SyM Lab

Synthetic Biology & Microbiology合成生物学与微生物学

Yi-Ming Shi (PI) 石一鸣（课题组长）

Publications发表论文

Marker area ∝ annual publication count圆点面积 ∝ 当年发表论文数
Publication statistics by year
YearPublications that yearCumulative publicationsCumulative citations
2010 1 1 0
2011 3 4 2
2012 5 9 13
2013 9 18 43
2014 5 23 84
2015 7 30 193
2016 4 34 297
2017 4 38 437
2018 4 42 591
2019 7 49 786
2020 2 51 1,029
2021 1 52 1,319
2022 3 55 1,646
2023 3 58 1,917
2024 3 61 2,232
2025 2 63 2,568
2026 4 67 2,832

Sources: SyM Lab Publications (67 records) and Google Scholar (accessed 23 Sep 2026). Values for 2010–2011 were reconstructed from the four early-publication detail charts (0 and 2 citations). The line totals 2,832 dated citations; 24 citations without an attributable year are excluded from the 2,856 all-time total.

Selected publications代表性论文

(*corresponding author, #equal contributions)（*通讯作者，#共同第一作者）

01 · Chemical Science

Ying Chen#, Yunsheng Chen#, Hao Xiang#, Changqi Luo, Jiaqi Duan, Kun Hu, Xiaohong Zheng, Jing Liu, Yongbo Xue*, Yi-Ming Shi*

Lipid-donor-anchored genome mining uncovers dioxanopeptins, antibacterial lipopeptides with a 1,3-dioxane functionalized polyunsaturated lipid tail.

Chem. Sci. 2026, 17, 8229-8241.

Press release新闻报道: ：
·CAS | 中科院：马克斯·普朗克—中国科学院合成生物化学联合研究中心双成果首发：提出天然产物四象限框架，并发现让细菌“断电”的新型抗生素
·ScienceNet | 科学网：科学家给“未知”画地图，探索抗生素研究“盲区”
·Shenzhen News | 深圳新闻网：马克斯·普朗克–中国科学院合成生物化学联合研究中心成立刚“满月”即迎来双成果

03 · Nature Chemistry

Shi, Y.-M.*; Hirschmann, M.; Shi, Y.-N.; Ahmed, S; Abebew, D.; Tobias, N. J.; Grün, P.; Crames, J. J.; Pöschel, L.; Kuttenlochner, W.; Richter, C.; Herrmann, J.; Müller, R; Thanwisai, A; Pidot, S. J.; Stinear, T. P.; Groll, M; Kim, Y.; Bode, H. B.*

Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteria.

Nat. Chem. 2022, 14, 701-712.

Press release:新闻报道： Finding New Weapons in Nature’s Battlesites

04 · Angewandte Chemie International Edition

Shi, Y.-M.*#; Crames, J. J.#; Czech, L.; Bozhüyük, K. A. J.; Shi, Y.-N.; Hirschmann, M.; Lamberth, S.; Paczia, N.; Rückert, C.; Kalinowski, J.; Bange, G.; Bode, H. B.*

Genome mining enabled by biosynthetic characterization uncovers a widespread class of benzoxazolinate-containing natural products.

Angew. Chem. Int. Ed. 2022, 61, e202206106.

Press release:新闻报道： Revealing Biochemical “Rings of Power”

05 · Nature Chemical Biology

Shi, Y.-M.; Brachmann, A. O; Westphalen, M. A.; Neubacher, N.; Tobias, N. J.; Bode, H. B.*

Dual phenazine gene clusters enable diversification during biosynthesis.

Nat. Chem. Biol. 2019, 15, 331-339.

