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24046-71-7

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24046-71-7 Usage

General Description

H-TRP-ALA-OH is a chemical compound consisting of the amino acids tryptophan (TRP) and alanine (ALA) linked together. Tryptophan is an essential amino acid that plays a key role in the production of serotonin and melatonin, while alanine is a non-essential amino acid involved in converting glucose to energy. The compound H-TRP-ALA-OH may have potential therapeutic and pharmaceutical applications due to the specific properties and functions of tryptophan and alanine. However, further research and studies are needed to fully understand the potential uses and effects of H-TRP-ALA-OH in biological and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 24046-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24046-71:
(7*2)+(6*4)+(5*0)+(4*4)+(3*6)+(2*7)+(1*1)=87
87 % 10 = 7
So 24046-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H17N3O3/c1-8(14(19)20)17-13(18)11(15)6-9-7-16-12-5-3-2-4-10(9)12/h2-5,7-8,11,16H,6,15H2,1H3,(H,17,18)(H,19,20)

24046-71-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name H-TRP-ALA-OH

1.2 Other means of identification

Product number -
Other names L-tryptophyl-L-alanine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24046-71-7 SDS

24046-71-7Downstream Products

24046-71-7Relevant articles and documents

Heavy atom induced phosphorescence study on the influence of internal structural factors on the photophysics of tryptophan in aqueous solutions

Kowalska-Baron, Agnieszka,Ga??cki, Krystian,Rozniakowski, Kamil,Kolesińska, Beata,Kamiński, Zbigniew J.,Wysocki, Stanis?aw

, p. 830 - 837 (2014/04/17)

In this study the effect of alanyl residue insertion into tryptophan and to some extent the effect of peptide bond on the photophysics of tryptophan chromophore has been studied. The photophysical parameters crucial in triplet state decay mechanism of aqueous AW, WA and AWA peptides have been determined applying our previously proposed methodology based on the heavy atom effect and compared with the previously reported values for tryptophan (Kowalska-Baron et al., 2012). The obtained results clearly indicated that the presence of alanyl residue and the peptide bond results in the changes in the fluorescence and phosphorescence decay kinetics of tryptophan. The fluorescence decays of the oligopeptides studied at pH 7 were biexponential. The longer lifetime component of WA arises from anionic form of this dipeptide, while the shorter one may be assigned to the zwitterionic form of WA. The observed invariance of the lifetimes of anionic and zwitterionic forms of WA throughout the pH studied supports the idea that these two components of WA fluorescence decay correspond to nearly independent species, possibly interconverting but at a rate slower than the fluorescence decay rates. Comparing the determined phosphorescence spectra of the oligopeptides studied with that of tryptophan, a slight blue-shift and more evident red-shift was observed in the spectrum of AW and WA, respectively. On the basis of the results of the phosphorescence measurements performed at pH 10, the 170 μs lifetime of WA, observed even at pH 7, may be assigned to the anionic form of the compound. It may be suggested that at pH 7 during the excited triplet state lifetime of WA there is a shift in the equilibrium towards the anionic form of this dipeptide. In the case of AW and AWA at pH 7 the obtained monoexponential decay kinetics, most probably, arise from zwitterionic forms of these peptides. The determined triplet quantum yield of AWA is slightly lower than that of tryptophan, while the quantum yield of AW is twofold lower than that of tryptophan. The highest value of the determined triplet quantum yield of WA confirms the presence of anionic form of this dipeptide at pH 7.

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