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经验公式(希尔记法):
C9H9I2NO3 · 2H2O
化学文摘社编号:
分子量:
469.01
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
206-092-0
MDL number:
Beilstein/REAXYS Number:
2218691
产品名称
3,5-二碘- L -酪氨酸 二水合物, crystalline
InChI key
NYPYHUZRZVSYKL-ZETCQYMHSA-N
InChI
1S/C9H9I2NO3/c10-5-1-4(2-6(11)8(5)13)3-7(12)9(14)15/h1-2,7,13H,3,12H2,(H,14,15)/t7-/m0/s1
SMILES string
N[C@@H](Cc1cc(I)c(O)c(I)c1)C(O)=O
assay
≥98.0% (HPLC)
form
crystalline
technique(s)
ligand binding assay: suitable
color
white
mp
200 °C (dec.) (lit.)
solubility
4 M NH4OH in methanol: 50 mg/mL, clear, yellow-green
storage temp.
−20°C
Quality Level
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Application
用于测定卤化酪氨酸和甲状腺激素转氨酶的底物。 甲状腺激素生物合成和替代代谢途径中的中间体。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Sangeeta Kumari et al.
Journal of the American Society for Mass Spectrometry, 18(8), 1516-1524 (2007-06-26)
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 investigating the collision-induced dissociation spectra of the trimeric complex [Cu(II)(ref)(2)(A)
Jana Frýdlová et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 863(1), 135-140 (2008-02-08)
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-tyrosine via its amino group. Immobilized l-tyrosine was iodinated
Yining Zheng et al.
Talanta, 69(1), 107-112 (2008-10-31)
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 3,3',5,5'-tetraiodo-L-thyronine (T(4))] was described by using capillary electrophoresis with photodiode-array ultraviolet-visible detection (CE-UV). The
M. Nakano
Methods in Enzymology, 17A, 660-660 (1970)
Purification and properties of halogenated tyrosine and thyroid hormone transaminase from rat kidney mitochondria.
M Nakano
The Journal of biological chemistry, 242(1), 73-81 (1967-01-10)
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