首页> 外国专利> AL-F-18-LABELED, AL-F-19-LABELED AND GA-68-LABELED GASTRIN-RELEASING PEPTIDE RECEPTOR (GRPR)-ANTAGONISTS FOR IMAGING OF PROSTATE CANCER

AL-F-18-LABELED, AL-F-19-LABELED AND GA-68-LABELED GASTRIN-RELEASING PEPTIDE RECEPTOR (GRPR)-ANTAGONISTS FOR IMAGING OF PROSTATE CANCER

机译:AL-F-18标记,AL-F-19标记和GA-68标记的释放胃泌素肽受体(GRPR)-拮抗剂对前列腺癌的成像

摘要

The present application discloses compositions and methods of synthesis and use of 18F-, 19F- or 68Ga-labeled molecules of use in PET, SPECT and/or MRI imaging of prostate cancer. Preferably, the 18F, 19F or 68Ga is attached to a chelator moiety on a prostate cancer targeting molecule, more preferably a bombesin analog, more preferably a GRPR antagonist, most preferably JMV5132 or JMV4168. The 18F or 19F may form a complex with a group IIIA metal to promote binding to the chelators. The labeled molecules may be used to detect, diagnose and/or image prostate cancer, including metastatic prostate cancer, in vivo.
机译:本申请公开了在PET中使用的 18 F-, 19 F-或 68 Ga标记的分子的合成方法和用途。 ,前列腺癌的SPECT和/或MRI成像。优选地,将 18 F, 19 F或 68 Ga连接至前列腺癌靶向分子上的螯合剂部分,更优选地,蛙皮素类似物,更优选GRPR拮抗剂,最优选JMV5132或JMV4168。 18 F或 19 F可能与IIIA族金属形成络合物,从而促进与螯合剂的结合。标记的分子可以用于体内检测,诊断和/或成像前列腺癌,包括转移性前列腺癌。

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