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Publication number
JP2010037232A5
JP2010037232A5 JP2008199850A JP2008199850A JP2010037232A5 JP 2010037232 A5 JP2010037232 A5 JP 2010037232A5 JP 2008199850 A JP2008199850 A JP 2008199850A JP 2008199850 A JP2008199850 A JP 2008199850A JP 2010037232 A5 JP2010037232 A5 JP 2010037232A5
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Japan
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group
positron
compound
halogen atom
ability
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JP2008199850A
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Japanese (ja)
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JP2010037232A (en
JP5544550B2 (en
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Priority to JP2008199850A priority Critical patent/JP5544550B2/en
Priority claimed from JP2008199850A external-priority patent/JP5544550B2/en
Publication of JP2010037232A publication Critical patent/JP2010037232A/en
Publication of JP2010037232A5 publication Critical patent/JP2010037232A5/ja
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Publication of JP5544550B2 publication Critical patent/JP5544550B2/en
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Claims (10)

ポジトロン放出源の分布と集積度を測定するポジトロン断層撮影法において、当該ポジトロン放出源として、化合物(I)を用いることを特徴とするポジトロン断層撮影法。
化合物(I)
[式中、Rはポジトロン放出能を有するC1−6アルキル基又はポジトロン放出能を有する1−6フルオロアルキル基を示し、Rは水素原子、ヒドロキシ基、ハロゲン原子、アルコキシ基、アミノ基、アルキルアミノ基、アシルアミノ基、ジアルキルアミノ基、シアノ基、ニトロ基、又はポジトロン放出能を有するハロゲン原子を示す。]
Oite for positron tomography to measure the distribution and concentration of the positron-emitting source, as the positron-emitting source, positron tomography, which comprises using a compound (I).
Compound (I)
[Wherein, R 1 represents a C 1-6 alkyl group having a positron releasing ability or a C 1-6 fluoroalkyl group having a positron releasing ability , and R 2 represents a hydrogen atom, a hydroxy group, a halogen atom, an alkoxy group, amino A halogen atom having a group, an alkylamino group, an acylamino group, a dialkylamino group, a cyano group, a nitro group, or a positron emission ability; ]
ポジトロン放出源の分布と集積度を測定するポジトロン断層撮影法において、当該ポジトロン放出源として、化合物(II)を用いることを特徴とするポジトロン断層撮影法。
化合物(II)
[式中、Rはポジトロン放出能を有するC1−6アルキル基又はポジトロン放出能を有する1−6フルオロアルキル基を示し、RおよびRはそれぞれ独立して、水素原子、ヒドロキシ基、ハロゲン原子、アルコキシ基、アミノ基、アルキルアミノ基、アシルアミノ基、ジアルキルアミノ基、シアノ基、ニトロ基、又はポジトロン放出能を有するハロゲン原子を示す。]
A positron tomography method for measuring the distribution and integration degree of a positron emission source, wherein the compound (II) is used as the positron emission source.
Compound (II)
[Wherein, R 1 represents a C 1-6 alkyl group having a positron-releasing ability or a C 1-6 fluoroalkyl group having a positron-releasing ability , and R 2 and R 3 each independently represent a hydrogen atom, a hydroxy group, , A halogen atom, an alkoxy group, an amino group, an alkylamino group, an acylamino group, a dialkylamino group, a cyano group, a nitro group, or a halogen atom having a positron emission ability. ]
請求項1記載の化合物(I)におけるポジトロン放出源として、R11CであるC1−6アルキル基若しくは18FであるC1−6フルオロアルキル基、又はR18F、76Br若しくは124Iであることを特徴とする請求項1に記載のポジトロン断層撮影法。 As positron-emitting source in a compound according to claim 1 (I), C 1-6 fluoroalkyl group R 1 is a C 1-6 alkyl group or a 18 F a 11 C, or R 2 is 18 F, 76 Br The positron tomography method according to claim 1, wherein the positron emission tomography method is 124 I. 請求項2記載の化合物(II)におけるポジトロン放出源として、R11CであるC1−6アルキル基若しくは18FであるC1−6フルオロアルキル基、又はRおよびRがそれぞれ独立して、18F、76Br若しくは124Iであることを特徴とする請求項2に記載のポジトロン断層撮影法。 As positron-emitting source in compound of claim 2 (II), C 1-6 fluoroalkyl group R 1 is a C 1-6 alkyl group or a 18 F a 11 C, or independently R 2 and R 3 The positron tomography method according to claim 2, wherein the positron tomography method is 18 F, 76 Br, or 124 I. 以下の化学式で表される化合物(I)、その塩、又はそれらの水和物若しくは溶媒和物。
化合物(I)
[式中、Rはポジトロン放出能を有するC1−6アルキル基又はポジトロン放出能を有する1−6フルオロアルキル基を示し、Rは水素原子、ヒドロキシ基、ハロゲン原子、アルコキシ基、アミノ基、アルキルアミノ基、アシルアミノ基、ジアルキルアミノ基、シアノ基、ニトロ基、又はポジトロン放出能を有するハロゲン原子を示す。]
Compound (I) represented by the following chemical formula, salt thereof, or hydrate or solvate thereof.
Compound (I)
[Wherein, R 1 represents a C 1-6 alkyl group having a positron releasing ability or a C 1-6 fluoroalkyl group having a positron releasing ability , and R 2 represents a hydrogen atom, a hydroxy group, a halogen atom, an alkoxy group, amino A halogen atom having a group, an alkylamino group, an acylamino group, a dialkylamino group, a cyano group, a nitro group, or a positron emission ability; ]
以下の化学式で表される化合物(II)、その塩、又はそれらの水和物若しくは溶媒和物。
化合物(II)
[式中、Rはポジトロン放出能を有するC1−6アルキル基又はポジトロン放出能を有する1−6フルオロアルキル基を示し、RおよびRはそれぞれ独立して、水素原子、ヒドロキシ基、ハロゲン原子、アルコキシ基、アミノ基、アルキルアミノ基、アシルアミノ基、ジアルキルアミノ基、シアノ基、ニトロ基、又はポジトロン放出能を有するハロゲン原子を示す。]
Compound (II) represented by the following chemical formula, a salt thereof, or a hydrate or solvate thereof.
Compound (II)
[Wherein, R 1 represents a C 1-6 alkyl group having a positron-releasing ability or a C 1-6 fluoroalkyl group having a positron-releasing ability , and R 2 and R 3 each independently represent a hydrogen atom, a hydroxy group, , A halogen atom, an alkoxy group, an amino group, an alkylamino group, an acylamino group, a dialkylamino group, a cyano group, a nitro group, or a halogen atom having a positron emission ability. ]
以下の化学式で表される化合物(Ia)、その塩、又はそれらの水和物若しくは溶媒和物。
化合物(Ia)
Compound (Ia) represented by the following chemical formula, salt thereof, or hydrate or solvate thereof.
Compound (Ia)
ポジトロン放出源の分布と集積度を測定するポジトロン断層撮影法におけるポジトロン放出源として、以下の化学式で表される化合物(Ia)、その塩、又はそれらの水和物若しくは溶媒和物を用いることを特徴とするポジトロン断層撮影法。
化合物(Ia)

