No results for "Category:Fatty aldehydes" (auto) in titles.

Suggestions for article titles:

1. Aldehyde: In organic chemistry, an aldehyde (/ˈældɪhaɪd/) is an organic compound containing a functional group with the structure R−CH=O. The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be ... (1=Organic compound containing the functional group R−CH=O) [100%] 2023-11-01 [Aldehydes] [Functional groups]...
2. Aldehyde: Articles Most recent articles on Aldehyde Most cited articles on Aldehyde Review articles on Aldehyde Articles on Aldehyde in N Eng J Med, Lancet, BMJ Media Powerpoint slides on Aldehyde Images of Aldehyde Photos of Aldehyde Podcasts & MP3s on Aldehyde ... [100%] 2023-04-05 [Aldehydes] [functional groups]...
3. Aldehyde: An aldehyde is an organic compound containing a carbon to oxygen double bond (also known as the carbonyl group). The carbon atom must be attached to at least one hydrogen atom to be an aldehyde. [100%] 2023-02-26 [Organic Chemistry]
4. Aldehyde: An aldehyde is an organic compound containing a terminal carbonyl group. This functional group, called an aldehyde group, consists of a carbon atom bonded to a hydrogen atom with a single covalent bond and an oxygen atom with a double ... [100%] 2023-02-03
5. Aldehídos: Los aldehídos poseen un grupo carbonilo (=C=O) unido a una cadena carbonada y a un átomo de hidrógeno. Los aldehídos son compuestos orgánicos caracterizados por poseer el grupo funcional -CHO (carbonilo). Un grupo carbonilo es el que se obtiene ... [88%] 2023-05-17
6. Fatty aldehyde: Fatty aldehydes are aliphatic, long-chain aldehydes which may be mono- or polyunsaturated. The fatty aldehydes include compounds such as octanal, nonanal, decanal or dodecanal. (Chemistry) [70%] 2023-12-07 [Fatty aldehydes]
7. Cyclamen aldehyde: Cyclamen aldehyde is a fragrance molecule which has been used in soaps, detergents, lotions, and perfumes since the 1920s. It was granted generally recognized as safe (GRAS) status by Flavor and Extract Manufacturers Association (FEMA) in 1965 and is approved ... (Chemistry) [70%] 2023-08-29 [Aldehydes] [Perfume ingredients]...
8. Myristyl aldehyde: Myristyl aldehyde, also known as tetradecanal, is a reduced form of myristic acid. It is naturally produced by bioluminescent bacteria of the Vibrio genus and is one of two substrates produced and consumed by the Vibrio fischeri luciferase light emission ... (Chemistry) [70%] 2023-12-19 [Fatty aldehydes] [Alkanals]...
9. Aldehyde dehydrogenase: Aldehyde dehydrogenases (EC 1.2.1.3) are a group of enzymes that catalyse the oxidation of aldehydes. They convert aldehydes (R–C(=O)–H) to carboxylic acids (R–C(=O)–O–H). (Biology) [70%] 2022-04-07 [Enzymes] [EC 1.2.1]...
10. Aldehyde tag: The aldehyde tag is a short peptide tag that can be further modified to add fluorophores, glycans, PEG (polyethylene glycol) chains, or reactive groups for further synthesis. A short, genetically-encoded peptide with a consensus sequence LCxPxR is introduced into ... (Chemistry) [70%] 2024-01-05 [Peptides]
11. Abscisic aldehyde: Abscisic aldehyde is an intermediate in the biosynthesis of the plant hormone abscisic acid. It is produced by the dehydrogenation of xanthoxin by xanthoxin dehydrogenases, which is an NAD+ dependent short-chain dehydrogenase, followed by selective oxidation by abscisic aldehyde ... (Chemistry) [70%] 2023-04-30 [Cyclohexenes] [Cyclohexenols]...
12. Polyunsaturated aldehyde: Polyunsaturated aldehydes (PUAs) are a group of allelopathic chemicals typically associated with diatom-copepod predator-prey interactions. These compounds are classified by an aldehyde group covalently bound to long carbon chains containing two or more carbon-carbon double bonds. (Chemistry) [70%] 2023-09-14 [Biomolecules] [Aldehydes]...
13. Aldehyde oxidase: Aldehyde oxidase (AO) is a metabolizing enzyme, located in the cytosolic compartment of tissues in many organisms. AO catalyzes the oxidation of aldehydes into carboxylic acid, and in addition, catalyzes the hydroxylation of some heterocycles. [70%] 2023-05-15 [EC 1.2.3]
14. Protocatechuic aldehyde: Protocatechuic aldehyde is a phenolic aldehyde, a compound released from cork stoppers into wine. This molecule can be used as a precursor in the vanillin synthesis by biotransformation by cell cultures of Capsicum frutescens, a type of Chili pepper. (Chemistry) [70%] 2024-07-14 [Hydroxybenzaldehydes]
15. Aldehyde oxidase 1: Aldehyde oxidase 1 is an enzyme that in humans is encoded by the AOX1 gene. Aldehyde oxidase produces hydrogen peroxide and, under certain conditions, can catalyze the formation of superoxide. [57%] 2023-03-18 [EC 1.2.3]
16. Glycine betaine aldehyde: Glycine betaine aldehyde, often simply called betaine aldehyde, is an intermediate in the metabolism of glycine, serine and threonine. The human aldehyde dehydrogenase (EC 1.2.1.3) stimulates the transformation of betaine aldehyde to glycine betaine. [57%] 2023-09-01 [Aldehydes] [Quaternary ammonium compounds]...
17. Reactive aldehyde species: Reactive aldehyde species (RASP), also known as reactive aldehydes, refer to a class of electrophilic organic aldehyde molecules that are generally toxic or facilitate inflammation. RASP covalently react with amine groups (via Schiff base formation) and thiol groups (via Michael ... (Chemistry) [57%] 2023-04-05 [Aldehydes] [Inflammations]...
18. Stephen aldehyde synthesis: Stephen aldehyde synthesis, a named reaction in chemistry, was invented by Henry Stephen (OBE/MBE). This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using tin(II) chloride (SnCl2), hydrochloric acid (HCl) and quenching the resulting ... (Chemistry) [57%] 2022-08-31 [Organic redox reactions] [Name reactions]...
19. Bouveault aldehyde synthesis: The Bouveault aldehyde synthesis (also known as the Bouveault reaction) is a one-pot substitution reaction that replaces an alkyl or aryl halide with a formyl group using a N,N-disubstituted formamide. For primary alkyl halides this produces the ... (Chemistry) [57%] 2023-11-19 [Addition reactions] [Carbon-carbon bond forming reactions]...
20. Wieland-Gumlich aldehyde: The so-called Wieland-Gumlich aldehyde (6) is an indoline derived by chemical degradation from strychnine. This compound is of some commercial interest as a chemical intermediate. (Chemistry) [57%] 2023-11-26 [Tryptamines] [Aldehydes]...