Year |
Citation |
Score |
2018 |
Nowotarski SL, Pachaiyappan B, Holshouser SL, Kutz CJ, Li Y, Huang Y, Sharma SK, Casero RA, Woster PM. Corrigendum to "Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures" [Bioorg. Med. Chem. 23 (2015) 1601-1612]. Bioorganic & Medicinal Chemistry. PMID 29859749 DOI: 10.1016/J.Bmc.2018.05.032 |
0.48 |
|
2016 |
Chen NH, Zhang YB, Huang XJ, Jiang L, Jiang SQ, Li GQ, Li YL, Wang GC. Drychampones A‒C: Three Meroterpenoids from Dryopteris championii. The Journal of Organic Chemistry. PMID 27583635 DOI: 10.1021/Acs.Joc.6B01720 |
0.346 |
|
2016 |
Luo W, Zhao T, Li Y, Wei J, Xu P, Li X, Wang Y, Zhang W, Elzatahry AA, Alghamdi A, Deng Y, Wang L, Jiang W, Liu Y, Kong B, et al. A Micelle Fusion-Aggregation Assembly Approach to Mesoporous Carbon Materials with Rich Active Sites for Ultra-Sensitive Ammo-nia Sensing. Journal of the American Chemical Society. PMID 27575996 DOI: 10.1021/Jacs.6B07355 |
0.305 |
|
2016 |
Zhang Y, Liu XH, Zhan YZ, Zhang LY, Li ZM, Li YH, Zhang X, Wang BL. Synthesis and biological activities of novel 5-substituted-1,3,4-oxadiazole Mannich bases and bis-Mannich bases as ketol-acid reductoisomerase inhibitors. Bioorganic & Medicinal Chemistry Letters. PMID 27575481 DOI: 10.1016/j.bmcl.2016.08.059 |
0.362 |
|
2015 |
Li Y, Woster PM. Discovery of a new class of histone deacetylase inhibitors with a novel zinc binding group. Medchemcomm. 6: 613-618. PMID 26005563 DOI: 10.1039/C4Md00401A |
0.663 |
|
2015 |
Nowotarski SL, Pachaiyappan B, Holshouser SL, Kutz CJ, Li Y, Huang Y, Sharma SK, Casero RA, Woster PM. Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures. Bioorganic & Medicinal Chemistry. 23: 1601-12. PMID 25725609 DOI: 10.1016/J.Bmc.2015.01.049 |
0.486 |
|
2015 |
Li Y, Woster PM. Discovery of a new class of histone deacetylase inhibitors with a novel zinc binding group Medchemcomm. 6: 613-618. DOI: 10.1039/c4md00401a |
0.564 |
|
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