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Succinyl-Coenzyme A (sodium salt)

Names

[ CAS No. ]:
108347-97-3

[ Name ]:
Succinyl-Coenzyme A (sodium salt)

[Synonym ]:
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

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]:

Research Areas >> Metabolic Disease
Research Areas >> Neurological Disease

Chemical & Physical Properties

[ Molecular Formula ]:
C25H38N7O19P3S

[ Molecular Weight ]:
865.59100

[ Exact Mass ]:
865.11600

[ PSA ]:
468.30000

[ Storage condition ]:
20°C

MSDS

Safety Information

[ Symbol ]:

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

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...


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Related Compounds