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For: Zaib S, Khan I. Synthetic and medicinal chemistry of phthalazines: Recent developments, opportunities and challenges. Bioorg Chem 2020;105:104425. [PMID: 33157344 DOI: 10.1016/j.bioorg.2020.104425] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Yang R, Ma S, Zhuo R, Xu L, Jia S, Yang P, Yao Y, Cao H, Ma L, Pan J, Wang J. Suppression of endoplasmic reticulum stress-dependent autophagy enhances cynaropicrin-induced apoptosis via attenuation of the P62/Keap1/Nrf2 pathways in neuroblastoma. Front Pharmacol 2022;13:977622. [DOI: 10.3389/fphar.2022.977622] [Reference Citation Analysis]
2 Akl L, Abd El-hafeez AA, Ibrahim TM, Salem R, Marzouk HMM, El-domany RA, Ghosh P, Eldehna WM, Abou-seri SM. Identification of novel piperazine-tethered phthalazines as selective CDK1 inhibitors endowed with in vitro anticancer activity toward the pancreatic cancer. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114704] [Reference Citation Analysis]
3 Hadsarung R, Thongnest S, Oekchuae S, Chaiyaveij D, Boonsombat J, Ruchirawat S. Facile synthesis of 1-substituted 4-H phthalazine, a versatile scaffold for chemically diverse phthalazines. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132920] [Reference Citation Analysis]
4 Mousavi H. A concise and focused overview upon arylglyoxal monohydrates-based one-pot multi-component synthesis of fascinating potentially biologically active pyridazines. Journal of Molecular Structure 2022;1251:131742. [DOI: 10.1016/j.molstruc.2021.131742] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
5 Malik MS, Alsantali RI, Alsharif MA, Aljayzani SI, Morad M, Jassas RS, Al-rooqi MM, Alsimaree AA, Altass HM, Asghar BH, Khder AS, Ahmed SA. Ionic liquid mediated four-component synthesis of novel phthalazinone based indole-pyran hybrids as cytotoxic agents. Arabian Journal of Chemistry 2022;15:103560. [DOI: 10.1016/j.arabjc.2021.103560] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
6 Mandal RD, Saha M, Das AR. Accessing oxy-functionalized N-heterocycles through rose bengal and TBHP integrated photoredox C(sp 3 )–O cross-coupling. Org Biomol Chem 2022;20:2939-63. [DOI: 10.1039/d2ob00381c] [Reference Citation Analysis]
7 Zaib S, Ibrar A, Ramay M, Zahra S, Hökelek T, Simpson J, Mcadam CJ, Awwad NS, Ibrahium HA, Frontera A, Khan I. Centroid⋯centroid and hydrogen bond interactions as robust supramolecular units for crystal engineering: X-ray crystallographic, computational and urease inhibitory investigations of 1,2,4-triazolo[3,4-a]phthalazines. CrystEngComm 2022;24:5324-39. [DOI: 10.1039/d2ce00351a] [Reference Citation Analysis]
8 Khedr F, Ibrahim MK, Eissa IH, Abulkhair HS, El-Adl K. Phthalazine-based VEGFR-2 inhibitors: Rationale, design, synthesis, in silico, ADMET profile, docking, and anticancer evaluations. Arch Pharm (Weinheim) 2021;354:e2100201. [PMID: 34411344 DOI: 10.1002/ardp.202100201] [Reference Citation Analysis]