基本信息
黎胜红  男  博导  中国科学院昆明植物研究所
办公电话: 0871-65223035
电子邮件: shli@mail.kib.ac.cn
通信地址: 昆明市蓝黑路132号

邮政编码: 650201

研究领域

主要运用植物化学、分析化学、生物化学、细胞和分子生物学等手段,以及首创单细胞植物化学研究新技术方法LMD-cryoNMR-UPLC/MS/MS,揭示植物特殊结构(如腺毛、分泌囊、乳汁器、特定细胞等)中的次生代谢产物及其生物功能,在此基础上发现独特天然活性物质。同时开展云南特色资源或药用植物的化学成分与生物活性研究,进行创新天然药物研究开发。

招生信息
100701-药物化学
招生方向
天然药物化学
天然产物生物合成
招生专业
100701-药物化学

教育背景

1996-09--2001-08   中国科学院昆明植物研究所   博士学位
1992-09--1996-07   云南大学   学士学位
学历
中科院昆明植物研究所 -- 研究生
学位
中科院昆明植物研究所 -- 博士

教授课程

天然药物化学
高级植物分子生物学
有机结构分析

指导学生

已指导学生

骆世洪  博士研究生  100701-药物化学  

周艳英  硕士研究生  077901-药物化学  

石伟  硕士研究生  071010-生物化学与分子生物学  

李春环  博士研究生  100701-药物化学  

黄春帅  硕士研究生  105500-药学硕士  

杨敏杰  硕士研究生  078001-药物化学  

王英  博士研究生  100701-药物化学  

景树溪  博士研究生  100701-药物化学  

匡策  硕士研究生  078001-药物化学  

李德森  硕士研究生  085238-生物工程  

谭艳云  硕士研究生  078001-药物化学  

肖朝江  博士研究生  100701-药物化学  

华娟  博士研究生  100701-药物化学  

凌伊  硕士研究生  105500-药学  

现指导学生

冯玲  博士研究生  100701-药物化学  

罗菲  硕士研究生  078001-药物化学  

郭凯  博士研究生  100701-药物化学  

李文渊  博士研究生  100701-药物化学  

耿浩  博士研究生  100701-药物化学  

王莹  博士研究生  100701-药物化学  

罗柳琼  硕士研究生  078001-药物化学  

黄庆谱  硕士研究生  078001-药物化学  

符然  硕士研究生  078001-药物化学  

高建雄  硕士研究生  078001-药物化学  

滕林琳  博士研究生  100701-药物化学  

工作经历

   
工作简历
2007-08~现在, 中国科学院昆明植物研究所, 研究员、引进国外杰出人才
2004-10~2008-01,德国马普化学生态研究所, 博士后(兼洪堡研究学者)
2004-03~2004-09,香港中文大学中医中药研究所, 博士后
2003-04~2004-02,中国科学院昆明植物研究所, 副研究员
2001-09~2003-03,中国科学院昆明植物研究所, 助理研究员
社会兼职
2018-09-22-今,中国植物保护学会化感作用专业委员会主任委员,
2017-01-20-今,Chemistry & Biodiversity编委,
2016-07-03-2021-07-02,中国中药协会中药材检测认证技术专业委员会委员,
2014-08-06-今,中国植物生理与分子生物学学会植物代谢专业委员会委员,
2013-12-01-2018-12-01,中国植物学会-植物化学与资源学专业委员会委员,
2012-12-31-2016-12-31,《植物生态学报》编委,
2012-10-22-2017-10-22,中国植物保护学会化感作用专业委员会副主任委员,
2012-03-05-今,《Natural Products and Bioprospectin》编委,
2011-11-01-今,《中华医学百科全书》天然药物化学卷编委,
2011-03-01-今,《广西植物》编委,
2010-11-25-2020-02-05,云南省植物学会理事,
2010-08-05-2018-11-10,广西植物功能物质研究与开发重点实验室学术委员会委员,
2008-07-14-2013-10-13,中国植物学会副秘书长,
2008-05-23-今,《The Open Bioactive Compounds Journal》编委,

