WO2003106439A1 - アミロイド蓄積性疾患の画像診断プローブ化合物、老人斑/びまん性老人斑染色用化合物、ならびにアミロイド蓄積性疾患の治療薬 - Google Patents
アミロイド蓄積性疾患の画像診断プローブ化合物、老人斑/びまん性老人斑染色用化合物、ならびにアミロイド蓄積性疾患の治療薬 Download PDFInfo
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- WO2003106439A1 WO2003106439A1 PCT/JP2003/007183 JP0307183W WO03106439A1 WO 2003106439 A1 WO2003106439 A1 WO 2003106439A1 JP 0307183 W JP0307183 W JP 0307183W WO 03106439 A1 WO03106439 A1 WO 03106439A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
- C07D277/66—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
Definitions
- Probe diagnostic imaging compound for amyloid-accumulating disease senile plaque Z Compound for diffuse senile plaque staining, and therapeutic agent for amyloid-accumulating disease
- the present invention relates to a probe for diagnostic imaging of a disease in which amyloid / 3 (A i3) protein is accumulated, in particular, a probe labeled with a positron-emitting nuclide, and a diagnostic imaging composition containing the probe.
- the compounds of the present invention are characterized by vividly staining senile plaques, especially diffuse senile plaques. Therefore, the present invention is characterized by using a composition and a kit containing the compound of the present invention, and a compound of the present invention, for staining A] 3, senile plaque, particularly diffuse senile plaque in a brain sample.
- the present invention relates to a method for staining A, senile plaques, especially diffuse senile plaques in a brain sample. Furthermore, the present invention relates to a composition containing the compound of the present invention for preventing and / or treating a disease in which one sheet structure of a protein causes or is a part of the etiology.
- Alzheimer's disease is currently regarded as one of the most difficult to treat, and accurate early diagnosis is desired.
- Alzheimer's disease is currently regarded as one of the most difficult diseases to treat, and a disease for which accurate early diagnosis is desired.
- Alzheimer's disease is a disease characterized by progressive dementia that mainly occurs from the elderly to the elderly. Pathologically, it is characterized by general atrophy of the cerebrum, marked degeneration and loss of nerve cells, neurofibrillary tangles and the appearance of senile plaques. It is known that the greatest risk factor for dementia represented by Alzheimer's disease is caro age. Therefore, the increase in the number of patients accompanying the aging population is particularly prominent in aging societies such as Japan, the United States, and European countries, and the cost of medical care for them has put the healthcare system in these countries at risk. I am concerned.
- the number of Alzheimer's disease patients in Japan is estimated to be about 100,000, and it is expected that the number of Alzheimer's disease patients will increase as the population ages in the future. Since the cost of patients with Waltz-heimer's disease, including nursing care costs, is considered to exceed 250 million yen per patient per year, socioeconomic costs exceeding 2.5 trillion yen have already been paid in Japan. Will be. It is now common knowledge in the world that treating Alzheimer's disease before or as soon as dementia manifests can have significant medical and economic benefits. However, it is extremely difficult at present to accurately diagnose these stages of Alzheimer's disease.
- Panorezheimer's disease In view of the above-mentioned progression characteristics of the disease state and the rapid increase in the number of patients, the necessity and significance of accurate early diagnosis of Panorezheimer's disease are extremely large.
- the histopathology of Alzheimer's disease is represented by two main features. Senile plaques and neurofibrillary tangles.
- the main component of the former is amyloid] 3 protein with & sheet structure, and the latter is hyperphosphorylated tau protein. Determining Panorezheimer's disease relies on the appearance of these pathological features in the patient's brain.
- Amyloid J3 protein is characteristic of amyloid accumulation diseases, including Alzheimer's disease, and is closely related. Therefore, in the body, especially in the brain, The detection of amyloid protein with a salt structure as a marker is one of the important diagnostic methods for amyloid-accumulating diseases, particularly Alzheimer's disease.
- amyloid accumulation diseases such as Alheimer's disease
- a substance that specifically binds to and stains amyloid protein in the body, particularly in the brain has been conventionally searched.
- Such substances include Congo Red (Pachitra
- the present inventors have found various compounds having characteristics such as high specificity for amyloid 0 protein, high blood-brain barrier permeability, high solubility, and low toxicity (Japanese Patent Application No. 2000-080082, No. 2000-080083, No. 2001-076075, PCT / JP 01/02204, PCT ZJP 0 lZO 2205).
- amyloid 3 protein and tau protein have a zero-sheet structure, so that the protein itself is considered to be a pathogen or part of the pathogenesis.
- Yankner et al. Have reported for the first time that amyloid 3 protein exerts neurotoxicity by adopting a 3 sheet structure (Science, Vol. 245, pp. 417-420, 1989). After that, many additional tests were carried out, and it was confirmed that amyloid protein having a three-sheet structure had neurotoxicity.
- amyloid having a sheet structure in this way 3 protein and tau protein have neurotoxicity, and the compounds that suppress the cytotoxicity are caused by the protein itself having a sheet structure. It is suggested that it may be a therapeutic agent for diseases that become part of the disease, for example, Alzheimer's disease.
- Alzheimer's disease On the other hand, for research on Alzheimer's disease or diagnosis using biopsy or autopsy samples, brain sections have been prepared from Alzheimer's patients and stained. Conventional dyes have mainly been Congo Red or Thioflavin S. These stains are characterized by staining both the senile plaques and neurofibrillary tangles, the two pathological hallmarks of Alzheimer's disease.
- the present inventors have conducted intensive studies to solve the above-mentioned problems, and as a result, have found that the compound represented by the formula I or a salt or solvate thereof has a very high binding specificity to the amyloid j3 protein. Furthermore, they found that blood-brain barrier permeability was high, and completed the present invention. Therefore, the present invention provides a substance which can be used as a diagnostic probe for a disease in which amyloid protein is accumulated, having high binding specificity to amyloid 3 protein, and high blood-brain barrier permeability, particularly a probe for diagnostic imaging. Is what you do.
