Wen-Chuan Chen’s research while affiliated with National Taiwan University and other places

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Publications (3)


An Improved Oxidative Cleavage Method for Large Scale Preparation of Some Acid‐Labile Aglycones from Glycosides
  • Article

February 2002

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24 Reads

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13 Citations

Journal- Chinese Chemical Society Taipei

Perng‐Haur Wang

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Sheng‐Jye Jou

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Wen‐Chuan Chen

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AbstractA practical method for large‐scale preparation of acid‐labile aglycones including protopanaxadiol, protopanaxatriol, cycloastragenol, and jujubogenin from the corresponding glycoside containing fraction was developed. The key point of this improved method is to generate and maintain the critical reaction conditions, anhydrous and strongly basic, in situ. This effort over comes the weakness of the reported method for oxidative cleavage of glycones and scales up the preparation of these acid‐labile aglycones for further studies.


New Jujubogenin Glycosides from Colubrina asiatica

December 2000

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60 Reads

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11 Citations

Journal of Natural Products

Three new jujubogenin glycosides, namely, 3' '-O-acetylcolubrin (1); 3' ',2' "-O-diacetylcolubrin (2), and 3' '-O-acetyl-6' '-O-trans-crotonylcolubrin (3), were isolated from the leaves of Colubrina asiatica, in addition to the known colubrin, rutin, and kaempferol 3-O-rutinoside. Compounds 1-3 were isolated and purified via a combination of chromatographic procedures, and determined structurally using spectroscopic methods.


Preparation and Cytotoxic Effect of Ceanothic Acid Derivatives

October 1998

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29 Reads

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27 Citations

Journal of Natural Products

Six ceanothane and 1-norceanothane derivatives (1, 2, 8−11) were prepared from ceanothic acid dibenzyl ester. These ring-A homologues of betulinic acid exhibited cytotoxic effects. Among these, 1-decarboxy-3-oxo-ceanothic acid (2) was found to be the most cytotoxic against OVCAR-3 and HeLa cancer cell lines, with an IC50 of 2.8 and 6.6 μg/mL, respectively, and an IC50 of 11.3 μg/mL against normal cell line FS-5.

Citations (3)


... Synthesis of CAG CAG (Registry No. 84605-18-5; fig. 1 a) is a natural saponin of the Astragalus species found in small amounts [31,32] . CAG used in the present study was synthesized by acid hydrolysis of its glycoside astragaloside IV (Sigma-Aldrich, USA) as described previously [33] . The identity of CAG was determined and confirmed by 1 H-NMR, 13 C-NMR, and mass spectrometry. ...

Reference:

Cycloastragenol Is a Potent Telomerase Activator in Neuronal Cells: Implications for Depression Management
An Improved Oxidative Cleavage Method for Large Scale Preparation of Some Acid‐Labile Aglycones from Glycosides
  • Citing Article
  • February 2002

Journal- Chinese Chemical Society Taipei

... In treatment of cancer [64] 1-O-Galloylpedunculagin Antioxidant activity [65,66] ( +)-cis-5,6-Dihydro-5-hydroxy4-methoxy-6-(2-phenylethyl)-2H-pyran-2-on A triterpenoid, pharmacological activity not know yet Ellagic acid It affects lipid metabolism by promoting cholesterol efflux and decreasing LDL uptake, while also possessing antioxidant, liver-protective, antisteatotic, anticholestatic, antifibrogenic, antihepatocarcinogenic, and antiviral activity [31] Ganoderic acid C Anti-inflammatory (inhibition of TNF α) activity [35,36,67] Ceanothic acid Anticancer and antimicrobial activity [68,69] Asiatic acid Antioxidant, anti-inflammatory and antihyperlipidemia activity [37,70] Azukisapogenol Antibacterial and antifungal activity [71] Liquiritic acid Atheroprotective, anti-inflammatory activity [72,73] (3beta,19alpha)-3,19,23,24-Tetrahydroxy-12-oleanen-28-oic acid A terpenoid showing similar chemical structure to arjunic acid and arjunin acid whose pharmacological activity is not known yet Considering two independent factors concentration of polymer PVPK30 (1,1.5, and 2%) and mixing speed (1000, 1500, and 2000) at three levels each, 9 batches were analyzed using design of experiment software version 6 (Fig. 6). The analysis employed a linear model (Table 3) to examine the correlation between polymer concentration and mixing speed regarding particle size of ACEN. ...

Preparation and Cytotoxic Effect of Ceanothic Acid Derivatives
  • Citing Article
  • October 1998

Journal of Natural Products

... revealed by resonances observed at δ C 165.6 (C-1''), 146.8 (C-3''), 122.9 (C-2''), 51.5 (OMe), and 18.0 (C-4'')[25]. The HMBC correlations observed from H-4 (δ H 5.55, dd, J = 3.2, 1.4 Hz) to C-1'' (δ C 165.6) and from the OMe (δ H 3.20, s) to C-7 (δ C 104.4) evidenced the linkage of the methoxy and the crotonyl groups at C-7 and C-4, respectively. ...

New Jujubogenin Glycosides from Colubrina asiatica
  • Citing Article
  • December 2000

Journal of Natural Products