Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nirun Sornsongkhram"'
Autor:
Virapong Prachayasittikul, Somsak Ruchirawat, Apilak Worachartcheewan, Ratchanok Pingaew, Nirun Sornsongkhram, Supaluk Prachayasittikul
Publikováno v:
Molecules, Vol 14, Iss 8, Pp 2768-2779 (2009)
This study reports the synthesis of some substituted 5-iodouracils and their bioactivities. Alkylation of 5-iodouracils gave predominately N1-substituted-(R)-5-iodouracil compounds 7a-d (R = n-C4H9, s-C4H9, CH2C6H11, CH2C6H5) together with N1,N3-disu
Externí odkaz:
https://doaj.org/article/8ea26a84de174b0d82770b102a6d1313
Autor:
Nirun Sornsongkhram, Apilak Worachartcheewan, Somsak Ruchirawat, Supaluk Prachayasittikul, Virapong Prachayasittikul, Ratchanok Pingaew
Publikováno v:
Molecules, Vol 14, Iss 8, Pp 2768-2779 (2009)
Molecules
Volume 14
Issue 8
Pages 2768-2779
Molecules
Volume 14
Issue 8
Pages 2768-2779
This study reports the synthesis of some substituted 5-iodouracils and their bioactivities. Alkylation of 5-iodouracils gave predominately N1-substituted-(R)-5-iodouracil compounds 7a-d (R = n-C(4)H(9), s-C(4)H(9), CH(2)C(6)H(11), CH(2)C(6)H(5)) toge
Autor:
Apilak Worachartcheewan, Somsak Ruchirawat, Virapong Prachayasittikul, Maneekarn Chinworrungsee, Supaluk Prachayasittikul, Nirun Sornsongkhram, Chanin Nantasenamat
Publikováno v:
ChemInform. 42
Autor:
Apilak Worachartcheewan, Nirun Sornsongkhram, Maneekarn Chinworrungsee, Virapong Prachayasittikul, Chanin Nantasenamat, Somsak Ruchirawat, Supaluk Prachayasittikul
Publikováno v:
European journal of medicinal chemistry. 46(2)
Considering that some thiopyrimidines were previously reported as potential therapeutics, the present study achieved novel analogs of bioactive 2-substituted thiopyrimidines-4-(3H)-ones via base catalyzed alkylation reaction of 2-thiouracil using alk
Autor:
Prachayasittikul, Supaluk1 supaluk@swu.ac.th, Sornsongkhram, Nirun1, Pingaew, Ratchanok1, Worachartcheewan, Apilak2, Ruchirawat, Somsak3, Prachayasittikul, Virapong2 mtvpr@mahidol.ac.th
Publikováno v:
Molecules. Aug2009, Vol. 14 Issue 8, p2768-2779. 12p. 2 Diagrams, 6 Charts.