Jiang Du

Jiang Du


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 May 2018 in Molecules
Verified
Journal Article
Open access
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KHKang He
Kang He
JWJinxi Wang
Jinxi Wang
JZJuan Zou
Juan Zou
JWJichun Wu
Jichun Wu
SHShaojie Huo
Shaojie Huo
JDJiang Du
Jiang Du
Three new steroidal alkaloids with an unusual 3α tigloylamide group, named sarchookloides A–C (1–3), were isolated along with four known compounds (4–7) from the roots of Sarcococca hookeriana. Their structures and relative configuration were elucidated on the basis of spectroscopic methods including MS, UV, IR, 1D, and 2D NMR data. The isolated compounds were evaluated for their cytotoxicity against five human cancer cell lines: Hela, A549, MCF-7, SW480, and CEM in vitro. All three amide substituted steroidal alkaloids exhibited significant cytotoxic activities with IC50 values of 1.05–31.83 μM.

20 December 2018 in Molecules
Verified
Journal Article
Open access
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SHShaojie Huo
Shaojie Huo
JWJichun Wu
Jichun Wu
XHXicheng He
Xicheng He
LPLutai Pan
Lutai Pan
JDJiang Du
Jiang Du
Two new steroidal alkaloids, named hookerianine A (1) and hookerianine B (2) were isolated from the stems and roots of Sarcococca hookeriana Baill., along with two known compounds, sarcorucinine G (3) and epipachysamine D (4). On the basis of spectroscopic methods and by comparison with literature data, their structures were determined. As well as X-ray crystallography was performed to confirm compound 4. To identify novel antitumor inhibitors, all compounds were performed a CCK-8 assay against five human cancer cell lines SW480, SMMC-7721, PC3, MCF-7 and K562 in vitro. Compound 2 exhibited moderate cytotoxic activities to all cell lines with IC50 values in the range of 5.97–19.44 μM. Compound 3 was the most effective one against SW480 and K562 cell lines with IC50 values of 5.77 and 6.29 μM, respectively.

1 March 2010 in Journal of Asian Natural Products Research
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Journal Article
Closed access
KHKang He
Kang He
JDJiang Du
Jiang Du
Two new steroidal alkaloids, 20α-dimethylamino-2α-hydroxyl-3β-tigloylamino-5α-pregnane (1) and Δ16-20α-dimethylamino-3β,4α-diol-5α-pregnane (2), along with five known alkaloids, sarcovagine D (3), pachysamine G (4), pachysamine H (5), pachysamine A (6), and terminaline (20S)-20-(N,N-dimethylamino)-5α-pregn-3β,4α-diol (7), were isolated from the roots of Sarcococca ruscifolia. Their structures were elucidated on the basis of NMR and MS data, and the relative stereochemistry of 1 was finally determined by X-ray crystallographic analysis.

1 October 2013 in Zeitschrift für Kristallographie - New Crystal Structures
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Journal Article
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KHKang He
Kang He
JZJuan Zou
Juan Zou
JWJin Xi Wang
Jin Xi Wang
JDJiang Du
Jiang Du
C29H45Cl2N2O2, monoclinic, P21 (no. 4), a = 8.4429(4) Å, b = 19.6901(9) Å, c = 9.0259(4) Å, β = 100.700(2)°, V = 1474.4 Å3, Z = 2, Rgt(F) = 0.0492, wRref(F2) = 0.1437, T = 293 K.