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01310

N-乙酰基-L-蛋氨酸

Name: <I>N</I>-乙酰基-<SC>L</SC>-蛋氨酸
Brand: SIAL

≥98.5% (T)

别名:

N-acetyl-L-lysine

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关于此项目

线性分子式:

CH₃SCH₂CH₂CH(NHCOCH₃)CO₂H

化学文摘社编号:

65-82-7

分子量:

191.25

UNSPSC Code:

12352209

NACRES:

NA.22

PubChem Substance ID:

329747249

EC Number:

200-617-7

Beilstein/REAXYS Number:

1725552

MDL number:

MFCD00064441

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Quality Level

100

assay

≥98.5% (T), ≥98.5% (TLC)

form

powder or crystals

optical activity

[α]20/D -21.0±1.0°, c = 1% in H₂O

reaction suitability

reaction type: solution phase peptide synthesis

mp

103-106 °C (lit.)

solubility

methanol: 50 mg/mL, clear to very slightly hazy, colorless

application(s)

peptide synthesis

SMILES string

CSCC[C@H](NC(C)=O)C(O)=O

InChI

1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m0/s1

InChI key

XUYPXLNMDZIRQH-LURJTMIESA-N

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Physicochemical and catalytic properties of acylase I from aspergillus melleus immobilized on amino- and carbonyl-grafted stöber silica.

Agnieszka Kołodziejczak-Radzimska et al.

Biotechnology progress, 34(3), 767-777 (2018-01-10)

Acylase I from Aspergillus melleus was immobilized on supports consisting of unmodified and modified silica. Modification was performed using 3-aminopropyltriethoxysilane (APTES) and glutaraldehyde (GA). The effectiveness of immobilization was investigated using the standard Bradford method in addition to a number

Prevention of bromobenzene toxicity by N-acetylmethionine: correlation between toxicity and the impairment in O- and S-methylation of bromothiocatechols.

K Lertratanangkoon et al.

Toxicology and applied pharmacology, 122(2), 191-199 (1993-10-01)

Bromobenzene (800 mg/kg, ip) caused severe liver necrosis with massive hemorrhage in the golden Syrian hamster within the first 24 hr. Kidney injury was also observed. Treatment with N-acetylmethionine (NAM) at an ip dose of 1200 mg/kg at 5 hr

Evolution of enzymatic activity in the enolase superfamily: structural studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis.

James B Thoden et al.

Biochemistry, 43(19), 5716-5727 (2004-05-12)

Divergent evolution of enzyme function is commonly explained by a gene duplication event followed by mutational changes that allow the protein encoded by the copy to acquire a new function. An alternate hypothesis is that this process is facilitated when

Model sclerotization studies. 4. Generation of N-acetylmethionyl catechol adducts during tyrosinase-catalyzed oxidation of catechols in the presence of N-acetylmethionine.

M Sugumaran et al.

Archives of insect biochemistry and physiology, 38(1), 44-52 (1998-05-20)

Incubation of catechol with mushroom tyrosinase in the presence of N-acetylmethionine resulted in the generation of an adduct. This product was identified to be N-acetylmethionyl catechol, on the basis of spectral characteristics and well-characterized chemical reaction of o-benzoquinone with N-acetylmethionine.

X-ray spectroscopic approaches to the investigation and characterization of photochemical processes.

Pierre Kennepohl et al.

Journal of synchrotron radiation, 16(Pt 4), 484-488 (2009-06-19)

Despite a wealth of studies exemplifying the utility of the 2-5 keV X-ray range in speciation and electronic structure elucidation, the exploitation of this energy regime for the study of photochemical processes has not been forthcoming. Herein, a new endstation

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货号	GTIN
01310-5G	04061838608932
01310-25G	04061833416365

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