Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Hyoungsu Kim"'
Autor:
Jung Hee Kim, Sung-Eun Kim, Do Seon Song, Hee Yeon Kim, Eileen L. Yoon, Seong Hee Kang, Young-Kul Jung, Jung Hyun Kwon, Sung Won Lee, Seul Ki Han, Young Chang, Soung Won Jeong, Jeong Ju Yoo, Young-Joo Jin, Gab Jin Cheon, Byung Seok Kim, Yeon Seok Seo, Hyoungsu Kim, Ji Won Park, Tae Hyung Kim, Dong Hyun Sinn, Woo Jin Chung, Hwi Young Kim, Han Ah Lee, Seung Woo Nam, In Hee Kim, Ji Hoon Kim, Hee Bok Chae, Joo Hyun Sohn, Ju Yeon Cho, Jung Gil Park, Hyun Chin Cho, Yoon Jun Kim, Jin Mo Yang, Ki Tae Suk, Moon Young Kim, Sang Gyune Kim, Hyung Joon Yim, Won Kim, Jae-Young Jang, Dong Joon Kim
Publikováno v:
Diagnostics, Vol 14, Iss 1, p 14 (2023)
Background: The European Foundation for the Study of Chronic Liver Failure (EF-CLIF) consortium suggested that the clinical courses after acute decompensation (AD) stratify the long-term prognosis: stable decompensated cirrhosis (SDC), unstable decom
Externí odkaz:
https://doaj.org/article/42f2b0029cd74f80a04dbbd01f01683d
Autor:
Saroj Kumar Shrestha, Kyung Hyun Min, Se Woong Kim, Hyoungsu Kim, William H. Gerwick, Yunjo Soh
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1207 (2023)
Bone metastasis resulting from advanced breast cancer causes osteolysis and increases mortality in patients. Kalkitoxin (KT), a lipopeptide toxin derived from the marine cyanobacterium Moorena producens (previously Lyngbya majuscula), has an anti-met
Externí odkaz:
https://doaj.org/article/c62f2c8197834b8d86412dce6bc4acbc
Publikováno v:
Pharmaceutics, Vol 14, Iss 12, p 2684 (2022)
Tofacitinib, a Janus kinase 1 and 3 inhibitor, is used to treat rheumatoid arthritis. It is mainly metabolized by the cytochromes p450 (CYP) 3A1/2 and CYP2C11 in the liver. Chronic inflammation eventually leads to cirrhosis in patients with rheumatoi
Externí odkaz:
https://doaj.org/article/fe33308a8e25453a8c041e668fe8419d
Autor:
Seungchan An, Hyejin Ko, Hongjun Jang, In Guk Park, Sungjin Ahn, Seok Young Hwang, Junpyo Gong, Soyeon Oh, Soo Yeon Kwak, Yeonjin Lee, Hyoungsu Kim, Minsoo Noh
Publikováno v:
ACS Medicinal Chemistry Letters. 14:425-431
Autor:
Iljin Shin, Hongjun Jang, Soo Yeon Kwak, Youngjik Park, Dongjoo Lee, Hyoungsu Kim, Deukjoon Kim
Publikováno v:
Organic Letters. 24:8780-8785
Autor:
Hyejin Ko, Seungchan An, Hongjun Jang, Sungjin Ahn, In Guk Park, Seok Young Hwang, Junpyo Gong, Soyeon Oh, Soo Yeon Kwak, Won Jun Choi, Hyoungsu Kim, Minsoo Noh
Publikováno v:
Biomolecules & Therapeutics. 31:312-318
The natural flavonoid macakurzin C (
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
A highly efficient metal-free oxidative direct C(sp3)–H functionalization of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) with a wide range of electron-rich nucleophiles was accomplished under mild conditions through oxidation with DDQ a
Externí odkaz:
https://doaj.org/article/70cc5abbf3c84c5bbd477556cfb1480c
Autor:
Seong-Ryeol Kim, Myeong-Seon Jeong, Seo-Hyeon Mun, Jaewon Cho, Min-Duk Seo, Hyoungsu Kim, Jooeun Lee, Jae-Hyoung Song, Hyun-Jeong Ko
Publikováno v:
Viruses, Vol 13, Iss 7, p 1350 (2021)
Influenza viruses cause respiratory infections in humans and animals, which have high morbidity and mortality rates. Although several drugs that inhibit viral neuraminidase are used to treat influenza infections, the emergence of resistant viruses ne
Externí odkaz:
https://doaj.org/article/9f5070b4dfe14733b9db8988ad40cf36
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2303 (2021)
Osteoclasts, bone-specified multinucleated cells produced by monocyte/macrophage, are involved in numerous bone destructive diseases such as arthritis, osteoporosis, and inflammation-induced bone loss. The osteoclast differentiation mechanism suggest
Externí odkaz:
https://doaj.org/article/f5bf4d072ca5493ba1441ceae3de2d6d
Autor:
Thien Nhan Lu, Minjung Kwak, Mallesham Samala, Minji Son, Jungjoong Hwang, Suresh Mandava, Thuy Trang Pham, Haeil Park, Hyoungsu Kim, Deukjoon Kim, Jongkook Lee
Publikováno v:
Organic Letters. 24:1652-1656
A highly stereoselective asymmetric total synthesis of (-)-jimenezin (