专利与奖励

   
奖励信息
(1) 国家“万人计划”领军人才, 国家级, 2017
(2) 云南省高层次人才, , 省级, 2017
(3) 科技部中青年科技创新领军人才, 国家级, 2017
(4) 中科院特聘研究员核心骨干, 院级, 2017
(5) 云南省创新团队带头人, 省级, 2017
(6) 科技部中青年科技创新领军人才, 部委级, 2016
(7) 云南省科研标兵, 省级, 2016
(8) 国务院政府特殊津贴, 国家级, 2016
(9) 云南省自然科学奖, 一等奖, 省级, 2014
(10) 中国科学院优秀研究生指导教师奖, , 院级, 2013
(11) 中国科学院优秀导师奖, , 院级, 2011
(12) 中国科学院****, , 院级, 2010
(13) 云南省中青年学术和技术带头人, , 省级, 2008
(14) 德国洪堡(AvH)奖学金, , 其他, 2005
(15) 云南省自然科学奖, 一等奖, 省级, 2003
专利成果
[1] 黎胜红, 刘燕, 陈月桂, 凌伊, 刘艳春. 双功能二倍半萜/二萜合酶LcTPS2、编码基因及其产物和应用. CN: CN113186183A, 2021-07-30.
[2] 黎胜红, 郭凯, 刘艳春, 刘燕. 二倍半萜化合物及其制备方法和在制备抗炎药物和免疫抑制药物中的应用. CN: CN111302924B, 2021-04-06.
[3] 黎胜红, 景树溪, 刘燕, 刘艳春. 火把花烷二倍半萜化合物及其制备方法、药物组合物及应用和火把花总提物的应用. CN202110276052.1, 2021-03-15.
[4] 黎胜红, 刘燕, 罗菲, 凌伊, 刘艳春. 雪松醇合酶Lc-CedS编码基因及其应用. CN: CN109735523A, 2019-05-10.
[5] 黎胜红, 李春环, 骆世洪. 克罗烷二萜化合物及其提取物和其作为昆虫拒食剂. 中国: CN103923076A, 2014-07-16.
[6] 黎胜红, 景树溪. 苯并吡喃三萜,其药物组合物及其制备方法与应用. 中国: CN102898499A, 2013-01-30.
[7] 黎胜红, 李春环. 二倍半萜类化合物及其制备方法与应用. 中国: CN102659803A, 2012-09-12.
[8] 黎胜红, 华娟, 骆世洪. 昆虫拒食剂及其制备方法与应用. 中国: CN102657241A, 2012-09-12.
[9] 黎胜红, 骆世洪. 米团花醌,其制备方法与应用. 中国: CN102617435A, 2012-08-01.
[10] 黎胜红, 骆世洪. 二倍半萜化合物及其应用. 中国: CN101787007A, 2010-07-28.
[11] 黎胜红, 牛雪梅, 孙汉董, 林中文. 一种抗血小板药物及其用途. 中国: CN1218695, 2005-09-14.

科研活动

   
科研项目
( 1 ) 植物次生代谢产物化学生态学研究, 主持, 部委级, 2010-01--2015-04
( 2 ) 云南特征唇形科植物的萜类次生代谢产物化学及防御功能研究, 主持, 国家级, 2013-01--2016-12
( 3 ) 植物源杀线虫活性化合物的发掘及作用机制研究, 主持, 国家级, 2013-01--2017-12
( 4 ) 植物特殊结构中的次生代谢产物与生物功能, 主持, 国家级, 2016-01--2020-12
( 5 ) 活性天然产物发现与生物合成, 主持, 省级, 2017-08--2020-08
( 6 ) 重要药用唇形科植物腺毛中的活性天然产物研究, 主持, 国家级, 2018-01--2021-12
参与会议
(1)几种云南特色植物腺毛中的天然产物及二倍半萜生物合成研究   植物与微生物促大健康产业发展学术研讨会   2017-12-03
(2)植物二倍半萜多样性与生物合成   基因组学与植物生物技术暨第二届植物青年科学家论坛   2017-11-24
(3)Bioactive natural proudcts in plant glandular trichomes   2017-10-13
(4)Unusual specialized metabolites of two Himalayan Lamiaceae plants and their biological functions   2017-09-18
(5)植物特殊结构中的次生代谢产物及其生物功能   第八届植物化感作用学术研讨会   2017-09-12
(6)几种云南特色植物的次生代谢产物与生物功能   第9届西部地区植物科学与资源利用研讨会   2017-08-25
(7)Terpenoids in the glandular trichomes of several Himalayan Lamiaceae species and sesterterpenoid biosynthesis   2017-07-16
(8)The Unusual Secondary Metabolism of Two Himalayan Mint Species   2016-11-14
(9)植物二倍半萜:化学多样性、生物功能与生物合成   中国化学会第十一届全国天然有机化学学术会议   2016-09-25
(10)Chemistry and Biological Functions of Plant Secondary Metabolites   黎胜红   2014-05-22
(11)植物次生代谢产物化学与生物功能   中国植物学会第十五届会员代表大会暨80周年学术年会   黎胜红   2013-10-13
(12)Secondary Metabolites and Biological Functions of Two Lamiaceae Plants   第九届中美华人化学教授会议   黎胜红   2013-08-05
(13)Chemistry and Ecological Functions of Plant Secondary Metabolites   黎胜红   2011-10-04
(14)植物次生代谢产物化学及生态学功能   第八届全国化学生态学学术研讨会   黎胜红   2010-10-09
(15)Secondary metabolites of the invasive Eupatorium adebophorum and their possible ecological functions    黎胜红   2010-10-04
(16)Investigation on the Allelochemicals of the Invasive Eupatorium adenophotum   黎胜红   2009-09-25

