Pyrrole‐Fused Benzoxazinones/Quinoxalinones: Molecular Dynamic Simulation, Antiproliferative and Antibacterial Activities

[1]  Joydev K. Laha,et al.  Recent Advances in Functionalization of Pyrroles and their Translational Potential , 2021, Chemical record.

[2]  Saravanakumar Rajendran,et al.  Lewis acid-promoted synthesis of highly substituted pyrrole-fused benzoxazinones and quinoxalinones , 2020 .

[3]  Jonathan R Scheerer,et al.  Synthesis of Pyrrolopyrazinones by Construction of the Pyrrole Ring onto an Intact Diketopiperazine. , 2020, The Journal of organic chemistry.

[4]  E. Schmidt,et al.  Secondary Metabolites of the Genus Didemnum: A Comprehensive Review of Chemical Diversity and Pharmacological Properties , 2020, Marine drugs.

[5]  Ioannis Papanastasiou,et al.  Multicomponent reaction of aldehydes, amines and oxalacetate analogues leading to biologically attractive pyrrole derivatives. , 2020, Mini reviews in medicinal chemistry.

[6]  Arnab Ghosh,et al.  Synthesis and Biological Assessment of Pyrrolobenzoxazine Scaffold as a Potent Antioxidant. , 2019, Journal of medicinal chemistry.

[7]  T. Minko,et al.  Metastatic and triple-negative breast cancer: challenges and treatment options , 2018, Drug Delivery and Translational Research.

[8]  A. Garofalo,et al.  Benzopyrroloxazines containing a bridgehead nitrogen atom as promising scaffolds for the achievement of biologically active agents. , 2018, European journal of medicinal chemistry.

[9]  M. Radi,et al.  Identification of Breast Cancer Inhibitors Specific for G Protein‐Coupled Estrogen Receptor (GPER)‐Expressing Cells , 2017, ChemMedChem.

[10]  M. Balamurali,et al.  Synthesis, characterization and biological applications of new copper(II) complexes of aryl hydrazones , 2017 .

[11]  A. Ibezim,et al.  Experimental and In-Silico Investigation of Anti-Microbial Activity of 1-Chloro-2-Isocyanatoethane Derivatives of Thiomorpholine, Piperazine and Morpholine , 2017, PloS one.

[12]  Koichi Fukase,et al.  Discovery of a Novel Scaffold as an Indoleamine 2,3‐Dioxygenase 1 (IDO1) Inhibitor Based on the Pyrrolopiperazinone Alkaloid, Longamide B , 2016, ChemMedChem.

[13]  C. Rosano,et al.  Identification of two benzopyrroloxazines acting as selective GPER antagonists in breast cancer cells and cancer-associated fibroblasts. , 2015, Future medicinal chemistry.

[14]  Lin Ma,et al.  Synthesis, antioxidant, and antimicrobial evaluation of some 2-arylbenzimidazole derivatives. , 2013, Bioorganic & medicinal chemistry letters.

[15]  J. Tanaka,et al.  Total synthesis of the marine natural products lukianols A and B , 2013 .

[16]  Chen Ma,et al.  Recent progress in biological activities and synthetic methodologies of pyrroloquinoxalines. , 2013, Mini reviews in medicinal chemistry.

[17]  R. Capon,et al.  Lamellarins as inhibitors of P-glycoprotein-mediated multidrug resistance in a human colon cancer cell line. , 2012, Chemistry, an Asian journal.

[18]  A. Verkman,et al.  Potent, metabolically stable benzopyrimido-pyrrolo-oxazine-dione (BPO) CFTR inhibitors for polycystic kidney disease. , 2011, Journal of medicinal chemistry.

[19]  V. Shukla,et al.  Antibacterial and antifungal activities from leaf extracts of Cassia fistula l.: An ethnomedicinal plant , 2011, Journal of advanced pharmaceutical technology & research.

[20]  Eric F. Johnson,et al.  Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). , 2009, Bioorganic & medicinal chemistry letters.

[21]  N. Neamati,et al.  Synthesis and biological evaluation of novel hydrazide based cytotoxic agents , 2009 .

[22]  N. Neamati,et al.  Discovery of a novel quinoxalinhydrazide with a broad-spectrum anticancer activity , 2009, Cancer biology & therapy.

[23]  C. Jarry,et al.  Synthesis of New Pyrrolo[1,2-a]quinoxaline Derivatives as Potential Inhibitors of Akt Kinase , 2008, Journal of enzyme inhibition and medicinal chemistry.

[24]  Sonia Manzanaro,et al.  Phenolic marine natural products as aldose reductase inhibitors. , 2006, Journal of natural products.

[25]  M. Srinivasulu,et al.  New potent cytotoxic lamellarin alkaloids from Indian ascidian Didemnum obscurum , 2005 .

[26]  Heonjoong Kang,et al.  A Novel Cytotoxic Alkaloid of Lamellarin Class from a Marine Ascidian Didemnum sp. , 2002 .

[27]  C. Olsen,et al.  Streptopyrrole: An antimicrobial metabolite from Streptomyces armeniacus , 1998 .