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Chemical compound
16α-Hydroxyestrone (16α-OH-E1), or hydroxyestrone, also known as estra-1,3,5(10)-triene-3,16α-diol-17-one, is an endogenous steroidal estrogen and a major
16α-Hydroxyestrone
Chemical compound
2-Hydroxyestrone (2-OHE1), also known as estra-1,3,5(10)-trien-2,3-diol-17-one, is an endogenous, naturally occurring catechol estrogen and a major metabolite
2-Hydroxyestrone
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
16-Ketoestrone (16-keto-E1, or 16-oxoestrone, or 16-oxo-E1) is an endogenous estrogen related to 16α-hydroxyestrone and 16β-hydroxyestrone. In contrast
16-Ketoestrone
Class of hormones
2-Hydroxylated: 2-Hydroxyestradiol 2-Hydroxyestrone 2-Hydroxyestriol 4-Hydroxylated: 4-Hydroxyestradiol 4-Hydroxyestrone 4-Hydroxyestriol The most abundant
Catechol_estrogen
Group of cytochrome P450 enzymes
function is CYP123A9 from Rhodococcus sp, which catalysis estrone to 16-hydroxyestrone in the estradiol degradation pathway of bacteria. Ye, X; Peng, T;
CYP123_family
Chemical compound
16β-Hydroxyestrone (16β-OH-E1) is an endogenous estrogen which serves as a metabolite of estrone as well as a metabolic intermediate in the transformation
16β-Hydroxyestrone
Chemical compound
activity. 15α-Hydroxydehydroepiandrosterone 16α-Hydroxyandrostenedione 16α-Hydroxyestrone Cetadiol Raju U, Bradlow HL, Levitz M (1990). "Estriol-3-sulfate in
16α-Hydroxy-DHEA
Type of steroid hormone
→ Dihydrotestosterone → Androstanediol Estrogens 2-Hydroxyestrone ← Estrone → 16α-Hydroxyestrone 2-Hydroxyestradiol ← Estradiol → Estriol → Estetrol
Sex_hormone
Index of chemical compounds with the same molecular formula
formula C18H22O3 may refer to: Hydroxyestrones 2-Hydroxyestrone 4-Hydroxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol Methallenestril
C18H22O3
Chemical compound
Dehydroepiandrosterone sulfate 15α-Hydroxy-DHEA sulfate 16α-Hydroxyandrostenedione 16α-Hydroxyestrone Estrone sulfate Jerome F. Strauss, III; Robert L. Barbieri (13 September
16α-Hydroxy-DHEA_sulfate
Chemical compound
O-methyltransferase via the intermediate 2-hydroxyestrone. Unlike estrone but similarly to 2-hydroxyestrone and 2-methoxyestradiol, 2-methoxyestrone has
2-Methoxyestrone
Chemical compound
Hydroxyestrone diacetate (brand names Colpoginon, Colpormon, Hormobion, Hormocervix) (former developmental code name RD-310), or 16α-hydroxyestrone diacetate
Hydroxyestrone_diacetate
Chemical compound
Androstenone (5α-androst-16-en-3-one) is a 16-androstene class steroidal pheromone. It is found in boar's saliva, celery cytoplasm,[citation needed] and
Androstenone
Chemical compound
sulfate 16α-Hydroxydehydroepiandrosterone 16α-Hydroxyandrostenedione 16α-Hydroxyestrone Estrone sulfate C19H28O6S Roger Smith (Prof.) (1 January 2001). The
15α-Hydroxy-DHEA_sulfate
Chemical compound
(DHEA). 16α-Hydroxydehydroepiandrosterone 16α-Hydroxyandrostenedione 16α-Hydroxyestrone Roger Smith (Prof.) (1 January 2001). The Endocrinology of Parturition:
15α-Hydroxy-DHEA
Chemical compound
as 2-hydroxyestradiol, 16α-hydroxyestrone, estriol (16α-hydroxyestradiol), and 4-hydroxyestrone but unlike 2-hydroxyestrone. Estrogen conjugate Lipoidal
4-Hydroxyestradiol
Chemical compound
cytochrome P450 enzymes into catechol estrogens such as 2-hydroxyestrone and 4-hydroxyestrone or into estriol. Both of these transformations take place
Estrone
Chemical compound
(16α-OH-A4) and 16α-OH-A4 is converted by aromatase into 16α-hydroxyestrone (16α-OH-E1), which is subsequently converted into estriol by 17β-hydroxysteroid
Estriol
Class of corticosteroids
glucocorticoids–new mechanisms for old drugs". The New England Journal of Medicine. 353 (16): 1711–1723. doi:10.1056/NEJMra050541. PMID 16236742. S2CID 5744727. Botía
Glucocorticoid
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
6β-Hydroxycortisol
Human enzyme
Sciences of the United States of America. 84 (16): 5530–4. Bibcode:1987PNAS...84.5530G. doi:10.1073/pnas.84.16.5530. PMC 298896. PMID 3475690. Haycock JW
Tyrosine_hydroxylase
Chemical compound
"Quercetin dihydrate safety sheet". Archived from the original on September 16, 2011. "Flavonoids". Micronutrient Information Center, Linus Pauling Institute
Quercetin
Mammalian protein found in Homo sapiens
Phenylalanine hydroxylase (PAH) (EC 1.14.16.1) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine
