Year |
Citation |
Score |
2025 |
Chen J, Bai X, Peng W, Liu J, Jia Z, Cheng M, Li J, Guo W, Zheng Y. A thiocoumarin based self-reporting sulfide prodrug strategy with a favorable safety profile. European Journal of Medicinal Chemistry. 289: 117426. PMID 40015159 DOI: 10.1016/j.ejmech.2025.117426 |
0.321 |
|
2024 |
Peng W, Qin L, Wang T, Sun Y, Li Z, Lefer DJ, Luo C, Ye F, Wang B, Guo W, Zheng Y. A Highly Atom-Efficient Prodrug Approach to Generate Synergy between HS and Nonsteroidal Anti-inflammatory Drugs and Improve Safety. Journal of Medicinal Chemistry. 67: 17350-17362. PMID 39316761 DOI: 10.1021/acs.jmedchem.4c01254 |
0.559 |
|
2024 |
Tong X, Chen J, Wang M, Liu J, Li J, Wang X, Zuo Y, Xu X, Wang Y, Wang B, Guo W, Zheng Y. Development of a Bioorthogonal Click-to-Release Reaction for Hydrogen Polysulfide (HS) Detection. Analytical Chemistry. PMID 39287125 DOI: 10.1021/acs.analchem.4c02677 |
0.563 |
|
2020 |
Yuan ZN, Zheng YQ, Wang BH. Prodrugs of hydrogen sulfide and related sulfur species: recent development. Chinese Journal of Natural Medicines. 18: 296-307. PMID 32402407 DOI: 10.1016/S1875-5364(20)30037-6 |
0.533 |
|
2019 |
Anifowose A, Yuan Z, Yang X, Pan Z, Zheng Y, Zhang Z, Wang B. Upregulation of p53 through induction of MDM2 degradation: Amino acid prodrugs of anthraquinone analogs. Bioorganic & Medicinal Chemistry Letters. 126786. PMID 31753697 DOI: 10.1016/J.Bmcl.2019.126786 |
0.743 |
|
2019 |
Ji X, Pan Z, Yu B, De La Cruz LK, Zheng Y, Ke B, Wang B. Click and release: bioorthogonal approaches to "on-demand" activation of prodrugs. Chemical Society Reviews. PMID 30724944 DOI: 10.1039/C8Cs00395E |
0.782 |
|
2018 |
Yuan Z, Zheng Y, Yu B, Wang S, Yang X, Wang B. Esterase-Sensitive Glutathione Persulfide Donor. Organic Letters. PMID 30299967 DOI: 10.1021/Acs.Orglett.8B02611 |
0.768 |
|
2018 |
Li S, Yu B, Wang J, Zheng Y, Zhang H, Walker MJ, Yuan Z, Zhu H, Zhang J, Wang PG, Wang B. Biomarker-based Metabolic Labeling for Redirected and Enhanced Immune Response. Acs Chemical Biology. PMID 29792670 DOI: 10.1021/Acschembio.8B00350 |
0.72 |
|
2018 |
Zheng Y, Ji X, Yu B, Ji K, Gallo D, Csizmadia E, Zhu M, Choudhury MR, De La Cruz LKC, Chittavong V, Pan Z, Yuan Z, Otterbein LE, Wang B. Enrichment-triggered prodrug activation demonstrated through mitochondria-targeted delivery of doxorubicin and carbon monoxide. Nature Chemistry. PMID 29760413 DOI: 10.1038/S41557-018-0055-2 |
0.743 |
|
2017 |
Yu B, Zheng Y, Yuan Z, Li S, Zhu H, De La Cruz LK, Zhang J, Ji K, Wang S, Wang B. Toward Direct Protein S-Persulfidation: A Prodrug Approach That Directly Delivers Hydrogen Persulfide. Journal of the American Chemical Society. PMID 29211467 DOI: 10.1021/Jacs.7B09795 |
0.795 |
|
2017 |
Zhang J, Shi Y, Zheng Y, Pan C, Yang X, Dou T, Wang B, Lu W. Homing in on an intracellular target for delivery of loaded nanoparticles functionalized with a histone deacetylase inhibitor. Oncotarget. 8: 68242-68251. PMID 28978112 DOI: 10.18632/Oncotarget.20021 |
0.586 |
|
2017 |