出版信息

   
发表论文
[1] Guo, Kai, Ren, Xue, Mu, RongFang, Zhou, TingTing, Li, Dan, Hu, Hong, Liu, Yan, Li, ShengHong. Ecdysteroids and spirosterane steroids from the traditional Chinese medicine Paris polyphylla var. yunnanensis. PHYTOCHEMISTRY LETTERS[J]. 2021, 45: 117-120, http://dx.doi.org/10.1016/j.phytol.2021.08.008.
[2] Teng, Linlin, Mu, Rongfang, Liu, Yanchun, Xiao, Chaojiang, Li, Desen, Gao, Jiangxiong, Guo, Kai, Li, Xiaonian, Liu, Yan, Li, Shenghong. Immunosuppressive and Adipogenesis Inhibitory Seterterpenoids with a Macrocyclic Ether System from Eurysolen gracilis. ORGANIC LETTERS[J]. 2021, 23(6): 2232-2237, https://pubs.acs.org/doi/10.1021/acs.orglett.1c00369.
[3] Zhang, ManWen, Guo, Kai, Zhang, Yu, Teng, LinLin, Huang, QingPu, Liu, Yan, Li, ShengHong. Leucoabietenes A and B, rearranged abietane and ent-abietane diterpene hydrocarbons against resistant infectious fungus and bacterium from the leaves of Leucosceptrum canum. TETRAHEDRON LETTERS[J]. 2021, 81: http://dx.doi.org/10.1016/j.tetlet.2021.153356.
[4] Wang, Ying, Liu, YanChun, Li, WenYuan, Guo, Kai, Liu, Yan, Li, ShengHong. Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii. PHYTOCHEMISTRY[J]. 2021, 186: http://dx.doi.org/10.1016/j.phytochem.2021.112731.
[5] Hua, Juan, Liu, YanChun, Luo, ShiHong, Liu, Yan, Xiao, ChaoJiang, Li, XiaoNian, Li, ShengHong. Immunostimulatory 6/6/6/6 Tetracyclic Triterpenoid Saponins with the Methyl-30 Incorporated Cyclization from the Root of Colquhounia elegans. ORGANIC LETTERS[J]. 2021, 23(19): 7462-7466, http://dx.doi.org/10.1021/acs.orglett.1c02673.
[6] Gao, JianXiong, Chen, YueGui, Li, DeSen, Lin, Liang, Liu, Yan, Li, ShengHong. Cloning and Functional Characterization of a Squalene Synthase from Paris polyphylla var. yunnanensis. CHEMISTRY & BIODIVERSITY[J]. 2021, 18(7): http://dx.doi.org/10.1002/cbdv.202100342.
[7] Jing, ShuXi, Fu, Ran, Li, ChunHuan, Zhou, TingTing, Liu, YanChun, Liu, Yan, Luo, ShiHong, Li, XiaoNian, Zeng, Fang, Li, ShengHong. Immunosuppresive Sesterterpenoids and Norsesterterpenoids from Colquhounia coccinea var. mollis. JOURNAL OF ORGANIC CHEMISTRY[J]. 2021, 86(16): 11169-11176, http://dx.doi.org/10.1021/acs.joc.1c00374.
[8] Guo, Kai, Liu, Yan, Li, ShengHong. The untapped potential of plant sesterterpenoids: chemistry, biological activities and biosynthesis. NATURAL PRODUCT REPORTS. 2021, [9] Guo, Kai, Liu, YanChun, Liu, Yan, Zhang, Han, Li, WenYuan, Shi, QiuMei, Li, XiaoNian, Zeng, Fang, Li, ShengHong. Immunosuppressive gentianellane-type sesterterpenoids from the traditional Uighur medicine Gentianella turkestanorum. PHYTOCHEMISTRY[J]. 2021, 187: http://dx.doi.org/10.1016/j.phytochem.2021.112780.
[10] Chen, YueGui, Li, DeSen, Ling, Yi, Liu, YanChun, Zuo, ZhiLi, Gan, LiShe, Luo, ShiHong, Hua, Juan, Chen, DingYuan, Xu, Fan, Li, Man, Guo, Kai, Liu, Yan, Gershenzon, Jonathan, Li, ShengHong. A Cryptic Plant Terpene Cyclase Producing Unconventional 18-and 14-Membered Macrocyclic C-25 and C-20 Terpenoids with Immunosuppressive Activity. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION[J]. 2021, 60(48): 25468-25476, http://dx.doi.org/10.1002/anie.202110842.
