Year |
Citation |
Score |
2022 |
Fernandes S, Meyer ST, Shah JP, Adhikari AA, Kerr WG, Chisholm JD. -Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents. Molecules (Basel, Switzerland). 27. PMID 36500543 DOI: 10.3390/molecules27238451 |
0.735 |
|
2022 |
Li DK, Chaudhari SN, Lee Y, Sojoodi M, Adhikari AA, Zukerberg L, Shroff S, Barrett SC, Tanabe K, Chung RT, Devlin AS. Inhibition of microbial deconjugation of micellar bile acids protects against intestinal permeability and liver injury. Science Advances. 8: eabo2794. PMID 36026454 DOI: 10.1126/sciadv.abo2794 |
0.762 |
|
2021 |
Adhikari AA, Ramachandran D, Chaudhari SN, Powell CE, Li W, McCurry MD, Banks AS, Devlin AS. A Gut-Restricted Lithocholic Acid Analog as an Inhibitor of Gut Bacterial Bile Salt Hydrolases. Acs Chemical Biology. PMID 34279901 DOI: 10.1021/acschembio.1c00192 |
0.792 |
|
2020 |
Chaudhari SN, Luo JN, Harris DA, Aliakbarian H, Yao L, Paik D, Subramaniam R, Adhikari AA, Vernon AH, Kiliç A, Weiss ST, Huh JR, Sheu EG, Devlin AS. A microbial metabolite remodels the gut-liver axis following bariatric surgery. Cell Host & Microbe. PMID 33434516 DOI: 10.1016/j.chom.2020.12.004 |
0.749 |
|
2020 |
Adhikari AA, Seegar TCM, Ficarro SB, McCurry MD, Ramachandran D, Yao L, Chaudhari SN, Ndousse-Fetter S, Banks AS, Marto JA, Blacklow SC, Devlin AS. Development of a covalent inhibitor of gut bacterial bile salt hydrolases. Nature Chemical Biology. PMID 32042200 DOI: 10.1038/S41589-020-0467-3 |
0.791 |
|
2019 |
Pedicone C, Fernandes S, Dungan OM, Dormann SM, Viernes DR, Adhikari AA, Choi LB, De Jong EP, Chisholm JD, Kerr WG. Pan-SHIP1/2 inhibitors promote microglia effector functions essential for CNS homeostasis. Journal of Cell Science. PMID 31780579 DOI: 10.1242/Jcs.238030 |
0.722 |
|
2019 |
Suzuki T, Mate NA, Adhikari AA, Chisholm JD. Dialkylation of Indoles with Trichloroacetimidates to Access 3,3-Disubstituted Indolenines. Molecules (Basel, Switzerland). 24. PMID 31731742 DOI: 10.3390/Molecules24224143 |
0.766 |
|
2019 |
Mahajani NS, Meador RIL, Smith TJ, Canarelli SE, Adhikari AA, Shah JP, Russo CM, Wallach DR, Howard KT, Millimaci AM, Chisholm JD. Ester Formation via Symbiotic Activation Utilizing Trichloroacetimidate Electrophiles. The Journal of Organic Chemistry. PMID 31117564 DOI: 10.1021/Acs.Joc.9B00745 |
0.661 |
|
2018 |
Yao L, Seaton SC, Ndousse-Fetter S, Adhikari AA, DiBenedetto N, Mina AI, Banks AS, Bry L, Devlin AS. A selective gut bacterial bile salt hydrolase alters host metabolism. Elife. 7. PMID 30014852 DOI: 10.7554/Elife.37182 |
0.698 |
|
2018 |
Yao L, Seaton SC, Ndousse-Fetter S, Adhikari AA, DiBenedetto N, Mina AI, Banks AS, Bry L, Devlin AS. Author response: A selective gut bacterial bile salt hydrolase alters host metabolism Elife. DOI: 10.7554/Elife.37182.026 |
0.676 |
|
2017 |
Adhikari AA, Radal L, Chisholm JD. Synthesis of 3,3'-Disubstituted Indolenines Utilizing the Lewis Acid Catalyzed Alkylation of 2,3-Disubstituted Indoles with Trichloroacetimidates. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 28: 2335-2339. PMID 29033500 DOI: 10.1055/S-0036-1588491 |
0.67 |
|
2017 |
Adhikari AA, Suzuki T, Gilbert RJ, Linaburg MR, Chisholm JD. Rearrangement of Benzylic Trichloroacetimidates to Benzylic Trichloroacetamides. The Journal of Organic Chemistry. PMID 28323428 DOI: 10.1021/Acs.Joc.7B00245 |
0.755 |
|
2016 |
Adhikari AA, Chisholm JD. Lewis Acid Catalyzed Displacement of Trichloroacetimidates in the Synthesis of Functionalized Pyrroloindolines. Organic Letters. PMID 27486831 DOI: 10.1021/Acs.Orglett.6B02024 |
0.611 |
|
2015 |
Russo CM, Adhikari AA, Wallach DR, Fernandes S, Balch AN, Kerr WG, Chisholm JD. Synthesis and initial evaluation of quinoline-based inhibitors of the SH2-containing inositol 5'-phosphatase (SHIP). Bioorganic & Medicinal Chemistry Letters. 25: 5344-8. PMID 26453006 DOI: 10.1016/J.Bmcl.2015.09.034 |
0.754 |
|
2014 |
Adhikari AA, Shah JP, Howard KT, Russo CM, Wallach DR, Linaburg MR, Chisholm JD. Convenient Formation of Diphenylmethyl Esters Using Diphenylmethyl Trichloroacetimidate Synlett. 25: 283-287. DOI: 10.1055/S-0033-1340293 |
0.73 |
|
2014 |
Adhikari AA, Shah JP, Howard KT, Russo CM, Wallach DR, Linaburg MR, Chisholm JD. ChemInform Abstract: Convenient Formation of Diphenylmethyl Esters Using Diphenylmethyl Trichloroacetimidate. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201428065 |
0.766 |
|
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