- the present invention also provides a diagnostic imaging probe for a disease in which amyloid / 3 ( ⁇ ) protein is accumulated, specifically, a probe labeled with a positron-emitting nuclide, and a diagnostic imaging composition containing the probe.
- the compound of the present invention is characterized by vividly staining senile plaques, particularly diffuse senile plaques. Therefore, the present invention provides a composition and a kit containing the compound of the present invention for staining A, senile plaque, particularly diffuse senile plaque in a brain sample, and a brain characterized by using the compound of the present invention. It provides a method for staining A
- the present invention also provides a composition comprising a compound of the present invention, for preventing and / or treating a disease in which the] 3-sheet structure of a protein causes or is a part of the etiology. Furthermore, the present invention also provides a method for diagnosing and treating amyloid-accumulating disease using the present compound. The present invention also provides compounds in which mutagenicity is not detected or is extremely small.
- R 2 are independently hydrogen, halogen, OH, COOH, SO 3 H, NH 2 , NO 2 , anorealkyl having 1 to 4 carbon atoms, or S-halogen, Alkyl having 1 to 4 carbons, alkyl having 1 to 4 carbons which may be substituted by O-halogen, phenyl, or CONHR 6 , or
- R 3 and R 4 are independently hydrogen, or alkyl having 1 to 4 carbons which may be substituted with halogen, or together Or
- R 5 is hydrogen, CONH 2 , COC 6 H 5 , or CO—an alkyl having 1 to 4 carbon atoms;
- R 6 is OH N halogen, and 1 to 5 of which may phenylene also be Honoré substituted with a substituent selected from alkyl which may number 1 to 4 carbon substituted by halogen,
- X is S or O
- n and n are independently integers from 0 to 4.
- the 0 / ray emitting nuclide is selected from the group consisting of 9 ⁇ Tc, 11 1 ! !, ⁇ Ga ⁇ ⁇ TK 1 2 3 I and 1 3 3 Xe A compound or a salt or solvate thereof;
- a composition for diagnostic imaging of a disease in which amyloid is accumulated comprising the compound according to any one of (1) to (14) or a pharmaceutically acceptable salt or solvate thereof and a pharmaceutically acceptable carrier. object;
- composition according to (15) comprising the compound according to (14) or a pharmaceutically acceptable salt or solvate thereof, which is labeled with 18 F;
- a kit for imaging diagnosis of a disease in which amyloid is accumulated comprising the compound according to any of (1) to (14) or a pharmaceutically acceptable salt or solvate thereof as an essential component;
- 82 for staining of senile plaques and z or diffuse senile plaques in a brain sample, comprising a compound selected from the group consisting of 82 or a salt or solvate thereof;
- a compound selected from the group consisting of BF-124, BF_125, BF-133, BF-164, BF-168, BF-173, BF-180, BF-183, N-276 and N-282 A kit for staining senile plaques and Z or diffuse senile plaques in a brain sample, which comprises a salt or solvate thereof as an essential component;
- a method for staining amyloid protein or senile plaque and / or diffuse senile plaque in a brain sample which comprises using the compound according to (1) or a pharmaceutically acceptable salt or solvate thereof;
- a method for staining senile plaques and / or diffuse senile plaques in a brain sample which comprises using a salt or a solvate; and
- a disease comprising the compound of (1) or a pharmaceutically acceptable salt or solvate thereof and a pharmaceutically acceptable carrier, wherein the three-sheet structure of the protein has a etiology or a part of the etiology.
- the sheet structure of the protein is characterized by using the compound according to any one of (1) to (14) or a pharmaceutically acceptable salt or solvate thereof, and A method of diagnosing the disease;
- Figure 1 shows fluorescence microscopy of senile plaques in the Alzheimer's brain stained with BF-125.
- a micrograph (left panel) and a micrograph (right panel) of a senile plaque stained with BC05 (anti-A 1-42 antibody) in a sample adjacent to the left panel are shown.
- the senile plaque is shown by a ⁇ -shaped arrow, and the diffuse senile plaque is shown by a dashed circle.
- Figure 2 shows a fluorescence micrograph (left panel) of the tau protein of the Anoletzheimer brain stained with BF-125 (left panel), and tau stained with AT8 (anti-tau antibody) in the adjacent sample on the left panel.
- a photomicrograph (right panel) is shown.
- Tau protein is indicated by an arrow, and senile plaques are indicated by wedge-shaped arrows.
- Figure 3 shows fluorescence micrographs of the senile plaques of the Alzheimer's brain stained with N-282 (left panel) and 4G8 (anti-A3) antibody staining of senile plaques in adjacent samples on the left panel.
- a photomicrograph (right panel) is shown.
- Senile plaques are indicated by wedge-shaped arrows, and diffuse senile plaques are indicated by dashed circles.
- Figure 4 shows fluorescence microscopy photographs (left panel) of senile plaques in the Alzheimer brain stained with BF-133, and 4G8 (anti-A3) antibody staining of senile plaques in adjacent samples on the left panel.
- a photomicrograph (right panel) is shown.
- Senile plaques are indicated by wedge-shaped arrows, and diffuse senile plaques are indicated by dashed circles.
- Figure 5 shows fluorescence micrographs (left panel) of diffuse senile plaques of normal elderly brain stained with BF-133, and 4G8 (anti- ⁇ antibody) staining of senile plaques in adjacent samples on the left panel.
- a photomicrograph (right panel) is shown. Diffuse senile plaques are indicated by broken circles.
- FIG. 6 shows a comparison of staining between BF-125 and thioflavin S in a section adjacent to the brain of an Alzheimer's disease patient. Arrows indicate the location of neurofibrillary tangles, wedge-shaped arrows indicate the location of senile plaques.
- FIG. 7 shows a comparison of staining between N-282 and Thioflavin S in a section adjacent to the brain of a patient with Panorezheimer's disease. Arrows indicate the location of neurofibrillary tangles, wedge-shaped arrows indicate the location of senile plaques.
