O-SUCCINYL-L-HOMOSERINE

Modify Date: 2024-01-11 08:37:40

O-SUCCINYL-L-HOMOSERINE Structure
O-SUCCINYL-L-HOMOSERINE structure
Common Name O-SUCCINYL-L-HOMOSERINE
CAS Number 1492-23-5 Molecular Weight 219.19200
Density 1.392g/cm3 Boiling Point 492.8ºC at 760mmHg
Molecular Formula C8H13NO6 Melting Point N/A
MSDS Chinese USA Flash Point 251.8ºC

 Use of O-SUCCINYL-L-HOMOSERINE


O-Succinyl-L-homoserine is a homoserine derivative. O-Succinyl-L-homoserine is an intermediate in the biosynthesis of methionine in Escherichia coli and Salmonella typhimurium[1].

 Names

Name O-succinyl-L-homoserine
Synonym More Synonyms

 O-SUCCINYL-L-HOMOSERINE Biological Activity

Description O-Succinyl-L-homoserine is a homoserine derivative. O-Succinyl-L-homoserine is an intermediate in the biosynthesis of methionine in Escherichia coli and Salmonella typhimurium[1].
Related Catalog
References

[1]. Huang JF, et, al. Metabolic engineering of E. coli for the production of O-succinyl-l-homoserine with high yield. 3 Biotech. 2018 Jul;8(7):310.

 Chemical & Physical Properties

Density 1.392g/cm3
Boiling Point 492.8ºC at 760mmHg
Molecular Formula C8H13NO6
Molecular Weight 219.19200
Flash Point 251.8ºC
Exact Mass 219.07400
PSA 126.92000
Vapour Pressure 4.68E-11mmHg at 25°C
Index of Refraction 1.515
Storage condition -20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922509090

 Precursor & DownStream

Precursor  0

DownStream  2

 Customs

HS Code 2922509090
Summary 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles10

More Articles
The enzymology of cystathionine biosynthesis: strategies for the control of substrate and reaction specificity.

Arch. Biochem. Biophys. 433 , 166-175, (2005)

The ability of enzymes to catalyze specific reactions, while excluding others, is central to cellular metabolism. Control of reaction specificity is of particular importance for enzymes that employ ca...

Cloning and characterization of two Lactobacillus casei genes encoding a cystathionine lyase.

Appl. Environ. Microbiol. 74 , 99-106, (2008)

Volatile sulfur compounds are key flavor compounds in several cheese types. To better understand the metabolism of sulfur-containing amino acids, which certainly plays a key role in the release of vol...

Enzymatic characterization and inhibitor discovery of a new cystathionine {gamma}-synthase from Helicobacter pylori.

J. Biochem. 143 , 59-68, (2008)

Cystathionine gamma-synthase (CGS) catalyses the first step of the transsulfuration pathway that converts l-cysteine to l-homocysteine in bacteria, whereas this pathway is absent in human. In this rep...

 Synonyms

(2S)-2-amino-4-(3-carboxypropanoyloxy)butanoic acid
O-Succinyl-L-homoserine