Weight | 307.087 g/mol |
---|---|
Formula | C9H10INO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
3-Iodo-L-tyrosine (70-78-0)
3-iodotyrosine
Score:
#1588 in Biochemistry
,
#4569 in Chemistry
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- SPECT Studies of Brain Tumors with L-3-[123I]Iodo--Methyl Tyrosine: Comparison with PET, 124IMT and First Clinical Results (The Journal of Nuclear Medicine, 1990)
- Imaging of brain tumors with L-3-[123I]iodo--methyl tyrosine and SPECT (The Journal of Nuclear Medicine, 1989)
- Transport Mechanisms of 3-[123I]Iodo--Methyl-L-Tyrosine in a Human Glioma Cell Line: Comparison with [3H-methyl]-L-Methionine (The Journal of Nuclear Medicine, 2000)
- Brain and brain tumor uptake of L-3-[123I]iodo-alpha-methyl tyrosine: competition with natural L-amino acids. (The Journal of Nuclear Medicine, 1991)
- 3-[123I]Iodo--methyl-L-tyrosine: uptake mechanisms and clinical applications (Nuclear Medicine and Biology, 2002)
- Comparison of O-(2-18F-fluoroethyl)-L-tyrosine PET and 3-123I-iodo-a-methyl-L-tyrosine SPECT in brain tumors (The Journal of Nuclear Medicine, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-iodotyrosine
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SMILESC1=CC(=C(C=C1CC(C(=O)O)N)I)O
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InChIKeyUQTZMGFTRHFAAM-UHFFFAOYSA-N
- Pubchem - 3-Iodo-L-tyrosine
- Wikipedia - 3-Iodo-Tyrosine
Monoiodotyrosine is a precursor of thyroid hormone and results from halogenation of tyrosine at the meta-position of the benzene ring. Two units can combine to form 3,3'-diiodothyronine. One unit can combine with diiodotyrosine to form triiodothyronine, as occurs in the colloid of the thyroid follicle.
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