Euscaphic acid (BioDeep_00000000563)

   

human metabolite PANOMIX_OTCML-2023 Endogenous natural product


代谢物信息卡片


(1R,2R,4aS,6aS,6bR,8aR,10S,11R,12aR,12bR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

化学式: C30H48O5 (488.3502)
中文名称: 野鸦椿酸
谱图信息: 最多检出来源 Homo sapiens(otcml) 42.47%

分子结构信息

SMILES: CC1CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(C)C5CCC43C)C2C1(C)O
InChI: InChI=1S/C30H48O5/c1-17-10-13-30(24(33)34)15-14-27(5)18(22(30)29(17,7)35)8-9-21-26(4)16-19(31)23(32)25(2,3)20(26)11-12-28(21,27)6/h8,17,19-23,31-32,35H,9-16H2,1-7H3,(H,33,34)/t17-,19-,20+,21-,22-,23-,26+,27-,28-,29-,30+/m1/s1

描述信息

Euscaphic acid is a pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 19 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata. It has a role as a plant metabolite. It is a pentacyclic triterpenoid, a hydroxy monocarboxylic acid and a triol. It derives from a hydride of an ursane.
Euscaphic acid is a natural product found in Ternstroemia gymnanthera, Rhaphiolepis deflexa, and other organisms with data available.
A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 19 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata.
Euscaphic acid is found in herbs and spices. Euscaphic acid is a constituent of Coleus amboinicus (Cuban oregano).
Constituent of Coleus amboinicus (Cuban oregano). Euscaphic acid is found in loquat and herbs and spices.
Euscaphic acid, a DNA polymerase inhibitor, is a triterpene from the root of the R. alceaefolius Poir. Euscaphic inhibits calf DNA polymerase α (pol α) and rat DNA polymerase β (pol β) with IC50 values of 61 and 108 μM[1]. Euscaphic acid induces apoptosis[2].
Euscaphic acid, a DNA polymerase inhibitor, is a triterpene from the root of the R. alceaefolius Poir. Euscaphic inhibits calf DNA polymerase α (pol α) and rat DNA polymerase β (pol β) with IC50 values of 61 and 108 μM[1]. Euscaphic acid induces apoptosis[2].

同义名列表

23 个代谢物同义名

(1R,2R,4aS,6aS,6bR,8aR,10S,11R,12aR,12bR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid; (1S,2S,4AS,6AS,6AS,6BR,8AR,10S,11R,12AS,14BS)-1,2,6A,6B,9,9,12A-HEPTAMETHYL-1,10,11-TRIS(OXIDANYL)-2,3,4,5,6,6A,7,8,8A,10,11,12,13,14B-TETRADECAHYDROPICENE-4A-CARBOXYLIC ACID; (1R,2R,4aS,6aS,6bR,8aR,10S,11R,12aR,12bR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid; (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid; Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, (2.alpha.,3.alpha.)-; Urs-12-en-28-oic acid,3,19-trihydroxy-, (2.alpha.,3alpha.)-; (2alpha,3alpha)-2,3,19-trihydroxyurs-12-en-28-oic acid; 2alpha,3alpha,19alpha-Trihydroxyurs-12-en-28-oic acid; Urs-12-en-28-oic acid,2,3,19-trihydroxy-, (2a,3a)-; (2alpha,3beta)-isomer of euscaphic acid; 2alpha-acetyl tormentic acid; Jacarandic acid; Acuminatic acid; Euscaphic acid; Tormentic acid; Euscophic acid; Euscapic acid; Jacarandate; LG23EX5V2J; Tormentate; Euscaphate; SCHEMBL13629631; Euscaphic acid



