Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Suresh, Mandava"'
Autor:
Suresh Mandava, Jaun Koo, Jungjoong Hwang, Hari Krishna Nallapaneni, Haeil Park, Jongkook Lee
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
The cross-metathesis (CM) of methallyl halides catalyzed using four different ruthenium-based complexes—Grubbs catalyst, Grubbs second-generation catalyst, Hoveyda-Grubbs second-generation catalyst, and Stewart–Grubbs catalyst—was investigated.
Externí odkaz:
https://doaj.org/article/40d0cd6344c343c997d656c6ca583fdc
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 (
Autor:
Momna Rubab, Ramachandran Chellia, Kandasamy Saravanakumar, Suresh Mandava, Imran Khan, Charles Nkufi Tango, Mohammad Shakhawat Hussain, Eric Banan-Mwine Daliri, Se-Hun Kim, Sudha Rani Ramakrishnan, Myeong-Hyeon Wang, Jongkook Lee, Joong-Ho Kwon, Sangeeta Chandrashekar, Deog-Hwan Oh
Publikováno v:
PLoS ONE, Vol 13, Iss 10, p e0203306 (2018)
This study aimed at investigating the antimicrobial activity of different solvent extracts of Chinese cabbage Brassica rapa subsp. pekinensis (BRARP) and their antioxidant and cytotoxicity properties. Of the different solvents extracts, the chlorofor
Externí odkaz:
https://doaj.org/article/3859021bf220489ebf5160d4f841166a
Autor:
Ramu Sridhar, Perali, Suresh, Mandava, Venu Kumar, Patteti, Seshadri, Kalapati, Venkata Rao, Chunduri
Publikováno v:
In Carbohydrate Research 1 October 2012 360:40-46
Autor:
Suresh Mandava, Kyung Soo So, Sung-Hoon Ahn, Hyun Pyo Kim, Ki Sun Kwon, Jongkook Lee, Myung Ae Bae
Publikováno v:
Biomolecules & Therapeutics. 28:344-353
This study aims to develop new potential therapeutic moracin M prodrugs acting on lung inflammatory disorders. Potential moracin M prodrugs (KW01-KW07) were chemically synthesized to obtain potent orally active derivatives, and their pharmacological
Autor:
Myeong-Hyeon Wang, Elango Jeevithan, Deog-Hwan Oh, Suresh Mandava, Kandasamy Saravanakumar, Jongkook Lee, Ravi Shankar Babu Yelamanchi, Deepthi Mandava, Wu Wenhui, Kandasamy Kathiresan, Ramachandran Chellia
Publikováno v:
Microbial Pathogenesis. 126:19-26
The present study aimed to purify and identify the metabolites from T. atroviride using high-performance liquid chromatography (HPLC) and 1H and 13C nuclear magnetic resonance spectrometer (NMR) followed by analyzing their toxicological, antibacteria
Publikováno v:
Science & Justice. 58:447-454
A new sildenafil analogue was detected during routine screening of dietary supplements suspected to be adulterated with an erectile dysfunction drug(s) using HPLC-DAD. The UV spectrum of this compound was highly similar to that of sildenafil and almo
Autor:
Hari Krishna Nallapaneni, Jungjoong Hwang, Jongkook Lee, Jaun Koo, Suresh Mandava, Haeil Park
Publikováno v:
Frontiers in Chemistry
Frontiers in Chemistry, Vol 8 (2020)
Frontiers in Chemistry, Vol 8 (2020)
The cross-metathesis (CM) of methallyl halides catalyzed using four different ruthenium-based complexes-Grubbs catalyst, Grubbs second-generation catalyst, Hoveyda-Grubbs second-generation catalyst, and Stewart-Grubbs catalyst-was investigated. When
Autor:
Deukjoon Kim, Jungjoong Hwang, Donghoon Kim, Ganganna Bogonda, Mallesham Samala, Haeil Park, Suresh Mandava, Thien Nhan Lu, Jongkook Lee
Publikováno v:
Organic Letters. 20:6398-6402
A stereoselective protection-free asymmetric total synthesis of (+)-chamuvarinin (1), a potent anticancer and antitrypanosomal agent, has been accomplished. The adjacently linked [bis(tetrahydrofuran)]tetrahydropyran (THF-THF-THP) core of this natura
Autor:
Jongkook, Lee, Suresh, Mandava, Sung-Hoon, Ahn, Myung-Ae, Bae, Kyung Soo, So, Ki Sun, Kwon, Hyun Pyo, Kim
Publikováno v:
Biomolecules & Therapeutics
This study aims to develop new potential therapeutic moracin M prodrugs acting on lung inflammatory disorders. Potential moracin M prodrugs (KW01-KW07) were chemically synthesized to obtain potent orally active derivatives, and their pharmacological