Trilostane

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Trilostane
Clinical data
AHFS/Drugs.com	Monograph
Routes of; administration	oral
ATC code	H02CA01 (WHO) ;
Legal status
Legal status	UK: POM (Prescription only) ; Veterinary use (U.S.);
Pharmacokinetic data
Metabolism	Hepatic
Elimination half-life	8 hours
Identifiers
	IUPAC name (4α,5α,17β)-3,17-dihydroxy-4,5-epoxyandrost-2-ene-2-carbonitrile;
CAS Number	13647-35-3 ;
PubChem CID	656583;
DrugBank	DB01108 ;
ChemSpider	570949 ;
UNII	L0FPV48Q5R;
KEGG	D01180 ;
ChEBI	CHEBI:32260 ;
ChEMBL	ChEMBL1200907 ;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C20H27NO3
Molar mass	329.433 g/mol
3D model (JSmol)	Interactive image;
	SMILES N#C\C4=C(/O)[C@H]5O[C@]35[C@]([C@@H]2[C@H]([C@H]1[C@]([C@@H](O)CC1)(C)CC2)CC3)(C)C4;
	InChI InChI=1S/C20H27NO3/c1-18-7-6-14-12(13(18)3-4-15(18)22)5-8-20-17(24-20)16(23)11(10-21)9-19(14,20)2/h12-15,17,22-23H,3-9H2,1-2H3/t12-,13-,14-,15-,17+,18-,19+,20+/m0/s1 ; Key:KVJXBPDAXMEYOA-CXANFOAXSA-N ;
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase used in the treatment of Cushing's syndrome.^[1]^[2]

It was withdrawn from human use in the United States market in April 1994.^[3]^[4] The drug is available in the United Kingdom for use in humans under the brand name Modrenal and is used for treatment of Cushing's disease and for breast cancer treatment.^[5]^[6]^[7] It was approved in the United States in 2008 for the treatment of Cushing's disease (hyperadrenocorticism) in dogs under the brand name Vetoryl.^[8] It was available by prescription in the UK under the Vetoryl brand name for some time before it was approved in the US.^[9] The drug is also used to treat the skin disorder Alopecia X in dogs.^[3]^[10]^[11] It is also the first drug approved to treat both pituitary- and adrenal-dependent Cushing's in dogs. This prescription drug works by stopping the production of cortisol in the adrenal glands.^[12]^[13] In studies of the drug, the most common side effects were vomiting, lack of energy, diarrhea, and weight loss. Trilostane should not be given to a dog that:

has kidney or liver disease;^[9]^[14]
takes certain medications used to treat heart disease;^{[citation needed]}
is pregnant, nursing or intended for breeding ^[9]^[14]

The safety and effectiveness of trilostane were shown in several studies. Success was measured by improvements in both blood test results and physical symptoms (increased appetite and activity level, and decreased panting, thirst and urination).^[7]^[15]

Only one other drug, Anipryl (veterinary brand name) selegiline, is FDA-approved to treat Cushing's disease in dogs, but only to treat uncomplicated, pituitary-dependent Cushing's.^[16] The only previous treatment for the disease was the use of Mitotane (brand name Lysodren) off-label.^[15]^[17]

It has been used as a progesterone inhibitor.^[18]

A number of compounding pharmacies in the US sell the product. Since the US approval of Vetoryl in December 2008,^[8] compounding pharmacies are no longer able to use a bulk drug product for compounding purposes, but must prepare the compounded drug from Vetoryl.^[19]

It is a 3β-hydroxysteroid dehydrogenase inhibitor.^[20]

Chemistry

The compound is prepared from testosterone in a four-step synthesis.