数据库引用编号

18 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

218 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 15 AIMP2, AKR1B1, BCL2, CASP3, ESR1, FRK, IL33, MAP3K7, MAPK8, MTOR, PIK3CA, POLB, PTGS2, TLR4, TRAF6
Peripheral membrane protein 6 ACHE, ESR1, GORASP1, MAP3K7, MTOR, PTGS2
Endosome membrane 3 MAP3K7, TLR4, TRAF6
Endoplasmic reticulum membrane 4 BCL2, MAP3K7, MTOR, PTGS2
Nucleus 13 ACHE, AIMP2, BCL2, CASP3, CS, ESR1, FRK, IL33, MAP3K7, MAPK8, MTOR, POLB, TRAF6
cytosol 12 AIMP2, AKR1B1, BCL2, CASP3, ESR1, FRK, GPT, MAP3K7, MAPK8, MTOR, PIK3CA, TRAF6
dendrite 1 MTOR
phagocytic vesicle 1 MTOR
nucleoplasm 8 AKR1B1, CASP3, ESR1, FRK, IL33, MAPK8, MTOR, POLB
Cell membrane 4 ACHE, ESR1, MAP3K7, TLR4
Cytoplasmic side 4 ESR1, GORASP1, MAP3K7, MTOR
lamellipodium 1 PIK3CA
Golgi apparatus membrane 2 GORASP1, MTOR
Synapse 2 ACHE, MAPK8
cell cortex 1 TRAF6
cell surface 2 ACHE, TLR4
glutamatergic synapse 2 CASP3, TRAF6
Golgi apparatus 3 ACHE, ESR1, GORASP1
Golgi membrane 2 GORASP1, MTOR
lysosomal membrane 2 GAA, MTOR
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
Cytoplasm, cytosol 1 AIMP2
Cytoplasmic vesicle, secretory vesicle 1 IL33
Lysosome 2 GAA, MTOR
plasma membrane 8 ACHE, ESR1, FRK, GAA, MAP3K7, PIK3CA, TLR4, TRAF6
Membrane 9 ACHE, AIMP2, BCL2, CS, ESR1, GAA, IL33, MTOR, TLR4
axon 1 MAPK8
caveola 1 PTGS2
extracellular exosome 5 AKR1B1, CS, FRK, GAA, GPT
Lysosome membrane 2 GAA, MTOR
endoplasmic reticulum 2 BCL2, PTGS2
extracellular space 3 ACHE, AKR1B1, IL33
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 4 ACHE, PIK3CA, TLR4, TRAF6
intercalated disc 1 PIK3CA
mitochondrion 3 AKR1B1, BCL2, CS
protein-containing complex 5 BCL2, ESR1, POLB, PTGS2, TRAF6
intracellular membrane-bounded organelle 2 GAA, IL33
Microsome membrane 2 MTOR, PTGS2
postsynaptic density 1 CASP3
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 1 TLR4
Secreted 3 ACHE, GAA, IL33
extracellular region 4 ACHE, FRK, GAA, IL33
cytoplasmic side of plasma membrane 1 TRAF6
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, MTOR
Mitochondrion matrix 1 CS
mitochondrial matrix 1 CS
Extracellular side 1 ACHE
transcription regulator complex 1 ESR1
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
CD40 receptor complex 1 TRAF6
external side of plasma membrane 1 TLR4
Early endosome 1 TLR4
pore complex 1 BCL2
microtubule 1 POLB
cis-Golgi network 1 GORASP1
basement membrane 1 ACHE
Nucleus, PML body 1 MTOR
PML body 1 MTOR
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 1 TLR4
neuron projection 1 PTGS2
chromatin 1 ESR1
phagocytic cup 1 TLR4
Chromosome 1 IL33
Cytoplasm, cell cortex 1 TRAF6
Lipid-anchor, GPI-anchor 1 ACHE
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
Lipid droplet 1 TRAF6
tertiary granule membrane 1 GAA
euchromatin 1 ESR1
side of membrane 1 ACHE
myelin sheath 1 BCL2
lipopolysaccharide receptor complex 1 TLR4
endoplasmic reticulum lumen 1 PTGS2
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
specific granule lumen 1 FRK
transport vesicle 1 IL33
azurophil granule membrane 1 GAA
azurophil granule lumen 1 FRK
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 GORASP1
Golgi apparatus, cis-Golgi network membrane 1 GORASP1
[Isoform 1]: Nucleus 1 ESR1
extrinsic component of cytoplasmic side of plasma membrane 1 TRAF6
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
spindle microtubule 1 POLB
basal dendrite 1 MAPK8
death-inducing signaling complex 1 CASP3
ATAC complex 1 MAP3K7
aminoacyl-tRNA synthetase multienzyme complex 1 AIMP2
Cytoplasmic vesicle, phagosome 1 MTOR
autolysosome lumen 1 GAA
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


