Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cui-Qing Pang"'
Autor:
Mizuho Yonezawa, Tsutomu Inokuchi, Junzo Nokami, Ming-qi Wang, Cui-Qing Pang, Yu Zhang, Ning Wang, Kento Imai
Publikováno v:
Bulletin of the Chemical Society of Japan. 86:864-869
The treatment of 6-chloroindolo[3,2-c]quinoline 6 with NaH–MeI led to methylation at N-11, forming 8, while the reaction of 6 with MeI with heating gave the corresponding 5-methylated quinolinium s...
Autor:
Wei Peng, Marta Świtalska, Cui-Qing Pang, Zhen-Wu Mei, Yoshiki Edazawa, Joanna Wietrzyk, Tsutomu Inokuchi, Ibrahim El-Sayed, Li Wang
Publikováno v:
European Journal of Medicinal Chemistry. 58:441-451
To search for new biological activities of the chromeno[2,3-b]indoles, the 5-oxa analog of the indolo[2,3-b]quinolines that are known to have a potent antitumor activity, a series of 11-amino derivatives with various substituents at the C-2 position
Autor:
Tsutomu Inokuchi, Kento Imai, Ming-qi Wang, Cui-Qing Pang, Ning Wang, Mizuho Yonezawa, Yu Zhang, Junzo Nokami
Publikováno v:
ChemInform. 45
The treatment of 6-chloroindolo[3,2-c]quinoline 6 with NaH–MeI led to methylation at N-11, forming 8, while the reaction of 6 with MeI with heating gave the corresponding 5-methylated quinolinium s...
Synthesis and in vitro cytotoxic effect of 6-amino-substituted 11H- and 11Me-indolo[3,2-c]quinolines
Autor:
Marta Świtalska, Cui-Qing Pang, Kento Imai, Ning Wang, Tran Anh Ngoc, Ming-Yu Wu, Joanna Wietrzyk, Li Wang, Tsutomu Inokuchi
Publikováno v:
European journal of medicinal chemistry. 78
A series of 6-amino-11H- indolo[3,2-c]quinoline derivatives with various substituents on the quinoline ring were synthesized. A methyl group introduced to N-11 of the intermediate 4 to elaborate novel analog 7. The cytotoxic effect of these 6-amino-s
Autor:
Cui-Qing Pang, Tsukasa Maeda, Wei Peng, Marcel Kaiser, Ibrahim El Tantawy El Sayed, Zhen-Wu Mei, Tsutomu Inokuchi, Wen-Jie Lu, Li Wang
Publikováno v:
Journal of medicinal chemistry. 56(4)
To obtain a high antimalarial activity with neocryptolepine derivatives, modifying and changing the side chains at the C11 position with varying the substituents of an electron-withdrawing or electron-donating nature at the C2 position for a SAR stud