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  F-18 labeled amino acid analogsRelated Patent Categories: Drug, Bio-affecting And Body Treating Compositions, Radionuclide Or Intended Radionuclide Containing; Adjuvant Or Carrier Compositions; Intermediate Or Preparatory CompositionsF-18 labeled amino acid analogs description/claimsThe Patent Description & Claims data below is from USPTO Patent Application 20070081941, F-18 labeled amino acid analogs. Brief Patent Description - Full Patent Description - Patent Application Claims
FIELD OF THE INVENTION [0001] The present invention relates to amino acid analogues labelled with halogen atom, such as a radioactive fluorine atom, such as F-18, or a non-radioactive fluorine atom, such as F-19. The invention further relates to precursor compounds for and a method of preparing these analogues, to a pharmaceutical composition comprising these analogues and to the use of this composition for diagnosis, for example by means of Positron Emission Tomography or functional MRI. BACKGROUND OF THE INVENTION [0002] Whatever the new approaches for therapy of cancers will be in the future, an accurate and specific non-invasive diagnosis on bio-molecular level of tumours and metastases will remain of primary importance. Transformation of normal cells into malignant cells is caused by changes in the genetic material, resulting in subtle but fundamental metabolic changes like increased glucose metabolism and increased amino acid uptake and metabolism. These changes in the metabolic phenotype permit the in-vivo study of tumours using radioactive labelled tracers coupled to SPECT (Single Photon Emission Computed Tomography) or PET (Positron Emission Tomography). PET linked coincidence acquisition allows a better resolution and quantification than SPECT, needed for tumour tracing and dimensioning. [0003] Currently, the use of .sup.18F-FDG (fluoro-deoxyglucose) and PET is the most important technique in nuclear medicine for the study of oncology patients. Although this method is very sensitive, it has two major limitations, namely an avid accumulation in inflammatory lesions and high uptake in the brain, jeopardizing the diagnosis of brain tumours. [0004] It was shown that the use of radioactive amino acids for SPECT and PET could overcome these shortcomings for the larger part. In the late 80's, several .sup.11C-labelled amino acids like methionine and tyrosine, as well as 2-.sup.18F-tyrosine (2-.sup.18F-Tyr) of high specific activity were used for PET studies. At that time it was believed that a high specific activity was required and that for tumour specification the labelled amino acid had to be involved in a high rate protein incorporation. None of these amino acids has meanwhile been introduced into routine clinical PET because of the short half life and insufficient in vivo stability of C-11 or complicated radiochemical synthesis resulting in insufficient yield (such as for 2.sup.18F-Tyr) [0005] About the same time, L-3-.sup.123I-alpha-methyl-tyrosine (3.sup.123I-IMT) was introduced as a SPECT tracer for brain tumours and is used until now also for other tumours like sarcoma and lymphoma. The uptake of this tracer in tumours occurs for the larger part by the L transport system. The plasma membrane transport system L is in many cells the only (efficient) pathway for the import of large branched and aromatic neutral amino acids. The L-type amino acid transporter 1 (LAT1) is a Na.sup.+ independent amino acid transporter and is over-expressed in over-expressed in malignant cell as it plays a critical role in cell growth and proliferation. For functional expression LAT1 requires the heavy chain of the surface antigen 4F2 (heavy chain 4F2hc). The increased accumulation is mainly determined by strongly increased amino acid transport activity rather than incorporation into proteins. A major drawback limiting the applicability of this tracer is however the high renal accumulation. [0006] O-(2-.sup.18F-ethyl)-tyrosine (FET) and .sup.18F-alpha-methyl-tyrosine were proposed in 1999 as potential PET tracers. The compounds showed the same uptake properties as IMT. The preparation of these tracers still requires complicated and time consuming synthetic steps and HPLC steps limiting the overall radiochemical yield. They are therefore in practice not very useful. [0007] In the research that led to the invention two new potential SPECT tracers, 2-.sup.123I-tyrosine (2-.sup.123I-Tyr) and 2-.sup.123I-phenylalanine, were developed. When evaluated in vivo in R1M tumour (rhabdomyo-sarcoma)-bearing rats, these tracers showed high uptake in the tumours (comparable with IMT) while no renal accumulation (10 times less activity in the kidneys than IMT) or high brain uptake was observed. Kinetic studies also revealed that the uptake of radioactive amino acid reflected the amounts of amino acids in the tumour as compared to the blood pool compartment and that no high specific activity is required for the tracer. However, also these tracers are almost limited to SPECT as the positron emitting iodine isotopes 1241 and .sup.122I do not have the required radionuclide properties for routine patient PET diagnosis. SUMMARY OF THE INVENTION [0008] It was found that a .sup.18F-labelled amino acid as tumour tracer shows higher tumour specificity as compared to FDG and is better suited as brain tracer. The fact that within toxicity limits neither high specific activity nor non-carrier added preparation of the .sup.18F-tracer is required, should allow for electrophilic radio-fluorination making use of [.sup.18F]--F.sub.2. However, the radioisotope production yield with the currently available F.sub.2-targets is limited and even with an almost quantitative labelling yield, amounts comparable with those of the .sup.18F-FDG production are far from being reached and does not allow routine multi patient PET diagnosis. [0009] It is therefore the object of the present invention to provide new compounds and precursors therefor that can be easily and quickly synthesized and can thus also be labelled with F-18 which has a half-life of only 2 hours. It is a further object