Ki-Cheul Lee

发表

Structure--activity relationship studies of novel arylsulfonylimidazolidinones for their anticancer activity.

Hwan-Mook Kim, V. Sharma, J. Kang, 2011, European journal of medicinal chemistry.

Synthesis of Water Soluble Analogues of Arylsulfonylimidazolidinone (JSH-2282).

V. Sharma, Niti Sharma, Sang-hun Jung, 2013 .

Importance of Imidazolidinone Motif in 4-Phenyl-N-arylsulfonylimidazolidinone for their Anticancer Activity

V. Sharma, Niti Sharma, Sang-hun Jung, 2011 .

Effect of the isosteric replacement of the phenyl motif with furyl (or thienyl) of 4-phenyl-N-arylsulfonylimidazolones as broad and potent anticancer agents

V. Sharma, J. Kang, Sang-hun Jung, 2011 .

Synthesis and evaluation of novel chromone analogs for their inhibitory activity against interleukin-5.

Youngsoo Kim, V. Sharma, Sang-hun Jung, 2010, European journal of medicinal chemistry.

A convenient preparation of a disaccharide motif and its role in the cytotoxicity of the triterpenoid saponin, α-hederin

Sang-hun Jung, Ki-Cheul Lee, Hye-Rim Shin, 2008, Archives of pharmacal research.

Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity.

Youngsoo Kim, V. Sharma, Sang-hun Jung, 2010, Bioorganic & medicinal chemistry.

Structure-activity relationship of naphthaldehydethiosemicarbazones in melanogenesis inhibition.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2012, Bioorganic & medicinal chemistry letters.

Refinement of the pharmacophore of 3,4-dihydroquinazoline-2(1H)-thiones for their anti-melanogenesis activity.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2010, Bioorganic & medicinal chemistry letters.

Evaluation of 3,4-dihydroquinazoline-2(1H)-thiones as inhibitors of alpha-MSH-induced melanin production in melanoma B16 cells.

Sang-Hun Jung, Seong-Cheol Bang, Jee-Hyun Lee, 2010, Bioorganic & medicinal chemistry.

Structural requirement(s) of N-phenylthioureas and benzaldehyde thiosemicarbazones as inhibitors of melanogenesis in melanoma B 16 cells.

Sang-Hun Jung, Seong-Cheol Bang, B. Hwang, 2010, Bioorganic & medicinal chemistry letters.

Novel benzo[d]imidazole-2(3H)-thiones as potent inhibitors of the alpha-melanocyte stimulating hormone induced melanogenesis in melanoma B16 cells.

Sang-Hun Jung, Seong-Cheol Bang, Jee-Hyun Lee, 2010, Chemical & pharmaceutical bulletin.

Inhibitory effect of novel tetrahydropyrimidine-2(1H)-thiones on melanogenesis.

Sang-Hun Jung, Seong-Cheol Bang, Jee-Hyun Lee, 2010, Bioorganic & medicinal chemistry.

Design and synthesis of novel chromenone derivatives as interleukin-5 inhibitors.

Youngsoo Kim, V. Sharma, Sang-hun Jung, 2013, Bioorganic & medicinal chemistry.

Identification of novel chromenone derivatives as interleukin-5 inhibitors.

Youngsoo Kim, V. Sharma, Sang-hun Jung, 2013, European journal of medicinal chemistry.

Novel interleukin-5 inhibitors based on hydroxyethylaminomethyl-4H-chromen-4-one scaffold.

Youngsoo Kim, V. Sharma, Sang-hun Jung, 2012, Bioorganic & medicinal chemistry.

Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2011, Bioorganic & medicinal chemistry letters.

Structural requirements of (E)-6-benzylidene-4a-methyl-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one derivatives as novel melanogenesis inhibitors.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2011, Bioorganic & medicinal chemistry letters.

Identification of indoline-2-thione analogs as novel potent inhibitors of α-melanocyte stimulating hormone induced melanogenesis.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2011, Chemical & pharmaceutical bulletin.

Structural characteristics of thiosemicarbazones as inhibitors of melanogenesis.

Sang-Hun Jung, B. Hwang, Youngsoo Kim, 2010, Bioorganic & medicinal chemistry letters.

Ketonethiosemicarbazones: structure-activity relationships for their melanogenesis inhibition.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2011, Bioorganic & medicinal chemistry letters.

Study on anti-proliferative effect of benzoxathiole derivatives through inactivation of NF-κB in human cancer cells.

Youngsoo Kim, V. Sharma, Niti Sharma, 2012, Bioorganic & Medicinal Chemistry Letters.

Structure-activity relationship study of arylsulfonylimidazolidinones as anticancer agents.

V. Sharma, Niti Sharma, Sang-hun Jung, 2011, Bioorganic & medicinal chemistry letters.

Evaluation of anticancer activity of 4-vinyl-1-arylsulfonylimidazolidinones

Sang-hun Jung, Ki-Cheul Lee, Hye-Rim Shin, 2006, Archives of pharmacal research.

Investigation of amino acid conjugates of (S)-1-[1-(4-aminobenzoyl)-2,3-dihydro-1H-indol-6-sulfonyl]-4-phenyl-imidazolidin-2-one (DW2282) as water soluble anticancer prodrugs.

V. Sharma, Sang-hun Jung, Ki-Cheul Lee, 2014, European journal of medicinal chemistry.

A SAR study on a series of synthetic lipophilic chalcones as inhibitor of transcription factor NF-κB.

Youngsoo Kim, V. Sharma, Niti Sharma, 2012, European journal of medicinal chemistry.

A convenient preparation of a disaccharide motif and its role in the cytotoxicity of the triterpenoid saponin, α-hederin

Sang-hun Jung, Ki-Cheul Lee, Hye-Rim Shin, 2008, Archives of pharmacal research.