ChemicalBook--->CAS DataBase List--->104809-02-1

104809-02-1

104809-02-1 Structure

104809-02-1 Structure
IdentificationBack Directory
[Name]

METHYLMALONYL COENZYME A LITHIUM
[CAS]

104809-02-1
[Synonyms]

MM-CoA
Methylmalonyl-CoA
METHYLMALONYL COENZYME A LITHIUM
METHYLMALONYL COENZYME A TETRALITHIUM &
α-methylmalonyl coenzyme a tetralithium salt
coenzyme A methylmalonyl derivative, lithium salt
methylmalonyl coenzyme a tetralithium salt hydrate
Methylmalonyl coenzyme A hydrate tetralithium salt
coenzyme A methylmalonyl derivative, tetralithium hydrate
Methylmalonyl coenzyme A tetralithium salt hydrate >=90% (HPLC)
3-[2-[3-[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-2-hydroxy-3,3-dimethyl-butanoyl]aminopropanoylamino]ethylsulfanyl]-2-methyl-3-oxo-propanoic acid
[Molecular Formula]

C25H41LiN7O19P3S
[MDL Number]

MFCD10567443
[MOL File]

104809-02-1.mol
[Molecular Weight]

875.55
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: 50 mg/mL, clear, colorless
[form ]

Solid
[color ]

Off-white to light yellow
[InChIKey]

ANDKBBZIPFWODN-WLVKLPLXSA-J
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

22-26-36
[WGK Germany ]

3
[F ]

10-21
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

Methylmalonyl coenzyme A (CoA) has been used in the preparation of the calibration curve in ultra-performance liquid chromatography-mass spectrometry (UPLC-MS/MS). It has also been used in the measurement of methylmalonyl-CoA mutase and methylmalonyl-CoA epimerase activity.
[Biochem/physiol Actions]

Methylmalonyl coenzyme A (CoA) is a catabolite of odd-chain fatty acids, cholesterol and few amino acids like valine, isoleucine, methionine, threonine. It is produced by the activity of the enzyme propionyl-CoA carboxylase(PCC). Methylmalonyl coenzyme A (CoA) is converted to succinyl-CoA by the methylmalonyl-CoA mutase (MCM) and vitamin B12 as the cofactor. Either a low MCM activity or an altered metabolism of vitamin B12 causes the inherited metabolic disease methylmalonic acidemia (MMA).
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