Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Inkyu Choi"'
Autor:
Heejeong Choi, Il Young Ryu, Inkyu Choi, Sultan Ullah, Hee Jin Jung, Yujin Park, YeJi Hwang, Yeongmu Jeong, Sojeong Hong, Pusoon Chun, Hae Young Chung, Hyung Ryong Moon
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 20, Iss , Pp 899-912 (2022)
As part of our continuous search for novel tyrosinase inhibitors, we designed 5,6-dihydroimindazo[2,1-b]thiazol-3(2H)-one (DHIT) derivatives based on the structure of MHY773; a potent tyrosinase inhibitor with a 2-iminothiazolidin-4-one template. Of
Externí odkaz:
https://doaj.org/article/a5e454fd81fe488cbb1512c293b5c205
Autor:
Inkyu Choi, Yujin Park, Il Young Ryu, Hee Jin Jung, Sultan Ullah, Heejeong Choi, Chaeun Park, Dongwan Kang, Sanggwon Lee, Pusoon Chun, Hae Young Chung, Hyung Ryong Moon
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 19, Iss , Pp 37-50 (2021)
The β-phenyl-α,β-unsaturated carbonyl (PUSC) scaffold confers tyrosinase inhibitory activity, and in the present study, 16 (Z)-5-(substituted benzylidene)-3-phenyl-2-thioxooxazolidin-4-one analogues containing this scaffold were synthesized. Mushr
Externí odkaz:
https://doaj.org/article/89ae3e87421146fd846ffb9e9870e0f5
Autor:
Heejeong Choi, Il Young Ryu, Inkyu Choi, Sultan Ullah, Hee Jin Jung, Yujin Park, Yeongmu Jeong, YeJi Hwang, Sojeong Hong, In-Soo Yoon, Hwayoung Yun, Min-Soo Kim, Jin-Wook Yoo, Yunjin Jung, Pusoon Chun, Hyung Ryong Moon
Publikováno v:
Molecules, Vol 26, Iss 16, p 4963 (2021)
To confirm that the β-phenyl-α,β-unsaturated thiocarbonyl (PUSTC) scaffold, similar to the β-phenyl-α,β-unsaturated carbonyl (PUSC) scaffold, acts as a core inhibitory structure for tyrosinase, twelve (Z)-5-(substituted benzylidene)-4-thioxothi
Externí odkaz:
https://doaj.org/article/81fbfe9f798140849b5c9ab47083a2ed
Autor:
Hee Jin Jung, Dong Chan Choi, Sang Gyun Noh, Heejeong Choi, Inkyu Choi, Il Young Ryu, Hae Young Chung, Hyung Ryong Moon
Publikováno v:
Antioxidants, Vol 10, Iss 7, p 1078 (2021)
Thirteen (Z)-2-(substituted benzylidene)benzimidazothiazolone analogs were synthesized and evaluated for their inhibitory activity against mushroom tyrosinase. Among the compounds synthesized, compounds 1–3 showed greater inhibitory activity than k
Externí odkaz:
https://doaj.org/article/29f2891bd5414372a6bd9152ca867865
Autor:
Sanggwon Lee, Heejeong Choi, Yujin Park, Hee Jin Jung, Sultan Ullah, Inkyu Choi, Dongwan Kang, Chaeun Park, Il Young Ryu, Yeongmu Jeong, YeJi Hwang, Sojeong Hong, Pusoon Chun, Hyung Ryong Moon
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11, p 5616 (2021)
We previously reported (E)-β-phenyl-α,β-unsaturated carbonyl scaffold ((E)-PUSC) played an important role in showing high tyrosinase inhibitory activity and that derivatives with a 4-substituted resorcinol moiety as the β-phenyl group of the scaf
Externí odkaz:
https://doaj.org/article/4fc225a1cfae4f10bc6fdb83b82f3b4b
Publikováno v:
Applied Sciences, Vol 9, Iss 11, p 2302 (2019)
Audio event detection (AED) is a task of recognizing the types of audio events in an audio stream and estimating their temporal positions. AED is typically based on fully supervised approaches, requiring strong labels including both the presence and
Externí odkaz:
https://doaj.org/article/32a8c26516c04ef6ac5ae45c0830268b
Publikováno v:
Applied Sciences, Vol 9, Iss 11, p 2289 (2019)
Most of the recently proposed deep learning-based speech enhancement techniques have focused on designing the neural network architectures as a black box. However, it is often beneficial to understand what kinds of hidden representations the model ha
Externí odkaz:
https://doaj.org/article/9dbad5b4e881499b9ca4b25eeef3ab9b
Publikováno v:
Archives of Design Research. 35:245-261
Publikováno v:
Bulletin of the Korean Chemical Society. 41:1134-1139
Autor:
Heejeong, Choi, Il, Young Ryu, Inkyu, Choi, Sultan, Ullah, Hee, Jin Jung, Yujin, Park, YeJi, Hwang, Yeongmu, Jeong, Sojeong, Hong, Pusoon, Chun, Hae, Young Chung, Hyung, Ryong Moon
Publikováno v:
Computational and structural biotechnology journal. 20
As part of our continuous search for novel tyrosinase inhibitors, we designed 5,6-dihydroimindazo[2,1