Tiabendazole (INN, BAN), also known as thiabendazole (AAN, USAN) or TBZ and the trade names Mintezol, Tresaderm, and Arbotect, is a preservative,
Uses
Preservative
Tiabendazole is used primarily to control mold,
blight, and other fungal diseases in fruits (e.g. oranges) and vegetables; it is also used as a
prophylaxis treatment for Dutch elm disease.
Tiabendazole is also used as a food additive,[UK Food Standards Agency: ] Australia and New Zealand.[Australia New Zealand Food Standards Code]
Use in treatment of aspergillosis has been reported.
It is also used in anti-fungal as a mixture with azoxystrobin.
Parasiticide
As an antiparasitic, tiabendazole is able to control
(such as those causing
strongyloidiasis),
, and other
helminth species which infect wild animals,
livestock, and humans.
First approved for use in sheep in 1961 and horses in 1962, resistance to this drug was first found in
Haemonchus contortus in 1964, and then in the two other major small ruminant nematode parasites,
Teladorsagia circumcincta and
Trichostrongylus colubriformis.
Fungicide
Tiabendazole acts as a fungicide through binding fungal tubulin. Resistant
Aspergillus nidulans specimens were found to have a mutation in the gene coding for β-tubulin, which was reversible by a mutation in the gene for α-tubulin. This showed that thiabendazole binds to both α- and β-tubulin.
This chemical is also used as a pesticide, including to treat Beech Leaf Disease.
Other
In dogs and cats, tiabendazole is used to treat ear infections.
Tiabendazole is also a chelating agent, which means it is used medicinally to bind metals in cases of metal poisoning, such as lead poisoning, mercury, or antimony poisoning.
Research
Genes responsible for the maintenance of cell walls in yeast have been shown to be responsible for
angiogenesis in vertebrates. Tiabendazole serves to block angiogenesis in both frog embryos and human cells. It has also been shown to serve as a vascular disrupting agent to reduce newly established blood vessels. Tiabendazole has been shown to effectively do this in certain cancer cells.
Pharmacodynamics
Tiabendazole works by inhibition of the mitochondrial, helminth-specific enzyme, fumarate reductase, with possible interaction with endogenous quinone.
Safety
The substance appears to have a slight toxicity in higher doses, with effects such as liver and intestinal disorders at high exposure in test animals (just below level). Some reproductive disorders and decreasing weaning weight have been observed, also at high exposure. Effects on humans from use as a drug include nausea, vomiting, loss of appetite, diarrhea, dizziness, drowsiness, or headache; very rarely also ringing in the ears, vision changes, stomach pain, yellowing eyes and skin, dark urine, fever, fatigue, increased thirst and change in the amount of urine occur. Carcinogenic effects have been shown at higher doses.
Synthesis
Intermediate aryl
amidine (
2) is prepared by aluminium trichloride-catalyzed addition of
aniline to the nitrile of 4-cyanothiazole (
1).
The amidine (
2) is then converted to its
N-chloro derivative
3 with sodium hypochlorite (NaOCl). Upon treatment with base, this undergoes a
nitrene insertion reaction (
4) to produce tiabendazole (
5).
An alternative synthesis involves reacting 4-thiazolecarboxamide with o-phenylenediamine in polyphosphoric acid.
Derivatives
A number of derivatives of tiabendazole are also pharmaceutical drugs, including
albendazole,
cambendazole,
fenbendazole,
oxfendazole,
mebendazole, and
flubendazole.
See also
-
Fungicide use in the United States
-
List of fungicides
External links
