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List of androgen esters

August 29, 2023

This is a list of androgen esters, including esters (as well as ethers) of natural androgens like testosterone and dihydrotestosterone (DHT) and synthetic anabolic–androgenic steroids (AAS) like nandrolone (19-nortestosterone).

Testosterone, the base androgen of most androgen esters.

Esters of natural AAS Edit

Testosterone esters Edit

Marketed Edit

Many esters of testosterone have been marketed, including the following major esters:[1][2]

And the following less commonly used esters:[1][2]

Never marketed Edit

The following major testosterone ester has not been marketed:[1][2]

  • Testosterone buciclate (20 Aet-1, CDB-1781) – a very long-acting testosterone ester that was under development but ultimately did not reach the market[4][5]

And the following less commonly known testosterone esters have also not been marketed:[1][2]

Dihydrotestosterone esters Edit

Marketed Edit

Several esters of dihydrotestosterone (DHT; androstanolone, stanolone) have also been marketed, including the following:[8][9]

Never marketed Edit

The following esters of DHT have not been marketed:[8][9]

Testifenon (chlorphenacyl DHT ester) is a nitrogen mustard ester of DHT that was developed as a cytostatic antineoplastic agent but was never marketed.[10]

Esters of other natural AAS Edit

Marketed Edit

The following esters of other natural AAS have been marketed:

Never marketed Edit

And the following have not been marketed:

Sturamustine is a nitrosourea ester of dehydroepiandrosterone (DHEA) that was developed as a cytostatic antineoplastic agent but was never marketed.[12][13]

Ethers of natural AAS Edit

Marketed Edit

Although not esters, the following ethers of natural AAS have been marketed as well:

Never marketed Edit

And the following have not been marketed:

Esters of synthetic AAS Edit

Methandriol esters Edit

Marketed Edit

Never marketed Edit

Nandrolone esters Edit

Marketed Edit

Many esters of the synthetic AAS nandrolone (19-nortestosterone) have been marketed, including the following major esters:[14][15][16]

And the following less commonly used esters:[14][15][16]

Never marketed Edit

The following nandrolone esters exist but were never marketed:

LS-1727 is a nitrosocarbamate ester of nandrolone that was developed as a cytostatic antineoplastic agent but was never marketed.[19]

Trenbolone esters Edit

Marketed Edit

A few esters of the synthetic AAS trenbolone have been marketed, including the following esters:

Never marketed Edit

The following trenbolone esters exist but were never marketed:

Esters of other synthetic AAS Edit

Marketed Edit

Many esters of other synthetic AAS have been marketed as well, including the following:

Never marketed Edit

Whereas the following have not been marketed:

Ethers of synthetic AAS Edit

Marketed Edit

Although not esters, the following ethers of synthetic AAS have been marketed as well:

Never marketed Edit

And the following have not been marketed:

