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Items: 1 to 20 of 100

1.

A natural inhibitor from Alisma orientale against human carboxylesterase 2: Kinetics, circular dichroism spectroscopic analysis, and docking simulation.

Yi J, Bai R, An Y, Liu TT, Liang JH, Tian XG, Huo XK, Feng L, Ning J, Sun CP, Ma XC, Zhang HL.

Int J Biol Macromol. 2019 Apr 13;133:184-189. doi: 10.1016/j.ijbiomac.2019.04.099. [Epub ahead of print]

PMID:
30991064
2.

A bioactive new protostane-type triterpenoid from Alisma plantago-aquatica subsp. orientale (Sam.) Sam.

Wang YL, Zhao JC, Liang JH, Tian XG, Huo XK, Feng L, Ning J, Wang C, Zhang BJ, Chen G, Li N, Sun CP.

Nat Prod Res. 2019 Mar;33(6):776-781. doi: 10.1080/14786419.2017.1408106. Epub 2017 Nov 28.

PMID:
29183156
3.

Protostane Triterpenoids from the Rhizome of Alisma orientale Exhibit Inhibitory Effects on Human Carboxylesterase 2.

Mai ZP, Zhou K, Ge GB, Wang C, Huo XK, Dong PP, Deng S, Zhang BJ, Zhang HL, Huang SS, Ma XC.

J Nat Prod. 2015 Oct 23;78(10):2372-80. doi: 10.1021/acs.jnatprod.5b00321. Epub 2015 Oct 1.

PMID:
26425784
4.

Alismanin A, a Triterpenoid with a C34 Skeleton from Alisma orientale as a Natural Agonist of Human Pregnane X Receptor.

Wang C, Huo XK, Luan ZL, Cao F, Tian XG, Zhao XY, Sun CP, Feng L, Ning J, Zhang BJ, Ma XC.

Org Lett. 2017 Oct 20;19(20):5645-5648. doi: 10.1021/acs.orglett.7b02738. Epub 2017 Oct 10.

PMID:
29016144
5.

Phytochemical constituents from Uncaria rhynchophylla in human carboxylesterase 2 inhibition: Kinetics and interaction mechanism merged with docking simulations.

Wang YL, Dong PP, Liang JH, Li N, Sun CP, Tian XG, Huo XK, Zhang BJ, Ma XC, Lv CZ.

Phytomedicine. 2018 Dec 1;51:120-127. doi: 10.1016/j.phymed.2018.10.006. Epub 2018 Oct 10.

PMID:
30466609
6.

Two new protostane-type triterpenoids from Alisma orientalis.

Xin XL, Zhao XY, Huo XK, Tian XG, Sun CP, Zhang HL, Tian Y, Liu Y, Wang X.

Nat Prod Res. 2018 Jan;32(2):189-194. doi: 10.1080/14786419.2017.1344660. Epub 2017 Jun 26.

PMID:
28649858
7.

Chemical constituents from Alisma plantago-aquatica subsp. orientale (Sam.) Sam and their anti-inflammatory and antioxidant activities.

Zhao XY, Wang G, Wang Y, Tian XG, Zhao JC, Huo XK, Sun CP, Feng L, Ning J, Wang C, Zhang BJ, Wang X.

Nat Prod Res. 2017 Sep 28:1-7. doi: 10.1080/14786419.2017.1380024. [Epub ahead of print]

PMID:
28954548
8.

A new protostane-type triterpenoid from Alisma plantago-aquatica subsp. orientale (Sam.) Sam.

Li HM, Liu D, Dai WF, Chen XQ, Li RT.

Nat Prod Res. 2018 Nov 14:1-6. doi: 10.1080/14786419.2018.1519710. [Epub ahead of print]

PMID:
30427740
9.

Xylarianins A-D from the endophytic fungus Xylaria sp. SYPF 8246 as natural inhibitors of human carboxylesterase 2.

Zhang J, Liang JH, Zhao JC, Wang YL, Dong PP, Liu XG, Zhang TY, Wu YY, Shang DJ, Zhang YX, Sun CP.

