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公开(公告)号:US20230406847A1
公开(公告)日:2023-12-21
申请号:US18036584
申请日:2021-11-11
Applicant: ABX ADVANCED BIOCHEMICAL COMPOUNDS GMBH
Inventor: Alexander HOEPPING , Hans-Joachim LANKAU , Ronny HESSE , Klaus KOPKA , Ulrike BAUDER WÜST , Christian LIS , René SMITS , Jan MOLLITOR , Kristine SCHEIBE , Alexandra GEISSLER
IPC: C07D413/14 , C07D413/12 , C07D401/12 , C07D409/12 , C07D417/12 , A61K51/04
CPC classification number: C07D413/14 , C07D413/12 , C07D401/12 , C07D409/12 , C07D417/12 , A61K51/0497 , A61K2121/00 , A61K2123/00
Abstract: The present invention relates to novel compounds that bind to the prostate-specific membrane antigen (PSMA)-binding and their use in the diagnosis and treatment of certain diseases where PSMA is upregulated.
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公开(公告)号:US20200165204A1
公开(公告)日:2020-05-28
申请号:US16778155
申请日:2020-01-31
Applicant: ABX advanced biochemical compounds GmbH
Inventor: René MARTIN , René SMITS , Ronny HESSE , Alexander HOEPPING , Marco MÜLLER , Sandra HÜBNER
IPC: C07D213/82 , C07B59/00
Abstract: A method for producing a radiofluorinated compound having an aromatic or heteroaromatic ring carrying [18F] fluorine as first substituent, a bonding unit, which can bind to a peptide or peptide mimetic, and a spacer group connected via bond A1 to the bonding unit and via bond A2 to the ring, wherein the bonding unit has second substituent(s) —OH, —CONH, and/or —COOH. The steps include (a) providing a precursor having the ring carrying a substituent Y, bonding unit with the second substituent(s), and spacer group, wherein substituent Y is —N+(R1R2R3), —NO2, —Cl, —Br, —F, or —I, and R1, R2, and R3 are independently C1-C6 alkyl; and (b) reacting the precursor with a [18F] fluoride anion in the presence of an activation salt to the radiofluorinated compound, which has a cation N+(R4R5R6R7) with R4, R5, R6, and R7 being independently C1-C6 alkyl, wherein the substituent Y is replaced by [18F] fluoride.
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公开(公告)号:US20190263756A1
公开(公告)日:2019-08-29
申请号:US16348997
申请日:2017-11-17
Applicant: ABX ADVANCED BIOCHEMICAL COMPOUNDS GMBH
Inventor: René MARTIN , René SMITS , Ronny HESSE , Alexander HOEPPING , Marco MÜLLER , Sandra HÜBNER
IPC: C07D213/82 , C07B59/00
Abstract: A method for producing a radiofluorinated compound having an aromatic or heteroaromatic ring carrying [18F] fluorine as first substituent, a bonding unit, which can bind to a peptide or peptide mimetic, and a spacer group connected via bond A1 to the bonding unit and via bond A2 to the ring, wherein the bonding unit has second substituent(s) —OH, —CONH, and/or —COOH. The steps include (a) providing a precursor having the ring carrying a substituent Y, bonding unit with the second substituent(s), and spacer group, wherein substituent Y is —N+(R1R2R3), —NO2, —Cl, —Br, —F, or —I, and R1, R2, and R3 are independently C1-C6 alkyl; and (b) reacting the precursor with a [18F] fluoride anion in the presence of an activation salt to the radiofluorinated compound, which has a cation N+(R4R5R6R7) with R4, R5, R6, and R7 being independently C1-C6 alkyl, wherein the substituent Y is replaced by [18F] fluoride.
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