前往化源商城

L-Threonine-d2

更新时间:2025-08-26 18:14:07

L-Threonine-d2结构式
L-Threonine-d2结构式
品牌特惠专场
常用名 L-Threonine-d2 英文名 L-Threonine-d2
CAS号 1202936-45-5 分子量 121.13
密度 N/A 沸点 N/A
分子式 C4H7D2NO3 熔点 N/A
MSDS N/A 闪点 N/A

 L-Threonine-d2用途


L-苏氨酸-d2是氘标记的L-苏氨酸。L-苏氨酸是一种天然氨基酸,可通过微生物发酵产生,用于食品、医药或饲料[1]。

 L-Threonine-d2名称

英文名 L-Threonine-d2

 L-Threonine-d2生物活性

描述 L-苏氨酸-d2是氘标记的L-苏氨酸。L-苏氨酸是一种天然氨基酸,可通过微生物发酵产生,用于食品、医药或饲料[1]。
相关类别
体外研究 氢、碳和其他元素的稳定重同位素已被纳入药物分子中,主要作为药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注[1]。
参考文献

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

[2]. Zhao H, et al. Increasing L-threonine production in Escherichia coli by engineering the glyoxylate shunt and the L-threonine biosynthesis pathway. Appl Microbiol Biotechnol. 2018 Jul;102(13):5505-5518.

[3]. Zhao H, et al. Increasing L-threonine production in Escherichia coli by engineering the glyoxylate shunt and the L-threonine biosynthesis pathway. Appl Microbiol Biotechnol. 2018 Jul;102(13):5505-5518.

[4]. Zhao H, et al. Increasing L-threonine production in Escherichia coli by engineering the glyoxylate shunt and the L-threonine biosynthesis pathway. Appl Microbiol Biotechnol. 2018 Jul;102(13):5505-5518.

[5]. Zhao H, et al. Increasing L-threonine production in Escherichia coli by engineering the glyoxylate shunt and the L-threonine biosynthesis pathway. Appl Microbiol Biotechnol. 2018 Jul;102(13):5505-5518.

[6]. Zhao H, et al. Increasing L-threonine production in Escherichia coli by engineering the glyoxylate shunt and the L-threonine biosynthesis pathway. Appl Microbiol Biotechnol. 2018 Jul;102(13):5505-5518.

 L-Threonine-d2物理化学性质

分子式 C4H7D2NO3
分子量 121.13
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。
品牌现货直购
推荐供应商:

暂无推荐供应商。我要出现这里

相关化合物: 更多...
(2S,3R)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]-3-hydroxypropanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]propanoyl]amino]-3-hydroxybutanoic acid
444846-01-9
(2S,3R)-2-[[(2S,3S)-2-[[(2S)-2,4-diamino-4-oxobutanoyl]amino]-3-methylpentanoyl]amino]-3-hydroxybutanoic acid
350582-78-4
(2S,3R)-2-[[(2S)-6-amino-2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]hexanoyl]amino]-3-hydroxybutanoic acid
872713-13-8
L-Threonine tert-butyl ester hydrochloride
69320-90-7
L-Threonine-13C4,d5,15N
2378755-51-0
L-Threonine-d5
1217456-38-6
L-Threonine-13C4,15N
202468-39-1
(2S,3R)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2R)-2-amino-3-sulfanylpropanoyl]amino]-3-hydroxypropanoyl]amino]-3-phenylpropanoyl]amino]hexanoyl]amino]-3-methylbutanoyl]amino]-3-hydroxybutanoic acid
675108-63-1
(2S,3R)-2-[[2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]acetyl]amino]-3-hydroxybutanoic acid
872713-15-0
4-Hydroxypyrrolidin-3-one
1379340-03-0
Boc-N-Me-Asp(OBzl)-OH
141408-45-9
N-(4-{[1-(4-fluorophenyl)-1H-tetrazol-5-yl]methoxy}phenyl)acetamide
912900-94-8
2H-Pyran, 4-chloro-3-ethyltetrahydro-, trans-
25999-33-1
(2E)-2-[(1-methyl-1H-indol-3-yl)methylidene]-3-oxo-2,3-dihydro-1-benzofuran-6-yl cyclohexanecarboxylate
929380-25-6
2-(4-Benzylpiperazin-1-yl)-5-chloroaniline
893751-49-0
(2S,3S,4R,5R)-5-(6-amino-2-iodopurin-9-yl)-3,4-dihydroxyoxolane-2-carboxylic acid
141018-27-1
(2E)-2-[(5-methoxy-1-methyl-1H-indol-3-yl)methylidene]-3-oxo-2,3-dihydro-1-benzofuran-6-yl 3,4-dimethoxybenzoate
929418-29-1
3-(3-bromo-1H-1,2,4-triazol-5-yl)pyridine
1219571-83-1
(2Z)-7-[(dipropylamino)methyl]-6-hydroxy-2-[(2E)-3-(2-methoxyphenyl)prop-2-en-1-ylidene]-1-benzofuran-3(2H)-one
929398-21-0