[11] Li, DeSen, Hua, Juan, Luo, ShiHong, Liu, YanChun, Chen, YueGui, Ling, Yi, Guo, Kai, Liu, Yan, Li, ShengHong. An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids. PLANT COMMUNICATIONS[J]. 2021, 2(5): 106-119, http://dx.doi.org/10.1016/j.xplc.2021.100233.
[12] Guo, Kai, Zhou, TingTing, Ren, Xue, Li, Dan, Hu, Hong, Liu, YanChun, Liu, Yan, Li, ShengHong. Secoiridoids and triterpenoids from the traditional Tibetan medicine Gentiana veitchiorum and their immunosuppressive activity. PHYTOCHEMISTRY[J]. 2021, 192: http://dx.doi.org/10.1016/j.phytochem.2021.112961.
[13] Geng, Hao, Liu, YanChun, Li, DeSen, Xiao, ChaoJiang, Liu, Yan, Li, XiaoNian, Li, ShengHong. Unusual glycosidic labdane diterpenoids with cytotoxicity from the root of Phlomoides betonicoides. PHYTOCHEMISTRY[J]. 2020, 173: http://dx.doi.org/10.1016/j.phytochem.2020.112325.
[14] Li, WenYuan, Liu, Yan, Lin, YuTian, Liu, YanChun, Guo, Kai, Li, XiaoNian, Luo, ShiHong, Li, ShengHong. Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis. PHYTOCHEMISTRY[J]. 2020, 170: http://dx.doi.org/10.1016/j.phytochem.2019.112198.
[15] Guo, Kai, Liu, Xin, Zhou, TingTing, Liu, YanChun, Liu, Yan, Shi, QiuMei, Li, XiaoNian, Li, ShengHong. Gentianelloids A and B: Immunosuppressive 10,11-seco-Gentianellane Sesterterpenoids from the Traditional Uighur Medicine Gentianella turkestanorum. JOURNAL OF ORGANIC CHEMISTRY[J]. 2020, 85(8): 5511-5515, https://www.webofscience.com/wos/woscc/full-record/WOS:000607535100034.
[16] Liu, Yan, Luo, ShiHong, Hua, Juan, Li, DeSen, Ling, Yi, Luo, Qian, Li, ShengHong. Characterization of defensive cadinenes and a novel sesquiterpene synthase responsible for their biosynthesis from the invasive Eupatorium adenophorum. NEW PHYTOLOGIST. 2020, https://www.webofscience.com/wos/woscc/full-record/WOS:000579700500001.
[17] Luo, LiuQiong, Chen, YueGui, Li, DeSen, Liu, Yan, Li, ShengHong. Production of the Inaccessible Sesquiterpene (-)-5-Epieremophilene by Metabolically EngineeredEscherichia coli. CHEMISTRY & BIODIVERSITY[J]. 2020, 17(7): http://ir.kib.ac.cn/handle/151853/71946, http://www.irgrid.ac.cn/handle/1471x/6927894, http://ir.kib.ac.cn/handle/151853/71947, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000544183300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=3a85505900f77cc629623c3f2907beab.
[18] Huang, QingPu, Guo, Kai, Liu, Yan, Liu, YanChun, Li, WenYuan, Geng, Hao, Wang, Ying, Li, ShengHong. Diterpenoids and Flavonoids from the Twigs of Cephalotaxus fortunei var. alpina. CHEMISTRY & BIODIVERSITY[J]. 2020, 17(6): https://www.webofscience.com/wos/woscc/full-record/WOS:000536998400001.
