Year |
Citation |
Score |
2020 |
Chen W, Xian M. Washington Red (WR) dyes and their imaging applications. Methods in Enzymology. 640: 149-163. PMID 32560796 DOI: 10.1016/Bs.Mie.2020.04.027 |
0.303 |
|
2020 |
Hamsath A, Xian M. Chemistry and Chemical Biology of Selenenyl Sulfides (RSeSR) and Thioseleninic acids (RSeSH). Antioxidants & Redox Signaling. PMID 32151152 DOI: 10.1089/Ars.2020.8083 |
0.34 |
|
2020 |
Du F, Shuang S, Guo Z, Gong X, Dong C, Xian M, Yang Z. Rapid synthesis of multifunctional carbon nanodots as effective antioxidants, antibacterial agents, and quercetin nanoprobes. Talanta. 206: 120243. PMID 31514864 DOI: 10.1016/J.Talanta.2019.120243 |
0.339 |
|
2019 |
Xu S, Wang Y, Parent Z, Xian M. Diacyl disulfides as the precursors for hydrogen persulfide (HS). Bioorganic & Medicinal Chemistry Letters. 126903. PMID 31901381 DOI: 10.1016/J.Bmcl.2019.126903 |
0.345 |
|
2019 |
Hu Y, Li X, Fang Y, Shi W, Li X, Chen W, Xian M, Ma H. Reactive oxygen species-triggered off-on fluorescence donor for imaging hydrogen sulfide delivery in living cells. Chemical Science. 10: 7690-7694. PMID 31803407 DOI: 10.1039/C9Sc02323B |
0.325 |
|
2019 |
Shyaka C, Xian M, Park CM. Esterase-sensitive trithiane-based hydrogen sulfide donors. Organic & Biomolecular Chemistry. PMID 31750500 DOI: 10.1039/C9Ob02273B |
0.312 |
|
2019 |
Yang CT, Devarie-Baez N, Hamsath A, Fu XD, Xian M. S-Persulfidation: Chemistry, Chemical Biology, and Significance in Health and Disease. Antioxidants & Redox Signaling. PMID 31547682 DOI: 10.1089/Ars.2019.7889 |
0.335 |
|
2019 |
Wang Y, Yang CT, Xu S, Chen W, Xian M. Hydrogen Sulfide Mediated Tandem Reaction of Selenenyl Sulfides and Its Application in Fluorescent Probe Development. Organic Letters. 21: 7573-7576. PMID 31539932 DOI: 10.1021/Acs.Orglett.9B02844 |
0.387 |
|
2019 |
Chen W, Matsunaga T, Neill DL, Yang CT, Akaike T, Xian M. Rational Design of a Dual-Reactivity Based Fluorescent Probe for Visualizing Intracellular HSNO. Angewandte Chemie (International Ed. in English). PMID 31479578 DOI: 10.1002/Anie.201908950 |
0.392 |
|
2019 |
Neill DL, Chang YC, Chen W, Li L, Xian M. A smartphone based device for the detection of sulfane sulfurs in biological systems. Sensors and Actuators. B, Chemical. 292: 263-269. PMID 31303694 DOI: 10.1016/J.Snb.2019.04.099 |
0.303 |
|
2019 |
Hamsath A, Wang Y, Yang CT, Xu S, Cañedo D, Chen W, Xian M. Acyl Selenyl Sulfides as the Precursors for Reactive Sulfur Species (Hydrogen Sulfide, Polysulfide, and Selenyl Sulfide). Organic Letters. PMID 31264875 DOI: 10.1021/Acs.Orglett.9B02021 |
0.344 |
|
2019 |
Xian M, Yang CT, Wang Y, Marutani E, Ida T, Ni X, Xu S, Chen W, Zhang H, Akaike T, Ichinose F. Data-Driven Identification of Hydrogen Sulfide Scavengers. Angewandte Chemie (International Ed. in English). PMID 31194894 DOI: 10.1002/Anie.201905580 |
0.333 |
|
2019 |
Wang H, Xu Y, Rao L, Yang CT, Yuan H, Gao T, Chen X, Sun H, Xian M, Liu C, Liu C. A Ratiometric Fluorescent Probe for Monitoring Endogenous Methylglyoxal in Living Cells and Diabetic Blood Samples. Analytical Chemistry. PMID 30990019 DOI: 10.1021/Acs.Analchem.8B05426 |
0.335 |
|
2019 |
Luo Y, Song Y, Zhu C, Li S, Xian M, Wai CM, Lin Y, Du D. Visualization of endogenous hydrogen sulfide in living cells based on Au nanorods@silica enhanced fluorescence. Analytica Chimica Acta. 1053: 81-88. PMID 30712572 DOI: 10.1016/J.Aca.2018.12.008 |
0.313 |
|
2018 |
Liu C, Park CM, Wang D, Xian M. Phosphite Esters: Reagents for Exploring S-Nitrosothiol Chemistry. Organic Letters. PMID 30520644 DOI: 10.1021/Acs.Orglett.8B03393 |
0.325 |
|
2018 |
