3,5-Diiodo-L-tyrosine dihydrate
3,5-Diiodo-L-tyrosine dihydrate structure
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Common Name | 3,5-Diiodo-L-tyrosine dihydrate | ||
|---|---|---|---|---|
| CAS Number | 18835-59-1 | Molecular Weight | 469.012 | |
| Density | 2.405g/cm3 | Boiling Point | 410.5ºC at 760mmHg | |
| Molecular Formula | C9H13I2NO5 | Melting Point | 185ºC | |
| MSDS | Chinese USA | Flash Point | 202.1ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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M. Nakano
Meth. Enzymol. 17A , 660, (1970)
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Formation of diiodotyrosine from thyroxine. Ether-link cleavage, an alternate pathway of thyroxine metabolism.
J. Clin. Invest. 72 , 1234-1245, (1983) Studies were performed to elucidate the nature of the pathway of hepatic thyroxine (T4) metabolism that is activated by inhibitors of liver catalase. For this purpose, the metabolism of T4 in homogenates of rat liver was monitored with T4 labeled with 125I ei... |
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Purification and properties of halogenated tyrosine and thyroid hormone transaminase from rat kidney mitochondria.
J. Biol. Chem. 242 , 73, (1967)
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Chiral discrimination of D- and L-amino acids using iodinated tyrosines as chiral references: effect of iodine substituent.
J. Am. Soc. Mass Spectrom. 18 , 1516-1524, (2007) L-Tyrosine and iodinated L-tyrosines, i.e., 3-iodo-L-tyrosine and 3,5-diiodo-L-tyrosine, are successfully used as chiral references for the chiral discrimination of aliphatic, acidic, and aromatic amino acids. Chiral discrimination is achieved by investigatin... |
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Identification and quantitation of iodotyrosines and iodothyronines in hydrolysate of iodinated casein by capillary electrophoresis.
Talanta 69 , 107-112, (2006) In this paper, a new method for separation, identification and quantitation of iodotyrosines and iodothyronines [3-monoiodo-L-tyrosine (MIT), 3,5-diiodo-L-tyrosine (DIT), L-thyronine (T(0)), 3,5-diiodo-L-thyronine (T(2)), 3,5,3'-triiodo-L-thyronine (T(3)) and... |
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Interaction of pepsin with aromatic amino acids and their derivatives immobilized to Sepharose.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 863 , 135-140, (2008) The interaction of porcine pepsin A with immobilized derivatives of aromatic amino acids was investigated. Divinyl sulfone-activated Sepharose was used to immobilize N-acetyl-l-phenylalanine and 3,5-diiodo-l-tyrosine via their free carboxyl groups and l-tyros... |