Press release:新闻报道： Drug Diversity in Bacteria

Full publications全部论文

202667

Woonkee S. Jo, Zaynoun Attieh#, Jan Johannes Crames#, Carl Leonhard Knopp, Julie Connelly, Yi-Ming Shi, Christopher S. Wilson, Maryam Dehghan, Peter Grün, Sunna Chang, Fathima S. Refai, Fabio Piano, Kristin C. Gunsalus, Tanja Schneider, Helge B. Bode*, Alan R. Healy*

Total Synthesis and Structural Revision of Rhabdobranin Reveals a Cryptic Gram-Negative Antibiotic

J. Am. Chem. Soc. 2026, 148, 38069–38079.

66

Siqiang Chen, Hao Xiang, Ying Chen, Helge B. Bode, Yi-Ming Shi*

From known knowns to unknown unknowns: synthetic biology paths to antimicrobial discovery

Curr. Opin. Microbiol. 2026, 91, 102759. PDF

Press release新闻报道: ：
·CAS | 中科院：马克斯·普朗克—中国科学院合成生物化学联合研究中心双成果首发：提出天然产物四象限框架，并发现让细菌“断电”的新型抗生素
·ScienceNet | 科学网：科学家给“未知”画地图，探索抗生素研究“盲区”
·Shenzhen News | 深圳新闻网：马克斯·普朗克–中国科学院合成生物化学联合研究中心成立刚“满月”即迎来双成果

65

Ying Chen#, Yunsheng Chen#, Hao Xiang#, Changqi Luo, Jiaqi Duan, Kun Hu, Xiaohong Zheng, Jing Liu, Yongbo Xue*, Yi-Ming Shi*

Lipid-donor-anchored genome mining uncovers dioxanopeptins, antibacterial lipopeptides with a 1,3-dioxane functionalized polyunsaturated lipid tail.

Chem. Sci. 2026, 17, 8229-8241.

Press release新闻报道: ：
·CAS | 中科院：马克斯·普朗克—中国科学院合成生物化学联合研究中心双成果首发：提出天然产物四象限框架，并发现让细菌“断电”的新型抗生素
·ScienceNet | 科学网：科学家给“未知”画地图，探索抗生素研究“盲区”
·Shenzhen News | 深圳新闻网：马克斯·普朗克–中国科学院合成生物化学联合研究中心成立刚“满月”即迎来双成果

64

Edna Bode*, Julia Büllesbach#, Kevin Bauer#, Yan-Ni Shi#, Simon Reiners#, Ziheng Cui#, Petra Happel#, Yi-Ming Shi, Kevin Hoffmann, Peter Grün, Bianca Pommerenke, Uli Kazmaier, Martin Grininger, Helge B. Bode*

Pseudotetraivprolides from Pseudomonas entomophila Provide Insights into the Biosynthesis of Detoxin/Rimosamide-Like Anti-Antibiotics.

Angew. Chem. 2026, 65, e13287.

202563

Wipanee Meesil, Helge B. Bode, Christian Rückert-Reed, Yi-Ming Shi, Sacha J. Pidot, Paramaporn Muangpat, Triwit Rattanarojpong, Narisara Chantratita, Sutthirat Sitthisak, Apichat Vitta, Aunchalee Thanwisai*

Genomic analysis for the identification of bioactive compounds in Xenorhabdus stockiae strain RT25.5.

Sci. Rep. 2025, 15, 23672.

62

Lena Peters#, Moritz Drechsler#, Barbara Pees, Georgia Angelidou, Liesa Salzer, Karlis Arturs Moors, Nicole Paczia, Hinrich Schulenburg, Yi-Ming Shi, Christoph Kaleta, Michael Witting, Helge B. Bode*, Katja Dierking*

Polyketide synthase-derived sphingolipids determine microbiota-mediated protection against pathogens in C. elegans.

Nat. Commun. 2025, 16, 5151.

Press release新闻报道: ：New insights into microbiome-mediated protection against pathogens

202461

Juliana Effert#; Margaretha Westphalen#; Andrea Calderari#; Yi-Ming Shi; Isam Elamri; Soumaya Najah; Peter Grün; Yanyan Li; Arnaud Gruez; Kira J. Weissman*; Helge B. Bode*

Pyrrolizwilline, a unique bacterial alkaloid assembled by a nonribosomal peptide synthetase and non-enzymatic dimerization

Angew. Chem. 2024, 63, e202411258.

59

Zhao Xia#; Hao Xiang#; Yi-Ming Shi*

Bacterial secondary metabolites embedded in producer cell membranes and antibiotics targeting their biosynthesis. 

ChemMedChem 2024, 19, e202400469.

202358

Jing, S.-X.; Fu, R.; Li, C.-H.; Hugelshofer, C. L.; Shi, Y.-M.; Luo, S.-H.; Liu, Y.-C.; Liu, Y.; Li, S.-H.*

Discovery of Unusual Sesterterpenoids from Colquhounia coccinea var. mollis and Their Metabolic Implications.