See also Edit

References Edit

  1. ^ a b c d Index Nominum 2000: International Drug Directory. Taylor & Francis US. 2000. ISBN 978-3-88763-075-1. Retrieved 29 May 2012.
  2. ^ a b c d e f g J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 642–. ISBN 978-1-4757-2085-3.
  3. ^ William Llewellyn (2011). Anabolics. Molecular Nutrition Llc. pp. 437–. ISBN 978-0-9828280-1-4.
  4. ^ E. Nieschlag; H. M. Behre (1 April 2004). Testosterone: Action, Deficiency, Substitution. Cambridge University Press. pp. 692–. ISBN 978-1-139-45221-2.
  5. ^ Shalender Bhasin (13 February 1996). Pharmacology, Biology, and Clinical Applications of Androgens: Current Status and Future Prospects. John Wiley & Sons. pp. 471–. ISBN 978-0-471-13320-9.
  6. ^ . www.evestra.com. Archived from the original on 2017-09-29.
  7. ^ Ahmed G, Elger W, Meece F, Nair HB, Schneider B, Wyrwa R, Nickisch K (October 2017). "A prodrug design for improved oral absorption and reduced hepatic interaction". Bioorg. Med. Chem. 25 (20): 5569–5575. doi:10.1016/j.bmc.2017.08.027. PMID 28886996.
  8. ^ a b J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 640–. ISBN 978-1-4757-2085-3.
  9. ^ a b I.K. Morton; Judith M. Hall (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 261–. ISBN 978-94-011-4439-1.
  10. ^ Lagova ND, Sof'ina ZP, Shkodinskaia EN, Kurdiumova KN, Valueva IM (1988). "[The antineoplastic activity of testiphenon]". Vopr Onkol (in Russian). 34 (11): 1363–8. PMID 3201773.
  11. ^ George W.A Milne (8 May 2018). Drugs: Synonyms and Properties: Synonyms and Properties. Taylor & Francis. pp. 67–. ISBN 978-1-351-78989-9.
  12. ^ J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 1122. ISBN 978-1-4757-2085-3.
  13. ^ Chavis C, de Gourcy C, Borgna JL, Imbach JL (1982). "New steroidal nitrosoureas". Steroids. 39 (2): 129–47. doi:10.1016/0039-128x(82)90081-2. PMID 7071885. S2CID 21042994.
  14. ^ a b J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 660–. ISBN 978-1-4757-2085-3.
  15. ^ a b Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 716–717. ISBN 978-3-88763-075-1.
  16. ^ a b I.K. Morton; Judith M. Hall (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. ISBN 978-94-011-4439-1.
  17. ^ Lerner, Leonard J.; Holthaus, Fred J.; Thompson, Charles R. (1959). "A myotrophic agent and gonadotrophin inhibitor, 19-nortestosterone-17-benzoate". Endocrinology. 64 (6): 1010–1016. doi:10.1210/endo-64-6-1010. ISSN 0013-7227. PMID 13652918.
  18. ^ Boschann, H. -W. (1955). "Cytologische Untersuchungen über die Wirkung von Androgenen am atrophischen Vaginalepithel in Abhängigkeit von Dosierung und Applikationsart". Archiv für Gynäkologie. 187 (1): 39–64. doi:10.1007/BF00985845. ISSN 0003-9128. PMID 13303168. S2CID 30443548.
  19. ^ Hartley-Asp B, Wilkinson R, Venitt S, Harrap KR (1981). "Studies on the mechanism of action of LS 1727, a nitrosocarbamate of 19-nortestosterone". Acta Pharmacol Toxicol (Copenh). 48 (2): 129–38. doi:10.1111/j.1600-0773.1981.tb01598.x. PMID 6167141.