of the invention to provide the use of such compounds in diagnosis. [0010] The inventors considered based on the results obtained with .sup.18F-FET and their own results with 2-.sup.123I-Phe and 2-.sup.123I-Tyr that the aromatic amino acid properties are conserved after substitution of an O-ethyl group and even in the presence of a voluminous iodine atom. This invention is thus based on the new approach to introduce an alkyl side chain on the phenyl ring to facilitate introduction of the radioactive atom. They thus provided an .sup.18F-alkyl-phenyl structure in phenylalanine and tyrosine, either ortho, meta or para. Examples are .sup.18F--CH.sub.2-Phe or .sup.18F--CH.sub.2--CH.sub.2-Phe and 2-.sup.18F--CH.sub.2-Tyr or 2-.sup.18F--CH.sub.2--CH.sub.2-Tyr. This reduces the labelling chemistry to direct conventional nucleophilic aliphatic substitution on the alkylphenylic side branch of the L-amino acid. In this approach cumbersome stereospecific synthesis is not required. The same strategy was followed for the radio-fluorination of the aliphatic amino acids leucine and isoleucine. Preliminary uptake experiments in R1M cells in vitro in a buffer simulating in vivo conditions, showed for .sup.3H-leucine and .sup.3H-isoleucine results comparable with .sup.3H-Tyr and .sup.3H-Phe. Since aliphatic-substituted F hardly changes the pharmacology, it follows that these aliphatic amino acids are also suitable molecules for radio-fluorination. DETAILED DESCRIPTION OF THE INVENTION [0011] The invention thus relates to halogenated amino acid analogues having the he general formula wherein: R is (C.sub.1-C.sub.6)alkyl optionally substituted with thioether or ether oxygen atom when n=0, or a substituted aromatic or heteraromatic ring when n=1-6; and m=0 or 1; and X is a halogen atom. [0012] R is preferably an alkyl selected from methyl, ethyl, propyl, isopropyl, butyl, tertiary butyl or methyl thioethyl ether when n is 0 and R is preferably phenyl, hydroxyphenyl, pyridyl, hydroxypyridinyl when n is 1, 2 or 3. [0013] The radioactive halogen atom is preferably a radioactive fluorine, in particular .sup.18F because of its radionuclidic properties which makes it within the positron emitting isotopes the most interesting for labelling tracer molecules for diagnosis with PET. [0014] Suitable amino acid analogues of the invention are analogues of the aromatic or heteroaromatic amino acids phenylalanine, tyrosine and azatyrosine or the alkyl amino acids alanine, valine, leucine, isoleucine and methionine. The aromatic amino acids are preferably derivatized at the 2 position (phenyl) and 3 position (2-pyridyl analogue) with a (C.sub.1-C.sub.2)alkyl methyl and ethyl. The alkyl can also be present at the 3 and 4 position on the aromatic ring of phenylalanine and position in meta-tyrosine. [0015] Preferred analogues are selected from the group consisting of [.sup.18F] labelled .beta.-2-fluoromethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-3-fluoromethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-4-fluoromethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-2-fluoroethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-3-fluoroethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-4-fluoroethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-2-fluoromethylphenyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-3-fluoromethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-4-fluoromethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-5-fluoromethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-3-fluoroethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.-4-fluoroethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled .beta.5-fluoroethyl-2-pyridyl-.alpha.-aminopropionic acid, [.sup.18F] labelled 2-amino-3-(5-fluoromethyl-3-hydroxyphenyl)propanoic acid, [.sup.18F] labelled 2-amino-3-(6-fluoromethyl-3-hydroxyphenyl)propanoic acid, [.sup.18F] labelled 2-amino-3-(2-fluoromethyl-4-hydroxyphenyl) propanoic acid, [.sup.18F] labelled 2-amino-3-(2-fluoroethyl-5-hydroxypyridyl)propanoic acid, [.sup.18F] labelled 2-amino-3-(3-fluoroethyl-5-hydroxy-2-pyridyl)propanoic acid, [.sup.18F] labelled 2-amino-3-(5-fluoroethyl-3-hydroxyphenyl)propanoic acid, [.sup.18F] labelled alanine, [.sup.18F] labelled valine, [.sup.18F] labelled leucine, [.sup.18F] labelled isoleucine and [.sup.18F] labelled methionine. Of these the analogues of which the 2 OR 6 position of the aromatic ring is substituted with the alkyl are found to be preferred because the 4 position (para) is not sterically hampered for biochemical recognition. The invention also relates to all of the above compounds that carry a non-radioactive label, in particular a non-radioactive fluorine atom. [0016] The invention further relates to a pharmaceutical composition comprising one or more amino acid analogues as claimed and an excipient, carrier or diluent. The excipient, diluent or carrier can be any compound or composition in liquid form, that is sterile and non-pyrogenic and can be isotonic saline or an isotonic buffer. [0017] The pharmaceutical composition can be used as a tracer in Positron Emission Tomography (PET) and functional MRI. [0018] The invention further relates to the use of the amino acid analogues in the preparation of a pharmaceutical composition for the diagnosis of cancer. [0019] According to another aspect thereof the invention provides a method for diagnosing a patient for the presence of tumours and/or metastases, which comprises administration of a diagnostic effective amount of one or more of the amino acid analogues, and visualizing the localisation of the analogues in the patients body, such as by means of PET or functional MRI. [0020] The present invention further provides precursor compounds for preparing the amino acid analogues, which precursors have the general formula wherein: R is (C.sub.1-C.sub.4)alkyl when n=0 or phenyl or pyridyl when n=1, 2 or 3; X is a leaving group, in particular tosyl, mesityl triflate or a halogen; and NH.sub.2 and COOH are protected. Continue reading about F-18 labeled amino acid analogs... 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