Year |
Citation |
Score |
2021 |
Wei Q, Bai J, Yan D, Bao X, Li W, Liu B, Zhang D, Qi X, Yu D, Hu Y. Genome mining combined metabolic shunting and OSMAC strategy of an endophytic fungus leads to the production of diverse natural products. Acta Pharmaceutica Sinica. B. 11: 572-587. PMID 33643832 DOI: 10.1016/J.Apsb.2020.07.020 |
0.362 |
|
2019 |
Chen Q, Gao J, Jamieson C, Liu J, Ohashi M, Bai J, Yan D, Liu B, Che Y, Wang Y, Houk KN, Hu Y. Enzymatic Intermolecular Hetero-Diels-Alder Reaction in the Biosynthesis of Tropolonic Sesquiterpenes. Journal of the American Chemical Society. PMID 31461283 DOI: 10.1021/Jacs.9B06592 |
0.307 |
|
2019 |
Zeng H, Yin G, Wei Q, Li D, Wang Y, Hu Y, Hu C, Zou Y. Unprecedented [5.5.5.6]Dioxafenstrane Ring Construction in Fungal Insecticidal Sesquiterpene Biosynthesis. Angewandte Chemie (International Ed. in English). PMID 30908782 DOI: 10.1002/Anie.201813722 |
0.333 |
|
2019 |
Zhang L, Bai J, Yan D, Wang Y, Zhang Y, Li L, Liu B, Hu Y. Pleosporalesones A–B, two unique polyketides isolated from Pleosporales sp. Tetrahedron Letters. 60: 375-377. DOI: 10.1016/J.Tetlet.2018.12.057 |
0.372 |
|
2018 |
Wang YN, Mou YH, Dong Y, Wu Y, Liu BY, Bai J, Yan DJ, Zhang L, Feng DQ, Pei YH, Hu YC. Diphenyl Ethers from a Marine-Derived . Marine Drugs. 16. PMID 30453472 DOI: 10.3390/Md16110451 |
0.421 |
|
2018 |
Hu Y, Tang Y. Biotransformation and biosynthesis of natural products. Journal of Asian Natural Products Research. 1-2. PMID 30274529 DOI: 10.1080/10286020.2018.1497464 |
0.355 |
|
2018 |
Bai J, Mu R, Dou M, Yan D, Liu B, Wei Q, Wan J, Tang Y, Hu Y. Epigenetic modification in histone deacetylase deletion strain of leads to diverse diterpenoids. Acta Pharmaceutica Sinica. B. 8: 687-697. PMID 30109192 DOI: 10.1016/J.Apsb.2017.12.012 |
0.369 |
|
2018 |
Zhang T, Wan J, Zhan Z, Bai J, Liu B, Hu Y. Activation of an unconventional meroterpenoid gene cluster in leads to the production of new berkeleyacetals. Acta Pharmaceutica Sinica. B. 8: 478-487. PMID 29881687 DOI: 10.1016/J.Apsb.2017.12.005 |
0.309 |
|
2018 |
Ji YB, Xu F, Liu BY, Wei Q, Guo YZ, Dong Y, Sun Y, Hu YC. [Trace phenolic compounds from Red Yeast Rice]. Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica. 43: 755-759. PMID 29600651 DOI: 10.19540/J.Cnki.Cjcmm.20180104.014 |
0.382 |
|
2018 |
Wang MH, Hu YC, Sun BD, Yu M, Niu SB, Guo Z, Zhang XY, Zhang T, Ding G, Zou ZM. Highly Photosensitive Poly-Sulfur-Bridged Chetomin Analogues from Chaetomium cochliodes. Organic Letters. PMID 29537276 DOI: 10.1021/Acs.Orglett.8B00304 |
0.332 |
|
2018 |
Das B, Neilsen BK, Fisher KW, Gehring D, Hu Y, Volle DJ, Kim HS, McCall JL, Kelly DL, MacMillan JB, White MA, Lewis RE. A Functional Signature Ontology (FUSION) screen detects an AMPK inhibitor with selective toxicity toward human colon tumor cells. Scientific Reports. 8: 3770. PMID 29491475 DOI: 10.1038/S41598-018-22090-6 |
0.6 |
|
2018 |