Zheng Y, Yu B, Li Z, Yuan Z, Lefer DJ, Wang B, Wang S, Organ CL, Trivedi RK. A Novel Esterase-sensitive Prodrug Approach for Controllable Delivery of Persulfide Species. Angewandte Chemie (International Ed. in English). PMID 28700817 DOI: 10.1002/Anie.201704117 |
0.747 |
|
2017 |
Zheng Y, Yu B, De La Cruz LK, Roy Choudhury M, Anifowose A, Wang B. Toward Hydrogen Sulfide Based Therapeutics: Critical Drug Delivery and Developability Issues. Medicinal Research Reviews. PMID 28240384 DOI: 10.1002/Med.21433 |
0.77 |
|
2016 |
Wang K, Friscourt F, Dai C, Wang L, Zheng Y, Boons GJ, Wang S, Wang B. A metal-free turn-on fluorescent probe for the fast and sensitive detection of inorganic azides. Bioorganic & Medicinal Chemistry Letters. PMID 26944613 DOI: 10.1016/J.Bmcl.2016.02.069 |
0.71 |
|
2016 |
Ji X, Damera K, Zheng Y, Yu B, Otterbein LE, Wang B. Toward Carbon Monoxide-Based Therapeutics: Critical Drug Delivery and Developability Issues. Journal of Pharmaceutical Sciences. 105: 406-16. PMID 26869408 DOI: 10.1016/J.Xphs.2015.10.018 |
0.765 |
|
2016 |
Zheng Y, Yu B, Ji K, Pan Z, Chittavong V, Wang B. Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide. Angewandte Chemie (International Ed. in English). PMID 26822005 DOI: 10.1002/Anie.201511244 |
0.76 |
|
2016 |
Zheng Y, Duan Y, Ji K, Wang R, Wang B. Tuning the reaction rates of fluoride probes for detection in aqueous solution Rsc Advances. 6: 25242-25245. DOI: 10.1039/C6Ra03252D |
0.765 |
|
2016 |
Zheng Y, Yu B, Ji K, Pan Z, Chittavong V, Wang B. Inside Cover: Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide (Angew. Chem. Int. Ed. 14/2016) Angewandte Chemie International Edition. 55: 4370-4370. DOI: 10.1002/Anie.201602011 |
0.76 |
|
2016 |
Zheng Y, Yu B, Ji K, Pan Z, Chittavong V, Wang B. Innentitelbild: Esterase-Sensitive Prodrugs with Tunable Release Rates and Direct Generation of Hydrogen Sulfide (Angew. Chem. 14/2016) Angewandte Chemie. 128: 4444-4444. DOI: 10.1002/Ange.201602011 |
0.761 |
|
2015 |
Zheng Y, Ji X, Ji K, Wang B. Hydrogen sulfide prodrugs-a review. Acta Pharmaceutica Sinica. B. 5: 367-377. PMID 26579468 DOI: 10.1016/J.Apsb.2015.06.004 |
0.773 |
|
2015 |
Wang K, Wang D, Ji K, Chen W, Zheng Y, Dai C, Wang B. Post-synthesis DNA modifications using a trans-cyclooctene click handle. Organic & Biomolecular Chemistry. 13: 909-15. PMID 25407744 DOI: 10.1039/C4Ob02031F |
0.727 |
|
2014 |
Wang D, Chen W, Zheng Y, Dai C, Wang K, Ke B, Wang B. 3,6-Substituted-1,2,4,5-tetrazines: tuning reaction rates for staged labeling applications. Organic & Biomolecular Chemistry. 12: 3950-5. PMID 24806890 DOI: 10.1039/C4Ob00280F |
0.748 |
|
2013 |
Wang D, Chen W, Zheng Y, Dai C, Wang L, Wang B. A general and efficient entry to asymmetric tetrazines for click chemistry applications Heterocyclic Communications. 19. DOI: 10.1515/Hc-2013-0072 |
0.747 |
|
2012 |
Fang Y, Zheng Y, Wang Z. Direct Base-Assisted C-N Bond Formation between Aryl Halides and Aliphatic Tertiary Amines under Transition-Metal-Free Conditions European Journal of Organic Chemistry. 2012: 1495-1498. DOI: 10.1002/Ejoc.201101618 |
0.302 |
|
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