Name | h-his-gly-oh |
---|---|
Synonyms |
HIS-GLY
N-L-Histidylglycine L-His-Gly-OH N-Histidylglycine L-HIS-GLY His-Gly-OH MFCD00037863 (S)-2-(2-Amino-3-(1H-imidazol-4-yl)propanamido)acetic acid L-histidyl-glycine histidylglycine |
Description | (S)-2-(2-Amino-3-(1H-imidazol-4-yl)propanamido)acetic acid is a Glycine (HY-Y0966) 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 |
Density | 1.434g/cm3 |
---|---|
Boiling Point | 687.4ºC at 760mmHg |
Melting Point | 180-182℃ |
Molecular Formula | C8H12N4O3 |
Molecular Weight | 212.20600 |
Flash Point | 369.5ºC |
Exact Mass | 212.09100 |
PSA | 121.10000 |
Vapour Pressure | 7.73E-20mmHg at 25°C |
Index of Refraction | 1.604 |
Storage condition | −20°C |
WGK Germany | 3 |
---|---|
HS Code | 2933290090 |
~62% 2578-58-7 |
Literature: Foerster, Martin; Vahrenkamp, Heinrich Chemische Berichte, 1995 , vol. 128, # 6 p. 541 - 550 |
~% 2578-58-7 |
Literature: Helvetica Chimica Acta, , vol. 40, p. 187,190 Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 307, p. 23,31 |
~% 2578-58-7 |
Literature: Helvetica Chimica Acta, , vol. 40, p. 187,190 Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 307, p. 23,31 |
~% 2578-58-7 |
Literature: Helvetica Chimica Acta, , vol. 40, p. 187,190 Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 307, p. 23,31 |
Precursor 2 | |
---|---|
DownStream 0 |
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% |