文献列表

  • Huiqiang Wei, Jianghong Guo, Xiao Sun, Wenfeng Gou, Hongxin Ning, Haihua Shang, Qiang Liu, Wenbin Hou, Yiliang Li. Discovery of Natural Ursane-type SENP1 Inhibitors and the Platinum Resistance Reversal Activity Against Human Ovarian Cancer Cells: A Structure-Activity Relationship Study. Journal of natural products. 2022 05; 85(5):1248-1255. doi: 10.1021/acs.jnatprod.1c01166. [PMID: 35500202]
  • Yingying Shi, Dongdong Zhang, Shupei Li, Xiuxiu Xuan, Liuqiang Zhang, Yiming Li, Fujiang Guo. Inhibitors of BRD4 protein from the roots of Astilbe grandis stapf ex E.H. Wilson. Natural product research. 2021 Jun; 35(12):2044-2050. doi: 10.1080/14786419.2019.1655414. [PMID: 31437007]
  • Daniela Alejandra Torres-Ortiz, Rodríguez-deLeón Eloy, Bah Moustapha, Ibarra-Alvarado César, Mercado-Silva Edmundo, Castro-Ruiz Jesús Eduardo, Rivera-Pastrana Dulce María. Vasorelaxing effect and possible chemical markers of the flowers of the Mexican Crataegus gracilior. Natural product research. 2020 Dec; 34(24):3522-3525. doi: 10.1080/14786419.2019.1577833. [PMID: 30864868]
  • Yang Yang, Yawei Wang, Meng Zhao, Haobo Jia, Bing Li, Dan Xing. Tormentic acid inhibits IL-1β-induced chondrocyte apoptosis by activating the PI3K/Akt signaling pathway. Molecular medicine reports. 2018 03; 17(3):4753-4758. doi: 10.3892/mmr.2018.8425. [PMID: 29328385]
  • Wen-Ping Jiang, Shyh-Shyun Huang, Yoshikazu Matsuda, Hiroshi Saito, Naoto Uramaru, Hui-Ya Ho, Jin-Bin Wu, Guan-Jhong Huang. Protective Effects of Tormentic Acid, a Major Component of Suspension Cultures of Eriobotrya japonica Cells, on Acetaminophen-Induced Hepatotoxicity in Mice. Molecules (Basel, Switzerland). 2017 May; 22(5):. doi: 10.3390/molecules22050830. [PMID: 28524081]
  • Maria Ferhat, Zahia Kabouchea, Yoshinori Fujimoto, Hiroshi Araya. Two New Triterpenes and Other Compounds from Mentha aquatica (Lamiaceae). Natural product communications. 2017 Apr; 12(4):483-486. doi: ". [PMID: 30520576]
  • Yu-lu Li, Hua-nian Dai, Guo-xu Ma, Wen Zhang, Tong-yu Wu, Yun-qing Wang, Jie-ming Zou, Xiao-qing Zhong, Yan-lin Zhou, Jing-quan Yuan, Xu-dong Xu, Wei Yi. [A new triterpenic acid from the roots of Rosa laevigata]. Yao xue xue bao = Acta pharmaceutica Sinica. 2017 Mar; 52(3):425-9. doi: ". [PMID: 29979854]
  • Yu-Lun Wang, Gen-Yi Sun, Ying Zhang, Jia-Jun He, Shen Zheng, Jing-Na Lin. Tormentic acid inhibits H2O2-induced oxidative stress and inflammation in rat vascular smooth muscle cells via inhibition of the NF-κB signaling pathway. Molecular medicine reports. 2016 Oct; 14(4):3559-64. doi: 10.3892/mmr.2016.5690. [PMID: 27572426]
  • Dan Yang, Jian Liang, Haihui Xie, Xiaoyi Wei. Norsesquiterpenoids and triterpenoids from strawberry cv. Falandi. Food chemistry. 2016 Jul; 203(?):67-72. doi: 10.1016/j.foodchem.2016.02.036. [PMID: 26948590]