[19] Guo, Kai, Liu, Yan, Luo, ShiHong, Liu, YanChun, Li, DeSen, Li, WenYuan, Li, ShengHong. Detoxification of Plant Aromatic Abietanoids via Cleavage of the Benzene Ring into 11,12-Seco-diterpene Polyenes by a Specialist Insect of Leucosceptrum canum. ORGANIC LETTERS[J]. 2020, 22(1): 126-129, http://dx.doi.org/10.1021/acs.orglett.9b04044.
[20] Tang, Ting, Li, ChunHuan, Li, DeSen, Jing, ShuXi, Hua, Juan, Luo, ShiHong, Liu, Yan, Li, ShengHong. Peltate glandular trichomes of Colquhounia vestita harbor diterpenoid acids that contribute to plant adaptation to UV radiation and cold stresses. PHYTOCHEMISTRY[J]. 2020, 172: http://dx.doi.org/10.1016/j.phytochem.2020.112285.
[21] Kai Guo, YanChun Liu, Yan Liu, ShiHong Luo, WenYuan Li, XiaoNian Li, ShengHong Li. Diversified abietane family diterpenoids from the leaves of Leucosceptrum canum and their cytotoxic activity. Phytochemistry. 2019, 157: 43-52, http://dx.doi.org/10.1016/j.phytochem.2018.10.010.
[22] Ling Yi, Teng LinLin, Hua Juan, Li DeSen, Luo ShiHong, Liu YanChun, Liu Yan, Li ShengHong. Leucosceptroid B from glandular trichomes of Leucosceptrum canum reduces fat accumulation in Caenorhabditis elegans through suppressing unsaturated fatty acid biosynthesis. CHINESE JOURNAL OF NATURAL MEDICINES[J]. 2019, 17(12): 892-899, http://dx.doi.org/10.1016/S1875-5364(19)30109-8.
[23] Feng, Ling, Zhang, Yu, Liu, YanChun, Liu, Yan, Luo, ShiHong, Huang, ChunShuai, Li, ShengHong. Leucoflavonine, a new bioactive racemic flavoalkaloid from the leaves of Leucosceptrum canum. BIOORGANIC & MEDICINAL CHEMISTRY[J]. 2019, 27(2): 442-446, http://dx.doi.org/10.1016/j.bmc.2018.12.023.
[24] Chen, YongHong, He, JiangBo, Bai, Xue, Li, XiaoNian, Lu, LanFeng, Liu, YanChun, Zhang, KeQin, Li, ShengHong, Niu, XueMei. Unexpected Biosynthesis of Fluorescein-Like Arthrocolins against Resistant Strains in an Engineered Escherichia coli. ORGANIC LETTERS[J]. 2019, 21(16): 6499-6503, [25] Li, ChunHuan, Zhang, JiaYao, Zhang, XiuYun, Li, ShengHong, Gao, JinMing. An overview of grayanane diterpenoids and their biological activities from the Ericaceae family in the last seven years. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRYnull. 2019, 166: 400-416, http://ir.kib.ac.cn/handle/151853/65189.
[26] Liu, Yan, Jing, ShuXi, Luo, ShiHong, Li, ShengHong. Non-volatile natural products in plant glandular trichomes: chemistry, biological activities and biosynthesis. NATURAL PRODUCT REPORTSnull. 2019, 36(4): 626-665, http://ir.kib.ac.cn/handle/151853/66161.
[27] Luo, Fei, Ling, Yi, Li, DeSen, Tang, Ting, Liu, YanChun, Liu, Yan, Li, ShengHong. Characterization of a sesquiterpene cyclase from the glandular trichomes of Leucosceptrum canum for sole production of cedrol in Escherichia coli and Nicotiana benthamiana. PHYTOCHEMISTRY[J]. 2019, 162: 121-128, http://dx.doi.org/10.1016/j.phytochem.2019.03.009.
[28] Zheng, Guowei, Luo, Shihong, Li, Shifei, Hua, Juan, Li, Weiqi, Li, Shenghong. Specialized metabolites from Ageratina adenophora and their inhibitory activities against pathogenic fungi. PHYTOCHEMISTRY[J]. 2018, 148: 57-62, http://dx.doi.org/10.1016/j.phytochem.2018.01.013.