Bioorg Chem. 2018 Dec;81:350-355. doi: 10.1016/j.bioorg.2018.07.019. Epub 2018 Jul 17.

PMID:
30193143
10.

Alisma orientale extract exerts the reversing cholestasis effect by activation of farnesoid X receptor.

Huo XK, Liu J, Yu ZL, Wang YF, Wang C, Tian XG, Ning J, Feng L, Sun CP, Zhang BJ, Ma XC.

Phytomedicine. 2018 Mar 15;42:34-42. doi: 10.1016/j.phymed.2018.03.017. Epub 2018 Mar 8.

PMID:
29655695
11.

Protostane-Type Triterpenoids from Alisma orientale.

Li HM, Chen XJ, Luo D, Fan M, Zhang ZJ, Peng LY, Wu XD, Li RT, Ji X, Zhao QS.

Chem Biodivers. 2017 Dec;14(12). doi: 10.1002/cbdv.201700452.

PMID:
29139211
12.

Alisma orientale: Ethnopharmacology, Phytochemistry and Pharmacology of an Important Traditional Chinese Medicine.

Shu Z, Pu J, Chen L, Zhang Y, Rahman K, Qin L, Zheng C.

Am J Chin Med. 2016;44(2):227-51. doi: 10.1142/S0192415X16500142. Review.

PMID:
27080939
13.

Characterization and function of the 3-hydroxy-3-methylglutaryl-CoA reductase gene in Alisma orientale (Sam.) Juz. and its relationship with protostane triterpene production.

Gu W, Geng C, Xue W, Wu Q, Chao J, Xu F, Sun H, Jiang L, Han Y, Zhang S.

Plant Physiol Biochem. 2015 Dec;97:378-89. doi: 10.1016/j.plaphy.2015.10.031. Epub 2015 Oct 29.

PMID:
26546781
14.

Alisol B 23-acetate from the rhizomes of Alisma orientale is a natural agonist of the human pregnane X receptor.

Kanno Y, Yatsu T, Yamashita N, Zhao S, Li W, Imai M, Kashima M, Inouye Y, Nemoto K, Koike K.

Phytomedicine. 2017 Mar 15;26:22-27. doi: 10.1016/j.phymed.2017.01.003. Epub 2017 Jan 9.

PMID:
28257661
15.

A new triterpenoid from Alisma orientale and their antibacterial effect.

Jin HG, Jin Q, Ryun Kim A, Choi H, Lee JH, Kim YS, Lee DG, Woo ER.

Arch Pharm Res. 2012 Nov;35(11):1919-26. doi: 10.1007/s12272-012-1108-5. Epub 2012 Dec 4.

PMID:
23212633
16.

Structures and biological activities of the triterpenoids and sesquiterpenoids from Alisma orientale.

Ma Q, Han L, Bi X, Wang X, Mu Y, Guan P, Li L, Huang X.

Phytochemistry. 2016 Nov;131:150-157. doi: 10.1016/j.phytochem.2016.08.015. Epub 2016 Sep 9.

PMID:
27615692
17.

Protective Effects of Alisma orientale Extract against Hepatic Steatosis via Inhibition of Endoplasmic Reticulum Stress.

Jang MK, Han YR, Nam JS, Han CW, Kim BJ, Jeong HS, Ha KT, Jung MH.

Int J Mol Sci. 2015 Nov 2;16(11):26151-65. doi: 10.3390/ijms161125944.

18.
19.

Alisolide, alisols O and P from the rhizome of Alisma orientale.

Zhao M, Xu LJ, Che CT.

Phytochemistry. 2008 Jan;69(2):527-32. Epub 2007 Jul 26.

PMID:
17662315
20.

[Prokaryotic expression, functional identification of squalene synthase in Alisma orientale and its immunoassay study].

Liu QZ, Gu W, Wu QN, Chao JG, Sang XH, Liu Q, Wang XH.

Zhongguo Zhong Yao Za Zhi. 2017 Oct;42(19):3733-3738. doi: 10.19540/j.cnki.cjcmm.2017.0149. Chinese.

PMID:
29235288

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