J. Nat. Prod. 2023, 86, 2468-2473.

57

Meesil, W.; Muangpat, P.; Sitthisak, S.; Rattanarojpong, T.; Chantratita, N.; Machado, R. A. R.; Shi, Y.-M.; Bode, H. B.; Vitta, A.; Thanwisai, A.*

Genome mining reveals novel biosynthetic gene clusters in entomopathogenic bacteria.

Sci. Rep. 2023, 13, 20764.

56

Zolfaghariyan, S.; Shakeri, A.; Asili, J.; Tarighi, S.; Grün, P.; Shi, Y.-M.; Bode, H. B.; Karimi, J.*

Cyclic Depsipeptides and Linear Peptides With Cytotoxic and Antiphytopathogenic Activities From Symbiotic Bacteria of Xenorhabdus (Enterobacteriales: Morganellaceae) Genus.

Ann. Entomol. Soc. Am. 2023, 116, 114-124.

202255

Shi, Y.-M.*; Hirschmann, M.; Shi, Y.-N.; Ahmed, S; Abebew, D.; Tobias, N. J.; Grün, P.; Crames, J. J.; Pöschel, L.; Kuttenlochner, W.; Richter, C.; Herrmann, J.; Müller, R; Thanwisai, A; Pidot, S. J.; Stinear, T. P.; Groll, M; Kim, Y.; Bode, H. B.*

Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteria.

Nat. Chem. 2022, 14, 701-712.

Press release:新闻报道： Finding New Weapons in Nature’s Battlesites

54

Shi, Y.-M.*#; Crames, J. J.#; Czech, L.; Bozhüyük, K. A. J.; Shi, Y.-N.; Hirschmann, M.; Lamberth, S.; Paczia, N.; Rückert, C.; Kalinowski, J.; Bange, G.; Bode, H. B.*

Genome mining enabled by biosynthetic characterization uncovers a widespread class of benzoxazolinate-containing natural products.

Angew. Chem. Int. Ed. 2022, 61, e202206106.

Press release:新闻报道： Revealing Biochemical “Rings of Power”

53

Shi, Y.-M.*; Hirschmann, M.; Shi, Y.-N.; Bode, H. B.*

Cleavage off-loading and post-assembly-line conversions yield products with unusual termini during biosynthesis.

ACS Chem. Biol. 2022, 17, 2221-2228.

202152

Reyes-Fernández, E. Z.; Shi, Y.-M.; Grün, P.; Bode, H. B.*; Bölker, M.*

An Unconventional Melanin Biosynthetic Pathway in Ustilago maydis.

Appl. Environ. Microbiol. 2021, 87, AEM.01510-01520.

202051

Machado, R.*; Thönen, L.; Arce, C.; Theepan, V.; Prada, F.; Wüethrich, D.; Robert, C.; Vogiatzaki, E.; Shi, Y.-M.; Schaeren, O. P.; Dias, M. N.; Bruggmann, R.; Hapfelmeier, S.; Bode, H. B.; Erb, M.

Engineering bacterial symbionts of nematodes improves their biocontrol potential to counter the western corn rootworm.

Nat. Biotechnol. 2020, 38, 600-608.

50

Lee, J.; Shi, Y.-M.; Grün, P.; Gube, M.; Feldbrügge, M.; Bode, H.; Hennicke, F.*

Identification of Feldin, an Antifungal Polyyne from the Beefsteak Fungus Fistulina hepatica.

Biomolecules 2020, 10, 1502.

201949

Shi, Y.-M.; Brachmann, A. O; Westphalen, M. A.; Neubacher, N.; Tobias, N. J.; Bode, H. B.*,

Dual phenazine gene clusters enable diversification during biosynthesis.

Nat. Chem. Biol. 2019, 15, 331-339.