[29] Zheng, Yu, Xiao, ChaoJiang, Guo, Kai, Wang, Ying, Liu, Yan, Luo, ShiHong, Li, XiaoNian, Li, ShengHong. Lobarioid A, unusual antibacterial depsidone possessing an eight-membered diether ring from the edible lichen Lobaria sp.. TETRAHEDRON LETTERS[J]. 2018, 59(8): 743-746, http://dx.doi.org/10.1016/j.tetlet.2018.01.027.
[30] Teng, LinLin, Song, TianYang, Xu, ZiFei, Liu, Xiao, Dai, Rong, Chen, YongHong, Li, ShengHong, Zhang, KeQin, Niu, XueMei. Selected Mutations Revealed Intermediates and Key Precursors in the Biosynthesis of Polyketide-Terpenoid Hybrid Sesquiterpenyl Epoxy-cyclohexenoids. ORGANIC LETTERS[J]. 2017, 19(14): 3923-3926, [31] Shenghong Li. Localization of Two Bioactive Labdane Diterpenoids in the Peltate Glandular Trichomes of Leonurus japonicus by Laser Microdissection coupled with UPLC-MS/MS. Phytochemical Analysis. 2017, [32] Hua, Juan, Luo, ShiHong, Liu, Yan, Liu, YanChun, Tan, YanYun, Feng, Ling, Xiao, ChaoJiang, Zhang, KeQin, Li, ShengHong, Niu, XueMei. New Bioactive Macrocyclic Diterpenoids from Euphorbia helioscopia. CHEMISTRY & BIODIVERSITY[J]. 2017, 14(10): https://www.webofscience.com/wos/woscc/full-record/WOS:000417435200001.
[33] Hua, Juan, Liu, Yan, Xiao, ChaoJiang, Jing, ShuXi, Luo, ShiHong, Li, ShengHong. Chemical profile and defensive function of the latex of Euphorbia peplus. PHYTOCHEMISTRY[J]. 2017, 136: 56-64, http://dx.doi.org/10.1016/j.phytochem.2016.12.021.
[34] Ma, FengWei, Xia, Bing, Luo, ShiHong, Li, ShengHong, Zhou, Yan. Analysis of the lithiated leucosceptroids from Leucosceptrum canum to facilitate their identification and differentiation by electrospray ionization tandem mass spectrometry. RAPID COMMUNICATIONS IN MASS SPECTROMETRY[J]. 2016, 30: 100-110, http://www.irgrid.ac.cn/handle/1471x/1109615.
[35] Shenghong Li. Capitate gandular trichomes of Paragutzlaffia henryi harbor new phytotoxic labdane diterpenoids. Journal of Agricultural and Food Chemistry. 2015, [36] Hua, Juan, Liu, YanChun, Jing, ShuXi, Luo, ShiHong, Li, ShengHong. Macrocyclic Diterpenoids from the Latex of Euphorbia helioscopia. NATURAL PRODUCT COMMUNICATIONS[J]. 2015, 10(12): 2037-2039, http://ir.kib.ac.cn/handle/151853/25433.
[37] Luo, ShiHong, Hugelshofer, Cedric L, Hua, Juan, Jing, ShuXi, Li, ChunHuan, Liu, Yan, Li, XiaoNian, Zhao, Xu, Magauer, Thomas, Li, ShengHong. Unraveling the Metabolic Pathway in Leucosceptrum canum by Isolation of New Defensive Leucosceptroid Degradation Products and Biomimetic Model Synthesis. ORGANIC LETTERS[J]. 2014, 16(24): 6416-6419, http://www.irgrid.ac.cn/handle/1471x/959015.
[38] Jing, ShuXi, Luo, ShiHong, Li, ChunHuan, Hua, Juan, Wang, YanLi, Niu, XueMei, Li, XiaoNian, Liu, Yan, Huang, ChunShuai, Wang, Ying, Li, ShengHong. Biologically Active Dichapetalins from Dichapetalum gelonioides. JOURNAL OF NATURAL PRODUCTS[J]. 2014, 77(4): 882-893, http://dx.doi.org/10.1021/np400971r.