Wu YZ, Zhang HW, Sun ZH, Dai JG, Hu YC, Li R, Lin PC, Xia GY, Wang LY, Qiu BL, Zhang JF, Ge GB, Lin S. Bysspectin A, an unusual octaketide dimer and the precursor derivatives from the endophytic fungus Byssochlamys spectabilis IMM0002 and their biological activities. European Journal of Medicinal Chemistry. 145: 717-725. PMID 29353723 DOI: 10.1016/j.ejmech.2018.01.030 |
0.329 |
|
2017 |
Ma Z, Li W, Zhang P, Lyu H, Hu Y, Yin WB. Rational design for heterologous production of aurovertin-type compounds in Aspergillus nidulans. Applied Microbiology and Biotechnology. PMID 29098413 DOI: 10.1007/S00253-017-8606-9 |
0.399 |
|
2017 |
Wu XF, Li L, Li Y, Lv HN, Liu YB, Hu YC. Phloroglucinols with Antioxidant Activities Isolated from Lysidice rhodostegia. Molecules (Basel, Switzerland). 22. PMID 28545244 DOI: 10.3390/Molecules22060855 |
0.377 |
|
2017 |
Bai J, Yan D, Zhang T, Guo Y, Liu Y, Zou Y, Tang M, Liu B, Wu Q, Yu S, Tang Y, Hu Y. A Cascade of Redox Reactions Generates Complexity in the Biosynthesis of the Protein Phosphatase-2 Inhibitor Rubratoxin A. Angewandte Chemie (International Ed. in English). PMID 28370936 DOI: 10.1002/Anie.201701547 |
0.341 |
|
2017 |
Fan A, Mi W, Liu Z, Zeng G, Zhang P, Hu Y, Fang W, Yin WB. Deletion of a Histone Acetyltransferase Leads to the Pleiotropic Activation of Natural Products in Metarhizium robertsii. Organic Letters. PMID 28301168 DOI: 10.1021/Acs.Orglett.7B00476 |
0.343 |
|
2015 |
Mao XM, Xu W, Li D, Yin WB, Chooi YH, Li YQ, Tang Y, Hu Y. Epigenetic Genome Mining of an Endophytic Fungus Leads to the Pleiotropic Biosynthesis of Natural Products. Angewandte Chemie (International Ed. in English). 54: 7592-6. PMID 26013262 DOI: 10.1002/Anie.201502452 |
0.457 |
|
2015 |
Colosimo D, Cai F, Hu Y, Potts M, White M, Ready J, MacMillan J. The discoipyrroles: A multifaceted approach to understand a novel family of marine natural products Planta Medica. 81. DOI: 10.1055/S-0035-1556348 |
0.577 |
|
2013 |
Potts MB, Kim HS, Fisher KW, Hu Y, Carrasco YP, Bulut GB, Ou YH, Herrera-Herrera ML, Cubillos F, Mendiratta S, Xiao G, Hofree M, Ideker T, Xie Y, Huang LJ, et al. Using functional signature ontology (FUSION) to identify mechanisms of action for natural products. Science Signaling. 6: ra90. PMID 24129700 DOI: 10.1126/Scisignal.2004657 |
0.698 |
|
2013 |
Hu Y, Potts MB, Colosimo D, Herrera-Herrera ML, Legako AG, Yousufuddin M, White MA, MacMillan JB. Discoipyrroles A-D: Isolation, structure determination, and synthesis of potent migration inhibitors from Bacillus hunanensis Journal of the American Chemical Society. 135: 13387-13392. PMID 23984625 DOI: 10.1021/Ja403412Y |
0.703 |
|
2013 |
Yin WB, Chooi YH, Smith AR, Cacho RA, Hu Y, White TC, Tang Y. Discovery of cryptic polyketide metabolites from dermatophytes using heterologous expression in Aspergillus nidulans. Acs Synthetic Biology. 2: 629-34. PMID 23758576 DOI: 10.1021/Sb400048B |
0.309 |
|
2013 |
Hu Y, Wang K, MacMillan JB. Hunanamycin A, an antibiotic from a marine-derived Bacillus hunanensis Organic Letters. 15: 390-393. PMID 23305153 DOI: 10.1021/Ol303376C |
0.627 |
