Alison Ondrus
Affiliations: | 2003-2009 | Massachusetts Institute of Technology, Cambridge, MA, United States |
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"Alison Ondrus"Mean distance: 8.35 | S | N | B | C | P |
Parents
Sign in to add mentor| Mohammad Movassaghi | grad student | 2003-2009 | MIT |
| James K. Chen | post-doc | Stanford | |
| Justin Du Bois | post-doc | Stanford |
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Publications
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| Feng Z, Hom ME, Bearrood TE, et al. (2022) Targeting colorectal cancer with small-molecule inhibitors of ALDH1B1. Nature Chemical Biology |
| Cheng YS, Zhang T, Ma X, et al. (2021) A proteome-wide map of 20(S)-hydroxycholesterol interactors in cell membranes. Nature Chemical Biology. 17: 1271-1280 |
| Mafi A, Purohit R, Vielmas E, et al. (2021) Hedgehog proteins create a dynamic cholesterol interface. Plos One. 16: e0246814 |
| Chen JK, Hom ME, Ondrus AE, et al. (2020) Bicyclic imidazolium inhibitors of Gli transcription factor activity. Chemmedchem |
| Steinman JB, Santarossa CC, Miller RM, et al. (2017) Chemical structure-guided design of dynapyrazoles, potent cell-permeable dynein inhibitors with a unique mode of action. Elife. 6 |
| Ondrus AE, Lee HL, Iwanaga S, et al. (2012) Fluorescent saxitoxins for live cell imaging of single voltage-gated sodium ion channels beyond the optical diffraction limit. Chemistry & Biology. 19: 902-12 |
| Ondrus AE, Kaniskan HU, Movassaghi M. (2010) Dimerization of functional pyrroloindolizines for the synthesis of complex myrmicarin alkaloids. Tetrahedron. 66: 4784-4795 |
| Ondrus AE, Ümit Kaniskan H, Movassaghi M. (2010) Dimerization of functional pyrroloindolizines for the synthesis of complex myrmicarin alkaloids Tetrahedron. 66: 4784-4795 |
| Ondrus AE, Movassaghi M. (2009) Reversible dimerization of (+)-myrmicarin 215B Organic Letters. 11: 2960-2963 |
| Ondrus AE, Movassaghi M. (2009) Total synthesis and study of myrmicarin alkaloids Chemical Communications. 4151-4165 |