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Chemical compound
17α-Dihydroequilin, or α-dihydroequilin, also known as 7-dehydro-17α-estradiol, as well as estra-1,3,5(10),7-tetraene-3,17α-diol, is a naturally occurring
17α-Dihydroequilin
Chemical compound
17β-Dihydroequilin is a naturally occurring estrogen sex hormone found in horses as well as a medication. As the C3 sulfate ester sodium salt, it is a
17β-Dihydroequilin
Chemical compound
dehydrogenase, equilin can be converted into the more potent estrogen 17β-dihydroequilin in the body. This estrogen has about 113% and 108% of the relative binding
Equilin
Primary male sex hormone
Testosteron (Androsten-3-ol-17-ol) [The crystalline production of the testicle hormone, testosterone (Androsten-3-ol-17-ol)]". Helvetica Chimica Acta
Testosterone
Estrogens found in horses
Equilin (Δ7-estrone) Equilenin (Δ6,8-estrone) 17α-Dihydroequilin (Δ7-17α-estradiol) 17β-Dihydroequilin (Δ7-17β-estradiol) 17α-Dihydroequilenin (Δ6,8-17α-estradiol)
Equine_estrogen
Chemical compound
PMID 13531579. Janocko L, Larner JM, Hochberg RB (April 1984). "The interaction of C-17 esters of estradiol with the estrogen receptor". Endocrinology. 114 (4): 1180–6
Estradiol_17β-acetate
Human hormone
Endocrine Basis of Geriatric Psychiatry. Cambridge University Press. pp. 17–. ISBN 978-1-139-42645-9. Zouboulis CC, Chen WC, Thornton MJ, Qin K, Rosenfield
Dihydrotestosterone
Steroidal antiandrogen and antimineralocorticoid
3869–3903. doi:10.1210/jc.2017-01658. PMID 28945902. S2CID 3726467. Deutsch M (17 June 2016). "Guidelines for the Primary and Gender-Affirming Care of Transgender
Spironolactone
Organochloride known as an insecticide
Pollutants/United Nations Environment Programme. Archived from the original (PDF) on 17 December 2010. Retrieved 22 November 2008. Feachem RG, Sabot OJ (May 2007)
DDT
Chemical compound
pharmacology and biological characteristics of 3-tetrahydropyranyl ether of 17-beta-estradiol]". Minerva Ginecologica (in Italian). 24 (2): 70–81. PMID 4603402
Estradiol 17β-tetrahydropyranyl ether
Estradiol_17β-tetrahydropyranyl_ether
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Giredestrant
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estriol_phosphate
Chemical compound
a terminal half-life of 12 ± 5 hours. Abiraterone acetate, also known as 17-(3-pyridinyl)androsta-5,16-dien-3β-ol acetate, is a synthetic androstane steroid
Abiraterone_acetate
Chemical compound
estradiol-3-benzoate-17-n-butyrate]" [Modification of the endometrium during combined therapy with dihydroxyprogesterone acetophenide and estradiol-3-benzoate-17-n-butyrate]
Estradiol_benzoate_butyrate
Chemical compound
quality and effectiveness. Estrone, also known as estra-1,3,5(10)-trien-3-ol-17-one, is a naturally occurring estrane steroid with double bonds at the C1
Estrone
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
N,N-Didesmethyltamoxifen
Polycyclic organic compound having sterane as a core structure
generic terms, e.g., 17-oxo steroids. The term '17-keto steroids', often used in the medical literature, is incorrect because C-17 is specified twice,
Steroid
Chemical in plants
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Apigenin
Primary female sex hormone
response by stimulating IL-4 production and Th2 differentiation. Type 1 and type 17 immune responses are downregulated, likely to be at least partially due to
Estrogen
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Α-Zearalenol
Chemical compound
in "essentially all" patients in both groups. Leg edema occurred in 18% (17/95) of the estradiol undecylate group and 4.2% (4/96) of the cyproterone acetate
Estradiol_undecylate
Chemical compound
C-17 results in longer retarding effects than esterification at C-3. The optimal retarding effect (exceeding 29 days) may be obtained with the C-17 oenanthate
Estradiol_undecylenate
Catechin (polyphenol) in tea
Enforcement, and Criminal Investigations. Food and Drug Administration. 17 April 2017. Archived from the original on April 26, 2017. Retrieved 30 September
Epigallocatechin_gallate
Type of steroid hormone
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Sex_hormone
Anti-seizure medication
Retrieved 17 June 2024 – via Business Wire. "Dilantin". Pfizer. Retrieved 17 June 2024. "Brands". Viatris. 16 November 2020. Retrieved 17 June 2024.
