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Hexanoyl Coenzyme A Trilithium Salt Hydrate

Original price was: $1,595.00.Current price is: $795.00.

Catalog Number: B2017646 (1 mg)
Hexanoyl Coenzyme A Trilithium Salt Hydrate is a chemical compound used in biochemical research. It is a derivative of coenzyme A, which plays a crucial role in various metabolic pathways in the body. This specific compound is often used in studies related to lipid metabolism and fatty acid synthesis. The trilithium salt hydrate form indicates that it contains three lithium ions and water molecules in its structure. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

Hexanoyl Coenzyme A Trilithium Salt Hydrate
Catalog number: B2017646
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 mg
Molecular Weight or Concentration: 901.49 g/mol
Supplied as: POWDER
Applications: a molecular tool for various biochemical applications
Storage: -20 °C
Keywords: Caproyl Coenzyme A trilithium salt
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Luo X, Reiter MA, d’Espaux L, Wong J, Denby CM, Lechner A, Zhang Y, Grzybowski AT, Harth S, Lin W, Lee H, Yu C, Shin J, Deng K, Benites VT, Wang G, Baidoo EEK, Chen Y, Dev I, Petzold CJ, Keasling JD. Complete biosynthesis of cannabinoids and their unnatural analogues in yeast Nature. 2019 Mar;567(7746):123-126.
2: Katagiri H, Asano T, Yamada T, Aoyama T, Fukushima Y, Kikuchi M, Kodama T, Oka Y. Acyl-coenzyme A dehydrogenases are localized on GLUT4-containing vesicles via association with insulin-regulated aminopeptidase in a manner dependent on its dileucine motif Mol Endocrinol. 2002 May;16(5):1049-59.
3: Ohgusu H, Shirouzu K, Nakamura Y, Nakashima Y, Ida T, Sato T, Kojima M. Ghrelin O-acyltransferase (GOAT) has a preference for n-hexanoyl-CoA over n-octanoyl-CoA as an acyl donor Biochem Biophys Res Commun. 2009 Aug 14;386(1):153-8.
4: Cantu DC, Ardèvol A, Rovira C, Reilly PJ. Molecular mechanism of a hotdog-fold acyl-CoA thioesterase Chemistry. 2014 Jul 14;20(29):9045-51.
5: Stout JM, Boubakir Z, Ambrose SJ, Purves RW, Page JE. The hexanoyl-CoA precursor for cannabinoid biosynthesis is formed by an acyl-activating enzyme in Cannabis sativa trichomes Plant J. 2012 Aug;71(3):353-65.
6: Chang KH, Liang PH, Beck W, Scholten JD, Dunaway-Mariano D. Isolation and characterization of the three polypeptide components of 4-chlorobenzoate dehalogenase from Pseudomonas sp. strain CBS-3 Biochemistry. 1992 Jun 23;31(24):5605-10.
7: Dutta D, Bhattacharyya S, Roychowdhury A, Biswas R, Das AK. Crystal structure of hexanoyl-CoA bound to β-ketoacyl reductase FabG4 of Mycobacterium tuberculosis Biochem J. 2013 Feb 15;450(1):127-39.
8: Kinsella JE, Bruns D, Infante JP. Fatty acid synthetase of bovine mammary: Properties and products Lipids. 1975 Apr;10(4):227-37.
9: Niezen-Koning KE, Wanders RJ, Nagel GT, Sewell AC, Heymans HS. Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenase Clin Chim Acta. 1994 Sep;229(1-2):99-106.
10: Morales-Quintana L, Nuñez-Tobar MX, Moya-León MA, Herrera R. Molecular dynamics simulation and site-directed mutagenesis of alcohol acyltransferase: a proposed mechanism of catalysis J Chem Inf Model. 2013 Oct 28;53(10):2689-700.

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Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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