추천 제품
분석
≥99.0% (AT)
형태
powder
광학 활성
[α]20/D +10±1°, c = 2% in H2O
반응 적합성
reaction type: solution phase peptide synthesis
mp
220-225 °C (dec.)
응용 분야
peptide synthesis
SMILES string
Cl.CCOC(=O)[C@@H](N)Cc1c[nH]c2ccccc12
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
InChI key
PESYCVVSLYSXAK-MERQFXBCSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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
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
F L Tse et al.
The Journal of pharmacy and pharmacology, 36(9), 633-636 (1984-09-01)
Sandoz compound 57-118 is a mixture of tryptophan ethyl ester amide derivatives (analogues I-V) possessing one of five fatty acid chains which differ in chain length, configuration, or the degree of unsaturation. The relative absorption of each of the five
V Iu Shviadas et al.
Biokhimiia (Moscow, Russia), 45(4), 629-635 (1980-04-01)
The hydrolysis of L-tryptophane ethyl ester catalyzed by alpha-chymotrypsin and the effect of ethyl ster of D-tryptophane on the course of the reaction were studied. A kinetic pattern of a three-step enzymatic reaction based on the assumption that the enzyme
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
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