Press release:新闻报道： Drug Diversity in Bacteria

48

Wang, G.#; Zhao Z.#; Ke, J.#; Engel, Y.#; Shi, Y.-M.#; Zhang, Z.; Bingol, K.; Robinson, D.; Wang, B.; Evans, R.; Miyamoto, Y.; Cheng, K.; Bowen, B.; Louie, K.; Kosina, S.; de Raad, M.; Silva, L.; Luhrs, A.; Lubbe, A.; Hoyt, W. D.; Francavilla, C.; Otani, H.; Deutsch, S.; Washton, M. N.; Rubin, E. M.; Mouncey, N. J.; Visel, A.; Cheng, J.-F.; Northen, T.; Bode, H. B.*; Yoshikuni, Y.*

Chassis-independent recombinase-assisted genome engineering enables rapid activation of biosynthetic gene clusters in undomesticated bacteria.

Nat. Microbiol. 2019, 4, 2498-2510.

Press release:新闻报道： Unlocking the Biochemical Treasure Chest Within Microbes

47

Grammbitter, G. L. C.; Schmalhofer, M.; Karimi, K.; Shi, Y. M.; Schoner, T. A.; Tobias, N. J.; Morgner, N.; Groll, M.; Bode, H. B.*

An Uncommon Type II PKS Catalyzes Biosynthesis of Aryl Polyene Pigments.

J. Am. Chem. Soc. 2019, 141, 16615-16623.

46

Bode, E.; Heinrich, A. K.; Hirschmann, M.; Abebew, D.; Shi, Y.-N.; Vo, T. D.; Wesche, F.; Shi, Y.-M.; Grün, P.; Simonyi, S.; Keller, N.; Engel, Y.; Wenski, S.; Bennet, R.; Beyer, S.; Bischoff, I.; Buaya, A.; Brandt, S.; Cakmak, I.; Çimen, H.; Eckstein, S.; Frank, D.; Fürst, R.; Gand, M.; Geisslinger, G.; Hazir, S.; Henke, M.; Heermann, R.; Lecaudey, V.; Schäfer, W.; Schiffmann, S.; Schüffler, A.; Schwenk, R.; Skaljac, M.; Thines, E.; Thines, M.; Ulshöfer, T.; Vilcinskas, A.; Wichelhaus, T. A.; Bode, H. B.*

Promoter Activation in Δhfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing.

Angew. Chem. Int. Ed. 2019, 58, 18957-18963.

45

Tobias, N. J.#*; Parra-Rojas, C.#; Shi, Y.-N.; Shi, Y.-M.; Simonyi, S.; Thanwisai, A.; Vitta, A.; Chantratita, N.; Hernandez-Vargas, E. A.*; Bode, H. B.*

Cyclo(tetrahydroxybutyrate) production is sufficient to distinguish between Xenorhabdus and Photorhabdus isolates in Thailand.

Environ. Microbiol. 2019, 21, 292-2932.

44

Shi, Y.-N.; Pusch, S.; Shi, Y.-M.; Richter, C.; Maciá-Vicente, J. G.; Schwalbe, H.; Kaiser, M.; Opatz, T.; Bode, H. B.*

(±)-Alternarlactones A and B, Two Antiparasitic Alternariol-like Dimers from the Fungus Alternaria alternata P1210 Isolated from the Halophyte Salicornia sp.

The J. Org. Chem. 2019, 84, 11203-11209.

43

Drummond, L.; Kschowak, M. J.; Breitenbach, J.; Wolff, H.; Shi, Y.-M.; Schrader, J.; Bode, H. B.; Sandmann, G.; Buchhaupt, M.*

Expanding the Isoprenoid Building Block Repertoire with an IPP Methyltransferase from Streptomyces monomycini.

ACS Synth. Biol. 2019, 8, 1303-1313.

201842

Shi, Y.-M.; Richter, C.; Challinor, V. L.; Grün, P.; Girela del Rio, A.; Kaiser, M.; Schüffler, A.; Piepenbring, M.; Schwalbe, H.; Bode, H. B.*

Georatusin, a Specific Antiparasitic Polyketide–Peptide Hybrid from the Fungus Geomyces auratus.

Org. Lett. 2018, 20, 1563-1567.

Hot off the press | 热点:Hot off the press:热点： Natural Product Reports 2018

41

Shi, Y.-M.; Bode, H. B.*

Chemical language and warfare of bacterial natural products in bacteria-nematode-insect interactions.

