Daucosterol (BioDeep_00000343673)

Main id: BioDeep_00000000575

 

natural product PANOMIX_OTCML-2023


代谢物信息卡片


(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

化学式: C35H60O6 (576.4389659999999)
中文名称: β-Sitosterol β-D-glucoside, 西托糖苷, 胡萝卜甙, 胡萝卜苷
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C
InChI: InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1

描述信息

Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane.
Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available.
A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa.
C308 - Immunotherapeutic Agent
Daucosterol is a natural sterol compound.
Daucosterol is a natural sterol compound.

同义名列表

75 个代谢物同义名

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; BETA-SITOSTEROL GLUCOSIDE (DAUCOSTEROL) (CONSTITUENT OF STINGING NETTLE) [DSC]; BETA-SITOSTEROL GLUCOSIDE (DAUCOSTEROL) (CONSTITUENT OF STINGING NETTLE); .beta.-D-Glucopyranoside, (3.beta.)-stigmast-5-en-3-yl; Stigmast-5-ene, 3-beta-(beta-D-glucopyranosyloxy)-; beta-D-Glucopyranoside, (3beta)-stigmast-5-en-3-yl; 3.BETA.-(.BETA.-D-GLUCOPYRANOSYLOXY)STIGMAST-5-ENE; (3-beta)-Stigmast-5-en-3-yl-beta-D-glucopyranoside; (3beta)-stigmast-5-en-3-yl beta-D-glucopyranoside; 3-beta-(beta-D-Glucopyranosyloxy)stigmast-5-ene; 3beta-(beta-D-Glucopyranosyloxy)stigmast-5-ene; beta-sitosterol 3-O-beta-D-glucopyranoside; (-)-beta-Sitosterol-beta-D-glucopyranoside; Eleutheroside A;-Sitosterol -D-glucoside; SITOSTEROL 3-O-.BETA.-D-GLUCOPYRANOSIDE; beta-sitosteryl-beta-D-glucopyranoside; beta-sitosterol-beta-D-glucopyranoside; beta-sitosterol 3-O-beta-D-glucoside; .BETA.-SITOSTEROL-.BETA.-D-GLUCOSIDE; 3-O-beta-D-glucosyl-beta-sitosterol; beta-sitosterol-beta-D-glycoside; beta-Sitosterol beta-D-Glucoside; Sitosterol-3-O-beta-D-glucoside; beta-Sitosterol monoglucoside; sitosteryl 3-beta-D-glucoside; .beta.-sitosterol-glucoside; NPJICTMALKLTFW-OFUAXYCQSA-N; beta-sitosterol glucutonide; beta-Sitosterol D-glucoside; sitosterol beta-D-glucoside; b-Sitosterol b-D-glucoside; O-glucosyl-beta-sitosterol; beta-sitosterol glucoside; beta-SITOSTEROL-GLUCOSIDE; beta-Sitosteryl glucoside; Sitoglusido [INN-Spanish]; Sitoglusidum [INN-Latin]; sitosterol glucuronide; Sitogluside [USAN:INN]; Sitosterol D-glucoside; Sitogluside (USAN/INN); Sitosteryl glycoside; SITOGLUSIDE [USAN]; SITOGLUSIDE [INN]; beta-Daucosterol; UNII-U45VN859W3; eleutheroside A; Coriandrinol; Sitoglusidum; Daucosterine; Daucosterol; Sitoglusido; Sitogluside; Daucosterin; Alexandrin; U45VN859W3; Doursterol; lyoniside; AC1NX3NW; Sterolin; BSS-G; AW 10; AW-10; BSSG; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methylol-tetrahydropyran-3,4,5-triol; (2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; Sitogluside (USAN); AIDS-014857; AIDS014857; 474-58-8; D05848



数据库引用编号

14 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)

