esters

Caprylic/Capric Triglyceride, a compound consisting of triglycerides and esters derived from fractionated vegetable oil, and fatty acids from coconut and palm kernel oils, serves as a food additive and is utilized in cosmetics. This substance demonstrates outstanding oxidation stability.

Diisohexyl phthalate is a kind of dialkyl phthalate esters and a plasticizer.

1. Obtusifolin has antioxidant properties and improves chemically induced diabetes and its complications by modulation of oxidative stress. 2. Obtusifolin suppresses phthalate esters-mediated bone resorption, thus may be a novel anti-breast-cancer bone me

Pentacosanoic acid, belongs to the class of organic compounds known as very long-chain fatty acids.

DSS Crosslinker is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is a homobifunctional crosslinker that is cell membrane permeable, with amine-reactive NHS esters at both ends of an 8-atom [11.4 angstrom] spacer arm for conjugating proteins, including intracellular proteins.

Ethyl cis-4,7,10,13,16,19-Docosahexaenoate, the ethyl ester of Docosahexaenoate (DHA), is selectively enriched in the ethyl ester fraction through alcoholysis using fatty acid ethyl esters from tuna oil and lauryl alcohol.

Pitavastatin calcium (NK-104) is a potent inhibitor of HMG-CoA reductase (Ki: 1.7 nM). It lowers both total cholesterol and low-density lipoprotein cholesterol in animals and humans. Metabolism of pitavastatin by the cytochrome P450 system is minimal, reducing the risk of drug-drug interactions.

Succinic acid (1, 2-ethanedicarboxylic acid) is a product of anaerobic metabolism and an intermediate of the tricarboxylic acid cycle.

1,5,7-Triazabicyclo[4.4.0]dec-5-ene (Triazabicyclodecene) is an isotope exchange catalyst in CDCl, facilitating acyl transfer in cyclic esters and ring-opening polymerization.

Octanoic acid (Caprylic acid), found naturally in coconuts and breast milk, is an oily liquid with a slightly unpleasant rancid taste and minimal solubility in water. It is commercially utilized in the production of esters for perfumery and in dye manufacturing.

Nonanoic acid (Nonoic acid) is a fatty acid which occurs naturally as esters are the oil of pelargonium. Synthetic esters, such as methyl nonanoate, are used as flavorings. Pelargonic acid is an organic compound composed of a nine-carbon chain terminating in a carboxylic acid. It is an oily liquid with an unpleasant, rancid odor. It is nearly insoluble in water, but well soluble in chloroform and ether.

1-(cyclohexylmethyl)guanidine hydroiodide is a guanidine derivative that has been used as a reagent in the synthesis of a variety of compounds, including peptides, peptoids, and other bioactive molecules, and as a catalyst in the synthesis of other compounds, such as amides, esters, and ethers.

Cholesteryl behenate is a standard in electrospray ionization tandem mass spectrometry for the analysis of cholesteryl esters and cholesterol.

LRAT-IN-1 (compound 1) is an inhibitor of lecithin retinol acyltransferase (LRAT) with an IC50 value of 21.1 μM. This compound works by inhibiting the esterification of retinol to form retinyl esters, thereby increasing the availability of retinol in the skin to deliver anti-aging benefits. LRAT-IN-1 is under investigation for its potential use as an anti-aging ingredient in cosmetics.

15-Aminopentadecanoic acid serves as a linker in PROTAC synthesis. It features an alkane chain with terminal carboxylic acid and amino groups. The amino group (NH2) can react with carboxylic acids, activated NHS esters, and carbonyls (ketones, aldehydes). The terminal carboxylic acid can form stable amide bonds with the primary amine group of activated NHS esters.

tert-Butyl (8-aminooctyl)carbamate (1-Boc-1,8-diaminooctane) serves as a linker for PROTAC synthesis. This compound features an alkane chain with a terminal amine protected by a Boc group. The amine group can react with carboxylic acids, active NHS esters, and carbonyl groups such as ketones and aldehydes. The Boc group can be removed under mild acidic conditions to yield a free amine.

16-Aminohexadecanoic acid is an alkyl chain compound characterized by terminal carboxylic acid and amino groups. It serves as a PROTAC linker in PROTAC synthesis. The amino group (NH2) can react with carboxylic acids, activated NHS esters, and carbonyl groups (ketones, aldehydes). The terminal carboxylic acid can form stable amide bonds by reacting with primary amines of activated NHS esters.

10-Aminodecanoic acid is an alkane chain featuring terminal carboxylic acid and amino groups. This compound serves as a PROTAC linker in PROTAC synthesis and other conjugation applications. The amino group (NH2) can react with carboxylic acids, activated NHS esters, and carbonyls (ketones, aldehydes), while the terminal carboxylic acid can react with primary amines of activated NHS esters to form stable amide bonds.

tert-Butyl (10-aminodecyl)carbamate (1-Boc-1,10-diaminodecane) serves as a PROTAC linker in the synthesis of PROTACs and other binding applications. This compound contains an alkane chain with a terminal amine and a Boc-protected amino group. The amine group can react with carboxylic acids, activated NHS esters, and carbonyls (ketones and aldehydes). The Boc group can be removed under mild acidic conditions to yield a free amine.

9-Aminononanoic acid can serve as a PROTAC linker and in other conjugates for PROTAC synthesis. This compound consists of an alkyl chain featuring terminal carboxylic acid and amino groups. The amino group (NH2) can react with carboxylic acids, activated NHS esters, carbonyls (ketones, aldehydes), among others. The terminal carboxylic acid is able to react with primary amines of activated NHS esters to form stable amide bonds.

tert-Butyl (9-aminononyl)carbamate is an alkane chain featuring a terminal amine and a Boc-protected amino group. It serves as a PROTAC linker in the synthesis of PROTACs and various coupling applications. The amine can react with carboxylic acids, activated NHS esters, and carbonyl groups (ketones, aldehydes). The Boc group can be deprotected under mild acidic conditions to form a free amine.

N-Boc-undecane-1,11-diamine is an alkane chain featuring terminal amine and Boc-protected amino groups. It serves as a PROTAC linker in PROTAC synthesis and other conjugation applications. The amine group can react with carboxylic acids, activated NHS esters, and carbonyl groups (ketones, aldehydes). The Boc group can be deprotected under mild acidic conditions to yield a free amine.

Thalidomide-5-(PEG2-amine) is a Thalidomide analogue that includes an E3 ligase ligand substituted with a terminal amine group. The amine group can react with NHS esters or carboxylic acids in the presence of EDC or HATU. The PEG spacer enhances water solubility.

Sulphostin is a covalent inhibitor of dipeptidyl peptidase 4 (DPP4), dipeptidyl peptidase 9 (DPP9), and dipeptidyl peptidase 8 (DPP8), with IC50 values of 79, 1392, and 6930 nM, respectively. It induces phosphorylation of amino sulfamide esters, irreversibly inhibiting enzyme activity. Sulphostin is applicable in inflammation and cancer research.