Xu S, Hamsath A, Neill DL, Wang Y, Yang CT, Xian M. Strategies for the Design of Donors and Precursors of Reactive Sulfur Species. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30372550 DOI: 10.1002/Chem.201804895 |
0.342 |
|
2018 |
Yang X, Liu W, Tang J, Li P, Weng H, Ye Y, Xian M, Tang B, Zhao Y. A multi-signal mitochondria-targeted fluorescent probe for real-time visualization of cysteine metabolism in living cells and animals. Chemical Communications (Cambridge, England). PMID 30191239 DOI: 10.1039/C8Cc05418E |
0.31 |
|
2018 |
Bibli SI, Luck B, Zukunft S, Wittig J, Chen W, Xian M, Papapetropoulos A, Hu J, Fleming I. A selective and sensitive method for quantification of endogenous polysulfide production in biological samples. Redox Biology. 18: 295-304. PMID 30077923 DOI: 10.1016/J.Redox.2018.07.016 |
0.332 |
|
2018 |
Liu H, Radford MN, Yang CT, Chen W, Xian M. Inorganic Hydrogen Polysulfides: Chemistry, Chemical Biology, and Detection. British Journal of Pharmacology. PMID 29669174 DOI: 10.1111/Bph.14330 |
0.335 |
|
2018 |
Xian M, Kang J, Xu S, Radford MN, Zhang W, Kelly SS, Day JJ. O to S Relay Deprotection, A General Approach for the Design of Controllable Donors of Reactive Sulfur Species. Angewandte Chemie (International Ed. in English). PMID 29624822 DOI: 10.1002/Anie.201802845 |
0.354 |
|
2018 |
Kang J, Ferrell AJ, Chen W, Wang D, Xian M. Cyclic Acyl Disulfides and Acyl Selenylsulfides as the Precursors for Persulfides (RSSH), Selenylsulfides (RSeSH), and Hydrogen Sulfide (H2S). Organic Letters. PMID 29345467 DOI: 10.1021/Acs.Orglett.7B04005 |
0.387 |
|
2018 |
Xu S, Wang Y, Radford MN, Ferrell AJ, Xian M. Synthesis of Unsymmetric Trisulfides from 9-Fluorenylmethyl Disulfides. Organic Letters. PMID 29313692 DOI: 10.1021/Acs.Orglett.7B03846 |
0.302 |
|
2017 |
Xian M, Chen W, Xu S, Day JJ, Wang D. A General Strategy for Development of Near-Infrared Fluorescent Probes for Bioimaging. Angewandte Chemie (International Ed. in English). PMID 29134784 DOI: 10.1002/Anie.201710688 |
0.318 |
|
2017 |
Garai D, Ríos-González BB, Furtmüller PG, Fukuto JM, Xian M, López-Garriga J, Obinger CC, Nagy P. Mechanisms of myeloperoxidase catalyzed oxidation of H2S by H2O2 or O2 to produce potent protein Cys-polysulfide-inducing species. Free Radical Biology & Medicine. PMID 29097214 DOI: 10.1016/J.Freeradbiomed.2017.10.384 |
0.364 |
|
2017 |
Yang CT, Chen L, Xu S, Day JJ, Li X, Xian M. Recent Development of Hydrogen Sulfide Releasing/Stimulating Reagents and Their Potential Applications in Cancer and Glycometabolic Disorders. Frontiers in Pharmacology. 8: 664. PMID 29018341 DOI: 10.3389/Fphar.2017.00664 |
0.304 |
|
2017 |
Zhang C, Biggs TD, Devarie-Baez NO, Shuang S, Dong C, Xian M. S-Nitrosothiols: chemistry and reactions. Chemical Communications (Cambridge, England). PMID 28944382 DOI: 10.1039/C7Cc06574D |
0.392 |
|
2017 |
Kang J, Neill DL, Xian M. Phosphonothioate-Based Hydrogen Sulfide Releasing Reagents: Chemistry and Biological Applications. Frontiers in Pharmacology. 8: 457. PMID 28740467 DOI: 10.3389/Fphar.2017.00457 |
0.342 |
|
2017 |
Chen X, Wu H, Park CM, Poole TH, Keceli G, Devarie Baez NO, Tsang AW, Lowther WT, Poole LB, King SB, Xian M, Furdui CM. Discovery of Heteroaromatic Sulfones As A New Class of Biologically Compatible Thiol-Selective Reagents. Acs Chemical Biology. PMID 28687042 DOI: 10.1021/Acschembio.7B00444 |
0.684 |
|
2017 |
Day JJ, Neill DL, Xu S, Xian M. Benzothiazole Sulfinate: A Sulfinic Acid Transfer Reagent under Oxidation-Free Conditions. Organic Letters. PMID 28670905 DOI: 10.1021/Acs.Orglett.7B01693 |
0.352 |
|
2017 |
