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L-Tyrosine-d7 Sale

(Synonyms: L-酪氨酸 d7) 目录号 : GC64433

L-Tyrosine-d7 是 L-Tyrosine 的氘代物。L-Tyrosine 是一种非必需氨基酸,能抑制后部皮层中柠檬酸合成酶的活性。

L-Tyrosine-d7 Chemical Structure

Cas No.:130551-49-4

规格 价格 库存 购买数量
1 mg
¥990.00
现货
5 mg
¥3,060.00
现货
10 mg
¥4,860.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

L-Tyrosine-d7 is the deuterium labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex.

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

Chemical Properties

Cas No. 130551-49-4 SDF Download SDF
别名 L-酪氨酸 d7
分子式 C9H4D7NO3 分子量 188.23
溶解度 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 5.3126 mL 26.5632 mL 53.1265 mL
5 mM 1.0625 mL 5.3126 mL 10.6253 mL
10 mM 0.5313 mL 2.6563 mL 5.3126 mL
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Research Update

Quantitation of deuterated and non-deuterated phenylalanine and tyrosine in human plasma using the selective ion monitoring method with combined gas chromatography-mass spectrometry. Application to the in vivo measurement of phenylalanine-4-monooxygenase activity

J Chromatogr 1977 Nov 11;142:523-31.PMID:914934DOI:10.1016/s0021-9673(01)92065-5

A specific method is described for the quantitative analysis of deuterated and non-deuterated phenylalanine and tyrosine in human plasma by gas chromatography-mass spectrometry using selective ion monitoring. From the several derivatives investigated, the N- or N,O-trifluoroacetyl methyl esters were found to be the most suitable for our purposes. DL-Phenylalanine-4-d1 and L-Tyrosine-d7 were used as internal standards. The sensitivity of this method permits the measurement of amounts as small as ca. 2.5 ng/ml in plasma for both phenylalanine and tyrosine. The coefficients of variation were found to be ca. 1.6% (n = 12) for phenylalanine and 3.0% (n = 12) for tyrosine. Using this method, an in vivo determination of phenylalanine-4-monooxygenase activity in humans is possible by loading the subjects with deuterated L-phenylalanine-d5 (accepted as substrate by phenylalanine-4-monooxygenase E.C. 1.14.16.1) and the subsequent measuring of deuterated L-tyrosine-d4 formed and residual L-phenylalanine-d5.