Syntheses and biological activities of the proposed structure of apteniol A and its derivatives

References

• DellaGreca M, Di Marino C, Previtera L, Purcaro R, Zerrelli A. Apteniols A–F, oxyneolignans from the leaves of Aptenia cordifolia. Tetrahedron. 2005;61:11924–11929.10.1016/j.tet.2005.09.054
   Web of Science ®Google Scholar
• DellaGreca M, Fiorentino A, Izzo A, Napoli F, Purcaro R, Zerrelli A. Phytotoxicity of secondary metabolites from Aptenia cordifolia. Chem. Biodivers. 2007;4:118–128.
   PubMed Web of Science ®Google Scholar
• Devi P, Wahidullah S, Rodrigues C, Souza LD. The sponge-associated bacterium Bacillus licheniformis SAB1: a source of antimicrobial compounds. Mar. Drugs. 2010;8:1203–1212.10.3390/md8041203
   PubMed Web of Science ®Google Scholar
• Ma D, Cai Q. N,N-Dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides. Org. Lett. 2003;5:3799–3802.10.1021/ol0350947
   PubMed Web of Science ®Google Scholar
• Schimelpfenig CW, Ford RR. Synthesis and properties of two dioxadioxoparacyclophanes. J. Org. Chem. 1981;46:1210–1212.10.1021/jo00319a035
   Web of Science ®Google Scholar
• Boger DL, Patane MA, Zhou J. Total synthesis of bouvardin, O-methylbouvardin, and O-methyl-N9-desmethylbouvardin. J. Am. Chem. Soc. 1994;116:8544–8556.10.1021/ja00098a015
   Web of Science ®Google Scholar
• Chomcheon P, Wiyakrutta S, Sriubolmas N, Ngamrojanavanich N, Kengtong S, Mahidol C, Ruchirawat S, Kittakoop P. Aromatase inhibitory, radical scavenging, and antioxidant activities of depsidones and diaryl ethers from the endophytic fungus Corynespora cassiicola L36. Phytochemistry. 2009;70:407–413.10.1016/j.phytochem.2009.01.007
   PubMed Web of Science ®Google Scholar
• Akama T, Baker SJ, Zhang Y-K, Hernandez V, Zhou H, Sanders V, Freund Y, Kimura R, Maples KR, Plattner JJ. Discovery and structure–activity study of a novel benzoxaborole anti-inflammatory agent (AN2728) for the potential topical treatment of psoriasis and atopic dermatitis. Bioorg. Med. Chem. Lett. 2009;19:2129–2132.10.1016/j.bmcl.2009.03.007
   PubMed Web of Science ®Google Scholar
• Morikawa T, Tao J, Toguchida I, Matsuda H, Yoshikawa M. Structures of new cyclic diarylheptanoids and inhibitors of nitric oxide production from Japanese folk medicine Acer nikoense. J. Nat. Prod. 2003;66:86–91.10.1021/np020351m
   PubMed Web of Science ®Google Scholar
• Tamai S, Kaneda M, Nakamura S. Piperazinomycin, a new antifungal antibiotic. I. Fermentation, isolation, characterization and biological properties. J. Antibiot. 1982;35:1130–1136.10.7164/antibiotics.35.1130
   PubMed Web of Science ®Google Scholar
• Kaneda M, Tamai S, Nakamura S, Hirata T, Kushi Y, Suga T. Piperazinomycin, a new antifungal antibiotic. II. Structure determination by X-ray crystallography. J. Antibiot. 1982;35:1137–1140.10.7164/antibiotics.35.1137
   PubMed Web of Science ®Google Scholar
• Lakshmi Niranjan Reddy V, Ravinder K, Srinivasulu M, Venkateshwar Goud T, Malla Reddy S, Srujankumar D, Prabhakar Rao T, Suryanarayana Murty U, Venkateswarlu Y. Two new macrocyclic diaryl ether heptanoids from Boswellia ovalifoliolata. Chem. Pharm. Bull. 2003;51:1081–1084.10.1248/cpb.51.1081
   PubMed Web of Science ®Google Scholar
• Gawroński J, Brzostowska M, Kwit M, Plutecka A, Rychlewska U. Rhombimines – Cyclic tetraimines of trans-1,2-diaminocyclohexane shaped by the diaryl ether structural motif. J. Org. Chem. 2005;70:10147–10150.10.1021/jo051687e
   PubMed Web of Science ®Google Scholar
• Sengupta S, Sadhukhan SK, Bhattacharyya S, Guha J. Palladium-catalyzed reactions of bisarenediazonium salts: two-fold Heck reaction, carbonylation and cross-coupling regimen. J. Chem. Soc. Perkin Trans. 1998;1:407–410.10.1039/a707378j
   Google Scholar
• Macías FA, Castellano D, Molinillo JMG. Search for a standard phytotoxic bioassay for allelochemicals. selection of target species. J. Agric. Food. Chem. 2000;48:2512–2521.10.1021/jf9903051
   PubMed Web of Science ®Google Scholar
• Zhou X, Tai A, Yamamoto I. Enhancement of neurite outgrowth in PC12 cells stimulated with cyclic AMP and NGF by 6-acylated ascorbic acid 2-O-α-glucosides (6-Acyl-AA-2G), novel lipophilic ascorbate derivatives. Biol. Pharm. Bull. 2003;26:341–346.10.1248/bpb.26.341
   PubMed Web of Science ®Google Scholar
• Watanabe J, Shinmoto H, Tsushida T. Coumarin and flavone derivatives from estragon ant thyme as inhibitors of chemical mediator release from RBL-2H3 cells. Biosci. Biotechnol. Biochem. 2005;69:1–6.10.1271/bbb.69.1
   PubMed Web of Science ®Google Scholar
• Demo SD, Masuda E, Rossi AB, Throndset BT, Gerard AL, Chan EH, Armstrong RJ, Fox BP, Lorens JB, Payan DG, Scheller RH, Fisher JM. Quantitative measurement of mast cell degranulation using a novel flow cytometric annexin-V binding assay. Cytometry. 1999;36:340–348.10.1002/(ISSN)1097-0320
   PubMedGoogle Scholar