Prochloraz

Prochloraz
Clinical data
Trade names	Abavit, Ascurit, Dibavit, Mirage, Octave, Omega, Prelude, Rival, Sporgon, Sportak, Sprint, Tenor
Identifiers
	IUPAC name N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide;
CAS Number	67747-09-5;
PubChem CID	73665;
ChemSpider	159925;
UNII	99SFL01YCL;
KEGG	C11182;
ChEBI	CHEBI:8434;
ChEMBL	ChEMBL522782;
CompTox Dashboard (EPA)	DTXSID4024270 ;
ECHA InfoCard	100.060.885
Chemical and physical data
Formula	C15H16Cl3N3O2
Molar mass	376.66 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCN(CCOC1=C(C=C(C=C1Cl)Cl)Cl)C(=O)N2C=CN=C2;
	InChI InChI=1S/C15H16Cl3N3O2/c1-10(2)21(15(22)20-4-3-19-9-20)5-6-23-14-12(17)7-11(16)8-13(14)18/h3-4,7-10H,5-6H2,1-2H3; Key:XJABPYGRRIVUOG-UHFFFAOYSA-N;

Prochloraz, brand name Sportak, is an imidazole fungicide that was introduced in 1978^[3] and is widely used in Europe, Australia, Asia, and South America within gardening and agriculture to control the growth of fungi.^[4]^[5] It is not registered for use in the United States.^[5] Similarly to other azole fungicides, prochloraz is an inhibitor of the enzyme lanosterol 14α-demethylase (CYP51A1), which is necessary for the production of ergosterol – an essential component of the fungal cell membrane – from lanosterol.^[6] The agent is a broad-spectrum, protective and curative fungicide, effective against Alternaria spp., Botrytis spp., Erysiphe spp., Helminthosporium spp., Fusarium spp., Pseudocerosporella spp., Pyrenophora spp., Rhynchosporium spp., and Septoria spp.^[5]^[2]

Like many imidazole and triazole fungicides and antifungal medications, prochloraz is not particularly selective in its actions.^[4]^[6] In addition to inhibition of lanosterol 14α-demethylase, prochloraz has also been found to act as an antagonist of the androgen and estrogen receptors, as an agonist of the aryl hydrocarbon receptor, and as an inhibitor of enzymes in the steroidogenesis pathway such as CYP17A1 and aromatase.^[4]^[6] In accordance, it has been shown to produce reproductive malformations in mice.^[4]^[6] As such, prochloraz is considered to be an endocrine disruptor.^[4]^[6]

References

^ Anonymous AC05372279 (1997). Consolidated list of products whose consumption and/or sale have been banned, withdrawn, severely restricted or not approved by governments / Pharmaceuticals. United Nations Publications. pp. 576–. ISBN 978-92-1-130219-6.^{[permanent dead link‍]}
^ ^a ^b Milne GW (2 September 2005). Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties. John Wiley & Sons. pp. 517–. ISBN 978-0-471-73661-5.
^ Carlile B (28 September 2006). "Chapter 3.7: Broad-spectrum systemic fungicides". Pesticide Selectivity, Health and the Environment. Cambridge University Press. pp. 81–. ISBN 978-1-139-45756-9.
^ ^a ^b ^c ^d ^e Vinggaard AM, Hass U, Dalgaard M, Andersen HR, Bonefeld-Jørgensen E, Christiansen S, et al. (February 2006). "Prochloraz: an imidazole fungicide with multiple mechanisms of action". International Journal of Andrology. 29 (1): 186–192. doi:10.1111/j.1365-2605.2005.00604.x. PMID 16466539.
^ ^a ^b ^c Paranjape K, Gowariker V, Krishnamurthy VN, Gowariker S (22 December 2014). "Prochloraz fungicide". The Pesticide Encyclopedia. CABI. pp. 406–. ISBN 978-1-78064-014-3.
^ ^a ^b ^c ^d ^e Sanderson JT (21 March 2015). "Disruptors of Androgen Action and Synthesis". In Darbre PD (ed.). Endocrine Disruption and Human Health. Elsevier Science. pp. 86–. ISBN 978-0-12-801120-1.