Ikeda M, Ishima Y, Shibata A, Chuang VTG, Sawa T, Ihara H, Watanabe H, Xian M, Ouchi Y, Shimizu T, Ando H, Ukawa M, Ishida T, Akaike T, Otagiri M, et al. Quantitative determination of polysulfide in albumins, plasma proteins and biological fluid samples using a novel combined assays approach. Analytica Chimica Acta. 969: 18-25. PMID 28411626 DOI: 10.1016/J.Aca.2017.03.027 |
0.348 |
|
2016 |
Peng B, Liu C, Li Z, Day JJ, Lu Y, Lefer DJ, Xian M. Slow generation of hydrogen sulfide from sulfane sulfurs and NADH models. Bioorganic & Medicinal Chemistry Letters. PMID 28003140 DOI: 10.1016/J.Bmcl.2016.12.023 |
0.33 |
|
2016 |
Chen W, Pacheco A, Takano Y, Day JJ, Hanaoka K, Xian M. A Single Fluorescent Probe to Visualize Hydrogen Sulfide and Hydrogen Polysulfides with Different Fluorescence Signals. Angewandte Chemie (International Ed. in English). PMID 27410794 DOI: 10.1002/Anie.201604892 |
0.35 |
|
2016 |
Kang J, Li Z, Organ CL, Park CM, Yang CT, Pacheco A, Wang D, Lefer DJ, Xian M. pH-Controlled Hydrogen Sulfide Release for Myocardial Ischemia-Reperfusion Injury. Journal of the American Chemical Society. PMID 27172143 DOI: 10.1021/Jacs.6B01373 |
0.335 |
|
2016 |
Wedmann R, Onderka C, Wei S, Szijártó IA, Miljkovic JL, Mitrovic A, Lange M, Savitsky S, Yadav PK, Torregrossa R, Harrer EG, Harrer T, Ishii I, Gollasch M, Wood ME, ... ... Xian M, et al. Improved tag-switch method reveals that thioredoxin acts as depersulfidase and controls the intracellular levels of protein persulfidation. Chemical Science (Royal Society of Chemistry : 2010). 7: 3414-3426. PMID 27170841 DOI: 10.1039/C5Sc04818D |
0.349 |
|
2016 |
Xu S, Yang CT, Meng FH, Pacheco A, Chen L, Xian M. Ammonium tetrathiomolybdate as a water-soluble and slow-release hydrogen sulfide donor. Bioorganic & Medicinal Chemistry Letters. PMID 26898812 DOI: 10.1016/J.Bmcl.2016.02.005 |
0.327 |
|
2016 |
Park CM, Johnson BA, Duan J, Park JJ, Day JJ, Gang D, Qian WJ, Xian M. 9-Fluorenylmethyl (Fm) Disulfides: Biomimetic Precursors for Persulfides. Organic Letters. PMID 26870874 DOI: 10.1021/Acs.Orglett.5B03557 |
0.396 |
|
2016 |
Park CM, Biggs TD, Xian M. Proline-based phosphoramidite reagents for the reductive ligation of S-nitrosothiols. The Journal of Antibiotics. PMID 26758493 DOI: 10.1038/Ja.2015.144 |
0.382 |
|
2016 |
Holmila R, Wu H, Chen X, Poole T, Park C, Poole LB, Xian M, Tsang AW, Bruce King S, Furdui CM. Selective Reagents for Analysis of Redox Effects in Biological Systems Free Radical Biology and Medicine. 100: S23. DOI: 10.1016/J.Freeradbiomed.2016.10.054 |
0.37 |
|
2015 |
Wang W, Xian M, Xie Y, Zheng J, Li J. Aggravation of airway inflammation and hyperresponsiveness following nasal challenge with Dermatophagoides pteronyssinus in perennial allergic rhinitis without symptoms of asthma. Allergy. PMID 26595454 DOI: 10.1111/all.12808 |
0.321 |
|
2015 |
Chen W, Rosser EW, Matsunaga T, Pacheco A, Akaike T, Xian M. The Development of Fluorescent Probes for Visualizing Intracellular Hydrogen Polysulfides. Angewandte Chemie (International Ed. in English). PMID 26381762 DOI: 10.1002/Anie.201506887 |
0.358 |
|
2015 |
Zhao Y, Yang C, Organ C, Li Z, Bhushan S, Otsuka H, Pacheco A, Kang J, Aguilar HC, Lefer DJ, Xian M. Design, Synthesis, and Cardioprotective Effects of N-Mercapto-Based Hydrogen Sulfide Donors. Journal of Medicinal Chemistry. 58: 7501-11. PMID 26317692 DOI: 10.1021/Acs.Jmedchem.5B01033 |
0.363 |
|
2015 |
Zhao Y, Pacheco A, Xian M. Medicinal Chemistry: Insights into the Development of Novel H2S Donors. Handbook of Experimental Pharmacology. 230: 365-88. PMID 26162844 DOI: 10.1007/978-3-319-18144-8_18 |
0.335 |
|
2015 |
