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Items: 1 to 20 of 48

1.

Bioactive triterpenoid saponins from the tubers of Hemsleya amabilis Diels.

Jin Y, Zhou X, Yang J, Xu X, Zhang J, Ma G.

Fitoterapia. 2019 Nov;139:104404. doi: 10.1016/j.fitote.2019.104404. Epub 2019 Oct 30.

PMID:
31676394
2.

Polyhydroxy cucurbitane triterpenes from Hemsleya penxianensis tubers.

Sun Z, Hu M, Zhu N, Huo X, Zhou X, Sun Z, Yang J, Ma G, Xu X.

Sci Rep. 2019 Aug 14;9(1):11835. doi: 10.1038/s41598-019-48365-0.

3.

New naphtoquinones derivatives from the edible bulbs of Eleutherine americana and their protective effect on the injury of human umbilical vein endothelial cells.

Chen D, Qiao J, Sun Z, Liu Y, Sun Z, Zhu N, Xu X, Yang J, Ma G.

Fitoterapia. 2019 Jan;132:46-52. doi: 10.1016/j.fitote.2018.11.009. Epub 2018 Nov 26.

PMID:
30496808
4.

Quantitative Evaluation of Twelve Major Components of Sulfur-Fumigated Astragali Radix with Different Durations by UPLC-MS.

Xing X, Sun Z, Yang M, Zhu N, Yang J, Ma G, Xu X.

Molecules. 2018 Oct 11;23(10). pii: E2609. doi: 10.3390/molecules23102609.

5.

Pyrrole Alkaloids from the Edible Mushroom Phlebopus portentosus with Their Bioactive Activities.

Sun Z, Hu M, Sun Z, Zhu N, Yang J, Ma G, Xu X.

Molecules. 2018 May 17;23(5). pii: E1198. doi: 10.3390/molecules23051198.

6.

Cucurbitane-type triterpenes from the tubers of Hemsleya penxianensis and their bioactive activity.

Zhu N, Sun Z, Hu M, Li Y, Zhang D, Wu H, Tian Y, Li P, Yang J, Ma G, Xu X.

Phytochemistry. 2018 Mar;147:49-56. doi: 10.1016/j.phytochem.2017.12.014. Epub 2017 Dec 26.

PMID:
29287258
7.

Congmujingnosides B-G, triterpene saponins from the stem of Aralia chinensis and their protective effects against H2O2-induced myocardial cell injury.

Zhang W, Zhu N, Hu M, Yu S, Sun Z, Wu H, Li P, Yang J, Ma G, Xu X.

Nat Prod Res. 2019 Feb;33(4):500-505. doi: 10.1080/14786419.2017.1399384. Epub 2017 Nov 8.

PMID:
29115145
8.

New cucurbitane triterpenoids with cytotoxic activities from Hemsleya penxianensis.

Li P, Zhu N, Hu M, Wu H, Yu T, Wu T, Zhang D, Sun Z, Yang J, Ma G, Xu X.

Fitoterapia. 2017 Jul;120:158-163. doi: 10.1016/j.fitote.2017.06.009. Epub 2017 Jun 15.

PMID:
28625732
9.

Iterative ensemble feature selection for multiclass classification of imbalanced microarray data.

Yang J, Zhou J, Zhu Z, Ma X, Ji Z.

J Biol Res (Thessalon). 2016 Jul 4;23(Suppl 1):13. doi: 10.1186/s40709-016-0045-8. eCollection 2016 May.

10.

Cassane diterpenes with oxygen bridge from the seeds of Caesalpinia sappan.

Xu X, Yuan J, Zhou X, Li W, Zhu N, Wu H, Li P, Sun Z, Yang J, Ma G.

Fitoterapia. 2016 Jul;112:205-10. doi: 10.1016/j.fitote.2016.06.005. Epub 2016 Jun 14.

PMID:
27316975
11.

Role of Bai-Shao towards the antidepressant effect of Chaihu-Shu-Gan-San using metabonomics integrated with chemical fingerprinting.

Chang X, Jia H, Zhou C, Zhang H, Yu M, Yang J, Zou Z.

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Dec 1;1006:16-29. doi: 10.1016/j.jchromb.2015.10.007. Epub 2015 Oct 20.

PMID:
26540435
12.

Antimalarial and Antiproliferative Cassane Diterpenes of Caesalpinia sappan.

Ma G, Wu H, Chen D, Zhu N, Zhu Y, Sun Z, Li P, Yang J, Yuan J, Xu X.

J Nat Prod. 2015 Oct 23;78(10):2364-71. doi: 10.1021/acs.jnatprod.5b00317. Epub 2015 Sep 23.

PMID:
26398312
13.

Aphanamixins A-F, acyclic diterpenoids from the stem bark of Aphanamixis polystachya.

Zhang X, Tan Y, Li Y, Jin L, Wei N, Wu H, Ma G, Zheng Q, Tian Y, Yang J, Zhang J, Xu X.

Chem Pharm Bull (Tokyo). 2014;62(5):494-8.

14.

Antimalarial diterpene alkaloids from the seeds of Caesalpinia minax.

Ma G, Sun Z, Sun Z, Yuan J, Wei H, Yang J, Wu H, Xu X.

Fitoterapia. 2014 Jun;95:234-9. doi: 10.1016/j.fitote.2014.04.001. Epub 2014 Apr 13.

PMID:
24727083
15.

Daphniphyllum alkaloids: recent findings on chemistry and pharmacology.

Wu H, Zhang X, Ding L, Chen S, Yang J, Xu X.

Planta Med. 2013 Nov;79(17):1589-98. doi: 10.1055/s-0033-1351024. Epub 2013 Nov 8. Review.

16.

Three new phenolics and other constituents from the seeds of Lithocarpus pachylepis.

Xie Y, Ma G, Wei H, Yuan J, Wu H, Zhou X, Yang J, Xu X.

Molecules. 2013 Aug 28;18(9):10397-403. doi: 10.3390/molecules180910397.

17.

Triterpene saponins from Tabellae Clinopodii.

Wang S, Ma G, Zhong M, Yu S, Xu X, Hu Y, Zhang Y, Wei H, Yang J.

Fitoterapia. 2013 Oct;90:14-9. doi: 10.1016/j.fitote.2013.06.014. Epub 2013 Jun 27.

PMID:
23811431
18.

Caesalpins A-H, bioactive cassane-type diterpenes from the seeds of Caesalpinia minax.

Ma G, Yuan J, Wu H, Cao L, Zhang X, Xu L, Wei H, Wu L, Zheng Q, Li L, Zhang L, Yang J, Xu X.

J Nat Prod. 2013 Jun 28;76(6):1025-31. doi: 10.1021/np300918q. Epub 2013 Jun 12.

PMID:
23806110
19.

Two new triterpenoid saponins from the root of Platycodon grandiflorum.

Ma G, Guo W, Zhao L, Zheng Q, Sun Z, Wei J, Yang J, Xu X.

Chem Pharm Bull (Tokyo). 2013;61(1):101-4.

20.

Clerodendranoic acid, a new phenolic acid from Clerodendranthus spicatus.

Zheng Q, Sun Z, Zhang X, Yuan J, Wu H, Yang J, Xu X.

Molecules. 2012 Nov 19;17(11):13656-61. doi: 10.3390/molecules171113656.

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