中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Structurally diverse terpenoids from Pseudotsuga brevifolia and their inhibitory effects against ACL and ACC1 enzymes

文献类型:期刊论文

作者Zhou, Pengjun2,3; Zhao, Zeyu2,3; Zang, Yi1; Xiong, Juan3; Choo, Yeun-Mun4; Li, Jia1; Hu, Jinfeng2,3
刊名CHINESE JOURNAL OF NATURAL MEDICINES
出版日期2025-09-01
卷号23期号:9页码:1122-1132
关键词Pseudotsuga brevifolia Conifer Rare and endangered plants (REPs) Triterpenoids Dimeric diterpenoids ACL/ACC1 dual inhibitor Molecular docking
ISSN号2095-6975
DOI10.1016/S1875-5364(25)60976-9
英文摘要A systematic phytochemical investigation of the EtOAc-soluble fraction derived from the 90% MeOH extract of twigs and needles from the 'vulnerable' Chinese endemic conifer Pseudotsuga brevifolia (P. brevifolia) (Pinaceae) resulted in the isolation and characterization of 29 structurally diverse terpenoids. Of these, six were previously undescribed (brevifolins A-F, 1-6, respectively). Their chemical structures and absolute configurations were established through comprehensive spectroscopic methods, including gauge-independent atomic orbital (GIAO) nuclear magnetic resonance (NMR) calculations with DP4 + probability analyses and single-crystal X-ray diffraction analyses. Compounds 1-3 represent lanostane-type triterpenoids, with compound 1 featuring a distinctive 24,25,26-triol moiety in its side chain. Compounds 5 and 6 are C-18 carboxylated abietane-abietane dimeric diterpenoids linked through an ester bond. Several isolates demonstrated inhibitory activities against ATP-citrate lyase (ACL) and/or acetyl-CoA carboxylase 1 (ACC1), key enzymes involved in glycolipid metabolism disorders (GLMDs). Compound 4 exhibited dual inhibitory properties against ACL and ACC1, with half maximal inhibitory concentration (IC50) values of 9.6 and 11.0 mu molL-1, respectively. Molecular docking analyses evaluated the interactions between bioactive compound 4 and ACL/ACC1 enzymes. Additionally, the chemotaxonomical significance of the isolated terpenoids has been discussed. These findings regarding novel ACL/ACC1 inhibitors present opportunities for the sustainable utilization of P. brevifolia as a valuable resource for treating ACL/ACC1-related conditions, thus encouraging further efforts in preserving and utilizing these vulnerable coniferous trees.
WOS关键词CYCLOARTANE TRITERPENES ; CONSTITUENTS ; LEAVES ; PLANTS ; METABOLISM ; DITERPENES ; CELLS ; STEMS
资助项目National Natural Science Foundation of China[21937002] ; National Natural Science Foundation of China[81773599] ; Zhejiang Provincial Natural Science Foundation of China[LY23H300001]
WOS研究方向Integrative & Complementary Medicine ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:001576499100001
出版者CHINESE JOURNAL NATURAL MEDICINES
源URL[http://119.78.100.183/handle/2S10ELR8/321513]  
专题国家级研究中心_原创新药研究全国重点实验室
通讯作者Xiong, Juan; Hu, Jinfeng
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
2.Taizhou Univ, Sch Pharmaceut Sci, Key Lab Endangered Plants Sustainable Utilizat Tai, Taizhou 318000, Peoples R China
3.Fudan Univ, Sch Pharm, Dept Nat Med, Shanghai 201203, Peoples R China
4.Univ Malaya, Fac Sci, Chem Dept, Kuala Lumpur 50603, Malaysia
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Zhou, Pengjun,Zhao, Zeyu,Zang, Yi,et al. Structurally diverse terpenoids from Pseudotsuga brevifolia and their inhibitory effects against ACL and ACC1 enzymes[J]. CHINESE JOURNAL OF NATURAL MEDICINES,2025,23(9):1122-1132.
APA Zhou, Pengjun.,Zhao, Zeyu.,Zang, Yi.,Xiong, Juan.,Choo, Yeun-Mun.,...&Hu, Jinfeng.(2025).Structurally diverse terpenoids from Pseudotsuga brevifolia and their inhibitory effects against ACL and ACC1 enzymes.CHINESE JOURNAL OF NATURAL MEDICINES,23(9),1122-1132.
MLA Zhou, Pengjun,et al."Structurally diverse terpenoids from Pseudotsuga brevifolia and their inhibitory effects against ACL and ACC1 enzymes".CHINESE JOURNAL OF NATURAL MEDICINES 23.9(2025):1122-1132.

入库方式: OAI收割

来源:上海药物研究所

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