Biggs TD, Weerasinghe L, Park CM, Xian M. Phosphine Mediated Conjugation of S-Nitrosothiols and Aldehydes. Tetrahedron Letters. 56: 2741-2743. PMID 26089576 DOI: 10.1016/J.Tetlet.2015.04.017 |
0.396 |
|
2015 |
Park CM, Weerasinghe L, Day JJ, Fukuto JM, Xian M. Persulfides: current knowledge and challenges in chemistry and chemical biology. Molecular Biosystems. 11: 1775-85. PMID 25969163 DOI: 10.1039/C5Mb00216H |
0.34 |
|
2015 |
Chen W, Rosser EW, Zhang D, Shi W, Li Y, Dong WJ, Ma H, Hu D, Xian M. A specific nucleophilic ring-opening reaction of aziridines as a unique platform for the construction of hydrogen polysulfides sensors. Organic Letters. 17: 2776-9. PMID 25961957 DOI: 10.1021/Acs.Orglett.5B01194 |
0.377 |
|
2015 |
Park CM, Macinkovic I, Filipovic MR, Xian M. Use of the "tag-switch" method for the detection of protein S-sulfhydration. Methods in Enzymology. 555: 39-56. PMID 25747474 DOI: 10.1016/Bs.Mie.2014.11.033 |
0.358 |
|
2015 |
Park CM, Xian M. Use of phosphorodithioate-based compounds as hydrogen sulfide donors. Methods in Enzymology. 554: 127-42. PMID 25725520 DOI: 10.1016/Bs.Mie.2014.11.032 |
0.348 |
|
2015 |
Peng B, Xian M. Hydrogen sulfide detection using nucleophilic substitution-cyclization-based fluorescent probes. Methods in Enzymology. 554: 47-62. PMID 25725515 DOI: 10.1016/Bs.Mie.2014.11.030 |
0.374 |
|
2015 |
Peng B, Zhang C, Marutani E, Pacheco A, Chen W, Ichinose F, Xian M. Trapping hydrogen sulfide (H₂S) with diselenides: the application in the design of fluorescent probes. Organic Letters. 17: 1541-4. PMID 25723840 DOI: 10.1021/Acs.Orglett.5B00431 |
0.416 |
|
2015 |
Lin VS, Chen W, Xian M, Chang CJ. Chemical probes for molecular imaging and detection of hydrogen sulfide and reactive sulfur species in biological systems. Chemical Society Reviews. 44: 4596-618. PMID 25474627 DOI: 10.1039/C4Cs00298A |
0.375 |
|
2015 |
Miao Z, Reisz JA, Mitroka SM, Pan J, Xian M, King SB. A selective phosphine-based fluorescent probe for nitroxyl in living cells. Bioorganic & Medicinal Chemistry Letters. 25: 16-9. PMID 25465170 DOI: 10.1016/J.Bmcl.2014.11.041 |
0.548 |
|
2015 |
Loebsch S, Zhao Y, Xian M, Steiner G, Kloesch B. A8.22 Thiol-activated hydrogen sulfide donors and their anti-inflammatory potential in the mouse macrophage cell line RAW264 Annals of the Rheumatic Diseases. 74: A90.2-A90. DOI: 10.1136/Annrheumdis-2015-207259.207 |
0.342 |
|
2015 |
Zhang C, Peng B, Chen W, Shuang S, Xian M, Dong C. A ratiometric fluorescent probe for hydrogen sulfide based on the nucleophilic substitution-cyclization of diselenides Dyes and Pigments. 121: 299-304. DOI: 10.1016/J.Dyepig.2015.06.003 |
0.39 |
|
2014 |
Marutani E, Sakaguchi M, Chen W, Sasakura K, Liu J, Xian M, Hanaoka K, Nagano T, Ichinose F. Cytoprotective effects of hydrogen sulfide-releasing N-methyl-D-aspartate receptor antagonists are mediated by intracellular sulfane sulfur. Medchemcomm. 5: 1577-1583. PMID 25431645 DOI: 10.1039/C4Md00180J |
0.32 |
|
2014 |
Chen Y, Mo HZ, Zheng MY, Xian M, Qi ZQ, Li YQ, Hu LB, Chen J, Yang LF. Selenium inhibits root elongation by repressing the generation of endogenous hydrogen sulfide in Brassica rapa. Plos One. 9: e110904. PMID 25333279 DOI: 10.1371/Journal.Pone.0110904 |
0.311 |
|
2014 |
Yang CT, Zhao Y, Xian M, Li JH, Dong Q, Bai HB, Xu JD, Zhang MF. A novel controllable hydrogen sulfide-releasing molecule protects human skin keratinocytes against methylglyoxal-induced injury and dysfunction. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 34: 1304-17. PMID 25277151 DOI: 10.1159/000366339 |
0.303 |
|
2014 |
