3-Carbamimidamido-L-alanine hydrochloride (1:1)

Names

[ Name ]:
3-Carbamimidamido-L-alanine hydrochloride (1:1)

[Synonym ]:
Ethanaminium, 1-carboxy-2-[(diaminomethylene)amino]-, chloride (1:1)
1-Carboxy-2-[(diaminomethylene)amino]ethanaminium chloride
L-Alanine, 3-[(aminoiminomethyl)amino]-, hydrochloride (1:1)
(S)-2-Amino-3-guanidinopropanoic acid hydrochloride
L-2-Amino-3-guanidinopropionic acid hydrochloride
3-Guanidino-L-alanine hydrochloride
3-Carbamimidamido-L-alanine hydrochloride (1:1)
(2S)-2-amino-3-(diaminomethylideneamino)propanoic acid,hydrochloride

Biological Activity

[Description]:

(S)-2-amino-3-guanidinopropanoic acid hydrochloride is an alanine derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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):1793-1023.

Chemical & Physical Properties

[ Boiling Point ]:
370.8ºC at 760 mmHg

[ Melting Point ]:
-220ºC (dec.)

[ Molecular Formula ]:
C₄H₁₁ClN₄O₂

[ Molecular Weight ]:
182.609

[ Flash Point ]:
178.1ºC

[ Exact Mass ]:
182.057053

[ PSA ]:
125.22000

[ LogP ]:
0.57460

[ Vapour Pressure ]:
1.62E-06mmHg at 25°C

[ Storage condition ]:
2-8°C

MSDS

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Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Noncoded amino acid replacement probes of the aspartate aminotransferase mechanism.

Biochemistry 36 , 10517-10525, (1997)

The primary role of Tyr225 in the aspartate aminotransferase mechanism is to provide a hydrogen bond to stabilize the 3'O- functionality of bound pyridoxal phosphate. The strength of this hydrogen bon...

Binding of the unreactive substrate analog L-2-amino-3-guanidinopropionic acid (dinor-L-arginine) to human arginase I.

Acta Crystallogr. Sect. F Struct. Biol. Cryst. Commun. 68(Pt 8) , 889-93, (2012)

Human arginase I (HAI) is a binuclear manganese metalloenzyme that catalyzes the hydrolysis of L-arginine to form L-ornithine and urea through a metal-activated hydroxide mechanism. Since HAI regulate...

Analysis of 1- and 3-methylhistidines, aromatic and basic amino acids in rat and human urine. Feldhoff RC, Ledden DJ, et al.

J. Chromatogr. A. 311 , 267-276, (1984)