Phenytoin
Chemical compound
esters § Estradiol esters "Human Metabolome Database: Showing metabocard for 17-beta-Estradiol glucuronide (HMDB0010317)". Michael Oettel; Ekkehard Schillinger
Estradiol_glucuronide
Chemical compound
"Estrogen receptor binding radiopharmaceuticals: II. Tissue distribution of 17 alpha-methylestradiol in normal and tumor-bearing rats". Journal of Nuclear
Methylestradiol
Class of drugs
0–20 0.64 0.62 Estrogen 17β-Dihydroequilin 7-Dehydro-17β-estradiol 7.9–113 7.9–108 0.09 0.17 Estrogen 17α-Dihydroequilin 7-Dehydro-17α-estradiol 18.6
Antiestrogen
estradiol-3-furoate, estradiol dipropionate, estradiol-17-caprylate, estradiol-3-benzoate-17-caprylate in oil, and finally estradiol-3-benzoate in emulsion
Pharmacokinetics_of_estradiol
Herbicide
2018-05-02 at the Wayback Machine, Chemical Science International Journal 17(3): 1-10, 2016 Wackett, L. P.; Sadowsky, M. J.; Martinez, B.; Shapir, N. (January
Atrazine
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Finrozole
Chemical compound
(7β-hydroxy-DHEA; 7β-OH-DHEA), also known as 3β,7β-dihydroxyandrost-5-ene-17-one, is an endogenous, naturally occurring steroid and a metabolite of
7β-Hydroxy-DHEA
Chemical compound
testes, this drug may prove itself superior to other treatments." "EnCyzix". 17 September 2018. Mikkelson TJ, Kroboth PD, Cameron WJ, Dittert LW, Chungi V
Enclomifene
Combination drug
1517/14656566.5.12.2559. PMID 15571472. S2CID 24659973. Dando TM, Perry CM (2004). "17 beta-estradiol/levonorgestrel transdermal system". Treatments in Endocrinology
Estradiol/levonorgestrel
Pharmaceutical combination
pharmaceutical company" in 1971, but was found to produce short menstrual cycles of 17 to 18 days with once-monthly administration and 20 to 24 days with twice-monthly
Estradiol valerate/hydroxyprogesterone caproate
Estradiol_valerate/hydroxyprogesterone_caproate
Plant-derived xenoestrogen
plant compounds that, because of its structural similarity to estradiol (17-β-estradiol), have the ability to cause both estrogenic or antiestrogenic
Phytoestrogen
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estriol_acetate_benzoate
Chemical compound
activity, similarly to DHEA and 3β-androstanediol. It has approximately 6% and 17% of the affinity of estradiol at the ERα and ERβ, respectively. Although androstenediol
Androstenediol
Chemical compound
dehydroepiandrosterone and 17 beta-estradiol after intramuscular administration of Gynodian-Depot in 3 women". Hormone Research. 17 (2): 84–89. doi:10.1159/000179680
Estradiol_valerate
Pharmaceutical combination
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Conjugated estrogens/medroxyprogesterone acetate
Conjugated_estrogens/medroxyprogesterone_acetate
Estrogen medication
active forms of the equine estrogens in CEEs, such as equilin and 17β-dihydroequilin, have greater potency in the liver relative to bioidentical estradiol
Conjugated_estrogens
Controversy related to consumer products
pp. A03. Retrieved 17 September 2008. Szabo, Liz. "Scientists, FDA face off over safety of BPA in consumer plastics". USA Today. 17 September 2008. Retrieved
Health_effects_of_Bisphenol_A
Androgen and anabolic steroid
PMID 11440282. "Oxymetholone Powder Uses". aea.ltd. Retrieved 2022-12-17. Kicman AT (June 2008). "Pharmacology of anabolic steroids". British Journal
Oxymetholone
Steroidal hormone medication
DailyMed. 18 September 2023. Retrieved 17 May 2024. "Estring- estradiol system". DailyMed. 27 February 2024. Retrieved 17 May 2024. Rovinski D, Ramos RB, Fighera
Estradiol_(medication)
Chemical compound
0–20 0.64 0.62 Estrogen 17β-Dihydroequilin 7-Dehydro-17β-estradiol 7.9–113 7.9–108 0.09 0.17 Estrogen 17α-Dihydroequilin 7-Dehydro-17α-estradiol 18.6
Stilbestrol
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estradiol_17β-benzoate
Polyphenol with a stilbene skeleton
August 17, 2017. "GSK absorbs controversial 'longevity' company: News blog". Nature Blog. Archived from the original on 2013-12-17. Retrieved 2017-08-17..