August 29, 2023
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This is a list of androgen esters including esters as well as ethers of natural androgens like testosterone and dihydrotestosterone DHT and synthetic anabolic androgenic steroids AAS like nandrolone 19 nortestosterone Testosterone the base androgen of most androgen esters Contents 1 Esters of natural AAS 1 1 Testosterone esters 1 1 1 Marketed 1 1 2 Never marketed 1 2 Dihydrotestosterone esters 1 2 1 Marketed 1 2 2 Never marketed 1 3 Esters of other natural AAS 1 3 1 Marketed 1 3 2 Never marketed 1 4 Ethers of natural AAS 1 4 1 Marketed 1 4 2 Never marketed 2 Esters of synthetic AAS 2 1 Methandriol esters 2 1 1 Marketed 2 1 2 Never marketed 2 2 Nandrolone esters 2 2 1 Marketed 2 2 2 Never marketed 2 3 Trenbolone esters 2 3 1 Marketed 2 3 2 Never marketed 2 4 Esters of other synthetic AAS 2 4 1 Marketed 2 4 2 Never marketed 2 5 Ethers of synthetic AAS 2 5 1 Marketed 2 5 2 Never marketed 3 See also 4 ReferencesEsters of natural AAS EditTestosterone esters Edit Marketed Edit Many esters of testosterone have been marketed including the following major esters 1 2 Testosterone caproate component of Omnadren and Triormon Depositum Testosterone cypionate Depo Testosterone numerous others Testosterone decanoate component of Sustanon 250 Testosterone enanthate Delatestryl numerous others component of Testoviron Depot Testosterone isobutyrate Agovirin Depot Perandren M Testocryst Virex Cryst component of Femandren M Folivirin Testosterone isocaproate component of Omnadren Sustanon 100 and Sustanon 250 Testosterone phenylpropionate component of Omnadren Sustanon 100 and Sustanon 250 Testosterone propionate Testoviron numerous others component of Omnadren Sustanon 100 Sustanon 250 and Testoviron Depot Testosterone undecanoate Aveed Andriol Nebido Jatenzo numerous others And the following less commonly used esters 1 2 Testosterone acetate Aceto Sterandryl Aceto Testoviron Amolisin Androtest A Deposteron Farmatest Perandrone A Testosterone cyclohexylpropionate Andromar Femolone Telipex Retard component of Trioestrine Retard Testosterone enantate benzilic acid hydrazone component of Climacteron Testosterone furoate Furotest Testosterone hexahydrobenzoate Sterandryl Retard component of Trinestril AP Testosterone hexahydrobenzylcarbonate Lontanyl Testosterone hexyloxyphenylpropionate Andradurin Testosterone ketolaurate Androdurin component of Testosid Depot and Klimanosid R Depot Testosterone nicotinate Bolfortan Linobol Testosterone phenylacetate Perandren Androject Testosterone phosphate Telipex Aquosum Testosterone undecylenate component of Durasteron and Triolandren Testosterone valerate component of Deposterona and Triolandren 3 Never marketed Edit The following major testosterone ester has not been marketed 1 2 Testosterone buciclate 20 Aet 1 CDB 1781 a very long acting testosterone ester that was under development but ultimately did not reach the market 4 5 And the following less commonly known testosterone esters have also not been marketed 1 2 Polytestosterone phloretin phosphate Testosterone 17b 1 5 aminosulfonyl 2 pyridinyl carbonyl L proline EC586 6 7 Testosterone acetate butyrate Testosterone acetate propionate Testosterone benzoate Testosterone butyrate Testosterone diacetate Testosterone dipropionate Testosterone formate Testosterone isovalerate Testosterone palmitate Testosterone phenylbutyrate Testosterone stearate Testosterone succinate Testosterone sulfateDihydrotestosterone esters Edit Marketed Edit Several esters of dihydrotestosterone DHT androstanolone stanolone have also been marketed including the following 8 9 Androstanolone benzoate Ermalone Amp Hermalone Sarcosan Androstanolone enanthate Anaboleen Depot Androstanolone propionate Pesomax Androstanolone valerate Apeton Never marketed Edit The following esters of DHT have not been marketed 8 9 Dihydrotestosterone acetate Dihydrotestosterone butyrate Dihydrotestosterone formate Dihydrotestosterone undecanoateTestifenon chlorphenacyl DHT ester is a nitrogen mustard ester of DHT that was developed as a cytostatic antineoplastic agent but was never marketed 10 Esters of other natural AAS Edit Marketed Edit The following