1103 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。



文献列表

  • Sumin Lee, Jae-Hyun Kim, Minsun Kim, Sooyeon Hong, Hoyeon Park, Eom Ji Kim, Eun-Young Kim, Chungho Lee, Youngjoo Sohn, Hyuk Sang Jung. Exploring the Anti-Osteoporotic Potential of Daucosterol: Impact on Osteoclast and Osteoblast Activities. International journal of molecular sciences. 2023 Nov; 24(22):. doi: 10.3390/ijms242216465. [PMID: 38003654]
  • Feng Zhang, Mengyao Wang, Yang Zha, Jie Zhou, Jihong Han, Shuang Zhang. Daucosterol Alleviates Alcohol-Induced Hepatic Injury and Inflammation through P38/NF-κB/NLRP3 Inflammasome Pathway. Nutrients. 2023 Jan; 15(1):. doi: 10.3390/nu15010223. [PMID: 36615880]
  • Haoran Guo, Hongliang Zeng, Chuhan Fu, Jinhua Huang, Jianyun Lu, Yibo Hu, Ying Zhou, Liping Luo, Yushan Zhang, Lan Zhang, Jing Chen, Qinghai Zeng. Identification of Sitogluside as a Potential Skin-Pigmentation-Reducing Agent through Network Pharmacology. Oxidative medicine and cellular longevity. 2021; 2021(?):4883398. doi: 10.1155/2021/4883398. [PMID: 34603597]
  • Trang T T Nguyen, Ha V H Nguyen. Effects of Fermentation Conditions Using Lactobacillus plantarum on the Charantin, Stigmasterol Glucoside and β-sitosterol Glucoside Contents of Bitter Gourd (Momordica charantia L.) Juice. Plant foods for human nutrition (Dordrecht, Netherlands). 2020 Dec; 75(4):656-658. doi: 10.1007/s11130-020-00860-w. [PMID: 33009632]
  • Merline Ymele Nguedia, Alain Brice Tueche, Abel Joël Gbaweng Yaya, Vincent Yadji, Derek Tantoh Ndinteh, Dieudonné Njamen, Stéphane Zingue. Daucosterol from Crateva adansonii DC (Capparaceae) reduces 7,12-dimethylbenz(a)anthracene-induced mammary tumors in Wistar rats. Environmental toxicology. 2020 Oct; 35(10):1125-1136. doi: 10.1002/tox.22948. [PMID: 32449848]
  • Huiyuan Zhang, Yamin Song, Cong Feng. Improvement of cerebral ischemia/reperfusion injury by daucosterol palmitate-induced neuronal apoptosis inhibition via PI3K/Akt/mTOR signaling pathway. Metabolic brain disease. 2020 08; 35(6):1035-1044. doi: 10.1007/s11011-020-00575-6. [PMID: 32363473]
  • Bing Han, Lingmin Jiang, Pu Jiang, Deqi Zhou, Xiaoxin Jia, Xuegang Li, Xiaoli Ye. Daucosterol linolenate from Sweet Potato Suppresses MCF7-Xenograft-Tumor Growth through Regulating PI3K/AKT Pathway. Planta medica. 2020 Jul; 86(11):767-775. doi: 10.1055/a-1176-1884. [PMID: 32512614]
  • Stéphane Zingue, Abel Joël Gbaweng Yaya, Thomas Michel, Derek Tantoh Ndinteh, Jochen Rutz, Florence Auberon, Sebastian Maxeiner, Felix K-H Chun, Alembert Tiabou Tchinda, Dieudonné Njamen, Roman A Blaheta. Bioguided identification of daucosterol, a compound that contributes to the cytotoxicity effects of Crateva adansonii DC (capparaceae) to prostate cancer cells. Journal of ethnopharmacology. 2020 Jan; 247(?):112251. doi: 10.1016/j.jep.2019.112251. [PMID: 31560992]
  • Claudia Luna-Herrera, Irma A Martínez-Dávila, Luis O Soto-Rojas, Yazmin M Flores-Martinez, Manuel A Fernandez-Parrilla, Jose Ayala-Davila, Bertha A León-Chavez, Guadalupe Soto-Rodriguez, Victor M Blanco-Alvarez, Francisco E Lopez-Salas, Maria E Gutierrez-Castillo, Bismark Gatica-Garcia, America Padilla-Viveros, Cecilia Bañuelos, David Reyes-Corona, Armando J Espadas-Alvarez, Linda Garcés-Ramírez, Oriana Hidalgo-Alegria, Fidel De La Cruz-López, Daniel Martinez-Fong. Intranigral Administration of β-Sitosterol-β-D-Glucoside Elicits Neurotoxic A1 Astrocyte Reactivity and Chronic Neuroinflammation in the Rat Substantia Nigra. Journal of immunology research. 2020; 2020(?):5907591. doi: 10.1155/2020/5907591. [PMID: 33282962]