Ono K, Akaike T, Sawa T, Kumagai Y, Wink DA, Tantillo DJ, Hobbs AJ, Nagy P, Xian M, Lin J, Fukuto JM. Redox chemistry and chemical biology of H2S, hydropersulfides, and derived species: implications of their possible biological activity and utility. Free Radical Biology & Medicine. 77: 82-94. PMID 25229186 DOI: 10.1016/J.Freeradbiomed.2014.09.007 |
0.333 |
|
2014 |
Liu C, Zhang F, Munske G, Zhang H, Xian M. Isotope dilution mass spectrometry for the quantification of sulfane sulfurs. Free Radical Biology & Medicine. 76: 200-7. PMID 25152234 DOI: 10.1016/J.Freeradbiomed.2014.08.003 |
0.344 |
|
2014 |
Zhao Y, Kang J, Park CM, Bagdon PE, Peng B, Xian M. Thiol-activated gem-dithiols: a new class of controllable hydrogen sulfide donors. Organic Letters. 16: 4536-9. PMID 25141097 DOI: 10.1021/Ol502088M |
0.329 |
|
2014 |
Zhang D, Chen W, Kang J, Ye Y, Zhao Y, Xian M. Highly selective fluorescence off-on probes for biothiols and imaging in live cells. Organic & Biomolecular Chemistry. 12: 6837-41. PMID 25047799 DOI: 10.1039/C4Ob01031K |
0.317 |
|
2014 |
Zhao Y, Biggs TD, Xian M. Hydrogen sulfide (H2S) releasing agents: chemistry and biological applications. Chemical Communications (Cambridge, England). 50: 11788-805. PMID 25019301 DOI: 10.1039/C4Cc00968A |
0.357 |
|
2014 |
Liu C, Chen W, Shi W, Peng B, Zhao Y, Ma H, Xian M. Rational design and bioimaging applications of highly selective fluorescence probes for hydrogen polysulfides. Journal of the American Chemical Society. 136: 7257-60. PMID 24809803 DOI: 10.1021/Ja502968X |
0.362 |
|
2014 |
Ida T, Sawa T, Ihara H, Tsuchiya Y, Watanabe Y, Kumagai Y, Suematsu M, Motohashi H, Fujii S, Matsunaga T, Yamamoto M, Ono K, Devarie-Baez NO, Xian M, Fukuto JM, et al. Reactive cysteine persulfides and S-polythiolation regulate oxidative stress and redox signaling. Proceedings of the National Academy of Sciences of the United States of America. 111: 7606-11. PMID 24733942 DOI: 10.1073/Pnas.1321232111 |
0.353 |
|
2014 |
Zhang D, Chen W, Miao Z, Ye Y, Zhao Y, King SB, Xian M. A reductive ligation based fluorescent probe for S-nitrosothiols. Chemical Communications (Cambridge, England). 50: 4806-9. PMID 24658175 DOI: 10.1039/C4Cc01288G |
0.318 |
|
2014 |
Li YJ, Chen J, Xian M, Zhou LG, Han FX, Gan LJ, Shi ZQ. In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. Plos One. 9: e90340. PMID 24587333 DOI: 10.1371/Journal.Pone.0090340 |
0.304 |
|
2014 |
Peng B, Chen W, Liu C, Rosser EW, Pacheco A, Zhao Y, Aguilar HC, Xian M. Fluorescent probes based on nucleophilic substitution-cyclization for hydrogen sulfide detection and bioimaging. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1010-6. PMID 24339269 DOI: 10.1002/Chem.201303757 |
0.371 |
|
2014 |
Zhang D, Macinkovic I, Devarie-Baez NO, Pan J, Park CM, Carroll KS, Filipovic MR, Xian M. Detection of protein S-sulfhydration by a tag-switch technique. Angewandte Chemie (International Ed. in English). 53: 575-81. PMID 24288186 DOI: 10.1002/anie.201305876 |
0.527 |
|
2014 |
Kloesch B, Becker T, Zhao Y, Xian M, Steiner G. A8.8 Controllable hydrogen sulfide donors and their anti-inflammatory potential in the murine macrophage cell line RAW264.7 Annals of the Rheumatic Diseases. 73: A79.1-A79. DOI: 10.1136/Annrheumdis-2013-205124.182 |
0.321 |
|
2014 |
Kloesch B, Loebsch S, Zhao Y, Xian M, Steiner G. P40 Cysteine-activated hydrogen sulphide donors and their anti-inflammatory potential in the human leukemic monocyte cell line U937 Nitric Oxide. 39: S28. DOI: 10.1016/J.Niox.2014.03.090 |
0.304 |
|
2014 |