esters of other natural AAS have been marketed Androstenediol dipropionate Bisexovister Bisexovis Ginandrin Stenandiol Prasterone enantate DHEA enantate Gynodian Depot in combination with estradiol valerate Prasterone sulfate DHEA sulfate Astenile Mylis Teloin Never marketed Edit And the following have not been marketed Androstenediol 3b acetate Androstenediol 3b acetate 17b benzoate 11 Androstenediol 17b acetate Androstenediol diacetateSturamustine is a nitrosourea ester of dehydroepiandrosterone DHEA that was developed as a cytostatic antineoplastic agent but was never marketed 12 13 Ethers of natural AAS Edit Marketed Edit Although not esters the following ethers of natural AAS have been marketed as well Cloxotestosterone acetate Caprosem the 17 O chloral hemiacetal acetate ether of testosterone 2 Never marketed Edit And the following have not been marketed Cloxotestosterone the 17 O chloral hemiacetal ether of testosterone 2 Silandrone SC 16148 the 17 O trimethylsilyl ether of testosterone 2 Esters of synthetic AAS EditMethandriol esters Edit Marketed Edit Methandriol bisenanthoyl acetate Notandron Depot Methandriol dipropionate Arbolic Durabolic Or Bolic Probolik Protabolin Methandriol propionate Metilbisexovis Never marketed Edit Methandriol diacetateNandrolone esters Edit Marketed Edit Many esters of the synthetic AAS nandrolone 19 nortestosterone have been marketed including the following major esters 14 15 16 Nandrolone decanoate Deca Durabolin others Nandrolone phenylpropionate Durabolin others And the following less commonly used esters 14 15 16 Nandrolone caproate Anabolin Depot Nandrolone cyclohexanecarboxylate Nor Durandron Norlongandron Nandrolone cyclohexylpropionate Andol Fherbolico Megabolin Megabolin Retar Pluropon Proteron Depot Sanabolicum Nandrolone cypionate Anabo Depo Nortestonate Dynabol Nortestrionate Pluropon Sterocrinolo Nandrolone furylpropionate Demelon Nandrolone hexyloxyphenylpropionate Anador Anadur Anadurine Nandrolone hydrogen succinate Anabolico Menidrabol Nandrolone laurate Clinibolin Fortadex Laurabolin Nandrolone propionate Anabolicus Nor Anabol Nortesto Norbyol 19 Pondus Testobolin Nandrolone sulfate Keratyl Nandrol Nandain Colirio Ocul Nandrol Nandrolone undecanoate Dynabolin Dynabolon Psychobolan Never marketed Edit The following nandrolone esters exist but were never marketed Bolmantalate nandrolone 17b adamantoate Nandrolone acetate Nandrolone benzoate 17 Nandrolone cyclotate Nandrolone enanthate 18 Nandrolone formate Nandrolone nonanoateLS 1727 is a nitrosocarbamate ester of nandrolone that was developed as a cytostatic antineoplastic agent but was never marketed 19 Trenbolone esters Edit Marketed Edit A few esters of the synthetic AAS trenbolone have been marketed including the following esters Trenbolone acetate Revalor Finaplix Finajet Trenbolone hexahydrobenzylcarbonate Parabolan Hexabolan Never marketed Edit The following trenbolone esters exist but were never marketed Trenbolone enanthate Trenbolone undecanoateEsters of other synthetic AAS Edit Marketed Edit Many esters of other synthetic AAS have been marketed as well including the following Bolandiol dipropionate Anabiol Storinal Bolazine capronate bolazine caproate Roxilon Inject Boldenone acetate Equilon 100 Boldenone cypionate Equilon 100 Boldenone propionate Equilon 100 Boldenone undecylenate boldenone undecenoate Boldane Equilon 100 Equipoise Parenabol Vebonol others Clostebol acetate Macrobin Steranabol Alfa Trofodermin Megagrisevit Clostebol caproate Macrobin Depot Clostebol propionate Yonchlon Drostanolone propionate Masteron Drolban Masteril Mastisol Metormon Permastril Metenolone acetate Primobolan Primobolan S Primonabol Nibal Metenolone enantate Primobolan Depot Norclostebol acetate Anabol 4 19 Oxabolone cipionate Steranabol Depo Steranabol Ritardo Propetandrol norethandrolone 3b propionate Solevar Stenbolone acetate Stenobolone Anatrofin Never marketed Edit Whereas the following have not been marketed 11b Methyl 19 nortestosterone dodecylcarbonate Dimethandrolone buciclate Dimethandrolone dodecylcarbonate Dimethandrolone undecanoate Mesterolone cypionate Nisterime acetate Trestolone acetate Trestolone enantateEthers of synthetic