  • Samia Baatouche, Thamere Cheriet, Djamel Sarri, Ratiba Mekkiou, Ouahiba Boumaza, Samir Benayache, Fadila Benayache, Ignacio Brouard, Francisco León, Ramdane Seghiri. Centaurea microcarpa Coss. & Dur. (Asteraceae) extracts: New cyanogenic glucoside and other constituents. Natural product research. 2019 Nov; 33(21):3070-3076. doi: 10.1080/14786419.2018.1517343. [PMID: 30445872]
  • Herminia López-Salazar, Brenda Hildeliza Camacho-Díaz, Sandra Victoria Ávila-Reyes, Ma Dolores Pérez-García, Manases González-Cortazar, Martha L Arenas Ocampo, Antonio R Jiménez-Aparicio. Identification and Quantification of β-Sitosterol β-d-Glucoside of an Ethanolic Extract Obtained by Microwave-Assisted Extraction from Agave angustifolia Haw. Molecules (Basel, Switzerland). 2019 Oct; 24(21):. doi: 10.3390/molecules24213926. [PMID: 31683500]
  • Navneet Kishore, Pradeep Kumar, Karuna Shanker, Akhilesh Kumar Verma. Human disorders associated with inflammation and the evolving role of natural products to overcome. European journal of medicinal chemistry. 2019 Oct; 179(?):272-309. doi: 10.1016/j.ejmech.2019.06.034. [PMID: 31255927]
  • Tamilselvam Rajavel, Gunasekeran Banu Priya, Venkatesan Suryanarayanan, Sanjeev Kumar Singh, Kasi Pandima Devi. Daucosterol disturbs redox homeostasis and elicits oxidative-stress mediated apoptosis in A549 cells via targeting thioredoxin reductase by a p53 dependent mechanism. European journal of pharmacology. 2019 Jul; 855(?):112-123. doi: 10.1016/j.ejphar.2019.04.051. [PMID: 31059712]
  • Ali M El-Halawany, Samir M Osman, Hossam M Abdallah. Cytotoxic constituents from Vicia monantha subsp. monantha seeds. Natural product research. 2019 Jun; 33(12):1783-1786. doi: 10.1080/14786419.2018.1434638. [PMID: 29411647]
  • Jian-Hua Shao, Jia Chen, Xiao-Qing Xu, Chun-Chao Zhao, Zi-Ling Dong, Wen-Yan Liu, Jie Shen. Chemical constituents and biological activities of Viburnum macrocephalum f. keteleeri. Natural product research. 2019 Jun; 33(11):1612-1616. doi: 10.1080/14786419.2018.1428593. [PMID: 29368956]
  • Ping Gao, Xiaopeng Huang, Tingting Liao, Guangsen Li, Xujun Yu, Yaodong You, Yuxing Huang. Daucosterol induces autophagic-dependent apoptosis in prostate cancer via JNK activation. Bioscience trends. 2019 May; 13(2):160-167. doi: 10.5582/bst.2018.01293. [PMID: 30944266]
  • Abdelaaty A Shahat, Syed Hidayathulla, Azmat A Khan, Amer M Alanazi, Osaid T Al Meanazel, Ali S Alqahtani, Mansour S Alsaid, Ahmed A Hussein. Phytochemical profiling, antioxidant and anticancer activities of Gastrocotyle hispida growing in Saudi Arabia. Acta tropica. 2019 Mar; 191(?):243-247. doi: 10.1016/j.actatropica.2019.01.013. [PMID: 30659804]
  • Nuan Ma, Qin Tang, Wan-Ting Wu, Xin-An Huang, Qin Xu, Guang-Li Rong, Song Chen, Jian-Ping Song. Three Constituents of Moringa oleifera Seeds Regulate Expression of Th17-Relevant Cytokines and Ameliorate TPA-Induced Psoriasis-Like Skin Lesions in Mice. Molecules (Basel, Switzerland). 2018 Dec; 23(12):. doi: 10.3390/molecules23123256. [PMID: 30544700]