Resveratrol
Chemical compound
Psychiatry. Lippincott Williams & Wilkins. ISBN 978-1-4511-7861-6. Genazzani AR (17 January 2006). Postmenopausal Osteoporosis: Hormones & Other Therapies. Taylor
Methyltestosterone
Anabolic steroid
and Oxandrolone in the Management of Male Health". Current Urology Reports. 17 (10): 72. doi:10.1007/s11934-016-0629-8. PMID 27535042. S2CID 43199715. Pan
Nandrolone_phenylpropionate
Antiretroviral medication
water (<10 μg/mL). Efavirenz was approved by the FDA on 21 September 1998. On 17 February 2016, the FDA approved the generic tablet formulation to be produced
Efavirenz
Chemical used in plastics, xenoestrogen
polymerization, and thermal stability". Designed Monomers and Polymers. 17 (1): 47–57. doi:10.1080/15685551.2013.797216. S2CID 94255723. Ghosh NN, Kiskan
Bisphenol_A
Combination drug
U.S. National Library of Medicine. Archived from the original on January 17, 2017. "Dydrogesterone". Drug Information Portal. U.S. National Library of
Estradiol/dydrogesterone
Chemical compound
Stavchansky SA (1988). "Human pharmacokinetics of ethynyl estradiol 3-sulfate and 17-sulfate". Steroids. 51 (1–2): 63–79. doi:10.1016/0039-128x(88)90185-7. PMID 3242167
Ethinylestradiol_sulfate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Oleuropein
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Testosterone_cypionate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Boldenone_undecylenate
Chemical compound
Administration. Archived from the original on 16 November 2016. Retrieved 17 December 2016. "Testosterone enanthate". Drugbank. Archived from the original
Testosterone_enanthate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Diethylstilbestrol_disulfate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estrone_sulfamate
Chemical compound
Cloxestradiol (INNTooltip International Nonproprietary Name), also known as 17-(2,2,2-trichloroethoxy)estradiol, is a synthetic, steroidal estrogen which
Cloxestradiol
Chemical compound
do Tocantins [Journal of Pathology of Tocantins] (in Portuguese). 5 (1): 17. doi:10.20873/uft.2446-6492.2018v5n1p17. ISSN 2446-6492. Moguilevsky JA, Wiemeyer
Estradiol_enanthate
Combination drug
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estradiol benzoate/testosterone propionate
Estradiol_benzoate/testosterone_propionate
Chemical compound
Characterization of the estrogenic activity of a synthetic adrenal steroid 17-α ethinyl androstenediol and its potential use in hormone replacement therapy
Ethinylandrostenediol
Pharmaceutical combination
December 2018. "Lolo Product information". Health Canada. 6 May 2024. Retrieved 17 February 2025. Rowan JP, Simon JA, Speroff L, Ellman H (June 2006). "Effects
Ethinylestradiol/norethisterone acetate
Ethinylestradiol/norethisterone_acetate
Antimicrobial agent
2023-08-17. "The FDA will ban antibacterial ingredients from soaps. What about Canada?". The Globe and Mail. 2016-09-06. Retrieved 2023-08-17. Consumer
Triclosan
Combination medication
Castration-Resistant Prostate Cancer" (Press release). Janssen. 11 August 2023. Retrieved 17 August 2023 – via PR Newswire. "Akeega: Pending EC decision". European Medicines
Niraparib/abiraterone_acetate
Chemical compound
Temperature Variations". Journal of Agricultural and Food Chemistry. 56 (17): 8066–8073. Bibcode:2008JAFC...56.8066C. doi:10.1021/jf801461h. PMID 18681442
Rotenone
Discontinued oral cancer remedy
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Brilanestrant
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estrone_benzoate
Pharmaceutical combination
placebo-controlled study". Journal of Bone and Mineral Research. 17 (10): 1904–12. doi:10.1359/jbmr.2002.17.10.1904. PMID 12369794. S2CID 29312298. "CombiPatch
Estradiol/norethisterone acetate
Estradiol/norethisterone_acetate
Chemical compound
therapy in women: a review". International Journal of Impotence Research. 17 (5): 399–408. doi:10.1038/sj.ijir.3901334. PMID 15889125. S2CID 6461717. Becker
Testosterone_propionate
Combination drug
FA (17 April 2013). Klinische Endokrinologie für Frauenärzte. Springer-Verlag. pp. 533–. ISBN 978-3-662-08110-5. Knörr K, Beller FK, Lauritzen C (17 April
Estradiol benzoate/hydroxyprogesterone caproate
Estradiol_benzoate/hydroxyprogesterone_caproate
Main polyphenol in grapefruit
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Naringenin
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Biochanin_A