  • Shi-jun Liu, Zhi-xin Liao, Zhi-shu Tang, Chun-li Cui, Hong-bo Liu, Yan-ni Liang, Yu Zhang. [Chemical Constituents from Rubus stans]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 May; 39(5):1045-8. doi: . [PMID: 30133048]
  • Luis F Julio, Alejandro F Barrero, M Mar Herrador del Pino, Jesús F Arteaga, Jesús Burillo, Maria Fe Andres, Carmen E Díaz, Azucena González-Coloma. Phytotoxic and Nematicidal Components of Lavandula luisieri. Journal of natural products. 2016 Feb; 79(2):261-6. doi: 10.1021/acs.jnatprod.5b00501. [PMID: 26797293]
  • Qing Wang, Qiaomei Sun, Xiangling Ma, Zaisheng Rao, Hui Li. Probing the binding interaction of human serum albumin with three bioactive constituents of Eriobotrta japonica leaves: Spectroscopic and molecular modeling approaches. Journal of photochemistry and photobiology. B, Biology. 2015 Jul; 148(?):268-276. doi: 10.1016/j.jphotobiol.2015.04.030. [PMID: 25985147]
  • Flora Tolentino, Priscila Alves de Araújo, Eduardo de Souza Marques, Marcel Petreanu, Sérgio Faloni de Andrade, Rivaldo Niero, Fábio F Perazzo, Paulo César Pires Rosa, Edson Luis Maistro. In vivo evaluation of the genetic toxicity of Rubus niveus Thunb. (Rosaceae) extract and initial screening of its potential chemoprevention against doxorubicin-induced DNA damage. Journal of ethnopharmacology. 2015 Apr; 164(?):89-95. doi: 10.1016/j.jep.2015.02.013. [PMID: 25681544]
  • Pan Chen, Zhi-jian Fang, Han-jing Yan, Hong-bo Zhou, Quan-xi Mei. [Study on Chemical Constituents of Petroleum Ether Fraction from Rubus alceaefolius]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Jan; 38(1):93-6. doi: . [PMID: 26214876]
  • Jin-Bin Wu, Yueh-Hsiung Kuo, Cheng-Hsiu Lin, Hui-Ya Ho, Chun-Ching Shih. Tormentic acid, a major component of suspension cells of Eriobotrya japonica, suppresses high-fat diet-induced diabetes and hyperlipidemia by glucose transporter 4 and AMP-activated protein kinase phosphorylation. Journal of agricultural and food chemistry. 2014 Nov; 62(44):10717-26. doi: 10.1021/jf503334d. [PMID: 25317836]
  • Man-Man Li, Xiao-Qin Su, Jing Sun, Yu-Fan Gu, Zheng Huang, Ke-Wu Zeng, Qian Zhang, Yun-Fang Zhao, Daneel Ferreira, Jordan K Zjawiony, Jun Li, Peng-Fei Tu. Anti-inflammatory ursane- and oleanane-type triterpenoids from Vitex negundo var. cannabifolia. Journal of natural products. 2014 Oct; 77(10):2248-54. doi: 10.1021/np500509q. [PMID: 25245917]
  • Chao Wang, Jing Yang, Ping Zhao, Qi Zhou, Zhinan Mei, Guangzhong Yang, Xinzhou Yang, Yunjiang Feng. Chemical constituents from Eucalyptus citriodora Hook leaves and their glucose transporter 4 translocation activities. Bioorganic & medicinal chemistry letters. 2014 Jul; 24(14):3096-9. doi: 10.1016/j.bmcl.2014.05.014. [PMID: 24894556]
  • Xiao-lu Chen, Quan-xi Mei, Hong-bo Zhou, Zhi-jian Fang, Ying-xin Zhu. [Chemical constituents from roots of Rubus parvifolius]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2014 Jun; 37(6):995-7. doi: . [PMID: 25470966]
