Carboxylic acid

About: Carboxylic acid is a research topic. Over the lifetime, 48544 publications have been published within this topic receiving 605696 citations.

Cannabidiolic acid as a selective cyclooxygenase-2 inhibitory component in cannabis.

Abstract: In the present study it was revealed that cannabidiolic acid (CBDA) selectively inhibited cyclooxygenase (COX)-2 activity with an IC(50) value (50% inhibition concentration) around 2 microM, having 9-fold higher selectivity than COX-1 inhibition. In contrast, Delta(9)-tetrahydrocannabinolic acid (Delta(9)-THCA) was a much less potent inhibitor of COX-2 (IC(50) > 100 microM). Nonsteroidal anti-inflammatory drugs containing a carboxyl group in their chemical structures such as salicylic acid are known to inhibit nonselectively both COX-1 and COX-2. CBDA and Delta(9)-THCA have a salicylic acid moiety in their structures. Thus, the structural requirements for the CBDA-mediated COX-2 inhibition were next studied. There is a structural difference between CBDA and Delta(9)-THCA; phenolic hydroxyl groups of CBDA are freed from the ring formation with the terpene moiety, although Delta(9)-THCA has dibenzopyran ring structure. It was assumed that the whole structure of CBDA is important for COX-2 selective inhibition because beta-resorcylic acid itself did not inhibit COX-2 activity. Methylation of the carboxylic acid moiety of CBDA led to disappearance of COX-2 selectivity. Thus, it was suggested that the carboxylic acid moiety in CBDA is a key determinant for the inhibition. Furthermore, the crude extract of cannabis containing mainly CBDA was shown to have a selective inhibitory effect on COX-2. Taken together, these lines of evidence in this study suggest that naturally occurring CBDA in cannabis is a selective inhibitor for COX-2.

Viscosity index improver - dispersant additive useful in oil compositions

Abstract: Hydrocarbon polymers such as ethylene copolymers may be reacted with unsaturated nitrogen-containing monomers or unsaturated carboxylic acids in the presence of a free radical catalyst such as a peroxide or azo free radical initiator and a chain stopping agent, e.g. a mercaptan to inhibit excessive cross-linking and branching. The copolymer grafted directly with the nitrogen-containing monomers may be utilized as an additive for oil and fuel compositions, particularly lubricating oil compositions as a V.I.-dispersant additive. The polymer reacted with carboxylic acid may be further reacted with amines, polyols, amino-alcohols, etc. to also form a V.I.-dispersant additive.

Attachment of human keratinocytes to plasma co-polymers of acrylic acid/octa-1,7-diene and allyl amine/octa-1,7-diene

Abstract: Plasma co-polymers (PCPs) of acrylic acid/octa-1,7-diene and allyl amine/octa-1,7-diene have been prepared and characterised using X-ray photoelectron spectroscopy (XPS). The use of a hydrocarbon diluent in the monomer feed allowed the deposition of films with controlled concentrations of carboxylic acid and nitrogen-containing functional groups. Human keratinocytes were cultured on these PCP surfaces, tissue culture poly(styrene) (TCPS) and collagen I. The level of keratinocyte attachment over 24 h was measured. PCP surfaces containing low concentrations of carboxylic acid groups (2.3%) were found to promote keratinocyte attachment. The performance of these PCPs was similar to collagen I, a well established substratum for attachment. Nitrogen-containing PCP surfaces were found to promote attachment at higher functional group concentrations, although the attachment did not attain the level achieved on the acid functionalised PCP surfaces.