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Methods Based on global patent data from 1945 to 2025, social network analysis method is used to construct and analyze the innovation cooperation network in this field. According to the theory of technology lifecycle, four development stages are divided for dynamic comparison. Results The cooperative network structure presents a phased evolution, from a closed “core small world” in its infancy to a long-term expansion, ultimately converging into a “strategic focused” tight structure; The national innovation strategy is divided into three types of paths: “sustained openness”“first rising and then falling”“low-level stability”. The intensity of international cooperation decreases in an “inverted U-shape” as technology matures; There is a significant “structural fragmentation” among micro entities, with the industry forming a high-density collaborative closed loop, while key academic institutions are often in a “bilateral isolation” state at the edge of the network, leading to an ecological imbalance of “industry academia decoupling”. Conclusion This study systematically reveals the dynamic evolution mechanism of innovation cooperation networks in the field of pentacyclic triterpenoids from three levels: network structure, national strategy, and subject behavior. It deepens the theoretical understanding of cooperation and competition relationships in the technology lifecycle and provides empirical evidence and policy implications for building a more resilient innovation ecosystem., authors=GAO Yi, NAN Minlun, XU Haowei, ZHANG Kaiyue, GAO Yuan, HE Yufang, authorsList=GAO Yi, NAN Minlun, XU Haowei, ZHANG Kaiyue, GAO Yuan, HE Yufang, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304388113715974226, articleId=1304388113455927377, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=五环三萜类化合物全球创新合作网络的图谱构建与演化研究, columnId=1304140194819629763, journalTitle=中草药, columnName=数据挖掘与循证医学, runingTitle=null, highlight=null, articleAbstract=目的 揭示五环三萜类化合物领域全球创新合作网络的动态演化规律,解析网络结构、国家创新策略与主体行为在技术生命周期不同阶段的协同演变机制。方法 基于1945—2025年全球专利数据,运用社会网络分析方法,构建并分析该领域的创新合作网络,依据技术生命周期理论划分4个发展阶段进行动态比较。结果 合作网络结构呈现阶段性演变,从萌芽期封闭的“核心小世界”经成长期扩张最终收敛为“战略聚焦型”紧密结构;国家创新策略分为“持续开放型”“先升后降型”“低位平稳型”3类路径,国际合作强度随技术成熟呈“倒U型”衰减;微观主体存在显著的“结构性割裂”,产业界形成高密度协作闭环,而关键学术机构多处于网络边缘的“双边孤立”状态,导致“产学脱钩”的生态失衡。结论 从网络结构、国家创新策略与主体行为3个层面,系统揭示五环三萜类化合物领域创新合作网络的动态演进机制,深化对技术生命周期中合作竞争关系的理论认识,为构建更具韧性的创新生态系统提供实证依据与政策启示。, authors=高艺1, 南敏伦2, 胥皓为1, 张凯月2, 高原2, 赫玉芳1, authorsList=高艺, 南敏伦, 胥皓为, 张凯月, 高原, 赫玉芳, authorCompany=1 长春中医药大学管理学院, 吉林 长春 130117;
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Hoever G, Baltina L, Michaelis M, et al. Antiviral activity of glycyrrhizic acid derivatives against SARS-coronavirus [J]. J Med Chem, 2005, 48(4): 1256-1259.
Csuk R, Schwarz S, Kluge R, et al. Synthesis and biological activity of some antitumor active derivatives from glycyrrhetinic acid [J]. Eur J Med Chem, 2010, 45(12): 5718-5723.
Csuk R, Schwarz S, Siewert B, et al. Synthesis and antitumor activity of ring A modified glycyrrhetinic acid derivatives [J]. Eur J Med Chem, 2011, 46(11): 5356-5369.
Schwarz S, Siewert B, Xavier N M, et al. A “natural” approach: Synthesis and cytoxicity of monodesmosidic glycyrrhetinic acid glycosides [J]. Eur J Med Chem, 2014, 72: 78-83.
