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经验公式(希尔记法):
C4H9NO3
化学文摘社编号:
分子量:
119.12
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
211-171-8
MDL number:
Beilstein/REAXYS Number:
1721643
产品名称
D -苏氨酸, ≥98% (TLC)
InChI
1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m0/s1
InChI key
AYFVYJQAPQTCCC-STHAYSLISA-N
SMILES string
C[C@H](O)[C@@H](N)C(O)=O
assay
≥98% (TLC)
form
powder or crystals
technique(s)
UHPLC: suitable
color
white
mp
274 °C
solubility
H2O: soluble
Quality Level
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Application
在超高效液相色谱系统 UHPLC)系统中,使用 D -苏氨酸作为标准混合物的组分,以定量氨基酸外消旋。
General description
D -苏氨酸性味甘 ,有毒。作为 L-苏氨酸脱水酶的抑制剂。
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Taste Chemistry (2012)
R Contestabile et al.
European journal of biochemistry, 268(24), 6508-6525 (2001-12-12)
Serine hydroxymethyltransferase (SHMT) is a member of the fold type I family of vitamin B6-dependent enzymes, a group of evolutionarily related proteins that share the same overall fold. The reaction catalysed by SHMT, the transfer of Cbeta of serine to
J Q Liu et al.
Journal of bacteriology, 179(11), 3555-3560 (1997-06-01)
We have isolated the gene encoding L-allo-threonine aldolase (L-allo-TA) from Aeromonas jandaei DK-39, a pyridoxal 5'-phosphate (PLP)-dependent enzyme that stereospecifically catalyzes the interconversion of L-allo-threonine and glycine. The gene contains an open reading frame consisting of 1,014 nucleotides corresponding to
J Q Liu et al.
Applied microbiology and biotechnology, 54(1), 44-51 (2000-08-22)
The dtaAX gene encoding a pyridoxal 5'-phosphate (pyridoxal-P)-dependent low-specificity D-threonine aldolase was cloned from the chromosomal DNA of Alcaligenes xylosoxidans IFO 12669. It contains an open reading frame consisting of 1,134 nucleotides corresponding to 377 amino acid residues. The predicted
Kateryna Fesko et al.
Bioorganic & medicinal chemistry letters, 18(22), 5987-5990 (2008-09-02)
The Y265A mutant of alanine racemase (alrY265A) was evaluated as a catalyst for the synthesis of beta-hydroxy-alpha-amino acids. It promotes the PLP-dependent aldol condensation of glycine with a range of aromatic aldehydes. The desired products were obtained with complete stereocontrol
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