|
2013 |
Sun Q, Carrasco YP, Hu Y, Guo X, Mirzaei H, Macmillan J, Chook YM. Nuclear export inhibition through covalent conjugation and hydrolysis of Leptomycin B by CRM1. Proceedings of the National Academy of Sciences of the United States of America. 110: 1303-8. PMID 23297231 DOI: 10.1073/Pnas.1217203110 |
0.694 |
|
2012 |
Hu Y, Martinez ED, MacMillan JB. Anthraquinones from a marine-derived streptomyces spinoverrucosus Journal of Natural Products. 75: 1759-1764. PMID 23057874 DOI: 10.1021/Np3004326 |
0.642 |
|
2012 |
Hu Y, MacMillan JB. A new peptide isolated from a marine derived Streptomyces bacillaris Natural Product Communications. 7: 211-214. PMID 22474960 DOI: 10.1177/1934578X1200700224 |
0.599 |
|
2012 |
Hu Y, Legako AG, Espindola APDM, MacMillan JB. Erythrolic acids A-E, meroterpenoids from a marine-derived erythrobacter sp. Journal of Organic Chemistry. 77: 3401-3407. PMID 22384985 DOI: 10.1021/Jo300197Z |
0.61 |
|
2012 |
Li Y, Liu Y, Yu S, Chen X, Wu X, Ma S, Qu J, Hu Y, Liu J, Lv H. Cytotoxic cardenolides from the stems of Periploca forrestii. Steroids. 77: 375-381. PMID 22212302 DOI: 10.1016/J.Steroids.2011.12.013 |
0.415 |
|
2011 |
Hu Y, MacMillan JB. Erythrazoles A-B, cytotoxic benzothiazoles from a marine-derived erythrobacter sp. Organic Letters. 13: 6580-6583. PMID 22106936 DOI: 10.1021/Ol202944G |
0.603 |
|
2011 |
Hu Y, Espindola APDM, Stewart NA, Wei S, Posner BA, MacMillan JB. Chromomycin SA analogs from a marine-derived Streptomyces sp. Bioorganic and Medicinal Chemistry. 19: 5183-5189. PMID 21807523 DOI: 10.1016/J.Bmc.2011.07.013 |
0.651 |
|
2011 |
Wu X, Wang Y, Yu S, Jiang N, Ma J, Tan R, Hu Y, Qu J. Antioxidative acylphloroglucinols from the roots of Lysidice rhodostegia Tetrahedron. 67: 8155-8159. DOI: 10.1016/J.Tet.2011.08.034 |
0.378 |
|
2010 |
Ma SG, Tang WZ, Liu YX, Hu YC, Yu SS, Zhang Y, Chen XG, Qu J, Ren JH, Liu YB, Xu S, Liu J, Liu YY, Li Y, Lü HN, et al. Prenylated C6-C3 compounds with molecular diversity from the roots of Illicium oligandrum. Phytochemistry. 72: 115-25. PMID 21112063 DOI: 10.1016/J.Phytochem.2010.10.021 |
0.388 |
|
2010 |
Hu Y, Ma S, Yu S, Wu X, Li Y. Phenolic glycosides isolated from the bark of Lysidice brevicalyx Wei. Journal of Asian Natural Products Research. 12: 516-521. PMID 20552492 DOI: 10.1080/10286020.2010.489818 |
0.379 |
|
2010 |
Wu XF, Hu YC, Yu SS, Jiang N, Ma J, Tan RX, Li Y, Lv HN, Liu J, Ma SG. Lysidicins F-H, three new phloroglucinols from Lysidice rhodostegia. Organic Letters. 12: 2390-3. PMID 20420380 DOI: 10.1021/Ol100735F |
0.388 |
|
2009 |
Liu J, Liu Y, Si Y, Yu S, Qu J, Xu S, Hu Y, Ma S. New vernocuminosides from the stem barks of Vernonia cumingiana Benth. Steroids. 74: 51-61. PMID 18840454 DOI: 10.1016/J.Steroids.2008.09.005 |
0.389 |
|
2008 |
Hu Y, Ma S, Li J, Yu S, Qu J, Liu J, Du D. Targeted isolation and structure elucidation of stilbene glycosides from the bark of Lysidice brevicalyx Wei guided by biological and chemical screening. Journal of Natural Products. 71: 1800-5. PMID 18847246 DOI: 10.1021/Np800083X |