Song H, Sun Y X, Xu G L, et al. Synthesis and biological evaluation of novel hydrogen sulfide releasing glycyrrhetic acid derivatives [J]. J Enzyme Inhib Med Chem, 2016, 31(6): 1457-1463.
Li Y, Feng L, Song Z F, et al. Synthesis and anticancer activities of glycyrrhetinic acid derivatives [J]. Molecules, 2016, 21(2): 199.
Moustafa G O, Shalaby A, Naglah A M, et al. Synthesis, characterization, in vitro anticancer potentiality, and antimicrobial activities of novel peptide-glycyrrhetinic-acid-based derivatives [J]. Molecules, 2021, 26(15): 4573.
Parra A, Rivas F, Lopez P E, et al. Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides [J]. Bioorg Med Chem, 2009, 17(3): 1139-1145.
Siewert B, Pianowski E, Csuk R. Esters and amides of maslinic acid trigger apoptosis in human tumor cells and alter their mode of action with respect to the substitution pattern at C-28[J]. Eur J Med Chem, 2013, 70: 259-272.
Siewert B, Pianowski E, Obernauer A, et al. Towards cytotoxic and selective derivatives of maslinic acid [J]. Bioorg Med Chem, 2014, 22(1): 594-615.
Meira C S, Barbosa-Filho J M, Lanfredi-Rangel A, et al. Antiparasitic evaluation of betulinic acid derivatives reveals effective and selective anti-Trypanosoma cruzi inhibitors [J]. Exp Parasitol, 2016, 166: 108-115.
Yang S J, Liu M C, Xiang H M, et al. Synthesis and in vitro antitumor evaluation of betulin acid ester derivatives as novel apoptosis inducers [J]. Eur J Med Chem, 2015, 102: 249-255.
Bo T Y, Li X Y, Juan F Z, et al. Research progress of resource distribution of bioactive compound ursolic acid [J]. Chem Ind Forest Prod, 2012, 32:119-126.
Do Nascimento P G G, Lemos T L G, Bizerra A M C, et al. Antibacterial and antioxidant activities of ursolic acid and derivatives [J]. Molecules, 2014, 19(1): 1317-1327.
Li W, Zhang H X, Nie M X, et al. A novel synthetic ursolic acid derivative inhibits growth and induces apoptosis in breast cancer cell lines [J]. Oncol Lett, 201815(2):2323-2329.
Sycz Z, Tichaczek-Goska D, Jezierska-Domaradzka A, et al. Are uropathogenic bacteria living in multispecies biofilm susceptible to active plant ingredient: Asiatic acid? [J]. Biomolecules, 2021, 11(12): 1754.
Nagoor Meeran M F, Goyal S N, Suchal K, et al. Pharmacological properties, molecular mechanisms, and pharmaceutical development of asiatic acid: A pentacyclic triterpenoid of therapeutic promise [J]. Front Pharmacol, 2018, 9: 892.
Liew K Y, Hafiz M F, Chong Y J, et al. A review of Malaysian herbal plants and their active constituents with potential therapeutic applications in sepsis [J]. Evid Based Complementary Altern Med, 2020, 2020: 8257817.
Sun B J, Wu L L, Wu Y, et al. Therapeutic potential of Centella asiatica and its triterpenes: A review [J]. Front Pharmacol, 2020, 11: 568032.
Brinker A M, Ma J, Lipsky P E, et al. Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae) [J]. Phytochemistry, 2007, 68(6): 732-766.
Lan G C, Zhang J, Ye W B, et al. Celastrol as a tool for the study of the biological events of metabolic diseases [J]. Sci China Chem, 2019, 62(4): 409-416.
Ng S W, Chan Y H, Chellappan D K, et al. Molecular modulators of celastrol as the keystones for its diverse pharmacological activities [J]. Biomed Pharmacother, 2019, 109: 1785-1792.
韦春玲, 肖瑾, 肖珊, 等. 具有抗菌活性的天然五环三萜类化合物研究进展[J]. 中成药, 2023, 45(4): 1231-1240.