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estrone_acetate
Chemical compound
parathion and methylparathion, pentachlorophenol, and 2,4,5-T. This took force on 17 May 2004. Australia ratified the Convention only three days later and became
Dieldrin
Chemical compound
(October 1967). "The synthesis of 3beta-hydroxyestr-4-en-17-one and 3beta-hydroxyandrost-4-en-17-one". Steroids. 10 (4): 411–24. doi:10.1016/0039-128X(67)90119-5
Etynodiol
Transdermal delivery system for estrogens
1136/bjsports-2018-099723. PMC 6686188. PMID 30301734. Deutsch, Madeline B. (2016-07-17). "Overview of feminizing hormone therapy | Gender Affirming Health Program"
Estrogen_patch
Chemical compound
4-Hydroxyestrone (4-OHE1), also known as estra-1,3,5(10)-triene-3,4-diol-17-one, is an endogenous, naturally occurring catechol estrogen, neuroestrogen
4-Hydroxyestrone
Chemical compound
Wilkins. pp. 1185–. ISBN 978-0-7817-1750-2. Archived from the original on 17 May 2020. Retrieved 3 January 2018. Llewellyn W (2011). Anabolics. Molecular
Testosterone_undecanoate
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Gq-mER
Combination drug
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estradiol cypionate/testosterone enanthate
Estradiol_cypionate/testosterone_enanthate
Proteins activated by the hormone estrogen
signaling pathways". Molecular and Cellular Biology. 24 (17): 7681–7694. doi:10.1128/MCB.24.17.7681-7694.2004. PMC 506997. PMID 15314175. Du Z, Wang H
Estrogen_receptor
Polyphenol compound
PMID 19074529. S2CID 285706. Archived from the original (PDF) on 2008-12-17. Retrieved 2009-02-19. Tarragó T, Kichik N, Claasen B, Prades R, Teixidó M
Baicalein
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estradiol_dicypionate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estriol_triacetate
Chemical compound
16α-hydroxyestrone diacetate, also known as 3,16α-dihydroxyestra-1,3,5(10)-trien-17-one 3,16α-diacetate, is a synthetic, steroidal estrogen which has been marketed
Hydroxyestrone_diacetate
Chemical compound
Improvement in arterial blood flow has been demonstrated in coronary arteries. 17-beta-estradiol (E2) is considered the most potent estrogen found in humans
Estradiol
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Guggulsterone
Chemical compound
ORG-817), also known as 3-methoxy-17-epiestriol, is a synthetic, steroidal estrogen and an estrogen ether and prodrug of 17-epiestriol. It has been used as
Epimestrol
Combination drug
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Estradiol cypionate/testosterone cypionate
Estradiol_cypionate/testosterone_cypionate
Combination formulation of aclobifene and prasterone
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Acolbifene/prasterone
Anabolic steroid
and Oxandrolone in the Management of Male Health". Current Urology Reports. 17 (10) 72. doi:10.1007/s11934-016-0629-8. PMID 27535042. S2CID 43199715. Pan
Nandrolone_decanoate
Chemical compound
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Taleranol
Chemical compound
premarin in men with coronary heart disease". Circulation. 17 (6): 1035–1040. doi:10.1161/01.CIR.17.6.1035. PMID 13547367. Spencer H, Kabakow B, Samachson
Mytatrienediol
Combination drug
(16β-hydroxy-17α-estradiol) 17α-Estradiol (alfatradiol) 17α-Dihydroequilenin 17α-Dihydroequilin 17α-Epiestriol (16α-hydroxy-17α-estradiol) 17α-Ethynyl-3α-androstanediol
Ethinylestradiol/drospirenone
Chemical compound
Agard-Jones, Vanessa (1 November 2013). "Bodies in the System". Small Axe. 17 (3(42)): 182–192. doi:10.1215/07990537-2378991. S2CID 145642259. Chlordécone :
Chlordecone
Pharmaceutical combination
2018. "First Generic Drug Approvals". U.S. Food and Drug Administration. 17 October 2022. Archived from the original on 26 January 2021. Retrieved 28
Estradiol/progesterone
Combination drug
Unions, Regional Office for Asia and the Pacific. p. 15. ISBN 978-967-9973-17-4. Synergon. 10 mg progesterone. 1 mg folliculine [estrone]. "Synergon Indications"
Estrone/progesterone
Chemical compound
CM (1999). "Design of an intravaginal ring for the controlled delivery of 17 beta-estradiol as its 3-acetate ester". J Control Release. 61 (3): 319–28
Estradiol_3-propionate
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17 DIHYDROEQUILIN
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17 DIHYDROEQUILIN
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17 DIHYDROEQUILIN
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