As a positron emission source in positron tomography for measuring the distribution and accumulation degree of a positron emission source, a compound (Ia) represented by the following chemical formula, a salt thereof, or a hydrate or solvate thereof is used. Characteristic positron tomography.
Compound (Ia)

以下の化学式で表される化合物(IIa)、その塩、又はそれらの水和物若しくは溶媒和物。
化合物(IIa)
Compound (IIa) represented by the following chemical formula, salt thereof, or hydrate or solvate thereof.
Compound (IIa)
ポジトロン放出源の分布と集積度を測定するポジトロン断層撮影法におけるポジトロン放出源として、以下の化学式で表される化合物(IIa)、その塩、又はそれらの水和物若しくは溶媒和物を用いることを特徴とするポジトロン断層撮影法。
化合物(IIa)





As a positron emission source in the positron tomography method for measuring the distribution and accumulation degree of the positron emission source, a compound (IIa) represented by the following chemical formula, a salt thereof, or a hydrate or solvate thereof is used. Characteristic positron tomography.
Compound (IIa)





JP2008199850A 2008-08-01 2008-08-01 Positron tomography and positron emitting compounds used in the method Expired - Fee Related JP5544550B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008199850A JP5544550B2 (en) 2008-08-01 2008-08-01 Positron tomography and positron emitting compounds used in the method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008199850A JP5544550B2 (en) 2008-08-01 2008-08-01 Positron tomography and positron emitting compounds used in the method

Publications (3)

Publication Number Publication Date
JP2010037232A JP2010037232A (en) 2010-02-18
JP2010037232A5 true JP2010037232A5 (en) 2011-09-15
JP5544550B2 JP5544550B2 (en) 2014-07-09

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JP2008199850A Expired - Fee Related JP5544550B2 (en) 2008-08-01 2008-08-01 Positron tomography and positron emitting compounds used in the method

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Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897766B2 (en) * 2005-09-23 2011-03-01 Abbott Laboratories Amino-aza-adamantane derivatives and methods of use
JP2007217370A (en) * 2006-02-17 2007-08-30 Nard Inst Ltd Positron tomography and positron emitting compounds used in the method

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