Filipovic MR, Macinkovic I, Zhang D, Devarie-Baez NO, Park C, Xian M. S7-5 The mechanism(s) of protein persulfide formation: Detection of protein S-sulfhydration by a tag-switch assay Nitric Oxide. 39: S9-S10. DOI: 10.1016/J.Niox.2014.03.035 |
0.387 |
|
2014 |
Xian M. S4-5 New chemistry and chemical tools for hydrogen sulfide research Nitric Oxide. 39. DOI: 10.1016/J.Niox.2014.03.020 |
0.373 |
|
2014 |
Peng B, Xian M. Fluorescent probes for hydrogen sulfide detection Asian Journal of Organic Chemistry. 3: 914-924. DOI: 10.1002/Ajoc.201402064 |
0.35 |
|
2013 |
Park CM, Zhao Y, Zhu Z, Pacheco A, Peng B, Devarie-Baez NO, Bagdon P, Zhang H, Xian M. Synthesis and evaluation of phosphorodithioate-based hydrogen sulfide donors. Molecular Biosystems. 9: 2430-4. PMID 23917226 DOI: 10.1039/C3Mb70145J |
0.352 |
|
2013 |
Chen W, Liu C, Peng B, Zhao Y, Pacheco A, Xian M. New fluorescent probes for sulfane sulfurs and the application in bioimaging. Chemical Science (Royal Society of Chemistry : 2010). 4: 2892-2896. PMID 23750317 DOI: 10.1039/C3Sc50754H |
0.36 |
|
2013 |
Devarie-Baez NO, Zhang D, Li S, Whorton AR, Xian M. Direct methods for detection of protein S-nitrosylation. Methods (San Diego, Calif.). 62: 171-6. PMID 23639867 DOI: 10.1016/J.Ymeth.2013.04.018 |
0.334 |
|
2013 |
Talipov MR, Khomyakov DG, Xian M, Timerghazin QK. Computational design of S-nitrosothiol "click" reactions. Journal of Computational Chemistry. 34: 1527-30. PMID 23553289 DOI: 10.1002/Jcc.23279 |
0.367 |
|
2013 |
Zhao Y, Bhushan S, Yang C, Otsuka H, Stein JD, Pacheco A, Peng B, Devarie-Baez NO, Aguilar HC, Lefer DJ, Xian M. Controllable hydrogen sulfide donors and their activity against myocardial ischemia-reperfusion injury. Acs Chemical Biology. 8: 1283-90. PMID 23547844 DOI: 10.1021/Cb400090D |
0.338 |
|
2013 |
Zhang D, Macinkovic I, Devarie-Baez NO, Pan J, Park C, Carroll KS, Filipovic MR, Xian M. Detektion von Persulfidbildung an Proteinen (S-Sulfhydrierung) mithilfe einer Tag-Switch-Technik Angewandte Chemie. 126: 586-592. DOI: 10.1002/Ange.201305876 |
0.539 |
|
2012 |
Park CM, Niu W, Liu C, Biggs TD, Guo J, Xian M. A proline-based phosphine template for Staudinger ligation. Organic Letters. 14: 4694-7. PMID 22924811 DOI: 10.1021/Ol3022484 |
0.326 |
|
2012 |
Zhang D, Devarie-Baez NO, Li Q, Lancaster JR, Xian M. Methylsulfonyl benzothiazole (MSBT): a selective protein thiol blocking reagent. Organic Letters. 14: 3396-9. PMID 22681565 DOI: 10.1021/Ol301370S |
0.344 |
|
2012 |
Liu C, Peng B, Li S, Park CM, Whorton AR, Xian M. Reaction based fluorescent probes for hydrogen sulfide. Organic Letters. 14: 2184-7. PMID 22486842 DOI: 10.1021/Ol3008183 |
0.393 |
|
2012 |
Li S, Wang H, Xian M, Whorton AR. Identification of protein nitrosothiols using phosphine-mediated selective reduction. Nitric Oxide : Biology and Chemistry / Official Journal of the Nitric Oxide Society. 26: 20-6. PMID 22100619 DOI: 10.1016/J.Niox.2011.11.001 |
0.388 |
|
2012 |
Devarie Baez NO, Zhang D, Liu C, Peng B, Zhao Y, Xian M. P64 Chemical approaches for the detection of hydrogen sulfide (H2S) Nitric Oxide. 27: S40. DOI: 10.1016/J.Niox.2012.08.065 |
0.342 |
|
2012 |
Zhao Y, Stein J, Park C, Devarie Baez NO, Xian M. P40 Development of new H2S donors Nitric Oxide. 27: S30. DOI: 10.1016/J.Niox.2012.08.041 |
0.365 |
|
2011 |
Liu C, Pan J, Li S, Zhao Y, Wu LY, Berkman CE, Whorton AR, Xian M. Capture and visualization of hydrogen sulfide by a fluorescent probe. Angewandte Chemie (International Ed. in English). 50: 10327-9. PMID 21898737 DOI: 10.1002/Anie.201104305 |
0.562 |
|
2011 |
Pan J, Devarie-Baez NO, Xian M. Facile amide formation via S-nitrosothioacids. Organic Letters. 13: 1092-4. PMID 21271725 DOI: 10.1021/Ol1031393 |
