N-乙酰基-L-蛋氨酸 | 65-82-7
中文名称:
N-乙酰基-L-蛋氨酸
英文名称:
N-Acetyl-L-methionine
CAS No.:
65-82-7
分子式:
C7 H1 3 NO3 S
分子量:
191.2480
名称和标识符
MDL
MFCD00064441
InChIKey
XUYPXLNMDZIRQH-LURJTMIESA-N
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
SMILES
S(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]([H])(C(=O)O[H])N([H])C(C([H])([H])[H])=O
BRN
1725552
别名信息
- 中文别名 -
N-乙酰基-L-蛋氨酸
醋酸基甲硫氨酸
N-乙酰-L-蛋氨酸
L(-)-N-乙酰甲硫氨基丁酸
L(-)-N-乙酰甲硫氨酸
N-乙酰-L(-)-蛋氨酸
N-乙酰-L-甲硫氨基酸
N-乙酰-L(DL)-蛋氨酸
(S)-2-乙酰氨基-4-(甲硫基)丁酸
N-Acetyl-L-methionine N-乙酰-L-蛋氨酸
N-乙酰-L-蛋氨酸(NAM)
N-乙酰-L-蛋氨酸及合成技术
N-乙酰-L-甲硫氨酸
乙酰蛋氨酸
L-(-)-N-乙酰甲硫氨基丁酸
-乙酰-L-蛋氨酸
- 英文别名 -
N-Acetyl-L-methionine
NAM
L-Methionine-15N, N-Acetyl Derivative
ACETYL-L-METHIONINE
AC-MET-OH
AC-METHIONINE
N-ACETYL-L-MET
N-AC-L-MET
N-AC-L-METHIONINE
N-ALPHA-ACETYL-L-METHIONINE
N-Acetyl-L-methionine (NAM)
(2S)-2-acetamido-4-methylsulfanylbutanoic acid
(S)-2-Acetylamino-4-methylsulfanyl-butyric acid
N-Acety-L-Methionine
N-Acetylmethionine
L-Methionine, N-acetyl-
L-(N-Acetyl)methionine
Acetylmethionine
Methionamine
(S)-2-acetamido-4-(methylthio)butanoic acid
Methionine, N-acetyl-, L-
Thiomedon
AcMet
N-Ac-Met
Nalpha-acetyl-L-methionine
Acetylmethionin
XUYPXLNMDZIRQH-LURJTMIESA-N
Methionine, N-acetyl-, L- (8CI)
Methionin
(2S)-2-acetamido-4-(methylsu
Ac-Met-OH
(2S)-2-acetamido-4-(methylsulfanyl)butanoic acid
Acetyl-L-methionine
物化性质
实验特性
LogP
0.71970
PSA
91.70000
Merck
96
折射率
-21 ° (C=1, H2O)
沸点
453.6℃ at 760 mmHg
熔点
103-106 °C (lit.)
闪点
228.1℃
溶解度
methanol: soluble100mg/mL, clear, colorless
颜色与性状
无色或有光泽的白色晶体或白色粉末。无臭或几乎无臭
稳定性
Stable. Incompatible with strong oxidizing agents.
溶解性
溶于水、乙醇、碱性溶液和稀无机酸,几乎不溶于乙醚
比旋光度
-20 º (c=4 H2O)
光学活性
[α]20/D -21.0±1.0°, c = 1% in H2O
密度
1.2684 (rough estimate)
计算特性
精确分子量
191.06200
氢键供体数量
2
氢键受体数量
4
可旋转化学键数量
5
同位素质量
191.062
重原子数量
12
复杂度
172
同位素原子数量
0
确定原子立构中心数量
1
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
0.1
互变异构体数量
2
表面电荷
0
拓扑分子极性表面积
91.7
海关数据
海关编码
29309070
海关数据
中国海关编码:
29309070
相关文献
1.
Reactivity of a cationic square-planar palladium(II) chloro complex containing bis[2-(diphenylphosphino)ethyl]amine: chloro substitutions by anionic ligands and formation of neutral digold(I) compounds possessing linear PAuX fragments. The X-Ray crystal structure of Au2[Ph2P(CH2)2N(NO)(CH2)2PPh2]Cl2
M. Inés García-Seijo,Abraha Habtemariam,Simon Parsons,R. O. Gould,M. Esther García-Fernández New J. Chem. 2002 26 636
2.
Targeted metabolomics reveals dynamic portrayal of amino acids and derivatives in triple-negative breast cancer cells and culture media
Fang Kou,Bangjie Zhu,Wenbin Zhou,Chunming Lv,Yu Cheng,Hai Wei Mol. Omics 2021 17 142
3.
Spectroscopic and potentiometric studies on the interaction of trans-[(MeH2N)2Pt(mcyt)2PdCl]NO3(mcyt = 1-methylcytosinate) with derivatives of amino acids
Imre Sóvágó,Attila Kiss,Bernhard Lippert J. Chem. Soc. Dalton Trans. 1995 489
4.
A highly selective and simultaneous determination of ascorbic acid, uric acid and nitrite based on a novel poly-N-acetyl-l-methionine (poly-NALM) thin film
Ayyadurai Kannan,Arumugam Sivanesan,Govindasamy Kalaivani,Arumugam Manivel,Ranganathan Sevvel RSC Adv. 2016 6 96898
5.
Stabilization of monofunctional platinum–nucleotide adducts: reactions of N-acetyl-L-methionine complexes with guanosine 5′-monophosphate and guanylyl(3′–5′)guanosine
Kevin J. Barnham,Zijian Guo,Peter J. Sadler J. Chem. Soc. Dalton Trans. 1996 2867
6.
Gold(I)-induced chelate ring-opening of palladium(II) and platinum(II) triphos complexes
Paloma Sevillano,Abraha Habtemariam,Simon Parsons,Alfonso Casti?eiras,M. Esther García,Peter J. Sadler J. Chem. Soc. Dalton Trans. 1999 2861
7.
Gold(I)-induced chelate ring-opening of palladium(II) and platinum(II) triphos complexes
Paloma Sevillano,Abraha Habtemariam,Simon Parsons,Alfonso Casti?eiras,M. Esther García,Peter J. Sadler J. Chem. Soc. Dalton Trans. 1999 2861
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Experimental and quantum chemical study of photochemical properties of 4-hydroxyquinoline
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Green light-induced apoptosis in cancer cells by a tetrapyridyl ruthenium prodrug offering two trans coordination sites
V. H. S. van Rixel,B. Siewert,S. L. Hopkins,S. H. C. Askes,A. Busemann,M. A. Siegler,Sylvestre Bonnet Chem. Sci. 2016 7 4922
10.
Ligand-centred redox activation of inert organoiridium anticancer catalysts
Wen-Ying Zhang,Samya Banerjee,George M. Hughes,Hannah E. Bridgewater,Ji-Inn Song,Ben G. Breeze,Guy J. Clarkson,James P. C. Coverdale,Carlos Sanchez-Cano,Fortuna Ponte,Emilia Sicilia,Peter J. Sadler Chem. Sci. 2020 11 5466
参考资料
Reaxys RN
1725552
Beilstein
1725552
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