Boc-Met-OSu

Names

[ Name ]:
Boc-Met-OSu

[Synonym ]:
BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER
Boc-Met-OSu
N-(tert-Butoxycarbonyl)-L-Methionine N-SucciniMidyl Ester
N-Boc-L-methionine N-Succinimidyl Ester
BOC-Met-ONsu
BOC-METHIONINE-OSU
2,5-Dioxo-1-pyrrolidinyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}methioninate
n-hydroxysuccinimidylt-butoxycarbonylmethionine
BOC-L-METHIONINE HYDROXYSUCCINIMIDE ESTER
Methionine, N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester
t-Boc-Met-OSu
N-tert-butyloxycarbonyl-L-methionine N-succinimidoyl ester
TBM-NHS
Boc-L-Met-OSu
Boc-L-methionine hydeoxysuccinimide ester
N-Boc-L-methionine N-Succinimidyl EsterBoc-Met-OSu
BOC-L-METHIONINE HYDROXYSUCCINIMIDESTER
tert-butyloxycarbonylmethionine N-hydroxysuccinimide ester
N-Boc-L-methionine N-hydroxysuccinimide ester

Biological Activity

[Description]:

Boc-Met-OSu is a Methionine (HY-13694) 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):1793-1144.

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Melting Point ]:
120-126ºC

[ Molecular Formula ]:
C₁₄H₂₂N₂O₆S

[ Molecular Weight ]:
346.399

[ Exact Mass ]:
346.119843

[ PSA ]:
127.31000

[ LogP ]:
0.63

[ Appearance of Characters ]:
Solid

[ Index of Refraction ]:
1.536

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29309090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

High affinity binding of a glycopeptide elicitor to tomato cells and microsomal membranes and displacement by specific glycan suppressors.

J. Biol. Chem. 268(20) , 14724-31, (1993)

We have previously isolated glycopeptides derived from yeast invertase that acted as highly potent elicitors in suspension-cultured tomato cells, inducing ethylene biosynthesis and phenylalanine ammon...

Peracylation of nucleosides with methionine: foundation for a method to detect carcinogen adducts.

Chem. Res. Toxicol. 7(5) , 650-8, (1994)

We report the chemical foundation for a new method to detect carcinogen-DNA adducts, which we have designated adduct detection by acylation with methionine (ADAM). The method is based on reaction of D...