Gly-His

Modify Date: 2024-01-03 19:18:32

Gly-His Structure
Gly-His structure
Common Name Gly-His
CAS Number 2489-13-6 Molecular Weight 212.20600
Density 1.56g/cm3 Boiling Point N/A
Molecular Formula C8H12N4O3 Melting Point N/A
MSDS Chinese USA Flash Point N/A

 Use of Gly-His


(S)-2-(2-Aminoacetamido)-3-(1H-imidazol-4-yl)propanoic acid is a histidine derivative[1].

 Names

Name h-gly-his-oh
Synonym More Synonyms

 Gly-His Biological Activity

Description (S)-2-(2-Aminoacetamido)-3-(1H-imidazol-4-yl)propanoic acid is a histidine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Density 1.56g/cm3
Molecular Formula C8H12N4O3
Molecular Weight 212.20600
Exact Mass 212.09100
PSA 121.10000
Vapour Pressure 3.33E-18mmHg at 25°C
Index of Refraction 1.604
Storage condition -20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 1
HS Code 2933290090

 Synthetic Route

~82%

Gly-His Structure

Gly-His

CAS#:2489-13-6

Literature: Chemische Berichte, , vol. 128, # 6 p. 541 - 550

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Gly-His Structure

Gly-His

CAS#:2489-13-6

Literature: Journal of the American Chemical Society, , vol. 75, p. 2388

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Gly-His Structure

Gly-His

CAS#:2489-13-6

Literature: Journal of the American Chemical Society, , vol. 75, p. 2388

~%

Gly-His Structure

Gly-His

CAS#:2489-13-6

Literature: Chemistry - A European Journal, , vol. 14, # 8 p. 2536 - 2541

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Gly-His Structure

Gly-His

CAS#:2489-13-6

Literature: Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 307, p. 23,31

 Customs

HS Code 2933290090
Summary 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles17

More Articles
Effect of carnosine and related compounds on the inactivation of human Cu,Zn-superoxide dismutase by modification of fructose and glycolaldehyde.

Biosci. Biotechnol. Biochem. 66 , 36-43, (2002)

Glycolaldehyde, an intermediate of the Maillard reaction, and fructose, which is mainly derived from the polyol pathway, rapidly inactivate human Cu,Zn-superoxide dismutase (SOD) at the physiological ...

Reduction of vanadium(V) to vanadium(IV) by NADPH, and vanadium(IV) to vanadium(III) by cysteine methyl ester in the presence of biologically relevant ligands.

Biochim. Biophys. Acta 1770(8) , 1212-8, (2007)

To better understand the mechanism of vanadium reduction in ascidians, we examined the reduction of vanadium(V) to vanadium(IV) by NADPH and the reduction of vanadium(IV) to vanadium(III) by L-cystein...

A comparative study of complex formation in the reactions of gold(III) with Gly-Gly, Gly-L-Ala and Gly-L-His dipeptides.

Bioorg. Chem. 38(4) , 144-8, (2010)

Proton NMR spectroscopy was applied to study the reactions of the dipeptides glycyl-glycine (Gly-Gly) and glycyl-L-alanine (Gly-L-Ala) with hydrogen tetrachloridoaurate(III) (H[AuCl(4)]). All reaction...

 Synonyms

GLY-HIS
N-Glycyl-L-histidine
Gly-L-His-L-Lis-OH
L-Gly-L-His-OH
Gly-L-His-OH
gly-his free base
glycylhistidine
Gly-His-OH
(2S)-2-(glycylamino)-3-(4H-imidazol-4-yl)propionic acid
glycyl-L-histidine
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