0.574 |
|
2011 |
Zhao Y, Wang H, Xian M. Cysteine-activated hydrogen sulfide (H2S) donors. Journal of the American Chemical Society. 133: 15-7. PMID 21142018 DOI: 10.1021/Ja1085723 |
0.34 |
|
2011 |
Wang H, Xian M. Chemical methods to detect S-nitrosation. Current Opinion in Chemical Biology. 15: 32-7. PMID 21036657 DOI: 10.1016/J.Cbpa.2010.10.006 |
0.343 |
|
2011 |
Pan J, Xian M. Disulfide formation via sulfenamides. Chemical Communications (Cambridge, England). 47: 352-4. PMID 20730241 DOI: 10.1039/C0Cc02076A |
0.558 |
|
2011 |
Liu X, Wang Y, Cao Y, Yadama V, Xian M, Zhang J. Study of dextrin-derived curing agent for waterborne epoxy adhesive Carbohydrate Polymers. 83: 1180-1184. DOI: 10.1016/J.Carbpol.2010.09.019 |
0.312 |
|
2010 |
Zhang D, Devarie-Baez NO, Pan J, Wang H, Xian M. One-pot thioether formation from S-nitrosothiols. Organic Letters. 12: 5674-6. PMID 21080645 DOI: 10.1021/Ol102491N |
0.562 |
|
2010 |
Zhang J, Li S, Zhang D, Wang H, Whorton AR, Xian M. Reductive ligation mediated one-step disulfide formation of S-nitrosothiols. Organic Letters. 12: 4208-11. PMID 20731371 DOI: 10.1021/Ol101863S |
0.377 |
|
2010 |
Devarie-Baez NO, Xian M. Facile preparation of 3-substituted benzisothiazoles from o-mercaptoacylphenones. Organic Letters. 12: 752-4. PMID 20078088 DOI: 10.1021/Ol9028447 |
0.326 |
|
2009 |
Wang H, Zhang J, Xian M. Facile formation of dehydroalanine from S-nitrosocysteines. Journal of the American Chemical Society. 131: 13238-9. PMID 19715315 DOI: 10.1021/Ja905558W |
0.347 |
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2009 |
Pan J, Downing JA, McHale JL, Xian M. A fluorogenic dye activated by S-nitrosothiols. Molecular Biosystems. 5: 918-20. PMID 19668853 DOI: 10.1039/B822283E |
0.55 |
|
2009 |
Devarie-Baez NO, Kim WS, Smith AB, Xian M. Multicomponent type II anion relay chemistry (ARC): one-pot syntheses of 2,3-disubstituted furans and thiophenes. Organic Letters. 11: 1861-4. PMID 19301924 DOI: 10.1021/Ol900434K |
0.486 |
|
2009 |
Zhang J, Wang H, Xian M. An unexpected Bis-ligation of S-nitrosothiols. Journal of the American Chemical Society. 131: 3854-5. PMID 19256495 DOI: 10.1021/Ja900370Y |
0.369 |
|
2009 |
Zhang J, Wang H, Xian M. Exploration of the "traceless" reductive ligation of S-nitrosothiols. Organic Letters. 11: 477-80. PMID 19128195 DOI: 10.1021/Ol802663Q |
0.353 |
|
2008 |
Wang H, Liu B, Liu X, Zhang J, Xian M. Synthesis of biobased epoxy and curing agents using rosin and the study of cure reactions Green Chemistry. 10: 1190-1196. DOI: 10.1039/B803295E |
0.35 |
|
2007 |
Smith AB, Kim DS, Xian M. Anion relay chemistry extended. Synthesis of a gorgonian sesquiterpene. Organic Letters. 9: 3307-9. PMID 17637030 DOI: 10.1021/Ol071281J |
0.529 |
|
2007 |
Xian M, Shuhler BJ. Study of the synthesis of poecillanosine Tetrahedron Letters. 48: 1209-1212. DOI: 10.1016/J.Tetlet.2006.12.059 |
0.302 |
|
2006 |
Smith AB, Xian M, Kim WS, Kim DS. The [1,5]-Brook rearrangement: an initial application in anion relay chemistry. Journal of the American Chemical Society. 128: 12368-9. PMID 16984158 DOI: 10.1021/Ja065033E |
0.608 |
|
2006 |
Smith AB, Xian M. Anion relay chemistry: an effective tactic for diversity oriented synthesis. Journal of the American Chemical Society. 128: 66-7. PMID 16390124 DOI: 10.1021/Ja057059W |
0.307 |
|
2005 |
Smith AB, Xian M. Design, synthesis, and biological evaluation of simplified analogues of (+)-discodermolide. Additional insights on the importance of the diene, the C7 hydroxyl, and the lactone. Organic Letters. 7: 5229-32. PMID 16268545 DOI: 10.1021/Ol052070M |
0.366 |