  • Bing Han, Pu Jiang, Wuyang Liu, Heshan Xu, Yuanfeng Li, Zhaoxing Li, Hang Ma, Yang Yu, Xuegang Li, Xiaoli Ye. Role of Daucosterol Linoleate on Breast Cancer: Studies on Apoptosis and Metastasis. Journal of agricultural and food chemistry. 2018 Jun; 66(24):6031-6041. doi: 10.1021/acs.jafc.8b01387. [PMID: 29878766]
  • Dinara Satmbekova, Radhakrishnan Srivedavyasasri, Yerkebulan Orazbekov, Roza Omarova, Ubaidilla Datkhayev, Samir A Ross. Chemical and biological studies on Cichorium intybus L. Natural product research. 2018 Jun; 32(11):1343-1347. doi: 10.1080/14786419.2017.1343319. [PMID: 28629227]
  • Lashyn Kiyekbayeva, Nesma M Mohamed, Orazbekov Yerkebulan, Enas I Mohamed, Datkhayev Ubaidilla, Akhtayeva Nursulu, Mamurova Assem, Radhakrishnan Srivedavyasasri, Samir A Ross. Phytochemical constituents and antioxidant activity of Echinops albicaulis. Natural product research. 2018 May; 32(10):1203-1207. doi: 10.1080/14786419.2017.1323213. [PMID: 28475371]
  • Radhakrishnan Srivedavyasasri, Miriah B White, Tatyana S Kustova, Nadezhda G Gemejiyeva, Charles L Cantrell, Samir A Ross. New tetranorlabdanoic acid from aerial parts of Salvia aethiopis. Natural product research. 2018 Jan; 32(1):14-17. doi: 10.1080/14786419.2017.1324961. [PMID: 28475363]
  • Shikha Mishra, Vidhu Aeri. Biotransformation of lignan glycoside to its aglycone by Woodfordia fruticosa flowers: quantification of compounds using a validated HPTLC method. Pharmaceutical biology. 2017 Dec; 55(1):360-366. doi: 10.1080/13880209.2016.1238948. [PMID: 27931157]
  • Jerald J Nair, Anke Wilhelm, Susanna L Bonnet, Johannes van Staden. Antibacterial constituents of the plant family Amaryllidaceae. Bioorganic & medicinal chemistry letters. 2017 11; 27(22):4943-4951. doi: 10.1016/j.bmcl.2017.09.052. [PMID: 29033234]
  • Sibylle Schäfer, Stefan Schwaiger, Hermann Stuppner. Aristolic Acid Derivatives from the Bark of Antidesma ghaesembilla. Planta medica. 2017 Aug; 83(12-13):1097-1102. doi: 10.1055/s-0043-110141. [PMID: 28499305]
  • Xuejiao Li, Chengcheng Zhao, Songsong Jing, Jiachen Sun, Xia Li, Shuli Man, Ying Wang, Wenyuan Gao. Novel phenanthrene and isocoumarin from the rhizomes of Dioscorea nipponica Makino subsp. rosthornii (Prain et Burkill) C. T. Ting (Dioscoreaceae). Bioorganic & medicinal chemistry letters. 2017 08; 27(15):3595-3601. doi: 10.1016/j.bmcl.2017.03.095. [PMID: 28606759]
  • Tamilselvam Rajavel, Ramar Mohankumar, Govindaraju Archunan, Kandasamy Ruckmani, Kasi Pandima Devi. Beta sitosterol and Daucosterol (phytosterols identified in Grewia tiliaefolia) perturbs cell cycle and induces apoptotic cell death in A549 cells. Scientific reports. 2017 06; 7(1):3418. doi: 10.1038/s41598-017-03511-4. [PMID: 28611451]
  • Xu Wang, Hong-lei Zhou, Rong Rong. [Chemical Constituents of Lonicerae Japonicae Flos]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Sep; 39(9):2030-2. doi: ". [PMID: 30209907]
