Z-Gly-Gly-Leu-pNA

PRODUCT IDENTIFICATION

CAS RN

53046-98-3

EINECS RN

FORMULA

MOLE WEIGHT

H.S CODE

SMILES

CLASSIFICATION

Tripeptide

EXTRA NOTES

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE.

white powder

MELTING POINT

BOILING POINT

DENSITY

SOLUBILITY IN WATER

VAPOR DENSITY

log P(octanol-water)

VAPOR PRESSURE

AUTOIGNITION TEMP

REFRACTIVE INDEX

FLASH POINT

INCOMPATIBLE MATERIALS

Strong oxidizing agents

Has not been reported

NFPA RATINGS

Health: 1; Flammability: 0; Instability: 0;

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking - Tripeptide

Google Scholar Search

PubChem Compound Summary - Z-Gly-Gly-Leu-pNA

http://www.ncbi.nlm.nih.gov/ - Z-Gly-Gly-Leu-pNA

http://www.peptideguide.com/
Application of Synthetic Peptides: Synthetic peptides are widely used for the following purposes: - To verify the structure of naturally occurring peptides as determined by degradation techniques
- To study the relationship between structure and activity of biologically active protein and peptides and establish their molecular mechanisms
- To develop new peptide-based immunogens, hormones, vaccines, etc
Peptide Drugs: Peptide drugs are either naturally-occurring peptides or altered natural peptides. There are many naturally-occurring peptides that are biologically active. If a patient does not naturally produce a peptide that they need, this peptide can be synthesized and given to them. In addition, the amino acids in an active peptide can be altered to make analogues of the original peptide. If the analogue is more biochemical active than the original peptide it is known as an agonist and if it has the reverse effect is known as an antagonist.
Diagnostic Peptides: Peptides can be designed that change color under certain conditions, and these can be used for diagnostic purposes. For example, a chromogenic peptide substrate can readily detect the presence, absence and varying blood levels of enzymes that control blood pressure and blood clotting ability.

Local:
Peptide is the members of the compounds composed of two or more amino acids joined by the linking between one amino acid residue and the carboxyl group of the next amino acid by hydrolysis into linear, branched or cyclical structures. The link is an amide bond, and is sometimes referred to as a peptide bond. Peptides are playing a promising role in the molecular biology and in the creating medicines. Peptides are used in the study of protein structure and function, antibodies for the inhibition of cancer, for the study of protein structure and function research. Peptides are also used as instrumental in mass spectrometry. Biological activities of peptide are applicable in the fields of nutrition, medicine, and cosmetics.

• Dipeptide: a molecule consisting of two amino acids
• Tripeptide a molecule consisting of three amino acids
• Octapeptide: a molecule consisting of eight amino acids
• Oligopeptide: a polypeptide composed of approximately 2-12 amino acids length (or 3 to 40 component amino acids)
• Polypeptide: a single molecule composed of approximately 13 or more amino acids.
• Protein: a linear polypeptides that are normally synthesized on ribosomes.

SALES SPECIFICATION

APPEARANCE

white powder

PURITY

98.0% min (HPLC)

TRANSPORT & REGULATORY INFORMATION

UN NO.

Not regulated

HAZARD SYMBOL

SAFETY INFORMATION

HAZARD OVERVIEW

Not known

GHS

SIGNAL WORD

PICTOGRAMS

HAZARD STATEMENTS

P STATEMENTS

RISK PHRASES

SAFETY PHRASES

PACKING

PRICE INFORMATION