班玉娟, 陈瑞, 张宇, 等. 五环三萜类化合物的口服吸收与代谢研究进展[J]. 化学试剂, 2021, 43(7): 11.
李传旺, 张贺, 饶攀, 等. 植物五环三萜类化合物生物合成途径研究进展[J]. 中草药, 2021, 52(11): 3436-3452.
何诗能, 张清, 谭珍媛, 等. 三萜类化合物结构修饰及活性研究进展[J]. 化学试剂, 2023, 45(5): 41-50.
赵青峰, 孙大洋, 何毓新. 湖泊沉积脱-A-三萜类化合物在环境重建中的研究进展与展望[J]. 地球科学进展, 2023, 38(3): 256-269.
保继栋, 党景丽, 张龙. 基于科技创新情报平台的生物农药领域专利分析[J]. 草业科学, 2017, 34(10): 2164-2170.
孙传良, 孙立冰. 基于incoPat的中国药科大学专利分析[J]. 中国药科大学学报, 2019, 50(3): 374-378.
熊焰, 李祥宇, 胡锴. 全球芯片产业创新态势与合作网络动态演变研究: 以逻辑芯片为例[J]. 中国科技论坛, 2025(12): 177-188.
乔永忠. 基于专利数据测度技术创新的指标准确性研究[J]. 中国科技论坛, 2025(6): 46-54.)
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中草药 |数据挖掘与循证医学 2026 , 57 (10) : 3912 -3925
五环三萜类化合物全球创新合作网络的图谱构建与演化研究
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高艺1, 南敏伦2, 胥皓为1, 张凯月2, 高原2, 赫玉芳1
作者信息
    1 长春中医药大学管理学院, 吉林 长春 130117;
    2 吉林省中医药科学院中药化学研究所, 吉林 长春 130012
通讯作者:
赫玉芳
作者简介:
高艺: 高艺,硕士研究生,研究方向为社会发展与管理药学。E-mail:19805484600@163.com
Mapping construction and evolution research of global innovation cooperation network of pentacyclic triterpenoids
  • GAO Yi, NAN Minlun, XU Haowei, ZHANG Kaiyue, GAO Yuan, HE Yufang
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.10.020
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    目的 揭示五环三萜类化合物领域全球创新合作网络的动态演化规律,解析网络结构、国家创新策略与主体行为在技术生命周期不同阶段的协同演变机制。方法 基于1945—2025年全球专利数据,运用社会网络分析方法,构建并分析该领域的创新合作网络,依据技术生命周期理论划分4个发展阶段进行动态比较。结果 合作网络结构呈现阶段性演变,从萌芽期封闭的“核心小世界”经成长期扩张最终收敛为“战略聚焦型”紧密结构;国家创新策略分为“持续开放型”“先升后降型”“低位平稳型”3类路径,国际合作强度随技术成熟呈“倒U型”衰减;微观主体存在显著的“结构性割裂”,产业界形成高密度协作闭环,而关键学术机构多处于网络边缘的“双边孤立”状态,导致“产学脱钩”的生态失衡。结论 从网络结构、国家创新策略与主体行为3个层面,系统揭示五环三萜类化合物领域创新合作网络的动态演进机制,深化对技术生命周期中合作竞争关系的理论认识,为构建更具韧性的创新生态系统提供实证依据与政策启示。
    五环三萜类化合物  /  创新合作网络  /  社会网络分析  /  演化机制  /  专利分析  /  技术生命周期
    Objective To reveal the dynamic evolution of the global innovation cooperation network in the field of pentacyclic triterpenoids, and analyze the collaborative evolution mechanism of network structure, national innovation strategies and individual behaviors at different stages of the technology lifecycle. Methods Based on global patent data from 1945 to 2025, social network analysis method is used to construct and analyze the innovation cooperation network in this field. According to the theory of technology lifecycle, four development stages are divided for dynamic comparison. Results The cooperative network structure presents a phased evolution, from a closed “core small world” in its infancy to a long-term expansion, ultimately converging into a “strategic focused” tight structure; The national innovation strategy is divided into three types of paths: “sustained openness”“first rising and then falling”“low-level stability”. The intensity of international cooperation decreases in an “inverted U-shape” as technology matures; There is a significant “structural fragmentation” among micro entities, with the industry forming a high-density collaborative closed loop, while key academic institutions are often in a “bilateral isolation” state at the edge of the network, leading to an ecological imbalance of “industry academia decoupling”. Conclusion This study systematically reveals the dynamic evolution mechanism of innovation cooperation networks in the field of pentacyclic triterpenoids from three levels: network structure, national strategy, and subject behavior. It deepens the theoretical understanding of cooperation and competition relationships in the technology lifecycle and provides empirical evidence and policy implications for building a more resilient innovation ecosystem.
