B Z Ahn

Summary

Country: Korea

Publications

  1. ncbi Inhibitory effect of bupleuri radix saponins on adhesion of some solid tumor cells and relation to hemolytic action: screening of 232 herbal drugs for anti-cell adhesion
    B Z Ahn
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Planta Med 64:220-4. 1998
  2. ncbi Naphthazarin derivatives (VII): antitumor action against ICR mice bearing ascitic S-180 cells
    G Y Song
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Arch Pharm Res 24:35-8. 2001
  3. ncbi Syntheses of certain 3-aryl-2-propenoates and evaluation of their cytotoxicity
    N H Nam
    College of Pharmacy, Chungnam National University, Taejon, South Korea
    Bioorg Med Chem Lett 11:1173-6. 2001
  4. ncbi Naphthazarin derivatives (VII): antitumor action against ICR mice bearing ascitic S-180 cells
    G Y Song
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Arch Pharm Res 24:190-3. 2001
  5. ncbi Naphthazarin derivatives (VIII): Synthesis, inhibitory effect on DNA topoisomerase-I, and antiproliferative activity of 6-(1-acyloxyalkyl)-5,8-dimethoxy-1,4-naphthoquinones
    Y Kim
    College of Pharmacy, Chungnam National University, Taejon 305-764, Korea
    Arch Pharm (Weinheim) 334:318-22. 2001
  6. ncbi Combretoxazolones: synthesis, cytotoxicity and antitumor activity
    N H Nam
    College of Pharmacy, Chungnam National University, Taejon 305-764, Republic of Korea
    Bioorg Med Chem Lett 11:3073-6. 2001

Collaborators

  • H M Kim
  • Y Kim
  • Y J You
  • N H Nam
  • G Y Song
  • H Cho
  • D H Hong

Detail Information

Publications6

  1. ncbi Inhibitory effect of bupleuri radix saponins on adhesion of some solid tumor cells and relation to hemolytic action: screening of 232 herbal drugs for anti-cell adhesion
    B Z Ahn
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Planta Med 64:220-4. 1998
    ..Taken together, it is suggested that the mechanism for anti-cell adhesive activity of saikosaponin may resemble that for their hemolytic action...
  2. ncbi Naphthazarin derivatives (VII): antitumor action against ICR mice bearing ascitic S-180 cells
    G Y Song
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Arch Pharm Res 24:35-8. 2001
    ..Some of 6-(1-propyloxyalkyl)-DMNQ derivatives with an alkyl group of butyl to octyl moiety showed T/C values of >400%..
  3. ncbi Syntheses of certain 3-aryl-2-propenoates and evaluation of their cytotoxicity
    N H Nam
    College of Pharmacy, Chungnam National University, Taejon, South Korea
    Bioorg Med Chem Lett 11:1173-6. 2001
    ..It was found that the ortho- or para-dihydroxy funtionality on the aryl ring was essential for the cytotoxicity of cinnamates. Compounds 8ba, 8bb and 9aa, 9ab showed potent cytotoxicity against various tumor cell lines...
  4. ncbi Naphthazarin derivatives (VII): antitumor action against ICR mice bearing ascitic S-180 cells
    G Y Song
    College of Pharmacy, Chungnam National University, Taejon, Korea
    Arch Pharm Res 24:190-3. 2001
    ..Some of 6-(1-propyloxyalkyl)-DMNQ derivatives with an alkyl group of butyl to octyl moiety showed T/C values of >400%...
  5. ncbi Naphthazarin derivatives (VIII): Synthesis, inhibitory effect on DNA topoisomerase-I, and antiproliferative activity of 6-(1-acyloxyalkyl)-5,8-dimethoxy-1,4-naphthoquinones
    Y Kim
    College of Pharmacy, Chungnam National University, Taejon 305-764, Korea
    Arch Pharm (Weinheim) 334:318-22. 2001
    ..It is noteworthy that 6-(1-heptanoyloxyethyl)-DMNQ exhibited both the most potent Topo I inhibitory activity (IC50, 11.5 microM) and the greatest antiproliferative activity (ED50, 0.05 microM) upon L1210 cells...
  6. ncbi Combretoxazolones: synthesis, cytotoxicity and antitumor activity
    N H Nam
    College of Pharmacy, Chungnam National University, Taejon 305-764, Republic of Korea
    Bioorg Med Chem Lett 11:3073-6. 2001
    ..Compound 6g exhibited a significant antitumor activity in BDF1 mice bearing B16 murine melanoma cells with inhibition rates of 67 and 61% at 100 and 30 mg/kg/day, respectively...