References

↑ Komanicky P, Spark RF, Melby JC. (1978). "Treatment of Cushing's syndrome with trilostane (WIN 24,540), an inhibitor of adrenal steroid biosynthesis". Journal of Clinical Endocrinology and Metabolism. 47 (5): 1042–1051. doi:10.1210/jcem-47-5-1042. PMID 233687.
↑ Forney, Barbara. "Trilostane for Veterinary Use". Wedgewood Pharmacy. Retrieved 5 April 2011.
↑ ^3.0 ^3.1 Cook, Audrey K. (1 February 2008). "Trilostane: A therapeutic consideration for canine hyperadrenocorticism". DVM 360. Retrieved 5 April 2011.
↑ "Trilostane consumer information". Drugs.com. 4 January 2009. Archived from the original on 12 February 2008. Retrieved 3 April 2011.
↑ "Modrenal consumer information". Drugs.com UK. Retrieved 3 April 2011.
↑ "Modrenal". electronic Medicines Compendium UK. Retrieved 3 April 2011.
↑ ^7.0 ^7.1 Braddock, JA, Church, DB, Robertson, ID, Watson, ADJ (October 2003). "Trilostane treatment in dogs with pituitary-dependent hyperadrenocorticism" (PDF). Australian Veterinary Journal. pp. 18 of 63. Retrieved 5 April 2011. (PDF)
↑ ^8.0 ^8.1 "Vetoryl approval information". Food and Drug Administration. 5 December 2008. Retrieved 3 April 2011.
↑ ^9.0 ^9.1 ^9.2 "Vetoryl-Contraindications". NOAH Compendium of Animal Health-National Office of Animal Health UK. Retrieved 3 April 2011.
↑ Hillier, Andrew (2006). "Alopecia: Is an Endocrine Disorder Responsible?" (PDF). Ohio State University Endocrinology Symposium. p. 12 of 67. Retrieved 8 April 2011. (PDF)
↑ Cerundolo, Rosario, Lloyd, David H., Persechino, Angelo, Evans, Helen, Cauvin, Andria (2004). "Treatment of Canine Alopecia X with trilostane" (PDF). European Society of Veterinary Dermatology. Retrieved 16 May 2011. (PDF)
↑ Reusch, Claudia E. (2006). "Trilostane-5 Years of Clinical Experience for the Treatment of Cushing's Disease" (PDF). Ohio State University Endocrinology Symposium. pp. 17–19. Retrieved 5 April 2011. (PDF)
↑ Reusch, Claudia E. (2010). "Trilostane-A Review of a Success Story". World Small Animal Veterinary Association (WSAVA). Retrieved 5 April 2011.
↑ ^14.0 ^14.1 "Dechra US Datasheet-Vetoryl" (PDF). Dechra US. Retrieved 3 April 2011. (PDF)
↑ ^15.0 ^15.1 "Treating Cushing's Disease in Dogs". US Food and Drug Administration. Retrieved 3 April 2011.
↑ "Anipryl consumer information". Drugs.com Vet. Retrieved 3 April 2011.
↑ Reine, NJ. (2007). "Medical management of pituitary-dependent hyperadrenocorticism: mitotane versus trilostane". Clinical Tech-Small Animal Practice. Retrieved 5 April 2011.
↑ le Roux PA, Tregoning SK, Zinn PM, van der Spuy ZM (June 2002). "Inhibition of progesterone secretion with trilostane for mid-trimester termination of pregnancy: randomized controlled trials". Human reproduction (Oxford, England). 17 (6): 1483–9. doi:10.1093/humrep/17.6.1483. PMID 12042266.
↑ "VETORYL (trilostane) Capsules Letter - Pharmacy Professionals". Food and Drug Administration. 11 September 2009. Retrieved 3 April 2011.
↑ de Gier J, Wolthers CH, Galac S, Okkens AC, Kooistra HS (April 2011). "Effects of the 3β-hydroxysteroid dehydrogenase inhibitor trilostane on luteal progesterone production in the dog". Theriogenology. 75 (7): 1271–9. doi:10.1016/j.theriogenology.2010.11.041. PMID 21295836.

External links

Trilostane (Vetoryl) information from Veterinary Medicines Directorate, UK. Includes precautionary use regarding concurrent medical conditions, possible side effects, and possible interaction with other drugs. (PDF)

Template:Corticosteroids Template:Steroidergics

[1] Komanicky P, Spark RF, Melby JC. (1978). "Treatment of Cushing's syndrome with trilostane (WIN 24,540), an inhibitor of adrenal steroid biosynthesis". Journal of Clinical Endocrinology and Metabolism. 47 (5): 1042–1051. doi:10.1210/jcem-47-5-1042. PMID 233687.

[2] Forney, Barbara. "Trilostane for Veterinary Use". Wedgewood Pharmacy. Retrieved 5 April 2011.

[Cook-3] 3.0 ^3.1 Cook, Audrey K. (1 February 2008). "Trilostane: A therapeutic consideration for canine hyperadrenocorticism". DVM 360. Retrieved 5 April 2011.

[4] "Trilostane consumer information". Drugs.com. 4 January 2009. Archived from the original on 12 February 2008. Retrieved 3 April 2011.

[DrugsUK-5] "Modrenal consumer information". Drugs.com UK. Retrieved 3 April 2011.

[6] "Modrenal". electronic Medicines Compendium UK. Retrieved 3 April 2011.

