salicylic acid

Salicylic acid (2-Hydroxybenzoic acid), a natural compound extracted from Willow bark, is an anti-inflammatory inhibitor of activity cyclooxygenase.

6-(beta-D-glucopyranosyloxy)-Salicylic acid methyl ester is a natural product. The catalog number is TN3155 and the CAS number is 108124-75-0. 6-(beta-D-glucopyranosyloxy)-Salicylic acid methyl ester can be used as a reference standard.

2-Methoxybenzoic acid (o-Anisic acid) is a novel antiemetic which prevents nausea and vomiting in humans.

Sodium salicylate (2-Hydroxybenzoic acid sodium salt), a metabolite of acetylsalicylic acid, can inhibit NF-kB and reduce oxidative stress.

2,6-Dihydroxybenzoic acid, a secondary metabolite derived from salicylic acid, undergoes hydrolyzation by liver enzymes as part of phase I metabolism.

Salicyluric acid (2-Hydroxy Hippuric Acid) is a metabolite of Salicylic Acid.

2-Hydroxy-6-methoxybenzoic acid (6-Methoxysalicylic acid) may be employed as internal standard for the determination of acetylsalicylic acid (aspirin, ASA) and its major metabolite, salicylic acid (SA),and exhibits significant analgesic effects

Phenyl salicylate (NSC-33406) is a chemical substance. It is synthesized by heating salicylic acid with phenol.

2,5-Dihydroxybenzoic acid (Gentisic acid) is an active metabolite of salicylic acid degradation with a broad spectrum of biological activity, such as anti-inflammatory, antirheumatic and antioxidant properties.

Tremuloidin (Compound 2), a salicylic acid derivative from Homalium cochinchinensis, exhibits weak activity against HIV-1 [1].

Coronatine, synthesized by Pseudomonas syringae, mimics bioactive jasmonic acid conjugates or octadecanoid signal molecules in higher plants, inducing pathogenic symptoms. It enhances the virulence of Pseudomonas syringae by triggering a signaling cascade that suppresses salicylic acid accumulation, thereby promoting infection [1] [2] [3] [4].

Benzyl salicylate is a salicylic acid benzyl ester that can be used as a fragrance additive or UV light absorber.

1,2-Dihydroxynaphthalene, an intermediate isolated from naphthalene metabolism, is confirmed as a precursor to the formation of naphthoquinone. This compound can be further metabolized by certain bacteria (such as Pseudomonas spp.) into compounds like coumarin and salicylic acid.