- FIG. 8 shows a comparison of the staining properties of BF-164 and thioflavin S in a brain adjacent section of a patient with Alzheimer's disease.
- the wedge-shaped arrow indicates the location of the senile plaque.
- FIG. 9 shows a comparison of staining properties between BF-168 and 6FZ3D (anti-A ⁇ antibody) in a brain adjacent section of a patient with Alzheimer's disease.
- Kusa type arrow indicates the location of senile plaques You.
- FIG. 10 shows a comparison of the staining properties of BF-173 and Thioflavin S in a brain adjacent section of a patient with Alzheimer's disease.
- the wedge-shaped arrow indicates the location of the senile plaque.
- FIG. 11 shows a comparison of the staining property between BF-180 and 6FZ3D (anti-A] 3 antibody) in a brain adjacent section of a patient with Alzheimer's disease.
- the wedge-shaped arrow indicates the location of the senile plaque, and the broken circle indicates the location of the diffuse senile plaque.
- FIG. 12 shows a comparison of the staining properties of BF-183 and Thioflavin S in the brain adjacent sections of Alzheimer's disease patients.
- the Kusatsu-shaped arrow indicates the location of the senile plaque.
- Fig. 13 shows fluorescence microscopy images of BF-124 stained senile plaques in the Alzheimer's brain (left panel) and senile plaques stained with 4G8 (anti-A antibody) in adjacent samples on the left panel.
- the micrograph (right panel) of the case is shown.
- the senile plaques are indicated by wedge-shaped arrows, and the diffuse senile plaques are indicated by broken circles.
- FIG. 14 shows a comparison of staining between N-276 and thioflavin S in a brain adjacent section of an Alzheimer's disease patient. Neurofibrils are indicated by arrows, and senile plaques are indicated by wedge-shaped arrows. Detailed description of the invention
- the compound represented by the above general formula I of the present invention or a salt or solvate thereof may be used as a probe for diagnosis, particularly as a probe for diagnostic imaging, and further for staining A] 3 or senile plaque Z diffuse senile plaque, It is also a substance used for the treatment of amyloid-accumulating diseases.
- R 1 and R 2 are independently halogen, OH, COOH, S0 3 H , NH 2, N0 2, 1 ⁇ 4 carbon atoms alkyl, S- halogen carbon atoms, which may be substituted with 1 to 4 alkyls, alkyls having 1 to 4 carbons which may be substituted with 0-halogen, phenyl, or CONHR 6 , or
- ⁇ may be formed. Note that ⁇ and ⁇ in the above formula bind to the positions of ⁇ and ⁇ in the benzene ring in Formula I, respectively.
- R 1 and R 2 are fluorine, chlorine, OH, COOH, S0 3 H , NH 2, N0 2 , or methyl, Echiru,, n-propyl, i one propyl, Amino, nitro, methoxy, ethoxy, etc. Is mentioned.
- R 1 and R 2 hydrogen or methyl is preferable.
- R 2 may be a labeled halogen, and a positron-emitting nuclide, such as 18 F, is preferred.
- R 3 and R 4 are independently hydrogen or an alkyl having 1 to 4 carbons which may be substituted by halogen, or together
- R 3 and R 4 examples include hydrogen, methyl and the like.
- R 3 and R 4 are preferably methyl or ethyl.
- R 5 is hydrogen, CONH 2 , COC 6 H 5 , or CO—alkyl having 1 to 4 carbon atoms.
- the position of the phenyl group to R 5 with respect to the double bond cis may be either trans The cis position is preferred.
- R 6 is a phenyl which may be substituted with 1 to 5 substituents selected from OH, halogen, and alkyl having 1 to 4 carbon atoms which may be substituted with nodogen.
- alkyl having 1 to 4 carbon atoms includes methyl, ethyl, propyl, butyl, and structural isomers thereof.
- halogen refers to fluorine, chlorine, bromine or iodine.
- X is S or O.
- n and n are each independently an integer from 0 to 4.
- the R 1 substituent or the R 2 substituent may be present at any position on the benzene ring to which each is attached.
- R 1 substituents may be present at any position on the benzene ring to which each is attached.
- R 1 substituents may be the same or different. This is the same for the R 2 substituent.
- Specific examples of the compound represented by the formula I include the compounds shown in Table 1.
- Salts of the compounds of I are also included in the present invention. Salts may be formed with the nitrogen atom or any functional group in the compounds of formula I. For example, when a carboxyl group or a sulfonic acid group is present in a compound, a salt may be formed between the compound and a metal. Examples of salts and salts include salts with alkali metals such as lithium, sodium and potassium, and salts with alkaline earth metals such as magnesium, calcium and barium. When the compound of the formula I contains a hydroxyl group, a compound whose hydrogen is a metal such as sodium or potassium is also included in the present invention.
- a complex formed with a compound of the formula I and a metal salt is also included in the present specification as a salt of the compound of the formula I.
- a metal salt for example, a complex formed with a metal salt such as magnesium chloride or iron chloride
- the compound of the present invention is preferably a pharmaceutically acceptable salt.
- the compound of the present invention may form an ionic salt together with an anion depending on the type of the substituent to R 5. Examples of the anion include a halide ion, an organic acid ion, a sulfonate ion and Chlorate ion and the like.
- the strong potassium salt is also preferably pharmaceutically acceptable.
- Pharmaceutically acceptable salts of the compounds of formula I include, for example, salts with halide ions such as chlorine, bromine and iodine, or salts with metals such as sodium, potassium and calcium. Kakul salt is included in the present invention. Further, the compound of the present invention may form a complex with a metal salt such as iron chloride or cobalt salt, and a powerful complex is also included in the present invention.
- the present invention also includes a solvate of the compound of the formula I. Is done. Examples of the solvates include hydrates, methanol solvates, ethanol solvates, and ammonium solvates.
- a pharmaceutically acceptable solvate When used in the composition or kit of the present invention, a pharmaceutically acceptable solvate is also preferable, and a pharmaceutically acceptable solvate includes a hydrate, an ethanol solvate and the like.