Nat. Prod. Rep. 2018, 35, 309-335. (Cover article封面文章)

40

Shi, Y.-M.#; Hu, K.#; Pescitelli, G.*; Liu, M.; Li, X.-N.; Du, X.; Xiao, W.-L.; Sun, H.-D.; Puno, P.-T.*,

Schinortriterpenoids with Identical Configuration but Distinct ECD Spectra Generated by Nondegenerate Exciton Coupling.

Org. Lett. 2018, 20, 1500-1504.

Press release新闻报道

39

Tobias, N. J.; Shi, Y.-M.; Bode, H. B.*,

Refining the Natural Product Repertoire in Entomopathogenic Bacteria.

Trends Microbiol. 2018, 26, 833-840.

201738

Shi, Y.-M.; Bode, H. B.*

Microbiology: A new language for small talk.

Nat. Chem. Biol. 2017, 13, 453-454.

37

Cai, X.#; Shi, Y.-M.#; Pöhlmann, N.; Revermann, O.; Bahner, I.; Pidot, S. J.; Wesche, F.; Lackner, H.; Büchel, C.; Kaiser, M.; Richter, C.; Schwalbe, H.; Stinear, T. P.; Zeeck, A.; Bode, H. B.*

Structure and Biosynthesis of Isatropolones, Bioactive Amine-Scavenging Fluorescent Natural Products from Streptomyces Gö66.

Angew. Chem. Int. Ed. 2017, 56, 4945-4949.

36

Tobias, N. J.#; Wolff, H.#; Djahanschiri, B.#; Grundmann, F.; Kronenwerth, M.; Shi, Y.-M.; Simonyi, S.; Grün, P.; Shapiro-Ilan, D.; Pidot, S. J.; Stinear, T. P.; Ebersberger, I.; Bode, H. B.*

Natural product diversity associated with the nematode symbionts Photorhabdus and Xenorhabdus.

Nat. Microbiol. 2017, 2, 1676-1685.

35

Hu, Z.-X.; Li, X.-N.; Shi, Y.-M.; Wang, W.-G.; Du, X.; Li, Y.; Zhang, Y.-H.*; Pu, J.-X.*; Sun, H.-D.

Lanostane-type triterpenoids from Kadsura coccinea.

Tetrahedron 2017, 73, 2931-2937.

201634

Shi, Y. M.#; Cai, S. L.#; Li, X. N.; Liu, M.; Shang, S. Z.; Du, X.; Xiao, W. L.; Pu, J. X.*; Sun, H. D.*

LC–UV-Guided Isolation and Structure Determination of Lancolide E: A Nortriterpenoid with a Tetracyclo[5.4.0.02,4.03,7]undecane- Bridged System from a “Talented” Schisandra Plant.

Org. Lett. 2016, 18, 100-103.

33

Hu, Z.-X.#; Shi, Y.-M.#; Wang, W.-G.; Tang, J.-W.; Zhou, M.; Du, X.; Zhang, Y.-H.*; Pu, J.-X.*; Sun, H.-D.

Structural Characterization of Kadcoccinin A: A Sesquiterpenoid with a Tricyclo[4.4.0.03,10]decane Scaffold from Kadsura coccinea.

Org. Lett. 2016, 18, 2284-2287.

32

Gao, Z.-H.#; Shi, Y.-M.#; Qiang, Z.; Wang, X.; Shang, S.-Z.; Yang, Y.; Du, B.-W.; Peng, H.-P.; Ji, X.; Li, H.*; Wang, F.*; Xiao, W.-L.*

Plasiatine, an Unprecedented Indole–Phenylpropanoid Hybrid from Plantago asiatica as a Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2.

Sci. Rep. 2016, 6, 24945.

31

Hu, Z. X.; Hu, K.; Shi, Y. M.; Wang, W. G.; Du, X.; Li, Y.; Zhang, Y. H.*; Pu, J. X.*; Sun, H. D.

Rearranged 6/6/5/6-Fused Triterpenoid Acids from the Stems of Kadsura coccinea.

J. Nat. Prod. 2016, 79, 2590-2598.

201530

Shi, Y. M.; Xiao, W. L.; Pu, J. X.; Sun, H. D.*

Triterpenoids from the Schisandraceae family: an update.

