Year |
Citation |
Score |
2018 |
Koubek EJ, Weissenrieder JS, Neighbors JD, Hohl RJ. Schweinfurthins: Lipid Modulators with Promising Anticancer Activity. Lipids. PMID 30334267 DOI: 10.1002/Lipd.12088 |
0.358 |
|
2017 |
Stockdale DP, Titunick MB, Biegler JM, Reed JL, Hartung AM, Wiemer DF, McLaughlin PJ, Neighbors JD. Selective opioid growth factor receptor antagonists based on a stilbene isostere. Bioorganic & Medicinal Chemistry. PMID 28693915 DOI: 10.1016/J.Bmc.2017.06.035 |
0.531 |
|
2016 |
Hartung AM, Navarro HA, Wiemer DF, Neighbors JD. Corrigendum to "A selective delta opioid receptor antagonist based on a stilbene core" [Bioorg. Med. Chem. Lett. 25 (2015) 5532-5535]. Bioorganic & Medicinal Chemistry Letters. 26: 1645. PMID 28750745 DOI: 10.1016/J.Bmcl.2016.02.014 |
0.488 |
|
2015 |
Hartung AM, Navarro HA, Wiemer DF, Neighbors JD. A selective delta opioid receptor antagonist based on a stilbene core. Bioorganic & Medicinal Chemistry Letters. 25: 5532-5. PMID 26525865 DOI: 10.1016/J.Bmcl.2015.10.059 |
0.532 |
|
2015 |
Kuder CH, Weivoda MM, Zhang Y, Zhu J, Neighbors JD, Wiemer DF, Hohl RJ. 3-Deoxyschweinfurthin B Lowers Cholesterol Levels by Decreasing Synthesis and Increasing Export in Cultured Cancer Cell Lines. Lipids. PMID 26494560 DOI: 10.1007/S11745-015-4083-Z |
0.529 |
|
2014 |
Hartung AM, Beutler JA, Navarro HA, Wiemer DF, Neighbors JD. Stilbenes as κ-selective, non-nitrogenous opioid receptor antagonists. Journal of Natural Products. 77: 311-9. PMID 24456556 DOI: 10.1021/Np4009046 |
0.512 |
|
2012 |
Kuder CH, Sheehy RM, Neighbors JD, Wiemer DF, Hohl RJ. Functional evaluation of a fluorescent schweinfurthin: mechanism of cytotoxicity and intracellular quantification. Molecular Pharmacology. 82: 9-16. PMID 22461663 DOI: 10.1124/Mol.111.077107 |
0.528 |
|
2010 |
Topczewski JJ, Kuder CH, Neighbors JD, Hohl RJ, Wiemer DF. Fluorescent schweinfurthin B and F analogs with anti-proliferative activity. Bioorganic & Medicinal Chemistry. 18: 6734-41. PMID 20724169 DOI: 10.1016/J.Bmc.2010.07.056 |
0.699 |
|
2010 |
Topczewski JJ, Callahan MP, Neighbors JD, Wiemer DF. Synthesis of (+)-Angelichalcone Synfacts. 2010: 266-266. DOI: 10.1055/S-0029-1219253 |
0.601 |
|
2010 |
Topczewski JJ, Neighbors JD, Wiemer DF. ChemInform Abstract: Total Synthesis of (+)-Schweinfurthins B (I) and E (II). Cheminform. 41. DOI: 10.1002/chin.201005210 |
0.665 |
|
2009 |
Birt DF, Widrlechner MP, Hammer KD, Hillwig ML, Wei J, Kraus GA, Murphy PA, McCoy J, Wurtele ES, Neighbors JD, Wiemer DF, Maury WJ, Price JP. Hypericum in infection: Identification of anti-viral and anti-inflammatory constituents. Pharmaceutical Biology. 47: 774-782. PMID 19907671 DOI: 10.1080/13880200902988645 |
0.517 |
|
2009 |
Topczewski JJ, Callahan MP, Neighbors JD, Wiemer DF. A tandem cascade cyclization-electrophilic aromatic substitution: application in the total synthesis of (+)-angelichalcone. Journal of the American Chemical Society. 131: 14630-1. PMID 19824722 DOI: 10.1021/Ja906468V |
0.725 |
|
2009 |
Topczewski JJ, Neighbors JD, Wiemer DF. Total synthesis of (+)-schweinfurthins B and E. The Journal of Organic Chemistry. 74: 6965-72. PMID 19697910 DOI: 10.1021/Jo901161M |
