Carboxin

The first synthesis of carboxin was disclosed in patents filed by Uniroyal. : Ethyl 2-chloroacetoacetate is treated with 2-mercaptoethanol and base, followed by cyclisation and water removal under acidic conditions. The resultant ethyl ester of the 1,4-oxathiine heterocycle is then formed into an amide with aniline using standard conditions via the carboxylic acid and acid chloride. This gives carboxin in high overall yield. The compound has been crystallised in two polymorphic forms, which have equal biological activity. == Mechanism of action ==

The mechanism of action of carboxin was not established until several years after it was first reported in 1966. In the period 1971–1975, evidence grew that it acted by inhibition of succinate dehydrogenase (SDHI), and later work showed that it binds to the quinone reduction site of the enzyme complex, preventing ubiquinone from doing so. As a consequence, the tricarboxylic acid cycle and electron transport chain cannot function. The compound was an early example of a fungicide exhibiting systemic movement from its application site on the crop plant to protect newly-growing tissue. ==Usage==

Owing to its systemic properties, carboxin is suitable for use as a seed treatment to give fungal control on the growing crop. However, it controls a relatively narrow range of species: mainly Tilletia spp. (known as bunts and smuts) in cereal crops and Rhizoctonia in cotton and vegetables. The compound was used in Australia, the EU, the UK and the US but registration has lapsed in the EU. It was reported to have had a total worldwide sales of $75 million in 2014. == Human safety ==

Carboxin has low mammalian toxicity and is not persistent in the environment. One of its metabolites, the sulfone, is also active as an SDHI and has been sold as the fungicide oxycarboxin. ==Analogues==

Carboxin was the first SDHI-type fungicide and its invention triggered a search for compounds with improved properties, particularly for active ingredients which would control a broader range of economically-important diseases. Boscalid, introduced in 2003, retained the aniline amide part-structure but with a pyridine ring in place of the 1,4-oxathiine and with a second benzene ring attached to the aniline portion. By 2014, it had annual sales of $390 million. The Fungicides Resistance Action Committee (FRAC) assigns fungicides into classes so as to facilitate resistance management and SDHI form one group. ==Brands==

Carboxin is the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. Vitavax is the brand name originally used by Uniroyal but as the compound's patents expired it became available to many other manufacturers and has been sold under multiple names. ==References==