Nat. Prod. Rep. 2015, 32, 367-410. (Cover article封面文章)

Press release新闻报道

29

Hu, Z. X.#; Shi, Y. M.#; Wang, W. G.; Li, X. N.; Du, X.; Liu, M.; Li, Y.; Xue, Y. B.; Zhang, Y. H.*; Pu, J. X.*; Sun, H. D.

Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.

Org. Lett. 2015, 17, 4616-4619.

28

Wang, W.-G.; Tang, J.-W.; Shi, Y.-M.; Du, X.; Li, X.-N.; Wu, H.-Y.; Jiang, H.-Y.; Li, Y.; Pu, J.-X.*; Sun, H.-D.

Laxiflorol A, the first example of 7,8:15,16-di-seco-15-nor-21-homo-ent-kauranoid from Isodon eriocalyx var. laxiflora.

RSC Adv. 2015, 5, 6132-6135.

27

Shi, Y. N.; Yang, L.; Zhao, J. H.; Shi, Y. M.; Qu, Y.; Zhu, H. T.; Wang, D.; Yang, C. R.; Li, X. C.; Xu, M.*; Zhang, Y. J.*

Chemical constituents from Piper wallichii.

Nat. Prod. Res. 2015, 29, 1372-1375.

26

Shi, Y. N.; Shi, Y. M.; Yang, L.; Li, X. C.; Zhao, J. H.; Qu, Y.; Zhu, H. T.; Wang, D.; Cheng, R. R.; Yang, C. R.; Xu, M.*; Zhang, Y. J.*

Lignans and aromatic glycosides from Piper wallichii and their antithrombotic activities.

J. Ethnopharmacol. 2015, 162, 87-96.

25

Liu, M.; Luo, Y. Q.; Wang, W. G.; Shi, Y. M.; Wu, H. Y.; Du, X.; Pu, J. X.*; Sun, H. D.*

Two New 18-Norschiartane-type Schinortriterpenoids from Schisandra lancifolia.

Nat. Prod. Commun. 2015, 10, 2045-2047.

24

Liang, C.-Q.; Shi, Y.-M.; Wang, W.-G.; Hu, Z.-X.; Li, Y.; Zheng, Y.-T.; Li, X.-N.; Du, X.; Pu, J.-X.; Xiao, W.-L.; Zhang, H.-B.; Sun, H.-D.*

Kadcoccinic Acids A–J, Triterpene Acids from Kadsura coccinea.

J. Nat. Prod. 2015, 78, 2067-2073.

201423

Liu, Z.-K.; Wu, D.-R.; Shi, Y.-M.; Zeng, T.; Liu, S.-H.; Du, X.; Dang, Y.-J.*; Xiao, W.-L.*; Sun, H.-D.

Three New Diterpenoids from Leonurus japonicus.

Chin. Chem. Lett. 2014, 25, 677-679.

22

Liang, C. Q.; Luo, R. H.; Yan, J. M.; Li, Y.; Li, X. N.; Shi, Y. M.; Shang, S. Z.; Gao, Z. H.; Yang, L. M.; Zheng, Y. T.; Xiao, W. L.*; Zhang, H. B.; Sun, H. D.*

Structure and Bioactivity of Triterpenoids from the Stems of Schisandra sphenanthera.

Arch. Pharmacal Res. 2014, 37, 168-174.

21

Shi, Y.-M.; Wang, L.-Y.; Zou, X.-S.; Li, X.-N.; Shang, S.-Z.; Gao, Z.-H.; Liang, C.-Q.; Luo, H.-R.; Li, H.-L.; Xiao, W.-L.*; Sun, H.-D.*

Nortriterpenoids from Schisandra chinensis and Their Absolute Configurational Assignments by Electronic Circular Dichroism Study.

Tetrahedron 2014, 70, 859-868.

20

Shi, Y. M.; Zhong, W. M.; Chen, H.; Wang, R. R.; Shang, S. Z.; Liang, C. Q.; Gao, Z. H.; Zheng, Y. T.; Xiao, W. L.*; Sun, H. D.*

New Lignans from the Leaves and Stems of Schisandra chinensis and Their Anti-HIV-1 Activities.

Chin. J. Chem. 2014, 32, 734-740.

19

Shi, Y. M.#; Yang, J.#; Xu, L.; Li, X. N.; Shang, S. Z.; Cao, P.*; Xiao, W. L.*; Sun, H. D.*

Structural Characterization and Antioxidative Activity of Lancifonins: Unique Nortriterpenoids from Schisandra lancifolia.