0.74 |
|
2009 |
Maury W, Price JP, Brindley MA, Oh C, Neighbors JD, Wiemer DF, Wills N, Carpenter S, Hauck C, Murphy P, Widrlechner MP, Delate K, Kumar G, Kraus GA, Rizshsky L, et al. Identification of light-independent inhibition of human immunodeficiency virus-1 infection through bioguided fractionation of Hypericum perforatum. Virology Journal. 6: 101. PMID 19594941 DOI: 10.1186/1743-422X-6-101 |
0.475 |
|
2009 |
Kuder CH, Neighbors JD, Hohl RJ, Wiemer DF. Synthesis and biological activity of a fluorescent schweinfurthin analogue. Bioorganic & Medicinal Chemistry. 17: 4718-23. PMID 19464190 DOI: 10.1016/J.Bmc.2009.04.071 |
0.578 |
|
2009 |
Neighbors JD, Topczewski JJ, Swenson DC, Wiemer DF. Synthesis of the cis-fused hexahydroxanthene system via cationic cascade cyclization Tetrahedron Letters. 50: 3881-3884. DOI: 10.1016/J.Tetlet.2009.04.052 |
0.7 |
|
2008 |
Neighbors JD, Buller MJ, Boss KD, Wiemer DF. A concise synthesis of pawhuskin A. Journal of Natural Products. 71: 1949-52. PMID 18922035 DOI: 10.1021/Np800351C |
0.624 |
|
2008 |
Mente NR, Neighbors JD, Wiemer DF. BF3 x Et2O-mediated cascade cyclizations: synthesis of schweinfurthins F and G. The Journal of Organic Chemistry. 73: 7963-70. PMID 18795788 DOI: 10.1021/Jo800951Q |
0.722 |
|
2008 |
Hammer KD, Hillwig ML, Neighbors JD, Sim YJ, Kohut ML, Wiemer DF, Wurtele ES, Birt DF. Pseudohypericin is necessary for the light-activated inhibition of prostaglandin E2 pathways by a 4 component system mimicking an Hypericum perforatum fraction. Phytochemistry. 69: 2354-62. PMID 18707743 DOI: 10.1016/J.Phytochem.2008.06.010 |
0.515 |
|
2008 |
Neighbors JD, Mente NR, Boss KD, Zehnder DW, Wiemer DF. Synthesis of the schweinfurthin hexahydroxanthene core through Shi epoxidation Tetrahedron Letters. 49: 516-519. DOI: 10.1016/J.Tetlet.2007.11.086 |
0.727 |
|
2007 |
Mente NR, Wiemer AJ, Neighbors JD, Beutler JA, Hohl RJ, Wiemer DF. Total synthesis of (R,R,R)- and (S,S,S)-schweinfurthin F: differences of bioactivity in the enantiomeric series. Bioorganic & Medicinal Chemistry Letters. 17: 911-5. PMID 17236766 DOI: 10.1016/J.Bmcl.2006.11.096 |
0.686 |
|
2006 |
Neighbors JD, Salnikova MS, Beutler JA, Wiemer DF. Synthesis and structure-activity studies of schweinfurthin B analogs: Evidence for the importance of a D-ring hydrogen bond donor in expression of differential cytotoxicity. Bioorganic & Medicinal Chemistry. 14: 1771-84. PMID 16290161 DOI: 10.1016/J.Bmc.2005.10.025 |
0.612 |
|
2005 |
Neighbors JD, Beutler JA, Wiemer DF. Synthesis of nonracemic 3-deoxyschweinfurthin B. The Journal of Organic Chemistry. 70: 925-31. PMID 15675850 DOI: 10.1021/Jo048444R |
0.622 |
|
2005 |
Neighbors JD, Salnikova MS, Wiemer DF. Total synthesis of pawhuskin C: A directed ortho metalation approach Tetrahedron Letters. 46: 1321-1324. DOI: 10.1016/J.Tetlet.2004.12.114 |
0.582 |
|
2002 |
Treadwell EM, Neighbors JD, Wiemer DF. A cascade cyclization approach to schweinfurthin B. Organic Letters. 4: 3639-42. PMID 12375907 DOI: 10.1021/Ol0266368 |
0.757 |
|
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