0.39 |
|
2008 |
Qu J, Hu Y, Li J, Wang Y, Zhang J, Abliz Z, Yu S, Liu Y. Structural characterization of constituents with molecular diversity in fractions from Lysidice brevicalyx by liquid chromatography/diode-array detection/electrospray ionization tandem mass spectrometry and liquid chromatography/nuclear magnetic resonance Rapid Communications in Mass Spectrometry. 22: 755-765. PMID 18288769 DOI: 10.1002/Rcm.3419 |
0.376 |
|
2008 |
Liu Y, Qu J, Yu S, Tang W, Liu J, Hu Y, Ma S. Nine novel C-21 steroidal glycosides substituted with orthoacetate from Dregea sinensis var. corrugata. Steroids. 73: 184-92. PMID 18006029 DOI: 10.1016/J.Steroids.2007.09.009 |
0.336 |
|
2007 |
Su DM, Wang YH, Yu SS, Yu DQ, Hu YC, Tang WZ, Liu GT, Wang WJ. Glucosides from the roots of Capparis tenera. Chemistry & Biodiversity. 4: 2852-62. PMID 18081096 DOI: 10.1002/Cbdv.200790235 |
0.399 |
|
2007 |
Wu X, Hu Y, Gao S, Yu S, Pei Y, Tang W, Huang X. Two new compounds from the roots of Lysidice rhodostegia. Journal of Asian Natural Products Research. 9: 471-477. PMID 17701568 DOI: 10.1080/10286020701189161 |
0.407 |
|
2007 |
Gao W, Bussom S, Grill SP, Gullen EA, Hu YC, Huang X, Zhong S, Kaczmarek C, Gutierrez J, Francis S, Baker DC, Yu S, Cheng YC. Structure-activity studies of phenanthroindolizidine alkaloids as potential antitumor agents. Bioorganic & Medicinal Chemistry Letters. 17: 4338-42. PMID 17531481 DOI: 10.1016/J.Bmcl.2007.05.021 |
0.333 |
|
2007 |
Gao S, Liu J, Fu GM, Hu YC, Yu SS, Fan LH, Yu DQ, Qu J. Resveratrol/phloroglucinol glycosides from the roots of Lysidice rhodostegia. Planta Medica. 73: 163-6. PMID 17415877 DOI: 10.1055/S-2006-951770 |
0.37 |
|
2007 |
Liu Y, Qu J, Yu S, Hu Y, Huang X. Seven new steroidal glycosides from the roots of Cynanchum forrestii. Steroids. 72: 313-322. PMID 17300821 DOI: 10.1016/J.Steroids.2006.11.024 |
0.337 |
|
2007 |
Hu YC, Wu XF, Gao S, Yu SS, Liu Y, Qu J, Liu J, Liu YB. Novel phloroglucinol derivatives from the roots of Lysidice rhodostegia. Organic Letters. 8: 2269-72. PMID 16706503 DOI: 10.1021/Ol060514O |
0.386 |
|
2006 |
Fu G, Liu Y, Yu S, Huang X, Hu Y, Chen X, Zhang F. Cytotoxic oxygenated triterpenoid saponins from Symplocos chinensis. Journal of Natural Products. 69: 1680-6. PMID 17190442 DOI: 10.1021/np060160 |
0.4 |
|
2006 |
Qu J, Hu YC, Yu SS, Chen XG, Li Y. New cassaine diterpenoid amides with cytotoxic activities from the bark of Erythrophleum fordii. Planta Medica. 72: 442-9. PMID 16557459 DOI: 10.1055/S-2005-916264 |
0.411 |
|
2006 |
Liu Y, Hu Y, Yu S, Fu G, Huang X, Fan L. Steroidal glycosides from Cynanchum forrestii Schlechter. Steroids. 71: 67-76. PMID 16256157 DOI: 10.1016/J.Steroids.2005.08.007 |
0.372 |
|
2004 |
Tang M, Shen D, Hu Y, Gao S, Yu S. Cytotoxic triterpenoid saponins from Symplocos chinensis. Journal of Natural Products. 67: 1969-74. PMID 15620235 DOI: 10.1021/Np040013G |
0.43 |
|
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