    pentacyclic triterpenoids  /  innovation cooperation networks  /  social network analysis  /  evolutionary mechanisms  /  patent analysis  /  technology lifecycle
    高艺, 南敏伦, 胥皓为, 张凯月, 高原, 赫玉芳. 五环三萜类化合物全球创新合作网络的图谱构建与演化研究. 中草药, 2026 , 57 (10) : 3912 -3925 . DOI: 10.7501/j.issn.0253-2670.2026.10.020
    GAO Yi, NAN Minlun, XU Haowei, ZHANG Kaiyue, GAO Yuan, HE Yufang. Mapping construction and evolution research of global innovation cooperation network of pentacyclic triterpenoids[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (10) : 3912 -3925 . DOI: 10.7501/j.issn.0253-2670.2026.10.020

      吉林省科学技术厅资助项目 (20250601031RC)

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    Siewert B, Pianowski E, Obernauer A, et al. Towards cytotoxic and selective derivatives of maslinic acid [J]. Bioorg Med Chem, 2014, 22(1): 594-615.
    Meira C S, Barbosa-Filho J M, Lanfredi-Rangel A, et al. Antiparasitic evaluation of betulinic acid derivatives reveals effective and selective anti-Trypanosoma cruzi inhibitors [J]. Exp Parasitol, 2016, 166: 108-115.
    Yang S J, Liu M C, Xiang H M, et al. Synthesis and in vitro antitumor evaluation of betulin acid ester derivatives as novel apoptosis inducers [J]. Eur J Med Chem, 2015, 102: 249-255.
    Bo T Y, Li X Y, Juan F Z, et al. Research progress of resource distribution of bioactive compound ursolic acid [J]. Chem Ind Forest Prod, 2012, 32:119-126.
    Do Nascimento P G G, Lemos T L G, Bizerra A M C, et al. Antibacterial and antioxidant activities of ursolic acid and derivatives [J]. Molecules, 2014, 19(1): 1317-1327.
    Li W, Zhang H X, Nie M X, et al. A novel synthetic ursolic acid derivative inhibits growth and induces apoptosis in breast cancer cell lines [J]. Oncol Lett, 201815(2):2323-2329.
    Sycz Z, Tichaczek-Goska D, Jezierska-Domaradzka A, et al. Are uropathogenic bacteria living in multispecies biofilm susceptible to active plant ingredient: Asiatic acid? [J]. Biomolecules, 2021, 11(12): 1754.
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    Liew K Y, Hafiz M F, Chong Y J, et al. A review of Malaysian herbal plants and their active constituents with potential therapeutic applications in sepsis [J]. Evid Based Complementary Altern Med, 2020, 2020: 8257817.
    Sun B J, Wu L L, Wu Y, et al. Therapeutic potential of Centella asiatica and its triterpenes: A review [J]. Front Pharmacol, 2020, 11: 568032.
    Brinker A M, Ma J, Lipsky P E, et al. Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae) [J]. Phytochemistry, 2007, 68(6): 732-766.
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    班玉娟, 陈瑞, 张宇, 等. 五环三萜类化合物的口服吸收与代谢研究进展[J]. 化学试剂, 2021, 43(7): 11.
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    2026年第57卷第10期
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    鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
    多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
    小菇属 Mycena 11 5.26
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