1999-33-3

Basic information

• Product Name: H-GLY-ASN-OH
• Synonyms: NALPHA-GLYCYL-L-ASPARAGINE;H-GLY-ASN-OH;L-GLYCYL ASPARAGINE;GLYCYL-L-ASPARAGINE;N-glycyl-beta-asparagine;gly-asn;(S)-2-(Aminomethyl)carbonylamino-3-carbamoylpropionic acid;(S)-2-[(Aminoacetyl)amino]succinamidic acid
• CAS NO: 1999-33-3
• Molecular Formula: C₆H₁₁N₃O₄
• Molecular Weight: 189.17
• EINECS: 217-881-4
• Product Categories: Amino Acid Derivatives;Biochemistry;Oligopeptides;Peptide Synthesis
• Mol File: 1999-33-3.mol

Chemical Properties

• Boiling Point: 324.41°C (rough estimate)
• Flash Point: 333.8 °C
• Appearance: /
• Density: 1.4204 (rough estimate)
• Vapor Pressure: 2.13E-17mmHg at 25°C
• Refractive Index: -8 ° (C=1, H2O)
• Storage Temp.: -15°C
• Water Solubility: almost transparency in Water
• CAS DataBase Reference: H-GLY-ASN-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-GLY-ASN-OH(1999-33-3)
• EPA Substance Registry System: H-GLY-ASN-OH(1999-33-3)

Safety Data

• Hazardous Substances Data: 1999-33-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
H-GLY-ASN-OH is used as an active pharmaceutical ingredient for its potential therapeutic effects. The dipeptide structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetics Industry:
H-GLY-ASN-OH is used as a key ingredient in the formulation of cosmetics for its moisturizing and skin-conditioning properties. Its ability to improve skin hydration and texture makes it a valuable addition to skincare products.
Used in Food and Beverage Industry:
H-GLY-ASN-OH is used as a flavor enhancer and a nutritional supplement in the food and beverage industry. Its dipeptide structure can contribute to the overall taste and nutritional value of various products, such as sports drinks, energy bars, and dietary supplements.
Used in Research and Development:
H-GLY-ASN-OH is used as a research tool in the field of biochemistry and molecular biology. Its unique properties make it an ideal candidate for studying peptide-protein interactions, enzyme activity, and other biological processes.

InChI:InChI=1/C6H11N3O4/c7-2-5(11)9-3(6(12)13)1-4(8)10/h3H,1-2,7H2,(H2,8,10)(H,9,11)(H,12,13)

Upstream product

• 974-17-4 N-benzyloxycarbonylglycyl-L-asparagine 
• 896436-37-6 -benzylester 
• 35181-18-1 N²-(N,N-phthaloyl-glycyl)-L-asparagine 

Downstream Products

• 52661-99-1 ((S)-3,6-dioxo-piperazin-2-yl)-acetic acid amide 
• 70-47-3 L-asparagine 
• 56-40-6 glycine 
• 401942-23-2 C₄₈H₇₄N₁₀O₁₈ 
• 401942-22-1 ZThrLys(Boc)ProThrAspGlyAsnOH 
• 401942-25-4 ZεAhxAlaAlaThrLys(Boc)ProThrAspGlyAsnOH 
• 151545-29-8 N-benzyloxycarbonylglycyl-L-asparagylglycine benzyl ester 
• 401942-20-9 ZThrAsp(OBzl)GlyAsnOH 
• 974-17-4 N-benzyloxycarbonylglycyl-L-asparagine 

Relevant articles and documents

SYNTHESIS AND PROPERTIES OF PEPTIDE FRAGMENTS OF THE S-REGION OF THE SURFACE PROTEIN OF THE HEPTATITIS B VIRUS

A peptide fragment with the 140-146 sequence of the main component of the surface protein of the hepatitis B virus (HBsAG) and a number of its structural analogues have been synthesized by the classical method in solution.Conjugates of the peptides synthesized with bovine serum albumin and with a synthetic polypeptide analogue of polytuftsin have been obtained.The ability of the preparations to bind antibodies from the blood sera of hepatitis B patients has been studied.The possibility has been shown of their use for revealing antibodies to the heptatitis B virus in solid-phase enzyme-mediated immunoassay.

Novel substrate peptides

A peptide substrate for myristoylating enzymes is disclosed having an amino acid sequence selected from the group consisting of the following sequences or a physiologically acceptable amide or salt derivative thereof: STR1 wherein R=Ala, Asn, Gln or Ser; S=Ala, Arg, Gln, Glu, Phe or Ser; T=Ala or Lys; W=Ala or Ser; X=Ala, Tyr, or Lys; Y=Arg or Pro; and Z=Arg, Leu or Lys.