H-Leu-Gly-OH

Names

[ CAS No. ]:
686-50-0

[ Name ]:
H-Leu-Gly-OH

[Synonym ]:
(S)-2-(2-Amino-4-methylpentanamido)acetic acid
2-[[(2S)-2-amino-4-methylpentanoyl]amino]acetic acid,hydrate
MFCD00065940
EINECS 211-688-9
H-Leu-Gly-OH

Chemical & Physical Properties

[ Melting Point ]:
-245ºC (dec.)

[ Molecular Formula ]:
C₈H₁₆N₂O₃

[ Molecular Weight ]:
188.22400

[ Exact Mass ]:
188.11600

[ PSA ]:
92.42000

[ LogP ]:
0.65180

[ Index of Refraction ]:
86 ° (C=2, H2O)

[ Storage condition ]:
−20°C

MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

(2S)-2-(carbamoylamino)-4-methylpentanoic acid
Sodium Glycinate
Glycine
(S)-(-)-4-Isobutyloxazolidine-2,5-Dione
Z-Leu-Gly-OH
L-Valine
2-[(2-bromo-4-methyl-pentanoyl)amino]acetic acid
Benzyloxycarbonyl-L-leucyl-glycin-benzylester

DownStream

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Copper(II)- cis, cis-1,3,5-triaminocyclohexane complex-promoted hydrolysis of dipeptides: kinetic, speciation and structural studies.

J. Biol. Inorg. Chem. 7 , 843-851, (2002)

The hydrolysis of glycylglycine (GylGly), glycyl-L-leucine (GlyLeu), L-leucylglycine (LeuGly) and glycyl-DL-serine (GlySer) promoted by a copper(II)- cis, cis-1,3,5-triaminocyclohexane complex [Cu(II)...

Cleavage of L-leucine-containing dipeptides by Clostridium butyricum. Khelifa N, Brik M, Tessedre AC, et al.

Bioorg. Med. Chem. 9 , 109-112, (1999)