[Church-7] 7.0 ^7.1 Braddock, JA, Church, DB, Robertson, ID, Watson, ADJ (October 2003). "Trilostane treatment in dogs with pituitary-dependent hyperadrenocorticism" (PDF). Australian Veterinary Journal. pp. 18 of 63. Retrieved 5 April 2011. (PDF)

[Approval-8] 8.0 ^8.1 "Vetoryl approval information". Food and Drug Administration. 5 December 2008. Retrieved 3 April 2011.

[NOAH-9] 9.0 ^9.1 ^9.2 "Vetoryl-Contraindications". NOAH Compendium of Animal Health-National Office of Animal Health UK. Retrieved 3 April 2011.

[10] Hillier, Andrew (2006). "Alopecia: Is an Endocrine Disorder Responsible?" (PDF). Ohio State University Endocrinology Symposium. p. 12 of 67. Retrieved 8 April 2011. (PDF)

[11] Cerundolo, Rosario, Lloyd, David H., Persechino, Angelo, Evans, Helen, Cauvin, Andria (2004). "Treatment of Canine Alopecia X with trilostane" (PDF). European Society of Veterinary Dermatology. Retrieved 16 May 2011. (PDF)

[12] Reusch, Claudia E. (2006). "Trilostane-5 Years of Clinical Experience for the Treatment of Cushing's Disease" (PDF). Ohio State University Endocrinology Symposium. pp. 17–19. Retrieved 5 April 2011. (PDF)

[13] Reusch, Claudia E. (2010). "Trilostane-A Review of a Success Story". World Small Animal Veterinary Association (WSAVA). Retrieved 5 April 2011.

[Dechra-14] 14.0 ^14.1 "Dechra US Datasheet-Vetoryl" (PDF). Dechra US. Retrieved 3 April 2011. (PDF)

[FDA-15] 15.0 ^15.1 "Treating Cushing's Disease in Dogs". US Food and Drug Administration. Retrieved 3 April 2011.

[16] "Anipryl consumer information". Drugs.com Vet. Retrieved 3 April 2011.

[17] Reine, NJ. (2007). "Medical management of pituitary-dependent hyperadrenocorticism: mitotane versus trilostane". Clinical Tech-Small Animal Practice. Retrieved 5 April 2011.

[pmid12042266-18] Roux PA, Tregoning SK, Zinn PM, van der Spuy ZM (June 2002). "Inhibition of progesterone secretion with trilostane for mid-trimester termination of pregnancy: randomized controlled trials". Human reproduction (Oxford, England). 17 (6): 1483–9. doi:10.1093/humrep/17.6.1483. PMID 12042266.

[19] "VETORYL (trilostane) Capsules Letter - Pharmacy Professionals". Food and Drug Administration. 11 September 2009. Retrieved 3 April 2011.

[pmid21295836-20] Gier J, Wolthers CH, Galac S, Okkens AC, Kooistra HS (April 2011). "Effects of the 3β-hydroxysteroid dehydrogenase inhibitor trilostane on luteal progesterone production in the dog". Theriogenology. 75 (7): 1271–9. doi:10.1016/j.theriogenology.2010.11.041. PMID 21295836.

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Clinical data

AHFS/Drugs.com	Monograph
Routes of administration	oral
ATC code	H02CA01 (WHO)
Legal status
Legal status	UK: POM (Prescription only) Veterinary use (U.S.)
Pharmacokinetic data
Metabolism	Hepatic
Elimination half-life	8 hours
Identifiers
IUPAC name (4α,5α,17β)-3,17-dihydroxy-4,5-epoxyandrost-2-ene-2-carbonitrile
CAS Number	13647-35-3^N
PubChem CID	656583
DrugBank	DB01108^Y
ChemSpider	570949^Y
UNII	L0FPV48Q5R
KEGG	D01180^Y
ChEBI	CHEBI:32260^Y
ChEMBL	ChEMBL1200907^N
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C₂₀H₂₇NO₃
Molar mass	329.433 g/mol
3D model (JSmol)	Interactive image
SMILES N#C\C4=C(/O)[C@H]5O[C@]35[C@]([C@@H]2[C@H]([C@H]1[C@]([C@@H](O)CC1)(C)CC2)CC3)(C)C4
InChI InChI=1S/C20H27NO3/c1-18-7-6-14-12(13(18)3-4-15(18)22)5-8-20-17(24-20)16(23)11(10-21)9-19(14,20)2/h12-15,17,22-23H,3-9H2,1-2H3/t12-,13-,14-,15-,17+,18-,19+,20+/m0/s1^Y Key:KVJXBPDAXMEYOA-CXANFOAXSA-N^Y
^NY (what is this?) (verify)

Trilostane

Overview

Chemistry

References

External links

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