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H-GLN-ALA-OH, also known as L-Glutaminyl-L-alanine, is a dipeptide consisting of two amino acids, L-Glutamine and L-Alanine, connected by a peptide bond. This chemical compound is significant due to its role as a constituent in many proteins and in biological reactions in the body. The 'H' in the name indicates the presence of a hydrogen atom at the start of the compound, while 'OH' at the end indicates a hydroxyl group. H-GLN-ALA-OH is generally used in the field of biochemistry for research purposes and is soluble in water, requiring storage in a cool, dry place to maintain its chemical stability.

16874-70-7

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16874-70-7 Usage

Uses

Used in Biochemical Research:
H-GLN-ALA-OH is used as a research compound for studying the structure, function, and interactions of proteins and peptides in various biological processes. Its presence in many proteins and involvement in biological reactions make it a valuable tool for understanding the mechanisms of protein synthesis, folding, and stability.
Used in Pharmaceutical Development:
H-GLN-ALA-OH can be used as a building block for the development of novel pharmaceuticals targeting specific diseases and conditions. Its unique properties and interactions with other molecules can be harnessed to design drugs with improved efficacy, selectivity, and reduced side effects.
Used in Nutritional Supplements:
Due to its role in protein synthesis and its presence in many proteins, H-GLN-ALA-OH can be used as a nutritional supplement to support muscle growth, recovery, and overall health. It may be particularly beneficial for athletes and individuals with increased protein requirements.
Used in Cosmetics and Personal Care Products:
H-GLN-ALA-OH can be incorporated into cosmetics and personal care products for its potential skin-protecting and moisturizing properties. Its ability to interact with proteins and peptides in the skin may contribute to improved skin health, hydration, and barrier function.
Used in Food and Beverage Industry:
H-GLN-ALA-OH can be used as a flavor enhancer or a functional ingredient in food and beverage products. Its presence in proteins and its ability to interact with other molecules may contribute to improved taste, texture, and nutritional value of the products.

Check Digit Verification of cas no

The CAS Registry Mumber 16874-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16874-70:
(7*1)+(6*6)+(5*8)+(4*7)+(3*4)+(2*7)+(1*0)=137
137 % 10 = 7
So 16874-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H15N3O4/c1-4(9)7(13)11-5(8(14)15)2-3-6(10)12/h4-5H,2-3,9H2,1H3,(H2,10,12)(H,11,13)(H,14,15)

16874-70-7SDS

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-GLN-ALA-OH

1.2 Other means of identification

Product number -
Other names L-Glutaminyl=>L-alanin

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:16874-70-7 SDS

16874-70-7Downstream Products

16874-70-7Relevant academic research and scientific papers

Disulfide bridged cyclic peptides containing a cgridri sequence useful in control of hypertension

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, (2014/02/10)

Disulfide bridged cyclic peptides are described which are preferably 13 to 20 amino acid residues in length and which include the endocyclic sequence cys-gly-arg-ile-asp-arg-ile. Peptides of this class are selective for and show picomolar-range affinity for the non-guanyl cyclase-coupled atrial peptide receptor. Affinity for this receptor is associated with potentiation of the mean arterial pressure response to atrial peptide and these peptides are therefore useful in control of hypertension. Peptides of most interest are of the formula wherein X1 is the peptidic fragment ser-ser; wherein X2 is a peptidic fragment selected from gly-ser-gly-leu, gly-ala-gly-leu and gly-leu; wherein X3 is the peptidic fragment asn-ser-phe-arg; wherein m is zero or one, n is one and r is one; and wherein A represents an amino terminus or its pharmaceutically--acceptable salt, and B represents a carboxyl terminus or its pharmaceutically-acceptable ester, amide or salt.

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