Oxidative bromination of imidazoheterocycle bromohydrates*
摘要:
The behavior of imidazo[1,2-a]pyridinium, imidazo[1,2-a]pyrimidinium, and imidazo[2,1-b]thiazolium bromides derivatives in oxidative bromination reactions has been studied. It has been established that reaction products structures and their yields depend on the properties of the substituents in the bicycle and the oxidant concentration.
KUTROV, G. P.;VOLOVENKO, YU. M.;KURG, V. A.;MACHKOVSKAYA, E. N.;BABICHEV,+, DOKL. AN YCCP. B,(1984) N, S. 36-38
作者:KUTROV, G. P.、VOLOVENKO, YU. M.、KURG, V. A.、MACHKOVSKAYA, E. N.、BABICHEV,+
DOI:——
日期:——
KUTROV, G. P.;KOVALENKO, N. V.;GETMANCHUK, YU. P., YKP. XIM. ZH., 57,(1991) N, S. 187-191
作者:KUTROV, G. P.、KOVALENKO, N. V.、GETMANCHUK, YU. P.
DOI:——
日期:——
PRMT5 INHIBITORS AND USES THEREOF
申请人:[en]GILEAD SCIENCES, INC.
公开号:WO2024137852A1
公开(公告)日:2024-06-27
The present disclosure relates generally to compounds that inhibit PRMT5. The disclosure further relates to the use of the compounds for the preparation of a medicament for the treatment of diseases and/or conditions through inhibiting PRMT5. The disclosure further relates to the use of the compounds for the treatment of a disease or condition associated with chromosome 9p21 deletion or MTAP null. The disclosure further relates to the use of the compounds for the treatment of cancers.