16047-57-7Relevant articles and documents
Highly selective suppression of melanoma cells by inducible DNA cross-linking agents: Bis(catechol) derivatives
Bai, Minghui,Huang, Jing,Zheng, Xiaolong,Song, Zhibin,Tang, Miru,Mao, Wuxiang,Yuan, Libo,Wu, Jun,Weng, Xiaocheng,Zhou, Xiang
, p. 15321 - 15327 (2010)
A series of bis(catechol) quaternary ammonium derivatives were designed and synthesized. We investigated their ability to cross-link DNA induced by tyrosinase and found that the o-quinone is key intermediate in the process by using the nucleophile 3-methy
INHIBITORS OF ERYTHROCYTE BAND 3 TYROSINE PHOSPHORYLATION AND USES THEREOF
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Page/Page column 43-44, (2021/01/22)
Inhibitors of erythrocyte band 3 tyrosine phosphorylation, compositions comprising same, and methods of using the inhibitors and compositions to treat sickle cell diseases.
Synthesis of [2-13C, 4-13C]-(2R,3S)-catechin and [2-13C, 4-13C]-(2R,3R)-epicatechin
Sharma, Pradeep K.,He, Min,Romanczyk Jr., Leo J.,Schroeter, Hagen
experimental part, p. 605 - 612 (2011/08/21)
The first synthesis of doubly labeled, [2-13C, 4- 13C]-(2R,3S)-catechin 15 and [2-13C, 4- 13C]-(2R,3R)-epicatechin 18 starting from labeled 2-hydroxy-4, 6-bis(benzyloxy)acetophenone 3 and labeled 3, 4-bis(benzyloxy)-benzaldehyde 7 are described. Copyright