- the term "compound of the present invention” is intended to include the compound of the formula I, and salts and solvates thereof.
- reference to "BF_124” is intended to include compound BF-124, and when present, salts and solvates thereof.
- a diagnostic imaging probe for a disease in which ⁇ ⁇ accumulates a compound of formula I or a salt or solvate thereof that specifically binds to ⁇ in vivo
- the compound of the present invention stains senile plaques, particularly diffuse senile plaques, clearly.
- the term “disease in which [ ⁇ ] 3 accumulates” refers to a disease characterized by accumulation of ⁇ protein in the brain, and diagnosed using A protein, ie, senile plaque (particularly, diffuse senile plaque) as a marker. Possible diseases include Alzheimer's disease and Down's syndrome.
- the compounds of the present invention have specificity for A j3. Especially BF— 1 25 (4—
- 2-Inoleic 3- (4-Dimethinoleamino-1-phenylene) is a preferred compound because of its high ⁇ -structure recognition and specific recognition of ⁇ (see Table 1). . Therefore, these compounds are suitable as diagnostic probes for diseases in which ⁇ or senile plaques and ⁇ or diffuse senile plaques accumulate, and are useful in brain samples. A] It is also preferred for staining of 3 or senile plaques and of diabetic or diffuse senile plaques. In addition, these compounds can also be preferably used for the prevention and / or treatment of diseases in which the ⁇ -sheet structure of a protein causes or is a part of the pathogenesis. Details will be described later.
- N-276 (2- [4- (dimethinoleamino) styryl] benzothiazole) is also a preferred compound because of its high blood-brain barrier permeability.
- the compounds of the present invention stain senile plaques or diffuse senile plaques.
- the compounds BF-124, BF-125, BF-133, BF-164 (2- (4-aminostyryl) benzoxazole), BF-168 (2- (4-methinoleaminostyrino 1-6- (2-fluoroethoxy) benzo) Xazozonole), BF-173, BF-180, BF-183 (2- [4- (2-fluoroethylamino) styrenole] benzoxazole), N-276 and N-282 are brain samples It is a preferred compound that vividly stains senile plaques in it.
- amyloid] 3 ( ⁇ ] 3) protein the main component of senile plaques in Alzheimer's disease, is thought to begin to accumulate long before the onset of the disease (dementia symptoms become evident) (at least 10 years ago). This early accumulated image is considered to be diffuse senile plaque.
- early detection of diffuse senile plaques enables early detection'diagnosis of Alha-Immer's disease.
- the compounds BF-124, BF-125, BF-133, BF-180 and N_282 clearly stain diffuse senile plaques and are considered useful for early detection and diagnosis of Alzheimer's disease. It is a particularly preferred compound.
- Labels include fluorescent substances, affinity substances, enzyme substrates, and radionuclides.
- a radionuclide-labeled probe is used for diagnostic imaging of diseases in which the 3 protein accumulates.
- the compounds of the present invention can be labeled with various radionuclides by methods well known in the art. For example, 3 H, 14 C, 35 S, 13 I, etc. are radionuclides that have been used before, and are often used in the mouth.
- PET detects two gamma rays emitted from positron-emitting nuclides in opposite directions by a coincidence method using a pair of detectors, so that information with excellent resolving power and quantitative properties can be obtained.
- the use SPEC T be labeled 9 9 m Tc, 1 1 1 I n, 6 Ga s 2 0 1 T 1, 1 2 3 I, 1 3 3 X present invention compounds of ⁇ -ray emitting nuclides such as e it can. 9 9 m Tc and
- 1 2 3 I is commonly used for SPEC.
- the PET for may be labeled 1 1 C, 1 3 N, 1 5 0, 1 8 F, 6 2 Cu, 6 8 Ga, 7 6 B present compounds with positron emitting nuclide such as r.
- positron emitting nuclide half-life is appropriate, 1 1 c in terms of the labeled easiness, 1 3 N, 1 5 0 , 1 8 F are preferred, 1 8 F are particularly preferred.
- the labeling position of the compound of the present invention on a radiation-emitting nuclide such as a positron-emitting nuclide or a ⁇ -ray-emitting nuclide may be any position in Formula I.
- hydrogen on the ring may be replaced by a radiation-emitting nuclide such as a positron-emitting nuclide or a gamma-ray-emitting nuclide.
- Marker position of the compounds of formula I can be any position, but Preferred labels are those in the substituents 1 ⁇ or R 2. Strongly labeled compounds of formula I are also included in the present invention. For example, when the compound of the present invention is labeled with 18 F, any of the side chains may be labeled with 18 F, or hydrogen on the ring may be substituted with 18 F. The hydrogen contained in any of to R 6 may be substituted with 1 8 F.
- the substituent (R x or R 2 ) on the benzene ring portion of the thiazoline ring in the compound may be 18 F, or, for example, the substituent (1 ⁇ ) on the benzene ring portion of the oxazoline ring in the compound. or a R 2) force 8 F.
- these nuclides are produced by equipment called cyclotrons or generators. Those skilled in the art can select a production method and an apparatus according to a produced nuclide.
- the nuclide thus produced can be used to label the compound of the present invention.
- Methods for producing labeled compounds labeled with these radionuclides are well known in the art. Representative methods include chemical synthesis, isotope exchange, and biosynthesis.
- the chemical synthesis method has been widely used in the past, and is essentially the same as the ordinary chemical synthesis method except that a radioactive starting material is used. This method has been introduced into various nuclide compounds.
- Isotope exchange method is a simple 3 H in the compound of structure, 3 5 S, 1 2 4 I like transferred into compounds of complex structure, to give a compound of the complicated structure labeled with these radionuclides Is the way.
- Biosynthetic method is a 1 4 C, 3 5 how to obtain the metabolites of these nuclides were introduced a compound labeled given to cells such as microorganisms like S.
- the label can be introduced at a desired position by designing the synthesis scheme according to the purpose as in the ordinary synthesis. Such designs are well-known to those skilled in the art.
- the desired nuclide can be introduced into the desired position of the compound of the present invention and labeled by these methods known to those skilled in the art.