  • Jing-jing Li, Yi Li, Min Bai, Jing-fu Tan, Qiang Wang, Jie Yang. Simultaneous determination of corosolic acid and euscaphic acid in the plasma of normal and diabetic rat after oral administration of extract of Potentilla discolor Bunge by high-performance liquid chromatography/electrospray ionization mass spectrometry. Biomedical chromatography : BMC. 2014 May; 28(5):717-24. doi: 10.1002/bmc.3098. [PMID: 24311372]
  • Xing Lin, Shijun Zhang, Renbin Huang, Shimei Tan, Shuang Liang, Xiaoyan Wu, Lang Zhuo, Quanfang Huang. Protective effect of tormentic acid from Potentilla chinensis against lipopolysaccharide/D-galactosamine induced fulminant hepatic failure in mice. International immunopharmacology. 2014 Apr; 19(2):365-72. doi: 10.1016/j.intimp.2014.02.009. [PMID: 24560903]
  • Masateru Ono, Shin Yasuda, Haruki Komatsu, Yukio Fujiwara, Motohiro Takeya, Toshihiro Nohara. Triterpenoids from the fruits and leaves of the blackberry (Rubus allegheniensis) and their inhibitory activities on foam cell formation in human monocyte-derived macrophage. Natural product research. 2014; 28(24):2347-50. doi: 10.1080/14786419.2014.939087. [PMID: 25033392]
  • Monica R Loizzo, Marco Bonesi, Nicodemo G Passalacqua, Antoine Saab, Francesco Menichini, Rosa Tundis. Antiproliferative activities on renal, prostate and melanoma cancer cell lines of Sarcopoterium spinosum aerial parts and its major constituent tormentic acid. Anti-cancer agents in medicinal chemistry. 2013 Jun; 13(5):768-76. doi: 10.2174/1871520611313050011. [PMID: 23157592]
  • Min Yan, Yan Zhu, Hong-Jun Zhang, Wei-Hua Jiao, Bing-Nan Han, Zhao-Xi Liu, Feng Qiu, Wan-Sheng Chen, Hou-Wen Lin. Anti-inflammatory secondary metabolites from the leaves of Rosa laevigata. Bioorganic & medicinal chemistry. 2013 Jun; 21(11):3290-7. doi: 10.1016/j.bmc.2013.03.018. [PMID: 23632365]
  • Li-Jie Zhang, Jing-Jy Cheng, Chia-Ching Liao, Hui-Ling Cheng, Hung-Tse Huang, Li-Ming Yang Kuo, Yao-Haur Kuo. Triterpene acids from Euscaphis japonica and assessment of their cytotoxic and anti-NO activities. Planta medica. 2012 Sep; 78(14):1584-90. doi: 10.1055/s-0032-1315040. [PMID: 22814889]
  • Gleice da Graça Rocha, Marisol Simões, Rodrigo Rodrigues Oliveira, Maria Auxiliadora Coelho Kaplan, Cerli Rocha Gattass. 3β-acetyl tormentic acid induces apoptosis of resistant leukemia cells independently of P-gp/ABCB1 activity or expression. Investigational new drugs. 2012 Feb; 30(1):105-13. doi: 10.1007/s10637-010-9524-1. [PMID: 20814731]
  • Hyo-Jin An, In-Tae Kim, Hee-Juhn Park, Hyung-Min Kim, Jung-Hye Choi, Kyung-Tae Lee. Tormentic acid, a triterpenoid saponin, isolated from Rosa rugosa, inhibited LPS-induced iNOS, COX-2, and TNF-α expression through inactivation of the nuclear factor-κb pathway in RAW 264.7 macrophages. International immunopharmacology. 2011 Apr; 11(4):504-10. doi: 10.1016/j.intimp.2011.01.002. [PMID: 21237302]
