Succinyl-Coenzyme A (sodium salt)

Modify Date: 2024-01-08 19:59:30

Succinyl-Coenzyme A (sodium salt) Structure
Succinyl-Coenzyme A (sodium salt) structure
Common Name Succinyl-Coenzyme A (sodium salt)
CAS Number 108347-97-3 Molecular Weight 865.59100
Density N/A Boiling Point N/A
Molecular Formula C25H38N7O19P3S Melting Point N/A
MSDS Chinese USA Flash Point N/A
Symbol GHS07
GHS07
Signal Word Warning

 Use of Succinyl-Coenzyme A (sodium salt)


Succinyl-Coenzyme A (Succinyl-CoA) sodium is an intermediate of the citric acid cycle. Succinyl-Coenzyme A sodium can be converted to succinic acid and can also combines with glycine to form δ-ALA to synthesize porphyrins (heme). Succinyl-Coenzyme A sodium can be used in the study of metabolic, neurological and haematological abnormalities (such as porphyrias) caused by nutritional vitamin B12 deficiency (resulting in a deficiency in Succinyl-Coenzyme A synthesis)[1][2].

 Names

Name Succinyl coenzyme A sodium salt
Synonym More Synonyms

 Succinyl-Coenzyme A (sodium salt) Biological Activity

Description Succinyl-Coenzyme A (Succinyl-CoA) sodium is an intermediate of the citric acid cycle. Succinyl-Coenzyme A sodium can be converted to succinic acid and can also combines with glycine to form δ-ALA to synthesize porphyrins (heme). Succinyl-Coenzyme A sodium can be used in the study of metabolic, neurological and haematological abnormalities (such as porphyrias) caused by nutritional vitamin B12 deficiency (resulting in a deficiency in Succinyl-Coenzyme A synthesis)[1][2].
Related Catalog

 Chemical & Physical Properties

Molecular Formula C25H38N7O19P3S
Molecular Weight 865.59100
Exact Mass 865.11600
PSA 468.30000
Storage condition 20°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P280-P305 + P351 + P338-P337 + P313
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Risk Phrases 36/37/38
Safety Phrases 22-26-36
RIDADR NONH for all modes of transport

 Articles9

More Articles
Direct biosynthesis of adipic acid from a synthetic pathway in recombinant Escherichia coli.

Biotechnol. Bioeng. 111(12) , 2580-6, (2014)

The C6 dicarboxylic acid, adipic acid, is an important platform chemical in industry. Biobased production of adipic acid is a promising alternative to the current petrochemical route. Here, we report ...

Functional characterization of a vitamin B12-dependent methylmalonyl pathway in Mycobacterium tuberculosis: implications for propionate metabolism during growth on fatty acids.

J. Bacteriol. 190(11) , 3886-95, (2008)

Mycobacterium tuberculosis is predicted to subsist on alternative carbon sources during persistence within the human host. Catabolism of odd- and branched-chain fatty acids, branched-chain amino acids...

Acetate formation in the energy metabolism of parasitic helminths and protists.

Int. J. Parasitol. 40 , 387-397, (2010)

Formation and excretion of acetate as a metabolic end product of energy metabolism occurs in many protist and helminth parasites, such as the parasitic helminths Fasciola hepatica, Haemonchus contortu...

 Synonyms

4-[2-[3-[[4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-[hydroxy(oxido)phosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-4-oxobutanoate