- Administration of the labeled compound of the present invention to a subject may be local or systemic.
- Administration routes include intradermal, intraperitoneal, intravenous, arterial, or spinal fluid injection or infusion, etc., which can be selected according to the type of disease, nuclide used, compound used, target condition, test site, etc. .
- the test site can be examined by means such as PET or SPECT. These means can be appropriately selected according to factors such as the type of disease, nuclide used, conjugate used, condition of the subject, and site to be examined.
- the dose of the compound of the present invention labeled with a radionuclide varies depending on the type of disease, nuclide used, compound used, age of the subject, physical condition, gender, degree of the disease, test site, and the like. In particular, careful attention should be paid to the exposure of the target. For example, 1 1 C, 1 3 ⁇ , 1 5 0, 1 the invention of which has been labeled with 8 F positron emission such as
- the radioactivity of the compound is usually in the range from 3.7 megabecquerels to 3.7 gigabetalels, preferably from 18 megabecquerels to 74 megabecquerels.
- the present invention also provides a composition for diagnostic imaging of a disease in which A accumulates, comprising the compound of the present invention.
- the composition of the present invention comprises the compound of the present invention and a pharmaceutically acceptable carrier.
- the compound of the present invention in the composition is preferably labeled.
- radionuclide especially positron emitting nuclide such as 11 C, 13 N, 15 O, and 18 F
- the composition of the present invention is preferably in a form that allows injection or infusion.
- the pharmaceutically acceptable carrier is preferably a liquid, and is preferably an aqueous solvent such as potassium phosphate buffer, physiological saline, Ringer's solution, distilled water, or polyethylene glycol, vegetable oil, ethanol, glycerin.
- aqueous solvents such as, but not limited to, dimethylsnoreoxide, propylene glycol and the like.
- the mixing ratio of the carrier and the compound of the present invention can be appropriately selected depending on the application site, detection means, etc., but is usually 100,000 to 1 to 2: 1 and preferably 10,000 to 1 Or a ratio of 10: 1.
- composition of the present invention further comprises a known antibacterial agent (for example, an antibiotic), a local anesthetic (for example, pro-in hydrochloride, dibu-in hydrochloride, etc.), a buffer (for example, a tris-monochloride buffer, a heparin). Buffer) and osmotic pressure regulators (eg, glucose, sorbitol, sodium chloride, etc.).
- a known antibacterial agent for example, an antibiotic
- a local anesthetic for example, pro-in hydrochloride, dibu-in hydrochloride, etc.
- a buffer for example, a tris-monochloride buffer, a heparin. Buffer
- osmotic pressure regulators eg, glucose, sorbitol, sodium chloride, etc.
- the present invention further provides a kit for diagnosing a disease in which A] 3 protein is accumulated, comprising the compound of the present invention as an essential component.
- the kit contains the compound of the present invention, a solvent for dissolving the compound, a buffer, an osmotic agent, an antibacterial agent, a local anesthetic, and the like separately or in a container together. It is a collection of what you put in.
- the compound of the present invention may be unlabeled or labeled. If unlabeled, the compounds of the invention can be labeled before use by conventional methods as described above.
- the compound of the present invention may be provided as a solid such as a lyophilized powder, or may be provided after being dissolved in an appropriate solvent.
- the solvent may be the same as the carrier used in the composition of the present invention described above.
- Each component such as a buffer, an osmotic pressure regulator, an antibacterial agent, and a local anesthetic is also used in the composition of the present invention. It may be the same as what you do.
- Various containers can be selected as appropriate, but they can also be formed into a shape suitable for the operation of introducing the label into the compound of the present invention, and can be made of a light-shielding material according to the properties of the compound, or can be used for patients. For convenience of administration, it may be in the form of a vial or a syringe.
- the kit may appropriately include instruments necessary for diagnosis, for example, instruments used for a syringe, an infusion set, or a PET device. Usually, instructions are attached to the kit.
- the compound of the present invention since the compound of the present invention specifically binds to the A] 3 protein or senile plaque and Z or diffuse senile plaque, the compound of the present invention can be used without labeling or in vitro. Can be used for the detection, quantification, etc. of A] 3.
- the compound of the present invention may be used for A] 3 protein staining of a microscope specimen, colorimetric quantification of A protein in a sample, or quantification of A protein using a scintillation counter.
- the compound of the present invention specifically recognizes A ⁇ , it is a preferred compound as a stain for ⁇ or senile plaques and / or diffuse senile plaques.
- the present invention provides a composition for staining ⁇ protein or senile plaque and / or diffuse senile plaque in a brain sample, comprising a compound of formula I or a pharmaceutically acceptable salt or solvate thereof. I do.
- BF-125, N-275, N-282, BF_145, BF-173, BF-180, BF-124, N-284, and N-306 are preferred compounds with high structure recognition.
- the present invention relates to a method for staining A] 3 protein or senile plaque and / or diffuse senile plaque in a brain sample, which comprises a compound of the formula I or a pharmaceutically acceptable salt or solvate thereof as an essential component. Kits are also provided. Furthermore, the present invention provides a method for preparing a compound of formula I or a pharmaceutically acceptable salt or solvate thereof, wherein the A / 3 protein or senile plaque and / or diffuse senile plaque in a brain sample is used. It also provides a dyeing method.
- the present invention comprises BF-124, BF-125, BF-133, BF-164, BF-168, BF-173, BF_180, BF_183, N-276 and N-282.
- a composition for staining senile plaques in a brain sample comprising a compound selected from the group consisting of: or a pharmaceutically acceptable salt or solvate thereof.
- the present invention is selected from the group consisting of BF-124, BF-125, BF-133, BF_164, BF-168, BF-173, BF-180, BF-183, N-276 and N-282.
- a kit for staining senile plaques in a brain sample comprising a compound or a pharmaceutically acceptable salt or solvate thereof as an essential component.
- the present invention provides a compound selected from the group consisting of BF-124, BF_125, BF-133, BF-164, BF_168, BF-173, BF-180, BF-183, N-276 and N-282, or a compound thereof.