  • Cheng-qin Liang, Xiao-jian Su, Xian-li Zhou, Jiang-ke Qin, Qing Xu, Rong-gan Liang, Ming-po Zheng. [Studies on the chemical constituents of Rubus parvifolius]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2011 Jan; 34(1):64-6. doi: . [PMID: 21818969]
  • Zhenfeng Hong, Wang Chen, Jinyan Zhao, Zhisheng Wu, JianHeng Zhou, Tianjiao Li, Juan Hu. Hepatoprotective effects of Rubus aleaefolius Poir. and identification of its active constituents. Journal of ethnopharmacology. 2010 May; 129(2):267-72. doi: 10.1016/j.jep.2010.03.025. [PMID: 20362654]
  • You-sheng Cehn, Kun Zhang, Su-qing Zhao, Jian-hong Zhang. [Studies on the lowering blood sugar substances from agrimony (II)]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2010 May; 33(5):724-6. doi: . [PMID: 20873555]
  • Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, Kazuo Koike. Triterpenoid saponins from Rubus ellipticus var. obcordatus. Journal of natural products. 2009 Oct; 72(10):1755-60. doi: 10.1021/np900237a. [PMID: 19795885]
  • Anelize S Fogo, Eliane Antonioli, João B Calixto, Alexandre H Campos. Tormentic acid reduces vascular smooth muscle cell proliferation and survival. European journal of pharmacology. 2009 Aug; 615(1-3):50-4. doi: 10.1016/j.ejphar.2009.05.009. [PMID: 19464287]
  • Jian Chen, Wei-Lin Li, Ju-Lan Wu, Bing-Ru Ren, Han-Qing Zhang. Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae. Die Pharmazie. 2008 Oct; 63(10):765-7. doi: . [PMID: 18972842]
  • Zhi-jing Ma, Zhi-juan Zhao. [Studies on chemical constituents from stem barks of Fraxinus paxiana]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2008 Aug; 33(16):1990-3. doi: ". [PMID: 19086636]
  • Jong Min Kim, Dae Sik Jang, Yun Mi Lee, Jeong Lim Yoo, Young Sook Kim, Joo-Hwan Kim, Jin Sook Kim. Aldose-reductase- and protein-glycation-inhibitory principles from the whole plant of Duchesnea chrysantha. Chemistry & biodiversity. 2008 Feb; 5(2):352-6. doi: 10.1002/cbdv.200890034. [PMID: 18293434]
  • Gleice da Graça Rocha, Marisol Simões, Kelly Araujo Lúcio, Rodrigo Rodrigues Oliveira, Maria Auxiliadora Coelho Kaplan, Cerli Rocha Gattass. Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines. Bioorganic & medicinal chemistry. 2007 Dec; 15(23):7355-60. doi: 10.1016/j.bmc.2007.07.020. [PMID: 17889544]
  • Lucia Helena Martini, Fernanda Jung, Felix Antunes Soares, Liane Nanci Rotta, Deusa Aparecida Vendite, Marcos Emilio dos Santos Frizzo, Rosendo A Yunes, João Batista Calixto, Susana Wofchuk, Diogo O Souza. Naturally occurring compounds affect glutamatergic neurotransmission in rat brain. Neurochemical research. 2007 Nov; 32(11):1950-6. doi: 10.1007/s11064-007-9393-y. [PMID: 17577666]
