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Biotin - Wikipedia
https://en.wikipedia.org/wiki/Biotin
WEBBiotin is classified as a heterocyclic compound, with a sulfur-containing tetrahydrothiophene ring fused to a ureido group. A C5-carboxylic acid side chain is appended to the former ring. The ureido ring, containing the −N−CO−N− group, serves as the carbon dioxide carrier in carboxylation reactions. [7]
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Biotin | C10H16N2O3S | CID 171548 - PubChem
https://pubchem.ncbi.nlm.nih.gov/compound/biotin
WEBBiotin is a water-soluble B-complex vitamin which is composed of an ureido ring fused with a tetrahydrothiophene ring, which attaches a valeric acid substituent at one of its carbon atoms. Biotin is used in cell growth, the production of fatty …
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Biotin, a universal and essential cofactor: synthesis, ligation and
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371270/
WEBJan 11, 2021 · The chemical structure of biotin consists of a tetrahydroimidizalone ring fused with an organosulfur-containing tetrahydrothiophane ring that bears a valeric acid substituent (Fig. 1A). Biotin must be covalently attached to its cognate enzyme proteins (e.g. carboxylases) for function and attachment is mediated by formation of an amide linkage ...
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biotin | C10H16N2O3S | ChemSpider
https://www.chemspider.com/chemical-structure.149962.html
WEBBiotin is a coenzyme for carboxylase enzymes, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. In addition, biotin is widely used throughout the biotechnology industry to conjugate proteins for biochemical assays.
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Biotin | Vitamin B7, Hair Growth & Skin Health | Britannica
https://www.britannica.com/science/biotin
WEBFeb 28, 2024 · Biotin was first identified as a nutritive requirement of yeast. Originally called vitamin H, it was isolated in pure form in 1935; its structure was established in 1942, after it had been shown to be required by animals.
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Biotin: What is Biotin? - Journal Of Nutrition
https://journalofnutrition.org/encyclopedia/biotin-what-is-biotin/
WEBBiotin is composed of a ureido ring fused with a tetrahydrothiophene ring, and it contains a valeric acid substituent and a sulfur atom. This unique structure allows biotin to function as a coenzyme in many enzymatic reactions. Biotin can be found in a variety of food sources, both from plant and animal origins.
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Biotin - NIST Chemistry WebBook
https://webbook.nist.gov/cgi/cbook.cgi?ID=C58855&Mask=200
WEBChemical structure: This structure is also available as a 2d Mol file. Other names: 1H-Thieno [3,4-d]imidazole-4-pentanoic acid, hexahydro-2-oxo-, [3as- (3aα,4β,6aα)]-; (+)-Biotin; d-Biotin; Bioepiderm; Bios II; Coenzyme R; Factor S; Vitamin B7; Vitamin H; Factor S (vitamin); Injacom H; D- (+)-Biotin; (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno ...
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Biotin - PMC - National Center for Biotechnology Information
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757853/
WEBAbstract. Biotin is a water-soluble vitamin and serves as a coenzyme for five carboxylases in humans. Biotin is also covalently attached to distinct lysine residues in histones, affecting chromatin structure and mediating gene regulation.
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Biotin: Biochemical, Physiological and Clinical Aspects
https://link.springer.com/chapter/10.1007/978-94-007-2199-9_1
WEBJan 1, 2011 · The chemical structure of the biotin molecule (see Fig. 1.1 for the structure of biotin and related/relevant compounds) is composed of two rings to which a valeric acid moiety is attached as a side chain.
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The Structural Characteristics of Biotin - University of Wisconsin
https://www.chem.uwec.edu/webpapers2001/barkacs/Pages/structure.html
WEBBiotin (C10H16N2O3S1) is a colorless vitamin that, when crystallized, is orthorhombic (space group P 21 21 21). It has a molecular weight of 224.31 g/mol. It is also known as coenzyme R (CoR), Bios II, and Bioepiderm. Some studies refer to biotin as a growth factor present in small amounts in every living cell.
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