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For: Lim CJ, Kim SH, Lee BH, Oh K, Yi KY. 4-Arylphthalazin-1(2H)-one derivatives as potent antagonists of the melanin concentrating hormone receptor 1 (MCH-R1). Bioorganic & Medicinal Chemistry Letters 2012;22:427-30. [DOI: 10.1016/j.bmcl.2011.10.111] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.2] [Reference Citation Analysis]
Number Citing Articles
1 Lim G, You KY, Lee JH, Jeon MK, Lee BH, Ryu JY, Oh KS. Identification and New Indication of Melanin-Concentrating Hormone Receptor 1 (MCHR1) Antagonist Derived from Machine Learning and Transcriptome-Based Drug Repositioning Approaches. Int J Mol Sci 2022;23:3807. [PMID: 35409167 DOI: 10.3390/ijms23073807] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Ismael A, Skrydstrup T, Bayer A. Carbonylative Suzuki-Miyaura couplings of sterically hindered aryl halides: synthesis of 2-aroylbenzoate derivatives. Org Biomol Chem 2020;18:1754-9. [PMID: 32065204 DOI: 10.1039/d0ob00044b] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
3 Das P, Biswas P, Guin J. Palladium-Catalyzed Decarboxylative ortho-C(sp2 )-H Aroylation of N-Sulfoximine Benzamides at Room Temperature. Chem Asian J 2020;15:920-5. [PMID: 32039558 DOI: 10.1002/asia.201901759] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
4 Malinowski Z, Fornal E, Sierocińska B, Czeczko R, Nowak M. Synthesis of 4-alkylsulfanylphthalazin-1(2H)-ones via palladium catalyzed sulfanylation of substituted 4-bromophthalazin-1(2H)-ones. Tetrahedron 2016;72:7942-51. [DOI: 10.1016/j.tet.2016.10.022] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
5 Mennen SM, Mak-jurkauskas ML, Bio MM, Hollis LS, Nadeau KA, Clausen AM, Hansen KB. Synthesis of 4-Substituted Phthalazin-1(2 H )-ones from 2-Acylbenzoic Acids: Controlling Hydrazine in a Pharmaceutical Intermediate through PAT-Guided Process Development. Org Process Res Dev 2015;19:884-91. [DOI: 10.1021/acs.oprd.5b00135] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
6 Johansson A, Löfberg C. Novel MCH 1 receptor antagonists: a patent review. Expert Opinion on Therapeutic Patents 2014;25:193-207. [DOI: 10.1517/13543776.2014.993382] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 1.9] [Reference Citation Analysis]
7 Pathak S, Debnath K, Hossain ST, Mukherjee SK, Pramanik A. Synthesis of biologically important phthalazinones, 2,3-benzoxazin-1-ones and isoindolinones from ninhydrin and their antimicrobial activity. Tetrahedron Letters 2013;54:3137-43. [DOI: 10.1016/j.tetlet.2013.04.015] [Cited by in Crossref: 21] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
8 Miao J, Ge H. Palladium-Catalyzed Chemoselective Decarboxylative Ortho Acylation of Benzoic Acids with α-Oxocarboxylic Acids. Org Lett 2013;15:2930-3. [DOI: 10.1021/ol400919u] [Cited by in Crossref: 84] [Cited by in F6Publishing: 76] [Article Influence: 9.3] [Reference Citation Analysis]
9 Lim CJ, Kim JY, Lee BH, Oh KS, Yi KY. Synthesis and SAR study of pyrrolo[3,4-b]pyridin-7(6H)-one derivatives as melanin concentrating hormone receptor 1 (MCH-R1) antagonists. Bioorg Med Chem Lett 2013;23:1736-9. [PMID: 23411080 DOI: 10.1016/j.bmcl.2013.01.053] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
10 Högberg T, Frimurer TM, Sasmal PK. Melanin concentrating hormone receptor 1 (MCHR1) antagonists—Still a viable approach for obesity treatment? Bioorganic & Medicinal Chemistry Letters 2012;22:6039-47. [DOI: 10.1016/j.bmcl.2012.08.025] [Cited by in Crossref: 30] [Cited by in F6Publishing: 24] [Article Influence: 3.0] [Reference Citation Analysis]