  • Ying Cui, Xue-mei Zhang, Ji-jun Chen, Yan Zhang, Xiu-kun Lin, Le Zhou. [Chemical constituents from root of Actinidia chinensis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2007 Aug; 32(16):1663-5. doi: ". [PMID: 18027663]
  • Márcia Kanegusuku, Danúbia Sbors, Eliza Stefanelo Bastos, Márcia Maria de de Souza, Valdir Cechinel-Filho, Rosendo Augusto Yunes, Franco Delle Monache, Rivaldo Niero. Phytochemical and analgesic activity of extract, fractions and a 19-hydroxyursane-type triterpenoid obtained from Rubus rosaefolius (Rosaceae). Biological & pharmaceutical bulletin. 2007 May; 30(5):999-1002. doi: 10.1248/bpb.30.999. [PMID: 17473451]
  • William P Jones, Tatiana Lobo-Echeverri, Qiuwen Mi, Hee-Byung Chai, Djaja D Soejarto, Geoffrey A Cordell, Steven M Swanson, A Douglas Kinghorn. Cytotoxic constituents from the fruiting branches of Callicarpa americana collected in southern Florida. Journal of natural products. 2007 Mar; 70(3):372-7. doi: 10.1021/np060534z. [PMID: 17279798]
  • Qin Zhang, Zai Chang, Qiang Wang. Ursane triterpenoids inhibit atherosclerosis and xanthoma in LDL receptor knockout mice. Cardiovascular drugs and therapy. 2006 Oct; 20(5):349-57. doi: 10.1007/s10557-006-0509-4. [PMID: 17136324]
  • Jing Yan, Xiu-Wei Yang. [Studies on the chemical constituents in herb of Ludwigia octovalvis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2005 Dec; 30(24):1923-6. doi: ". [PMID: 16494025]
  • Norihiro Banno, Toshihiro Akihisa, Harukuni Tokuda, Ken Yasukawa, Hiroshi Higashihara, Motohiko Ukiya, Kenji Watanabe, Yumiko Kimura, Jun-Ichi Hasegawa, Hoyoku Nishino. Triterpene acids from the leaves of Perilla frutescens and their anti-inflammatory and antitumor-promoting effects. Bioscience, biotechnology, and biochemistry. 2004 Jan; 68(1):85-90. doi: 10.1271/bbb.68.85. [PMID: 14745168]
  • Jongwon Choi, Kyung-Tae Lee, Joohun Ha, Sei-Young Yun, Chang-Duk Ko, Hyun-Ju Jung, Hee-Juhn Park. Antinociceptive and antiinflammatory effects of Niga-ichigoside F1 and 23-hydroxytormentic acid obtained from Rubus coreanus. Biological & pharmaceutical bulletin. 2003 Oct; 26(10):1436-41. doi: 10.1248/bpb.26.1436. [PMID: 14519951]
  • Léslei B Bortalanza, Juliano Ferreira, Sonia C Hess, Franco Delle Monache, Rosendo A Yunes, João B Calixto. Anti-allodynic action of the tormentic acid, a triterpene isolated from plant, against neuropathic and inflammatory persistent pain in mice. European journal of pharmacology. 2002 Oct; 453(2-3):203-8. doi: 10.1016/s0014-2999(02)02428-7. [PMID: 12398905]
  • Chikako Murakami, Kiyomi Ishijima, Mitsuru Hirota, Kengo Sakaguchi, Hiromi Yoshida, Yoshiyuki Mizushina. Novel anti-inflammatory compounds from Rubus sieboldii, triterpenoids, are inhibitors of mammalian DNA polymerases. Biochimica et biophysica acta. 2002 Apr; 1596(2):193-200. doi: 10.1016/s0167-4838(02)00227-3. [PMID: 12007601]
