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D-ALA-ALA-ALA, also known as D-Alanyl-D-alanyl-D-alanine, is a tripeptide compound composed of three D-alanine amino acids. These D-enantiomeric amino acids have a specific spatial arrangement, which is less common in nature compared to their L-counterparts. The unique arrangement of the three D-alanine molecules in D-ALA-ALA-ALA may influence their interactions with other molecules or proteins, although the exact uses or roles of D-ALA-ALA-ALA are not clearly defined and may vary depending on the context in which it is utilized or studied.

5874-89-5

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5874-89-5 Usage

Uses

Used in Pharmaceutical Applications:
D-ALA-ALA-ALA is used as a pharmaceutical compound for its potential interactions with other molecules or proteins. The specific spatial arrangement of the D-alanine molecules in this tripeptide may contribute to its unique properties and applications in drug development.
Used in Metabolic Studies:
D-ALA-ALA-ALA is used as a research tool in metabolic studies, where its role in contributing to metabolism and energy production can be investigated. The presence of three D-alanine molecules in D-ALA-ALA-ALA may provide insights into the metabolic processes involving D-enantiomeric amino acids.
Used in Biochemical Research:
D-ALA-ALA-ALA is used as a biochemical research compound to study the interactions between D-enantiomeric amino acids and other biological molecules. The unique arrangement of the three D-alanine molecules in this tripeptide may help researchers understand the differences in properties and roles between Dand L-enantiomeric amino acids.
Used in Nutritional Supplements:
D-ALA-ALA-ALA is used as a nutritional supplement to provide the body with D-enantiomeric amino acids, which may have different roles in metabolism and energy production compared to their L-counterparts. The inclusion of this tripeptide in supplements may offer potential health benefits depending on the context of its use.
Used in Cosmetic Applications:
D-ALA-ALA-ALA is used as a cosmetic ingredient for its potential benefits in skincare and other beauty products. The unique properties of the D-enantiomeric amino acids in this tripeptide may contribute to the development of innovative cosmetic formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 5874-89-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5874-89:
(6*5)+(5*8)+(4*7)+(3*4)+(2*8)+(1*9)=135
135 % 10 = 5
So 5874-89-5 is a valid CAS Registry Number.

5874-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name H-D-Ala-Ala-Ala-OH

1.2 Other means of identification

Product number -
Other names D-Ala-L-Ala-L-Ala

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:5874-89-5 SDS

5874-89-5Upstream product

5874-89-5Downstream Products

5874-89-5Relevant academic research and scientific papers

A cell wall-active lipopeptide from the fungus Pochonia bulbillosa

Koehn, Frank E.,Kirsch, Donald R.,Feng, Xidong,Janso, Jeffrey,Young, Mairead

, p. 2045 - 2048 (2008)

Bioassay-directed fractionation of a fermentation of Pochonia bulbinosa, culture 38G272, led to the isolation of a series of structurally novel, prospective cell wall-active lipopeptides. The main component of this suite is 1, a linear hexapeptide with a δ-hydroxymyristic acid amide substituted N-terminus. The structure was deduced using high-field microsample NMR, Fourier transform mass spectrometry, and microscale chemical degradation. The potent cell wall activity and synthetically accessible structure of 1 make it a potential lead for further investigation.

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