- a method for staining senile plaques in a brain sample which comprises using a pharmaceutically acceptable salt or solvate, is also provided.
- BF-124, BF-125, BF-133, BF-180 and N-282 clearly stain diffuse senile plaques in brain samples.
- Compounds BF-124, BF-125, BF-133, BF-180, and N-282 are considered to be useful for early detection and diagnosis of Alzheimer's disease because they clearly stain diffuse senile plaques. It is. Accordingly, the present invention provides a brain comprising a compound selected from the group consisting of BF-124, BF-125, BF-133, BF-180 and N-282, or a pharmaceutically acceptable salt or solvate thereof.
- a composition for staining a diffuse senile plaque in a sample is provided.
- the present invention includes, as an essential component, a compound selected from the group consisting of BF-124, BF-125, BF-133, BF_180, and N-282, or a pharmaceutically acceptable salt or solvate thereof.
- a kit for staining diffuse senile plaques in a brain sample is provided. Further, the present invention uses a compound selected from the group consisting of BF-124, BF_125, BF-133, BF-180, and N-282, or a pharmaceutically acceptable salt or solvate thereof.
- a method for staining diffuse senile plaques in a brain sample characterized in that:
- the compounds of the invention of the formula I have specificity for A] 3, in a further embodiment of the invention the compounds of the formula I or pharmaceutically acceptable salts or solvates thereof and pharmaceutically acceptable Provided is a composition for preventing and / or treating a disease in which a protein sheet structure causes or is a part of the pathogen, which comprises a carrier.
- a 3 accumulates Alzheimer's disease, Down's syndrome, and the like can be mentioned as accumulated diseases.
- the compound of the present invention is considered to be useful as a stain for senile plaques and Z or diffuse senile plaques in brain sections of Alzheimer's disease patients in studies of Alzheimer's disease or diagnosis after death. Staining of a brain section using the compound of the present invention can be performed by an ordinary method.
- the present invention provides a composition for staining senile plaques and / or diffuse senile plaques in a brain sample containing the compound of the present invention or a pharmaceutically acceptable salt or solvate thereof, and the compound of the present invention or a pharmaceutically acceptable salt thereof.
- a kit for staining senile plaques and / or diffuse senile plaques in a brain sample comprising an acceptable salt or solvate as an essential component.
- the present invention further relates to a method for staining senile plaques and Z or diffuse senile plaques in a brain sample, which comprises using the compound of the present invention or a pharmaceutically acceptable salt or solvate thereof. .
- amyloid] 3 protein and tau protein having a [3 sheet structure] have neurotoxicity. Since the compound of the present invention is specific to the amyloid i3 protein, it is considered that the compound of the present invention suppresses the cytotoxicity of amyloid i3 protein having a three-sheet structure. Thus, it is considered that the compound of the present invention can be used as a therapeutic agent for pathogenesis or a disease that becomes a part of pathogenesis, for example, Alzheimer's disease, when the protein itself has a] 3 sheet structure.
- the present invention further provides a disease comprising a compound of the present invention or a pharmaceutically acceptable salt or solvate thereof and a pharmaceutically acceptable carrier, wherein the sheet structure of the protein is a cause or a part of the cause.
- the present invention relates to a medicament and a progenitor for preventing and / or treating Alzheimer's disease.
- a liquid formulation is preferred, and an injection formulation is particularly preferred.
- a powerful injection formulation can be injected directly into the brain, or the compound of the present invention has high blood / brain barrier permeability as shown in Example 3; It can also be formulated and administered for infusion. Preparation of such liquid formulations can be performed by methods known in the art.
- the solution is prepared by adding the compound of the present invention. It is dissolved in a suitable carrier, water for injection, physiological saline, Ringer's solution, etc., sterilized with a filter or the like, and then filled in a suitable container, for example, a vial or ampoule. It is also possible to freeze-dry the solution and prepare the solution again with a suitable carrier at the time of use.
- a suspension can be prepared by sterilizing the compound of the invention, for example, by exposure to ethylene oxide, and then suspending the suspension in a sterile liquid carrier.
- the dose of the compound of the present invention depends on the patient's condition, age, age, body weight, etc., but generally, for an adult weighing 70 kg, 0.1 mg to 1 g per day for an adult weighing 70 kg. Preferably it is 1 mg to 10 Omg, more preferably 5 mg to 5 Omg. Treatment may be performed at such dosages for a period of time, and the dosage may be increased or decreased depending on the results.
- the present invention provides a method for diagnosing a disease in which the] 3 sheet structure of a protein is a cause or a part of the cause, comprising using the compound of the present invention or a pharmaceutically acceptable salt or solvate thereof, and A method for preventing and / or treating a disease in which the [3] -sheet structure of a protein is an etiology or a part of the etiology, comprising using the compound of the present invention or a pharmaceutically acceptable salt or solvate thereof. Also provide.
- the diagnostic method may be in vivo or in vivo, and the compound may be labeled or unlabeled.
- the dosage and administration method of the compound of the present invention in the above treatment method are as described above.
- Amyloid] 3 protein (purchased from Peptide Laboratories) is a phosphate buffer (pH 7.
- the partition coefficient of the compound of the present invention was measured by the following method and used as an index of blood-brain barrier permeability. Specifically, the distribution coefficient of water Z1-octanol was measured according to the following procedure.
- 1-octanol was used for the oil phase
- phosphate buffer ( ⁇ 7.3) or ultrapure water was used for the aqueous phase.
- An appropriate amount of the test compound was dissolved in an oil phase or an aqueous phase, and both phases were placed in the same test tube and shaken vigorously at room temperature for 30 minutes. After leaving still at room temperature for 1 hour or more, it was centrifuged at 2,000 rpm for 10 minutes, and left still at room temperature for 1 hour. The aqueous phase and the oil phase were each sampled and transferred to a 96-well microplate.
- Microphone Mouth plate reader (Molecular Devices, Spectramax 250 ) was used to measure the absorbance at the maximum absorption wavelength of each test compound, and the concentration of the test compound was calculated from the calibration curve determined in advance.