[39] Li, ChunHuan, Liu, Yan, Hua, Juan, Luo, ShiHong, Li, ShengHong. Peltate glandular trichomes of Colquhounia seguinii harbor new defensive clerodane diterpenoids. JOURNAL OF INTEGRATIVE PLANT BIOLOGY[J]. 2014, 56(9): 928-940, http://lib.cqvip.com/Qikan/Article/Detail?id=662864376.
[40] Cai, JieYun, Chen, DuoZhi, Luo, ShiHong, Kong, NingChuan, Zhang, Yu, Di, YingTong, Zhang, Qiang, Hua, Juan, Jing, ShuXi, Li, ShunLin, Li, ShengHong, Hao, XiaoJiang, He, HongPing. Limonoids from Aphanamixis polystachya and Their Antifeedant Activity. JOURNAL OF NATURAL PRODUCTS[J]. 2014, 77(3): 472-482, http://www.irgrid.ac.cn/handle/1471x/842198.
[41] Luo, ShiHong, Hua, Juan, Li, ChunHuan, Liu, Yan, Li, XiaoNian, Zhao, Xu, Li, ShengHong. Unusual antifeedant spiro-sesterterpenoid from the flowers of Leucosceptrum canum. TETRAHEDRON LETTERS[J]. 2013, 54(3): 235-237, http://dx.doi.org/10.1016/j.tetlet.2012.11.010.
[42] Li, ChunHuan, Jing, ShuXi, Luo, ShiHong, Shi, Wei, Hua, Juan, Liu, Yan, Li, XiaoNian, Schneider, Bernd, Gershenzon, Jonathan, Li, ShengHong. Peltate Glandular Trichomes of Colquhounia coccinea var. mollis Harbor a New Class of Defensive Sesterterpenoids. ORGANIC LETTERS[J]. 2013, 15(7): 1694-1697, http://www.irgrid.ac.cn/handle/1471x/660279.
[43] Luo, ShiHong, Hua, Juan, Niu, XueMei, Liu, Yan, Li, ChunHuan, Zhou, YanYing, Jing, ShuXi, Zhao, Xu, Li, ShengHong. Defense sesterterpenoid lactones from Leucosceptrum canum. PHYTOCHEMISTRY[J]. 2013, 86: 29-35, http://dx.doi.org/10.1016/j.phytochem.2012.11.008.
[44] Zheng, Guowei, Jia, Yanxia, Zhao, Xu, Zhang, Fujuan, Luo, Shihong, Li, Shenghong, Li, Weiqi. o-Coumaric acid from invasive Eupatorium adenophorum is a potent phytotoxin. CHEMOECOLOGY[J]. 2012, 22(2): 131-138, http://www.irgrid.ac.cn/handle/1471x/431863.
[45] Luo, ShiHong, Hua, Juan, Li, ChunHuan, Jing, ShuXi, Liu, Yan, Li, XiaoNian, Zhao, Xu, Li, ShengHong. New Antifeedant C-20 Terpenoids from Leucosceptrum canum. ORGANIC LETTERS[J]. 2012, 14(22): 5768-5771, [46] Li, ShengHong, Nagy, Nina Elisabeth, Hammerbacher, Almuth, Krokene, Paal, Niu, XueMei, Gershenzon, Jonathan, Schneider, Bernd. Localization of Phenolics in Phloem Parenchyma Cells of Norway Spruce (Picea abies). CHEMBIOCHEM[J]. 2012, 13(18): 2707-2713, https://www.webofscience.com/wos/woscc/full-record/WOS:000312546300010.
[47] Shi Wei, Luo Shihong, Li Shenghong. Defensive Sesquiterpenoids from Leaves of Eupatorium adenophorum. CHINESE JOURNAL OF CHEMISTRY[J]. 2012, 30(6): 1331-1334, http://lib.cqvip.com/Qikan/Article/Detail?id=42601411.
[48] Luo, ShiHong, Liu, Yan, Hua, Juan, Niu, XueMei, Jing, ShuXi, Zhao, Xu, Schneider, Bernd, Gershenzon, Jonathan, Li, ShengHong. Unique Proline-Benzoquinone Pigment from the Colored Nectar of "Bird's Coca Cola Tree" Functions in Bird Attractions. ORGANIC LETTERS[J]. 2012, 14(16): 4146-4149, http://www.irgrid.ac.cn/handle/1471x/501443.