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2005 |
Smith AB, Xian M, Liu F. Design, total synthesis, and evaluation of C13-C14 cyclopropane analogues of (+)-discodermolide. Organic Letters. 7: 4613-6. PMID 16209492 DOI: 10.1021/Ol051691C |
0.35 |
|
2005 |
Shaw SJ, Sundermann KF, Burlingame MA, Myles DC, Freeze BS, Xian M, Brouard I, Smith AB. Toward understanding how the lactone moiety of discodermolide affects activity. Journal of the American Chemical Society. 127: 6532-3. PMID 15869264 DOI: 10.1021/Ja051185I |
0.713 |
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2005 |
Smith AB, Freeze BS, Xian M, Hirose T. Total synthesis of (+)-discodermolide: a highly convergent fourth-generation approach. Organic Letters. 7: 1825-8. PMID 15844916 DOI: 10.1021/Ol050455Z |
0.712 |
|
2005 |
Smith AB, Freeze BS, Lamarche MJ, Hirose T, Brouard I, Xian M, Sundermann KF, Shaw SJ, Burlingame MA, Horwitz SB, Myles DC. Design, synthesis, and evaluation of analogues of (+)-14-normethyldiscodermolide. Organic Letters. 7: 315-8. PMID 15646986 DOI: 10.1021/Ol0476873 |
0.747 |
|
2005 |
Smith AB, Freeze BS, Lamarche MJ, Hirose T, Brouard I, Rucker PV, Xian M, Sundermann KF, Shaw SJ, Burlingame MA, Horwitz SB, Myles DC. Design, synthesis, and evaluation of carbamate-substituted analogues of (+)-discodermolide. Organic Letters. 7: 311-4. PMID 15646985 DOI: 10.1021/Ol047686A |
0.754 |
|
2002 |
Cai T, Xian M, Wang PG. Electrochemical and peroxidase oxidation study of N'-hydroxyguanidine derivatives as NO donors. Bioorganic & Medicinal Chemistry Letters. 12: 1507-10. PMID 12031330 DOI: 10.1016/S0960-894X(02)00185-3 |
0.308 |
|
2002 |
Wang PG, Xian M, Tang X, Wu X, Wen Z, Cai T, Janczuk AJ. Nitric oxide donors: chemical activities and biological applications. Chemical Reviews. 102: 1091-134. PMID 11942788 DOI: 10.1021/Cr000040L |
0.301 |
|
2001 |
Xian M, Li X, Tang X, Chen X, Zheng Z, Galligan JJ, Kreulen DL, Wang PG. N-hydroxyl derivatives of guanidine based drugs as enzymatic NO donors. Bioorganic & Medicinal Chemistry Letters. 11: 2377-80. PMID 11527735 DOI: 10.1016/S0960-894X(01)00456-5 |
0.324 |
|
2001 |
Wu X, Tang X, Xian M, Wang PG. Glycosylated diazeniumdiolates: A novel class of enzyme-activated nitric oxide donors Tetrahedron Letters. 42: 3779-3782. DOI: 10.1016/S0040-4039(01)00614-1 |
0.313 |
|
2000 |
Xian M, Wang QM, Chen X, Wang K, Wang PG. S-nitrosothiols as novel, reversible inhibitors of human rhinovirus 3C protease. Bioorganic & Medicinal Chemistry Letters. 10: 2097-100. PMID 10999479 DOI: 10.1016/S0960-894X(00)00420-0 |
0.3 |
|
2000 |
Wang K, Zhang W, Xian M, Hou YC, Chen XC, Cheng JP, Wang PG. New chemical and biological aspects of S-nitrosothiols. Current Medicinal Chemistry. 7: 821-34. PMID 10828289 DOI: 10.2174/0929867003374633 |
0.339 |
|
2000 |
Xian M, Chen X, Liu Z, Wang K, Wang PG. Inhibition of papain by S-nitrosothiols. Formation of mixed disulfides. The Journal of Biological Chemistry. 275: 20467-73. PMID 10779505 DOI: 10.1074/Jbc.M001054200 |
0.328 |
|
1999 |
Zhu X, Xian M, Wang K, Cheng J. Is NO (Nitric Oxide) an Electron Acceptor or an Electrophile? A Detailed Thermodynamic Investigation on the Mechanisms of NO-Initiated Reactions with 3,6-Dibromocarbazolide Anion and Related Carbanion The Journal of Organic Chemistry. 64: 4187-4190. DOI: 10.1021/Jo982037W |
0.309 |
|
1999 |
Xian M, Zhu X, Li Q, Cheng J. A high-yielding and facile preparation of N-substituted thioureas by substitution of nitrosothioureas with alkylamines Tetrahedron Letters. 40: 1957-1960. DOI: 10.1016/S0040-4039(99)00093-3 |
0.314 |
|
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