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Results for "

Succinyl CoA

" in MedChemExpress (MCE) Product Catalog:

7

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4

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1

Recombinant Proteins

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-E70121
    Succinyl-CoA synthetase

    		Others Others
    Succinyl-CoA synthetase catalyzes the only substrate-level phosphoryl-ation step in the tricarboxylic acid cycle. Succinyl-CoA synthetase is a phosphate target for the activation of mitochondrial metabolism .
    Succinyl-CoA synthetase
  • HY-137808
    Succinyl-Coenzyme A sodium
    1 Publications Verification

    Succinyl-CoA sodium

    		 Endogenous Metabolite Neurological Disease Metabolic Disease
    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) .
    Succinyl-Coenzyme A sodium
  • HY-126791A
    Methylmalonyl-CoA tetralithium

    IsoSuccinyl coenzyme A tetralithium; Methylmalonyl coenzyme tetralithium

    		 Endogenous Metabolite Others
    Methylmalonyl-CoA (Methylmalonyl coenzyme A) tetralithium is a catabolite of valine, isoleucine, methionine, threonine, odd-chain fatty acids, and cholesterol. Methylmalonyl-CoA tetralithium is converted to succinyl-CoA by enzymatic reaction of methylmalonyl-CoA mutase (MCM) with coenzyme vitamin B12 .
    Methylmalonyl-CoA tetralithium
  • HY-148285
    Succinyl CoA

    		Endogenous Metabolite Metabolic Disease
    Succinyl CoA is an intermediate of the citric acid cycle. Succinyl CoA can be converted to succinic acid and can also combines with glycine to form δ-amino levulinic acid (ALA) to synthesize porphyrins (heme). Succinyl CoA 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 CoA synthesis) .
    Succinyl CoA
  • HY-CE00006
    (1-Methylpentyl)succinyl-CoA

    (1-Methylpentyl)Succinyl-coenzyme A

    		 Biochemical Assay Reagents Others
    (1-Methylpentyl)succinyl-CoA ((1-Methylpentyl)succinyl-coenzyme A) is a a higher alkylsuccinyl-CoA .
    (1-Methylpentyl)succinyl-CoA
  • HY-126791
    Methylmalonyl-CoA

    IsoSuccinyl coenzyme A; Methylmalonyl coenzyme A

    		 Endogenous Metabolite Others
    Methylmalonyl coenzyme A (Methylmalonyl-CoA) is a catabolite of valine, isoleucine, methionine, threonine, odd-chain fatty acids, and cholesterol. Methylmalonyl coenzyme A tetralithium is converted to succinyl-CoA by enzymatic reaction of methylmalonyl-CoA mutase (MCM) with coenzyme vitamin B12 .
    Methylmalonyl-CoA
  • HY-112540
    Acetoacetic acid

    		Endogenous Metabolite Neurological Disease Metabolic Disease
    Acetoacetic acid is an endogenous metabolite present in Cerebrospinal_Fluid and Blood that can be used for the research of Meningitis, Pregnancy, 3 Hydroxy 3 Methylglutaryl CoA Lyase Deficiency, Preeclampsia/Eclampsia, Diabetes Mellitus Type 2, Glucose Transporter Type 1 Deficiency Syndrome and Succinyl CoA:3 Oxoacid CoA Transferase Deficiency .
    Acetoacetic acid

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