- test compound binding specificity to amyloid] 3 protein and distribution coefficient (test compound blood-brain barrier permeability) is defined as a useful coefficient, this coefficient is actually It is considered that when the test compound is administered, the test compound penetrates the blood-brain barrier and serves as an index of how much the test compound binds to amyloid ⁇ protein in the brain.
- test compound of the present invention As a diagnostic probe for a disease in which amyloid is accumulated.
- Paraffin-embedded brain tissue is sliced to a thickness of 6 / zm or 8 / im, It was spread on a ride glass and dried. Paraffin brain sections were treated with xylene for 10 minutes X2, 100% ethanol for 5 minutes X2, and 95% ethanol for 5 minutes X2, and then deparaffinized in running water for 10 minutes.
- a treatment for removing autofluorescence due to lipofuscin was performed.
- the deparaffinized sections were immersed for 60 minutes in a 10% formalin solution, washed for 5 minutes with PBS, and immersed for 90 minutes in 0. 25% KM n O 4 solution. After washing 2 min X 2 times with PBS, 0. dipped 1% K 2 S 2 0 5 / Shuu acid solution for about 30 seconds in a further subjected to 2 minutes X 3 times washed with PBS.
- Amyloid] 3 protein specific antibody 4G8 Signet Human Amyloid Beta Protein Clone 4G8, 1: 100 dilution
- AT8 specific antibody for tau protein Tau protein, 1: 200 dilution
- BC05 WAK0, anti-amyloid J3 monoclonal antibody kit, undiluted
- 6FZ3D DAKO, monoclonal anti-human beta amyloid clone 6FZ3D, 1:50 dilution
- AT8 Inogenetics NV, anti-tau antibody, 1:20 (Dilution 0) was added dropwise at approximately 15 1, and the mixture was reacted at 37 ° C. for 1 hour.
- the acute toxicity of the compound of the present invention was examined by intravenous administration using mice.
- Crj Male CD1 male mice were used per group (average body weight of each group was 30-34 g). Each compound was dissolved in a single or mixed solution of physiological saline, 1N HC1, and polyethylene glycol 400, then diluted in physiological saline and administered via the tail vein, and observed up to 7B thereafter did.
- B Brain transfer test
- the compound of the present invention was intravenously administered to mice, and the brain distribution in in vivo was measured.
- mice used 30-40 g (7 weeks old, n 3) of S Ic: ICR (Japan SLC).
- test compound Dissolve the test compound in INHC 1, polyethylene glycol 400 alone or in a mixed solution, dilute with purified water, inject via tail vein, and 2 minutes after administration, heparin from abdominal aorta under ether anesthesia Blood was collected using a treated syringe and brain was collected.
- the brain was frozen, the wet weight was measured, physiological saline was added, and the brain was homogenized using a mixer (MM300, Retsch). The homogenate was centrifuged for 10 minutes, the supernatant was added to a conditioned C18 solid phase extraction cartridge, and eluted with chlorophonolem.
- Two- to three-day-old coronal sections (350 / zm thick) of the striatum of the cerebral cortex were prepared from the cerebral hemispheres of Wistar rats at 5 days per plate, and cultured on a Millicell-CM membrane, 5 per plate (1 plate) 30 sections were obtained from two or three pups).
- the medium was in vitro and used 50% minimum essential medium + 25% Hanks' balanced salt solution + 25% poma serum until 14th. From then on (including during drug treatment), serum-free Neurobasal + B-27 medium was used.
- the medium volume was 1 ml per 1 ⁇ l on the first day of the culture, and 0.7 ml after the first day in vitro, and the medium was replaced every other day.
- Treatment with test compound and A] 3 (1-40) resulted in 1.6 ml / well of medium (1.0 ml below membrane, 0.6 ml above) 1)
- the section was submerged. Twenty-four hours later, the culture medium was removed from the lower side of the membrane by 0.6 ml to eliminate the submerged state of the section. After a further 48 hours (total 72 hours of treatment starting force))
- the cultured sections were fixed with 4% paraformaldehyde and stained with Nissl with 0.1% toluidine blue.
- Example 1 Screening and amyloid for 0 structure recognition; 3 staining
- Table 1 shows the results obtained by examining the degree of structure recognition and the distribution coefficient of the compound of the present invention.
- ThT thioflavin T
- Compounds of the invention BF-125, N-282, BF_145, BF-173, BF-180, BF-124, N-284, N-306).
- the partition coefficient could not be measured for BF_125, N-282, BF-124 and N-276, indicating that the tendency to partition to the lipid layer was extremely large.
- the distribution coefficient of BF-133 was also large. Therefore, the useful coefficients of these compounds are so large that they cannot be calculated, and they can be said to be extremely suitable as diagnostic probes for diseases in which amyloid accumulates.
- BF-125 hydrochloride (hereinafter referred to simply as “BF_125” in Examples 1, 2 and 3) is a senile plaque recognized by BC05 which is a specific antibody for amyloid 131-42 protein. The diffuse senile plaque was stained.
- BF-125 was recognized by AT8, a specific antibody for tau protein, and the recognized tau protein did not stain. That is, BF-125 was found to be a probe that mainly recognizes senile plaques and diffuse senile plaques.
- N-282 is 4G8, a specific antibody for the amyloid] 3 protein. Recognized and senile plaques were stained. That is, it was found that N-282 was a probe that mainly recognized senile plaques and diffuse senile plaques.
- BF-133 is known to be a probe that mainly recognizes senile plaques and diffuse senile plaques, and the amyloid) 3 protein, which is the main component of senile plaques in Alzheimer's disease, causes the disease (dementia symptoms are evident) It is thought that accumulation begins long before (at least 10 years ago), and this early accumulation image is considered to be diffuse senile plaque. As shown in Figure 5, BF-133 also stained diffuse senile plaques in normal elderly. This indicates that BF-133 is extremely useful for early detection and diagnosis of Alzheimer's disease.
