93690
L-色氨酸乙酯 盐酸盐
≥99.0% (AT)
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关于此项目
经验公式（希尔记法）:
C13H16N2O2 · HCl
化学文摘社编号:
分子量:
268.74
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-786-0
Beilstein/REAXYS Number:
3919010
MDL number:
产品名称
L-色氨酸乙酯 盐酸盐, ≥99.0% (AT)
InChI key
PESYCVVSLYSXAK-MERQFXBCSA-N
InChI
1S/C13H16N2O2.ClH/c1-2-17-13(16)11(14)7-9-8-15-12-6-4-3-5-10(9)12;/h3-6,8,11,15H,2,7,14H2,1H3;1H/t11-;/m0./s1
SMILES string
Cl.CCOC(=O)[C@@H](N)Cc1c[nH]c2ccccc12
assay
≥99.0% (AT)
form
powder
optical activity
[α]20/D +10±1°, c = 2% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
220-225 °C (dec.)
application(s)
peptide synthesis
Quality Level
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wgk
WGK 3
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Kento Takayama et al.
Journal of natural medicines, 75(1), 116-128 (2020-10-21)
Indole is produced from dietary tryptophan by tryptophanase in intestinal bacteria, such as Escherichia coli. In the liver, indole is converted into indoxyl sulfate, a uremic toxin and risk factor for chronic kidney disease (CKD). Probiotics and prebiotics are currently
Diana E Schlamadinger et al.
The journal of physical chemistry. B, 113(44), 14769-14778 (2009-10-13)
Ultraviolet resonance Raman (UVRR) spectra of tryptophan compounds in various solvents and a model peptide are presented and reveal systematic changes that reflect solvent polarity, hydrogen bond strength, and cation-pi interaction. The commonly utilized UVRR spectral marker for environment polarity
Anikó Takátsy et al.
Journal of molecular recognition : JMR, 19(4), 270-274 (2006-05-17)
Studies of molecular recognition of chiral compounds by proteins are of importance from many points of view. The biological role of proteins in their interaction with small molecules is of fundamental interest and can be used in many different fields
Ting Sun et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 70(4), 676-680 (2011-12-27)
(18)F labeled natural amino acids have been introduced as promising tumor imaging agents. A novel [(18)F]fluoro amino acid analog 1-[(18)F]fluoroethyl-L-tryptophan (1-[(18)F]FETrp) was designed and synthesized by a two-pot three-step procedure, including the synthesis of 1-[(18)F]fluoro-2- (tosyloxy)ethane, the [(18)F]fluoroethylation of the
Jonathan E Meegan et al.
Soft matter, 13(35), 5922-5932 (2017-08-05)
Four novel amino acid-functionalised triphenylenes have been prepared with glycine, l-alanine, l-phenylalanine and l-tryptophan ethyl ester side-chains. The glycine derivative is a good gelator of chloroform, the alanine derivative gels ethanol and toluene, and the phenylalanine derivative gels benzene and
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