[49] Luo, ShiHong, Weng, LinHong, Xie, MingJin, Li, XiaoNian, Hua, Juan, Zhao, Xu, Li, ShengHong. Defensive Sesterterpenoids with Unusual Antipodal Cyclopentenones from the Leaves of Leucosceptrum canum. ORGANIC LETTERS[J]. 2011, 13(7): 1864-1867, https://www.webofscience.com/wos/woscc/full-record/WOS:000288691600074.
[50] Zhou, YanYing, Luo, ShiHong, Yi, TingShuang, Li, ChunHuan, Luo, Qian, Hua, Juan, Liu, Yan, Li, ShengHong. Secondary Metabolites from Glycine soja and Their Growth Inhibitory Effect against Spodoptera litura. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY[J]. 2011, 59(11): 6004-6010, http://dx.doi.org/10.1021/jf200821p.
[51] Shenghong Li. Novel polyesterified 3,4-seco-grayanane diterpenoids as antifeedants from Pieris formosa. Organic Letters. 2010, [52] Luo, ShiHong, Luo, Qian, Niu, XueMei, Xie, MingJin, Zhao, Xu, Schneider, Bernd, Gershenzon, Jonathan, Li, ShengHong. Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION[J]. 2010, 49(26): 4471-4475, https://www.webofscience.com/wos/woscc/full-record/WOS:000279219600023.
[53] Zhao, Xu, Zheng, GuoWei, Niu, XueMei, Li, WeiQi, Wang, FuSheng, Li, ShengHong. Terpenes from Eupatorium adenophorum and Their Allelopathic Effects on Arabidopsis Seeds Germination. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY[J]. 2009, 57(2): 478-482, https://www.webofscience.com/wos/woscc/full-record/WOS:000262665000024.
[54] Shenghong Li. Protonation of a neutral (S)-b-bisabolene intermediate is involved in (S)-b-macrocarpene formation by the maize sesquiterpene synthases TPS6 and TPS11. 2008, [55] Li, ShengHong, Niu, XueMei, Zahn, Stefan, Gershenzon, Jonathan, Weston, Jennie, Schneider, Bernd. Diastereomeric stilbene glucoside dimers from the bark of Norway spruce (Picea abies). PHYTOCHEMISTRY[J]. 2008, 69(3): 772-782, http://dx.doi.org/10.1016/j.phytochem.2007.08.033.
[56] Li Shenghong, Qiu Shengxiang, Yao Ping, Sun Handong, Fong Harry H. S., Zhang Hongjie. Compounds from the Fruits of the Popular European Medicinal Plant Vitex agnus-castus in Chemoprevention via NADP(H):Quinone Oxidoreductase Type 1 Induction. Evidence-based Complementary and Alternative Medicine : eCAM. 2013: http://www.irgrid.ac.cn/handle/1471x/660298.
[57] Liu Yan, Luo Shi-Hong, Schmidt Axel, Wang Guo-Dong, Sun Gui-Ling, Grant Marcus, Kuang Ce, Yang Min-Jie, Jing Shu-Xi, Li Chun-Huan, Schneider Bernd, Gershenzon Jonathan, Li Sheng-Hong. A Geranylfarnesyl Diphosphate Synthase Provides the Precursor for Sesterterpenoid (C 25 ) Formation in the Glandular Trichomes of the Mint Species Leucosceptrum canum. The Plant Cell. 28(3): 804-822, http://ir.kib.ac.cn/handle/151853/26225.
发表著作
(1) 《天然产物化学进展》——第1章:二萜化合物研究进展, Advances in Natural Product Chemistry, 化学工业出版社, 2005-05, 第 2 作者
(2) 《化学生态学前沿》——第16章:植物次生代谢产物化学生态学, Frontiers of Chemical Ecology, 高等教育出版社, 2010-07, 第 1 作者
(3) 《二萜化学》,  Chemistry of Diterpeniods, 化学工业出版社, 2012-01, 第 2 作者