Alison Ondrus - Publications

Affiliations: 
2003-2009 Massachusetts Institute of Technology, Cambridge, MA, United States 

16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.405
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  0.408
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  0.394
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  0.42
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  0.582
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  0.567
2009 Ondrus AE, Movassaghi M. Reversible dimerization of (+)-myrmicarin 215B Organic Letters. 11: 2960-2963. PMID 19586059 DOI: 10.1021/Ol9008552  0.534
2009 Ondrus AE, Movassaghi M. Total synthesis and study of myrmicarin alkaloids Chemical Communications. 4151-4165. PMID 19585010 DOI: 10.1039/B903995N  0.589
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  0.526
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  0.578
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  0.601
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  0.534
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  0.508
2005 Movassaghi M, Ondrus AE. Enantioselective total synthesis of tricyclic myrmicarin alkaloids Organic Letters. 7: 4423-4426. PMID 16178549 DOI: 10.1021/Ol051629F  0.537
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