AAS Edit Marketed Edit Although not esters the following ethers of synthetic AAS have been marketed as well Mepitiostane Thioderon 17b 1 methyloxycyclopentyl ether of epitiostanol Methyltestosterone 3 hexyl ether Androgenol Enoltestovis Enoltestovister 3 hexyl enol ether of methyltestosterone Penmesterol penmestrol Pandrocine Testopan 3 cyclopentyl enol ether of methyltestosterone Quinbolone Anabolicum Anabolvis 17b cyclopentenyl enol ether of boldenone D1 testosterone Never marketed Edit And the following have not been marketed Mesabolone 17b 1 methyloxycyclohexyl ether of 1 testosterone dihydroboldenone Methoxydienone methoxygonadiene 3 methyl ether of 17 dehydro 18 methyl 19 nor d2 5 10 testosterone Prostanozol 17b tetrahydropyran ether of the 17a demethylated analogue of stanozololSee also EditList of androgens anabolic steroids List of estrogen esters List of progestogen esters List of corticosteroid estersReferences Edit a b c d Index Nominum 2000 International Drug Directory Taylor amp Francis US 2000 ISBN 978 3 88763 075 1 Retrieved 29 May 2012 a b c d e f g J Elks 14 November 2014 The Dictionary of Drugs Chemical Data Chemical Data Structures and Bibliographies Springer pp 642 ISBN 978 1 4757 2085 3 William Llewellyn 2011 Anabolics Molecular Nutrition Llc pp 437 ISBN 978 0 9828280 1 4 E Nieschlag H M Behre 1 April 2004 Testosterone Action Deficiency Substitution Cambridge University Press pp 692 ISBN 978 1 139 45221 2 Shalender Bhasin 13 February 1996 Pharmacology Biology and Clinical Applications of Androgens Current Status and Future Prospects John Wiley amp Sons pp 471 ISBN 978 0 471 13320 9 R amp D Research www evestra com Archived from the original on 2017 09 29 Ahmed G Elger W Meece F Nair HB Schneider B Wyrwa R Nickisch K October 2017 A prodrug design for improved oral absorption and reduced hepatic interaction Bioorg Med Chem 25 20 5569 5575 doi 10 1016 j bmc 2017 08 027 PMID 28886996 a b J Elks 14 November 2014 The Dictionary of Drugs Chemical Data Chemical Data Structures and Bibliographies Springer pp 640 ISBN 978 1 4757 2085 3 a b I K Morton Judith M Hall 6 December 2012 Concise Dictionary of Pharmacological Agents Properties and Synonyms Springer Science amp Business Media pp 261 ISBN 978 94 011 4439 1 Lagova ND Sof ina ZP Shkodinskaia EN Kurdiumova KN Valueva IM 1988 The antineoplastic activity of testiphenon Vopr Onkol in Russian 34 11 1363 8 PMID 3201773 George W A Milne 8 May 2018 Drugs Synonyms and Properties Synonyms and Properties Taylor amp Francis pp 67 ISBN 978 1 351 78989 9 J Elks 14 November 2014 The Dictionary of Drugs Chemical Data Chemical Data Structures and Bibliographies Springer p 1122 ISBN 978 1 4757 2085 3 Chavis C de Gourcy C Borgna JL Imbach JL 1982 New steroidal nitrosoureas Steroids 39 2 129 47 doi 10 1016 0039 128x 82 90081 2 PMID 7071885 S2CID 21042994 a b J Elks 14 November 2014 The Dictionary of Drugs Chemical Data Chemical Data Structures and Bibliographies Springer pp 660 ISBN 978 1 4757 2085 3 a b Index Nominum 2000 International Drug Directory Taylor amp Francis January 2000 pp 716 717 ISBN 978 3 88763 075 1 a b I K Morton Judith M Hall 6 December 2012 Concise Dictionary of Pharmacological Agents Properties and Synonyms Springer Science amp Business Media ISBN 978 94 011 4439 1 Lerner Leonard J Holthaus Fred J Thompson Charles R 1959 A myotrophic agent and gonadotrophin inhibitor 19 nortestosterone 17 benzoate Endocrinology 64 6 1010 1016 doi 10 1210 endo 64 6 1010 ISSN 0013 7227 PMID 13652918 Boschann H W 1955 Cytologische Untersuchungen uber die Wirkung von Androgenen am atrophischen Vaginalepithel in Abhangigkeit von Dosierung und Applikationsart Archiv fur Gynakologie 187 1 39 64 doi 10 1007 BF00985845 ISSN 0003 9128 PMID 13303168 S2CID 30443548 Hartley Asp B Wilkinson R Venitt S Harrap KR 1981 Studies on the mechanism of action of LS 1727 a nitrosocarbamate of 19 nortestosterone Acta Pharmacol Toxicol Copenh 48 2 129 38 doi 10 1111 j 1600 0773 1981 tb01598 x PMID 6167141 Retrieved from https en wikipedia org w index php title List of androgen esters amp oldid 1166533328 Methandriol esters, wikipedia, wiki, book, books, library,

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