Search Results - "Thanigaimalai, P."

Structural requirement(s) of N-phenylthioureas and benzaldehyde thiosemicarbazones as inhibitors of melanogenesis in melanoma B 16 cells by Thanigaimalai, P., Le Hoang, Tuan Anh, Lee, Ki-Cheul, Bang, Seong-Cheol, Sharma, Vinay K., Yun, Cheong-Yong, Roh, Eunmiri, Hwang, Bang-Yeon, Kim, Youngsoo, Jung, Sang-Hun

“…To define the structural requirement of phenylthiourea, a series of thiourea and thiosemicarbazone analogs were prepared and evaluated as inhibitors of…”
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Inhibitory effect of novel tetrahydropyrimidine-2(1 H)-thiones on melanogenesis by Thanigaimalai, P., Lee, Ki-Cheul, Bang, Seong-Cheol, Lee, Jee-Hyun, Yun, Cheong-Yong, Roh, Eunmiri, Hwang, Bang-Yeon, Kim, Youngsoo, Jung, Sang-Hun

“…The series of imidazoldine-2-thiones 2 and tetrahydropyrimidine-2-thiones 3 were discovered as inhibitor of α-MSH-induced melanin production in melanoma B16…”
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Evaluation of 3,4-dihydroquinazoline-2(1H)-thiones as inhibitors of α-MSH-induced melanin production in melanoma B16 cells by Thanigaimalai, P., Lee, Ki-Cheul, Bang, Seong-Cheol, Lee, Jee-Hyun, Yun, Cheong-Yong, Roh, Eunmiri, Hwang, Bang-Yeon, Kim, Youngsoo, Jung, Sang-Hun

“…Novel 3,4-dihydroquinazoline-2(1H)-thiones (QNTs) 1 were found to be potent inhibitors of α-MSH-induced melanin production. The effect of QNTs to inhibit…”
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The scope of thallium nitrate oxidative cyclization of chalcones; synthesis and evaluation of isoflavone and aurone analogs for their inhibitory activity against interleukin-5 by Thanigaimalai, P., Yang, Hyun-Mo, Sharma, Vinay Kumar, Kim, Youngsoo, Jung, Sang-Hun

“…The oxidative cyclization of 2′-hydroxy-6′-cyclohexylmethoxychalcones 5 using thallium (III) nitrate (TTN) in alcoholic solvents produced isoflavones 2 and…”
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Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity by Thanigaimalai, P., Lee, Ki-Cheul, Sharma, Vinay K., Yun, Jun-Ho, Kim, Youngsoo, Jung, Sang-Hun

“…A new series of hydroxyalkylaminomethylchromones 3( a– p) were synthesized and demonstrated for their activity against intrerlukin-5. The most active analog 3d…”
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