  • Si-Hyung Park, Sei-Ryang Oh, Kyung-Seop Ahn, Jae-Gil Kim, Hyeong-Kyu Lee. Structure determination of a new lupane-type triterpene, tiarellic acid, isolated from Tiarella polyphylla. Archives of pharmacal research. 2002 Feb; 25(1):57-60. doi: 10.1007/bf02975262. [PMID: 11885693]
  • C L Cantrell, S G Franzblau, N H Fischer. Antimycobacterial plant terpenoids. Planta medica. 2001 Nov; 67(8):685-94. doi: 10.1055/s-2001-18365. [PMID: 11731906]
  • F Z Chen, S L Peng, L S Ding, Y H He, M K Wang. [Chemical constituents from the fruit of Rosa bella Rehd. et Wils]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2001 Aug; 26(8):549-51. doi: . [PMID: 12776369]
  • T H Lee, S S Lee, Y C Kuo, C H Chou. Monoterpene glycosides and triterpene acids from Eriobotrya deflexa. Journal of natural products. 2001 Jul; 64(7):865-9. doi: 10.1021/np0100237. [PMID: 11473413]
  • Y K Kim, S K Yoon, S Y Ryu. Cytotoxic triterpenes from stem bark of Physocarpus intermedius. Planta medica. 2000 Jun; 66(5):485-6. doi: 10.1055/s-2000-8585. [PMID: 10909277]
  • Y Kashiwada, H K Wang, T Nagao, S Kitanaka, I Yasuda, T Fujioka, T Yamagishi, L M Cosentino, M Kozuka, H Okabe, Y Ikeshiro, C Q Hu, E Yeh, K H Lee. Anti-AIDS agents. 30. Anti-HIV activity of oleanolic acid, pomolic acid, and structurally related triterpenoids. Journal of natural products. 1998 Sep; 61(9):1090-5. doi: 10.1021/np9800710. [PMID: 9748372]
  • L Gan, Y Zhao, J Zhang, F Jiang. [Isolation and identification of triterpenoids from Rubus alceaefolius Poir]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1998 Jun; 23(6):361-2, 383. doi: ". [PMID: 11601300]
  • X Lu, W Xu, J Shen, G Han. [Chemical studies on Campylotropis hirtella (Franch. Schindl.)]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1997 Nov; 22(11):680-2, 704. doi: . [PMID: 11243186]
  • S Valcic, G A Wächter, G Montenegro, B N Timmermann. Triterpenoids from Acaena pinnatifida R. et P. Zeitschrift fur Naturforschung. C, Journal of biosciences. 1997 Mar; 52(3-4):264-6. doi: 10.1515/znc-1997-3-420. [PMID: 9167278]
  • H X Xu, F Q Zeng, M Wan, K Y Sim. Anti-HIV triterpene acids from Geum japonicum. Journal of natural products. 1996 Jul; 59(7):643-5. doi: 10.1021/np960165e. [PMID: 8759159]
  • X Lu, H Luo. [Chemical studies on the root of Salvia trijuga Diels]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 1996 Jul; 21(7):424-5, 448. doi: ". [PMID: 9642393]
  • N De Tommasi, F De Simone, C Pizza, N Mahmood, P S Moore, C Conti, N Orsi, M L Stein. Constituents of Eriobotrya japonica. A study of their antiviral properties. Journal of natural products. 1992 Aug; 55(8):1067-73. doi: 10.1021/np50086a006. [PMID: 1279126]
  • Y H Pei, X Li, T R Zhu. [Studies on the structure of a new ellagic acid glycoside from the root-sprouts of Agrimonia pilosa Ledeb]. Yao xue xue bao = Acta pharmaceutica Sinica. 1990; 25(10):798-800. doi: ". [PMID: 2099598]