- Fig. 6 shows a comparison of staining between BF-125 and Thioflavin S
- Fig. 7 shows a comparison of N-282 and Thioflavin S in sections adjacent to the brain of a patient with Panorezheimer's disease.
- Thioflavin S stained both senile plaques and neurofibrillary tangles
- BF-125 ⁇ N-282 stained only senile plaques.
- BF-164 showed staining at the same position in senile plaques recognized by Thioflavin S, and was found to clearly stain senile plaques.
- BF-168 stained at the same position as the senile plaque recognized by the anti-A antibody 6FZ3D, indicating that the senile plaque was clearly stained.
- BF-173 showed staining at the same position as the senile plaque recognized by Thioflavin S, indicating that the senile plaque was clearly stained.
- BF-180 stained senile plaques and diffuse senile plaques recognized by the anti-Ai3 antibody 6F / 3D. That is, it was found that BF-180 was a probe that mainly recognized senile plaques and diffuse senile plaques.
- BF-183 showed staining at the same position as the senile plaque recognized by Thioflavin S, indicating that the senile plaque was clearly stained.
- BF-124 also stained diffuse senile plaques. This indicates that BF-124 is extremely useful for early detection and diagnosis of Alzheimer's disease. Is shown.
- Fig. 14 shows a comparison of staining between N-276 and Thioflavin S in a section adjacent to the brain of an Alzheimer's disease patient. N-276 stained only senile plaques, whereas Thioflavin S stained both senile plaques and neurofibrillary tangles.
- the compound of the present invention is considered to be useful as a stain for senile plaques and / or diffuse senile plaques in brain sections of Alzheimer's disease patients.
- BF-124 BF- 125 BF-133 BF-180 and N-282 vividly stain diffuse senile plaques in brain samples, and these compounds can be used for early detection and diagnosis of Alzheimer's disease. This is extremely useful.
- Table 2 shows the results of the acute toxicity test performed on the compound of the present invention by the above method (A).
- a brain penetration test was performed by the method described in (B) above.
- the figure shows brain migration 2 minutes after intravenous administration of the compound of the present invention in mice.
- the compound of the present invention is a compound having extremely high brain migration.
- Table 3 Brain transfer 2 minutes after intravenous administration of the compound of the present invention (mouse)
- Example 4 Inhibitory effect of the compound of the present invention on A ⁇ (1-40) neurotoxicity
- BF-124 and BF-125 were treated at a concentration of 1 ⁇ and hyumanin G at a concentration of 10 ⁇ simultaneously with 10 ⁇ AJ3 (1-40).
- Table 4 shows the results. Table 4 Inhibitory effect of the compound of the present invention on ⁇ (1-40) -induced cell death
- Hyumanin G 96.1 ⁇ 10.0
- the numerical values represent the number of surviving cells (mean soil standard error) in each group when the shara treatment group was 100%.
- sham is an untreated control
- Vehicle control is a control to which a solvent in which the drug was dissolved was added.
- the concentration of -125 is 1 ⁇ , which by itself is a concentration at which toxicity to cells is not a problem.
- the compound of the present invention was shown to suppress the neurotoxicity of A (1-40) at a safe concentration for cells. It is thought that it can be used as an effective and safe therapeutic agent for the etiology or a disease that is a part of the etiology, such as Panorezheimer's disease.
- Example 5 Reverse mutation test
- the compound of the present invention desirably has no mutagenicity or is a non-problematic Mosoré in view of its use.
- a reverse mutation test using histidine-requiring Salmonella typhimurium TA100 and TA98 strains was performed. The study was conducted twice: a dose-finding study and a main study.
- test compound was dissolved or suspended in DMSO, and then serially diluted to prepare test compound solutions of each concentration.
- test compound solution or negative control (DMSO) solution into a sterile test tube in a volume of 1 ⁇ . Then, in the absence of a metabolic activation system (one S9 mix), add 0.1 ml sodium phosphate. 500 ⁇ l of an acid buffer (pH 7.4) and 500 ⁇ l of S9 mix in the presence of a metabolic activation system (+ S 9 mix) were dispensed.
- DMSO negative control
- test strain suspension cultured with shaking at 37 ° C for 8 hours 100 ⁇ l was added, and the mixture was shaken at 37 ° C. C for 20 minutes. After completion of the shaking, 2 ml of top agar was added, and the contents were mixed.
- the mixture was poured onto a minimal glucose agar plate (plate), spread evenly, the top agar was solidified, the plate was transferred to a thermostat, and cultured at 37 ° C for 48 hours.
- the growth state of the test strain on the plate was observed using a stereoscopic microscope, and the state of deposition of the test substance was visually observed. Then, the number of colonies generated by reversion was counted.
- a colony analyzer was used to perform area correction and countdown correction to calculate the number of rollers.
- the use of a colony analyzer was inappropriate due to precipitation of the test compound or growth inhibition, etc., the cells were counted visually.
- the compound of the present invention has high specificity for the A 3 protein, high blood-brain barrier permeability, and extremely high safety.
- the present compound sharply stains senile plaques, especially diffuse senile plaques, and is extremely useful for early diagnosis' discovery of Alzheimer's disease.
- a composition and a kit for diagnostic imaging of a disease in which Ai3 protein is accumulated comprising the compound of the present invention.
- Use of such a compound, composition, or kit enables accurate diagnosis of disease at an early stage.
- the present invention also relates to A] 3 or aged Also provided are stains, kits, and methods for macula or diffuse senile plaques.
- the present invention provides a composition and a method for preventing or treating an amyloid-accumulating disease, comprising the compound of the present invention, and an amyloid-accumulating disease characterized by using the compound of the present invention.
- a diagnostic method is also provided.
Abstract
Description
Claims
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AU2003242233A AU2003242233A1 (en) | 2002-06-12 | 2003-06-06 | Probe compound for image diagnosis of disease with amyloid accumulation, compound for staining age spots/diffuse age spots, and remedy for disease with amyloid accumulation |
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JP2002-378812 | 2002-12-27 | ||
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