  • Shikha Mishra, Vidhu Aeri. Optimization of microwave-assisted extraction conditions for preparing lignan-rich extract from Saraca asoca bark using Box-Behnken design. Pharmaceutical biology. 2016 Jul; 54(7):1255-62. doi: 10.3109/13880209.2015.1066399. [PMID: 26428389]
  • 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]
  • Shi-jun Liu, Zhi-xin Liao, Zhi-shu Tang, Chun-li Cui, Hong-bo Liu, Yan-ni Liang, Yu Zhang. [Study on Chemical Constituents of Delphinium caeruleum]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Feb; 39(2):318-21. doi: ". [PMID: 30080366]
  • Fang-hui Xu, Yu-xiang Ding, Qiang Wang. [Chemical Constituents of Ethyl Acetate Fraction from Hypericum ascyron]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Feb; 39(2):322-5. doi: . [PMID: 30080367]
  • Shao-jun Wang, Chuang Wu, Gan Zhao. [Study on Chemical Constituents of Stalk from Pottsia laxifora]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Feb; 39(2):326-8. doi: ". [PMID: 30080368]
  • Narayan Dolai, Ashish Kumar, Aminul Islam, Pallab K Haldar. Apoptogenic effects of β-sitosterol glucoside from Castanopsis indica leaves. Natural product research. 2016; 30(4):482-5. doi: 10.1080/14786419.2015.1023201. [PMID: 25790168]
  • Li Zhang, Jun Dang, Li-juan Mei, Yun Shao, Qi-Ian Wang, Xue-juan Liu. [Chemical Constituents from Roots of Gentiana straminea of Tibetan Medicine]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Jan; 39(1):103-6. doi: . [PMID: 30080009]
  • Li Zhang, Dong Pei, Yan-ru Huang, Jian-teng Wei, Duo-long Di, Lan-xia Wang. [Chemical Constituents from Cynomorium songaricum]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2016 Jan; 39(1):74-7. doi: . [PMID: 30079707]
  • Jian Wang, Yang-min Ma, Meng-ru Yan, Qian Xu, Zi-rui Qu, Zhi Miao. [Chemical Compositions from Stems and Branches of Sorbaria arborea]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Oct; 38(10):2098-101. doi: . [PMID: 27254923]
  • Wei Yin, Zu-rong Song, Jin-qi Liu, Guo-sheng Zhang. [Chemical Constituents of Paris polyphylla var. chinensis Aerial Parts]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Sep; 38(9):1875-8. doi: ". [PMID: 26930982]
  • Zhi-jun Guo, Zhu-ya Yang, Wen-hong Tan, Zhi-hong Zhou, Xiao-xia Ma. [Chemical Constituents from Processed Products of Aconitum Vilmoriniani Radix]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 May; 38(5):988-91. doi: . [PMID: 26767293]
  • Yong Chen, Jian Zuo, Jian-wei Chen, Xiang Li. [Chemical Constituents from Claoxylon indicum Stems]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Apr; 38(4):761-3. doi: . [PMID: 26672343]
  • Ping Qiu, Qi-zhi Wang, Min Yin, Ming Wang, You-yi Zhao, Yu Shan, Xu Feng. [Chemical Constituents of Ethyl Acetate Fraction of Suaeda glauca]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Apr; 38(4):751-3. doi: . [PMID: 26672340]
  • Chun-ling Zhu. [Chemical Constituents from Mallotus paniculatus (II)]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Apr; 38(4):764-5. doi: . [PMID: 26672344]
  • Yan-ping Chen, Dao-peng Tan, Qi Zeng, Yu Wang, Qi-xin Yan, Ling-jie Zeng. [Chemical Constituents from Leaves of Acanthus ilicifolius and Their Anti-influenza Virus Activities]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Mar; 38(3):527-30. doi: . [PMID: 26495655]
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