Year |
Citation |
Score |
2024 |
Feng Z, Hom ME, Bearrood TE, Rosenthal ZC, Fernández D, Ondrus AE, Gu Y, McCormick AK, Tomaske MG, Marshall CR, Kline T, Chen CH, Mochly-Rosen D, Kuo CJ, Chen JK. Author Correction: Targeting colorectal cancer with small-molecule inhibitors of ALDH1B1. Nature Chemical Biology. PMID 39653787 DOI: 10.1038/s41589-024-01810-2 |
0.385 |
|
2022 |
Feng Z, Hom ME, Bearrood TE, Rosenthal ZC, Fernández D, Ondrus AE, Gu Y, McCormick AK, Tomaske MG, Marshall CR, Kline T, Chen CH, Mochly-Rosen D, Kuo CJ, Chen JK. Targeting colorectal cancer with small-molecule inhibitors of ALDH1B1. Nature Chemical Biology. PMID 35788181 DOI: 10.1038/s41589-022-01048-w |
0.417 |
|
2021 |
Cheng YS, Zhang T, Ma X, Pratuangtham S, Zhang GC, Ondrus AA, Mafi A, Lomenick B, Jones JJ, Ondrus AE. A proteome-wide map of 20(S)-hydroxycholesterol interactors in cell membranes. Nature Chemical Biology. 17: 1271-1280. PMID 34799735 DOI: 10.1038/s41589-021-00907-2 |
0.412 |
|
2021 |
Mafi A, Purohit R, Vielmas E, Lauinger AR, Lam B, Cheng YS, Zhang T, Huang Y, Kim SK, Goddard WA, Ondrus AE. Hedgehog proteins create a dynamic cholesterol interface. Plos One. 16: e0246814. PMID 33630857 DOI: 10.1371/journal.pone.0246814 |
0.393 |
|
2020 |
Chen JK, Hom ME, Ondrus AE, Sakata-Kato T, Rack PG. Bicyclic imidazolium inhibitors of Gli transcription factor activity. Chemmedchem. PMID 32268014 DOI: 10.1002/Cmdc.202000169 |
0.422 |
|
2017 |
Steinman JB, Santarossa CC, Miller RM, Yu LS, Serpinskaya AS, Furukawa H, Morimoto S, Tanaka Y, Nishitani M, Asano M, Zalyte R, Ondrus AE, Johnson AG, Ye F, Nachury MV, et al. Chemical structure-guided design of dynapyrazoles, potent cell-permeable dynein inhibitors with a unique mode of action. Elife. 6. PMID 28524820 DOI: 10.7554/Elife.25174 |
0.424 |
|
2012 |
Ondrus AE, Lee HL, Iwanaga S, Parsons WH, Andresen BM, Moerner WE, Du Bois J. Fluorescent saxitoxins for live cell imaging of single voltage-gated sodium ion channels beyond the optical diffraction limit. Chemistry & Biology. 19: 902-12. PMID 22840778 DOI: 10.1016/J.Chembiol.2012.05.021 |
0.467 |
|
2010 |
Ondrus AE, Kaniskan HU, Movassaghi M. Dimerization of functional pyrroloindolizines for the synthesis of complex myrmicarin alkaloids. Tetrahedron. 66: 4784-4795. PMID 20798891 DOI: 10.1016/J.Tet.2010.04.006 |
0.577 |
|
2010 |
Ondrus AE, Ümit Kaniskan H, Movassaghi M. Dimerization of functional pyrroloindolizines for the synthesis of complex myrmicarin alkaloids Tetrahedron. 66: 4784-4795. DOI: 10.1016/j.tet.2010.04.006 |
0.562 |
|
2009 |
Ondrus AE, Movassaghi M. Reversible dimerization of (+)-myrmicarin 215B Organic Letters. 11: 2960-2963. PMID 19586059 DOI: 10.1021/Ol9008552 |
0.53 |
|
2009 |
Ondrus AE, Movassaghi M. Total synthesis and study of myrmicarin alkaloids Chemical Communications. 4151-4165. PMID 19585010 DOI: 10.1039/B903995N |
0.584 |
|
2008 |
Guggenheim ER, Ondrus AE, Movassaghi M, Lippard SJ. Poly(ADP-ribose) polymerase-1 activity facilitates the dissociation of nuclear proteins from platinum-modified DNA Bioorganic and Medicinal Chemistry. 16: 10121-10128. PMID 18977144 DOI: 10.1016/J.Bmc.2008.09.074 |
0.53 |
|
2007 |
Movassaghi M, Ondrus AE, Chen B. Efficient and stereoselective dimerization of pyrroloindolizine derivatives inspired by a hypothesis for the biosynthesis of complex myrmicarin alkaloids Journal of Organic Chemistry. 72: 10065-10074. PMID 18020368 DOI: 10.1021/Jo701981Q |
0.573 |
|
2006 |
Ondrus AE, Movassaghi M. Dimerization of (+)-Myrmicarin 215B. A Potential Biomimetic Approach to Complex Myrmicarin Alkaloids. Tetrahedron. 62: 5287-5297. PMID 20640170 DOI: 10.1016/J.Tet.2006.01.108 |
0.596 |
|
2006 |
Ondrus AE, Movassaghi M. Dimerization of (+)-myrmicarin 215B. A potential biomimetic approach to complex myrmicarin alkaloids Tetrahedron. 62: 5287-5297. DOI: 10.1016/j.tet.2006.01.108 |
0.531 |
|
2005 |
Movassaghi M, Ondrus AE. Palladium-catalyzed synthesis of N-vinyl pyrroles and indoles Journal of Organic Chemistry. 70: 8638-8641. PMID 16209629 DOI: 10.1021/Jo051450I |
0.504 |
|
2005 |
Movassaghi M, Ondrus AE. Enantioselective total synthesis of tricyclic myrmicarin alkaloids Organic Letters. 7: 4423-4426. PMID 16178549 DOI: 10.1021/Ol051629F |
0.533 |
|
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