coa

Methylglutaric acid is a leucine metabolite. A large amount of methylglutaric acid is identified in urine of patients with deficiency of 3-methylglutaconyl coenzyme A hydratase (PMID 6181239 ). Methylglutaric acid is also found to be associated with 3-hyd

Dephospho-CoA (dpCoA) is an endogenous compound extracted from Escherichia coli and Lactobacillus plantarum, and is an intermediate in coenzyme A biosynthesis.

Palmitoyl CoA lithium (Palmitoyl coenzyme A lithium) is a major component of fatty acids involved in the carnitine shuttle system, beta-oxidation, and the tricarboxylic acid cycle, and can be used to study metabolic disorders in the body.

Caffeoyl-CoA can be isolated from the leaf tissues of Gramineae, exhibiting a Km value of 1.45 μM [1].

3-Hydroxybutyryl-CoA, a metabolite found in mice, E. coli, and others, contains 3-hydroxybutanoyl as the S-acyl component and serves as an intermediate in butyric acid fermentation and the metabolism of lysine and tryptophan [1].

CoA-S-S-CoA, an endogenous metabolite found in *P. furiousus*, serves as a substrate for NOXA2 [1].

Malonyl CoA tetralithium (Malonyl coenzyme A), serves as a substrate in fatty acid biosynthesis and functions as an inhibitor of fatty acid oxidation. Additionally, it acts as a reversible inhibitor of mitochondrial carnitine palmitoyltransferase (CPT) 1 [1] [2].

Methylmalonyl-CoA tetralithium, also known as Methylmalonyl coenzyme A, serves as a metabolic byproduct derived from the breakdown of valine, isoleucine, methionine, threonine, odd-chain fatty acids, and cholesterol. It is converted into succinyl-CoA through the enzymatic activity of methylmalonyl-CoA mutase (MCM) in the presence of the coenzyme vitamin B12 [1].

Coatline B is a useful organic compound for research related to life sciences. The catalog number is T124030 and the CAS number is 87441-89-2.

Coatline A is a useful organic compound for research related to life sciences. The catalog number is T124031 and the CAS number is 87441-88-1.

26-Desglucoavenacoside A is a useful organic compound for research related to life sciences. The catalog number is T124583 and the CAS number is 59795-21-0.

Glucoalyssin is a useful organic compound for research related to life sciences and the catalog number is T124765.

Coagulin L is a useful organic compound for research related to life sciences. The catalog number is T125335 and the CAS number is 216164-64-6.

Licoagroside B is a useful organic compound for research related to life sciences and the catalog number is T130375.

Licoagrochalcone B is a flavonoid isolated from Patrinia villosa.

Licoagrochalcone C, a flavonoid compound, demonstrates potent inhibitory effects on NF-κB transcription and significantly reduces LPS-induced NO production, showcasing its bioactive properties [1] [2].

Glucoamylase, an enzyme obtained from various sources such as plants, animals, and microorganisms, is utilized in industrial applications. It is extensively employed in starch saccharification processes and the brewing and distilling industries [1].

Glucoarabin, a bioactive glucosinolate, upregulates the phase II detoxification enzyme quinone reductase (NQO1) in Hepa1c1c7 cells when hydrolyzed (hGSL 9), without affecting cytochrome P450 (CYP) 1A1 activity [1].

Licoarylcoumarin is a strong inhibitor of adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase. Licoarylcoumarin has antibacterial effects on the VRE strains; it has anti-HIV activity, and it has inhibitory effects on xanthine oxidase.

Secoaristolenedioic acid (Compound 1) is a sesquiterpene identified in the ethanol extract of the roots and rhizomes of Nardostachys chinensis.

S-Secoantioquine (Secantioquine) is an open-ring derivative of dibenzylisoquinoline alkaloids. In experiments involving rat striatal membranes, it shows weak displacement activity at the [3H-SCH 23390] binding site but demonstrates some displacement activity at the [3H-raclopride] binding site.

Sterculic acid, a stearoyl-CoA desaturase-1 (SCD1) inhibitor, effectively suppresses delta-9 desaturase (Δ9D) activity in a dose-dependent manner, exhibiting an inhibition concentration (IC50) value of 0.9 μM [1].

Mevastatin (ML236B) is an HMG-CoA reductase inhibitor that was initially isolated from the mold Pythium ultimum. Mevastatin was the first statin to enter clinical trials.

Simvastatin (MK 733) is an HMG-CoA reductase inhibitor (Ki=0.2 nM) with oral activity. Simvastatin has hypolipidemic activity, inhibits hepatic production of cholesterol, and is also used for the prevention of cardiovascular disease.