Org. Lett. 2014, 16, 1370-1373.

201318

Shi, Y. M.#; Wang, X. B.#; Li, X. N.; Luo, X.; Shen, Z. Y.; Wang, Y. P.*; Xiao, W. L.*; Sun, H. D.*

Lancolides, Antiplatelet Aggregation Nortriterpenoids with Tricyclo[6.3.0.02,11]undecane-Bridged System from Schisandra lancifolia.

Org. Lett. 2013, 15, 5068-5071.

Hot off the pressHot off the press | 热点::热点： Natural Product Reports 2013

17

Shang, S.-Z.; Han, Y.-S.; Shi, Y.-M.; Du, X.; Liang, C.-Q.; Wainberg, M. A.; Gao, Z.-H.; Xiao, W.-L.*; Sun, H.-D.*

Four New Lignans from the Leaves and Stems of Schisandra propinqua var. sinensis.

Nat. Prod. Bioprospect. 2013, 3, 56-60.

16

Shang, S. Z.; Kong, L. M.; Yang, L. P.; Jiang, J.; Huang, J.; Zhang, H. B.; Shi, Y. M.; Zhao, W.; Li, H. L.; Luo, H. R.; Li, Y.; Xiao, W. L.*; Sun, H. D.*

Bioactive Phenolics and Terpenoids from Manglietia insignis.

Fitoterapia 2013, 84, 58-63.

15

Shang, S. Z.; Chen, H.; Liang, C. Q.; Gao, Z. H.; Du, X.; Wang, R. R.; Shi, Y. M.; Zheng, Y. T.; Xiao, W. L.*; Sun, H. D.*

Phenolic Constituents from Parakmeria yunnanensis and Their Anti-HIV-1 Activity.

Arch. Pharmacal Res. 2013, 36, 1223-1230.

14

Liang, C.-Q.; Hu, J.; Shi, Y.-M.; Shang, S.-Z.; Du, X.; Zhan, R.; Wang, W.-G.; Xiong, W.-Y.; Xiao, W.-L.; Zhang, H.-B.*; Sun, H.-D.*

Five New Nortriterpenoids from the Stems of Schisandra neglecta.

Helv. Chim. Acta 2013, 96, 1376-1385.

13

Liang, C. Q.; Shi, Y. M.; Li, X. Y.; Luo, R. H.; Li, Y.; Zheng, Y. T.; Zhang, H. B.; Xiao, W. L.*; Sun, H. D.*

Kadcotriones A–C: Tricyclic Triterpenoids from Kadsura coccinea.

J. Nat. Prod. 2013, 76, 2350-4.

12

Liang, C. Q.; Hu, J.; Shi, Y. M.; Shang, S. Z.; Du, X.; Zhan, R.; Xiong, W. Y.; Zhang, H. B.; Xiao, W. L.*; Sun, H. D.*

Schisphenlignans A–E: Five New Dibenzocyclooctadiene Lignans from Schisandra sphenanthera.

Chem. Pharm. Bull. 2013, 61, 96-100.

11

Liang, C. Q.; Hu, J.; Luo, R. H.; Shi, Y. M.; Shang, S. Z.; Gao, Z. H.; Wang, R. R.; Zheng, Y. T.; Xiong, W. Y.; Zhang, H. B.; Xiao, W. L.*; Sun, H. D.*

Six New Lignans from the Leaves and Stems of Schisandra sphenanthera.

Fitoterapia 2013, 86, 171-177.

10

He, F.; Bao, J.; Zhang, X. Y.; Tu, Z. C.; Shi, Y. M.; Qi, S. H.*

Asperterrestide A, a Cytotoxic Cyclic Tetrapeptide from the Marine-Derived Fungus Aspergillus terreus SCSGAF0162.

J. Nat. Prod. 2013, 76, 1182-1186.

20129

Zou, J.; Du, X.; Pang, G.; Shi, Y.-M.; Wang, W.-G.; Zhan, R.; Kong, L.-M.; Li, X.-N.; Li, Y.; Pu, J.-X.*; Sun, H.-D.*

Ternifolide A, a New Diterpenoid Possessing a Rare Macrolide Motif from Isodon ternifolius.

