangan K, Sriram D, Aoki S, Basavoju S. The design and green synthesis of novel benzotriazoloquinolinyl spirooxindolopyrrolizidines: antimycobacterial and antiproliferative studies. New J Chem 2019;43:17511-20. [DOI: 10.1039/c9nj03802g] [Cited by in Crossref: 5] [Article Influence: 1.7] [Reference Citation Analysis]
33 Barakat A, Soliman SM, Alshahrani S, Islam MS, Ali M, Al-majid AM, Yousuf S. Synthesis, X-ray Single Crystal, Conformational Analysis and Cholinesterase Inhibitory Activity of a New Spiropyrrolidine Scaffold Tethered Benzo[b]Thiophene Analogue. Crystals 2020;10:120. [DOI: 10.3390/cryst10020120] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
34 Fadaly WA, Elshaier YA, Hassanein EH, Abdellatif KR. New 1,2,4-triazole/pyrazole hybrids linked to oxime moiety as nitric oxide donor celecoxib analogs: Synthesis, cyclooxygenase inhibition anti-inflammatory, ulcerogenicity, anti-proliferative activities, apoptosis, molecular modeling and nitric oxide release studies. Bioorganic Chemistry 2020;98:103752. [DOI: 10.1016/j.bioorg.2020.103752] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 6.5] [Reference Citation Analysis]
35 Altowyan MS, Atef S, Al-agamy MH, Soliman SM, Ali M, Shaik MR, Choudhary MI, Ghabbour HA, Barakat A. Synthesis and characterization of a spiroindolone pyrothiazole analog via X-ray, biological, and computational studies. Journal of Molecular Structure 2019;1186:384-92. [DOI: 10.1016/j.molstruc.2019.03.032] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
36 Islam MS, Haukka M, Soliman SM, Al-majid AM, Rahman AM, Bari A, Barakat A. Regio- and stereoselective synthesis of spiro-heterocycles bearing the pyrazole scaffold via [3+2] cycloaddition reaction. Journal of Molecular Structure 2022;1250:131711. [DOI: 10.1016/j.molstruc.2021.131711] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
37 Singh K, Pal R, Khan SA, Kumar B, Akhtar MJ. Insights into the structure activity relationship of nitrogen-containing heterocyclics for the development of antidepressant compounds: An updated review. Journal of Molecular Structure 2021;1237:130369. [DOI: 10.1016/j.molstruc.2021.130369] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 9.0] [Reference Citation Analysis]
38 Aziz YMA, Lotfy G, Said MM, El Ashry ESH, El Tamany ESH, Soliman SM, Abu-Serie MM, Teleb M, Yousuf S, Dömling A, Domingo LR, Barakat A. Design, Synthesis, Chemical and Biochemical Insights Into Novel Hybrid Spirooxindole-Based p53-MDM2 Inhibitors With Potential Bcl2 Signaling Attenuation. Front Chem 2021;9:735236. [PMID: 34970530 DOI: 10.3389/fchem.2021.735236] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
39 Ferreira JMGDO, da Silva GA, Coelho MC, Junior CGL, Vale JA. Quick synthesis of isatin-derived knoevenagel adducts using only eco-friendly solvent. Results in Chemistry 2021;3:100135. [DOI: 10.1016/j.rechem.2021.100135] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
40 Ibrahim HM, Behbehani H. TFA-catalyzed Q-Tube Reactor-Assisted Strategy for the Synthesis of Pyrido[1,2-b][1,2,4]triazine and Pyrido[1',2':2,3][1,2,4]triazino[5,6-b]indole Derivatives. ACS Omega 2021;6:16086-99. [PMID: 34179654 DOI: 10.1021/acsomega.1c01980] [Reference Citation Analysis]
41 Boddy AJ, Bull JA. Stereoselective synthesis and applications of spirocyclic oxindoles. Org Chem Front 2021;8:1026-84. [DOI: 10.1039/d0qo01085e] [Cited by in Crossref: 20] [Article Influence: 20.0] [Reference Citation Analysis]
42 Hosseini S, Esmaeili AA, Khojastehnezhad A, Notash B. An efficient synthesis of novel spiro[indole-3,8′-pyrano[2,3- d ][1,3,4]thiadiazolo[3,2- a ]pyrimidine derivatives via organobase-catalyzed three-component reaction of malononitrile, isatin and heterocyclic-1,3-diones. Journal of Sulfur Chemistry 2021;42:628-44. [DOI: 10.1080/17415993.2021.1944144] [Reference Citation Analysis]