Org. Lett. 2012, 14, 3210-3213.

8

Shang, S.-Z.; Yan, J.-M.; Zhang, H.-B.; Shi, Y.-M.; Gao, Z.-H.; Du, X.; Li, Y.; Xiao, W.-L.*; Sun, H.-D.*

Two New Neolignans from Manglietia insignis.

Nat. Prod. Bioprospect. 2012, 2, 227-230.

7

Liang, C. Q.; Shi, Y. M.; Luo, R. H.; Li, X. Y.; Gao, Z. H.; Li, X. N.; Yang, L. M.; Shang, S. Z.; Li, Y.; Zheng, Y. T.; Zhang, H. B.; Xiao, W. L.*; Sun, H. D.*

Kadcoccitones A and B, Two New 6/6/5/5-Fused Tetracyclic Triterpenoids from Kadsura coccinea.

Org. Lett. 2012, 14, 6362-6365.

6

Gao, Z.-H.; Kong, L.-M.; Zou, X.-S.; Shi, Y.-M.; Shang, S.-Z.; Luo, H.-R.; Liang, C.-Q.; Li, X.-N.; Li, Y.; Du, X.; Xiao, W.-L.*; Sun, H.-D.*

Four new indole alkaloids from Plantago asiatica.

Nat. Prod. Bioprospect. 2012, 2, 249-254.

5

Luo, X.#; Shi, Y. M.#; Luo, R. H.; Luo, S. H.; Li, X. N.; Wang, R. R.; Li, S. H.; Zheng, Y. T.; Du, X.; Xiao, W. L.*; Pu, J. X.; Sun, H. D.*

Schilancitrilactones A–C: Three Unique Nortriterpenoids from Schisandra lancifolia.

Org. Lett. 2012, 14, 1286-1289.

20114

Shi, Y. M.; Li, X. Y.; Li, X. N.; Luo, X.; Xue, Y. B.; Liang, C. Q.; Zou, J.; Kong, L. M.; Li, Y.; Pu, J. X.; Xiao, W. L.*; Sun, H. D.*

Schicagenins A–C: Three Cagelike Nortriterpenoids from Leaves and Stems of Schisandra chinensis.

Org. Lett. 2011, 13, 3848-3851.

3

Yang, G.-Y.; Li, Y.-K.; Zhang, X.-J.; Li, X.-N.; Yang, L.-M.; Shi, Y.-M.; Xiao, W.-L.*; Zheng, Y.-T.; Sun, H.-D.*

Three New Nortriterpenoids from Schisandra wilsoniana and Their Anti-HIV-1 Activities.

Nat. Prod. Bioprospect. 2011, 1, 33-36.

2

Luo, X.; Pu, J. X.; Fan, P.; Shi, Y. M.; Yang, G. Y.; Li, X. N.; Lei, C.; Gao, X. M.; Zhang, H. B.; Xiao, W. L.*; Sun, H. D.*

Four New Dibenzocyclooctadiene Lignans from Schisandra rubriflora.

Chin. J. Nat. Med. 2011, 9, 167-172.

20101

王涛*; 吴爱芝; 陈传兵; 石一鸣; 王宁生; 宓穗卿.

抗疟活性化合物─3-[4-(7-氯喹啉-4-基)哌嗪-1-基]丙酸的合成与结构鉴定.

中国新药杂志 2010, 19, 2328-2330.

Book Chapter专著章节

  1. Xiao, W. L.; Shi, Y. M. Chapter 6: Macrocyclic and Miscellaneous Diterpenoids “Diterpenoids: Chemistry” (Editor Sun, H. D.; Li, S. H.), Chemical Industry Press, Beijing, p. 367–402, 2011.
    肖伟烈、石一鸣《二萜化学》第六章: 大环及其它类型二萜 (主编：孙汉董、黎胜红), 化学工业出版社, 北京, 2011年，367–402页。
  2. Zhang, S. R.; Xiao, W. L.; Zhu, X. X.; Wang, Y. W.; Shi, Y. M. et al. Volume 11: Medical Flora of China, Peking University Medical Press, Beijing, 2014.
    张树仁、肖伟烈、石一鸣等《中国药用植物志》第十一卷, 北京大学医学出版社, 北京, 2014年。