Phenylalanine_hydroxylase
Chemical compound
3β-Androstenol, also known as 5α-androst-16-en-3β-ol, is a naturally occurring mammalian pheromone known to be present in humans and pigs. It is thought
3β-Androstenol
Chemical compound
O-methyltransferase via the intermediate 4-hydroxyestrone. It has estrogenic activity similarly to estrone and 4-hydroxyestrone. 2-Methoxyestradiol 2-Methoxyestriol
4-Methoxyestrone
Chemical compound
Fishman J, Martucci C (September 1980). "Biological properties of 16 alpha-hydroxyestrone: implications in estrogen physiology and pathophysiology". The
2-Methoxyestriol
Primary female sex hormone
estrogens 2-hydroxyestradiol, 2-hydroxyestrone, 4-hydroxyestradiol, and 4-hydroxyestrone, as well as 16α-hydroxyestrone, are also estrogens with varying
Estrogen
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Etiocholanolone_glucuronide
Mammalian pheromone also found in truffles
Androstenol, also known as 5α-androst-16-en-3α-ol (shortened to 3α,5α-androstenol or 3α-androstenol), is a 16-androstene class steroidal pheromone and
Androstenol
Chemical compound
into 16α-hydroxy-DHEA sulfate, then desulfated and aromatized into 16α-hydroxyestrone, and finally converted into estriol by 17β-hydroxysteroid dehydrogenase
16α-Hydroxyandrostenedione
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Androstenetriol
Class of enzymes
Tryptophan hydroxylase (TPH) is an enzyme (EC 1.14.16.4) involved in the synthesis of the monoamine neurotransmitter serotonin. Tyrosine hydroxylase, phenylalanine
Tryptophan_hydroxylase
Pharmaceutical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
OSU-ERβ-12
Combination drug
"Bazedoxifene / conjugated estrogens (Duavee) Use During Pregnancy". Drugs.com. 16 February 2019. Retrieved 23 June 2020. "Duavive Product information". Health
Bazedoxifene/conjugated estrogens
Bazedoxifene/conjugated_estrogens
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
7α-Hydroxycholesterol
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Testosterone_sulfate
Chemical compound
estrogen. It is an estrogen ester, specifically, an ester of estrone. Hydroxyestrone diacetate Estradiol acetate Estriol triacetate Elks J (14 November 2014)
Estrone_acetate
Chemical compound
PMID 15500480. Archived from the original (PDF) on 1 May 2014. Retrieved 16 May 2011. (PDF) "Anipryl consumer information". Drugs.com Vet. Retrieved 3
Trilostane
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Fluoroestradiol_(18F)
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
11β-Hydroxydihydrotestosterone
11β-Hydroxydihydrotestosterone
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
18-Hydroxycortisol
Chemical compound
2-Hydroxyestradiol→2-Methoxyestradiol 2-Hydroxyestrone→2-Methoxyestrone 4-Hydroxyestradiol→4-Methoxyestradiol 4-Hydroxyestrone→4-Methoxyestrone Inhibitors: 2-Hydroxyestradiol
9-Methyl-β-carboline
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Tetrahydrocortisone
Chemical compound
hours 6 to 9 years: < 0.3 mg/24 hours 10 to 15 years: 0.1 to 0.6 mg/24 hours 16 years and older: 0 to 1.4 mg/ 24 hours. For males: 0 to 5 years: < 0.1 mg/24
Pregnanetriol
Chemical compound
Fishman J, Martucci C (September 1980). "Biological properties of 16 alpha-hydroxyestrone: implications in estrogen physiology and pathophysiology". The
2-Hydroxyestriol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Alestramustine
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Pregnanolone
Class of chemical compounds
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Adrenal_steroid
– GABAA receptor positive allosteric modulator 3α-Androstenol: 5α-androst-16-en-3α-ol – GABAA receptor positive allosteric modulator Androsterone:
List_of_neurosteroids
Organochloride known as an insecticide
com. Retrieved 16 December 2023. Johnson, Jenn (22 February 2018). "Her Heart's Home | Timeless New England". New England. Retrieved 16 December 2023.
DDT
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
7α-Hydroxyepiandrosterone
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
11-Ketotestosterone
Chemical compound
action". Journal of Molecular Endocrinology. 56 (3): R139–55. doi:10.1530/JME-16-0013. PMID 26908835. Watson RR (22 July 2011). DHEA in Human Health and Aging
Dehydroepiandrosterone
Experimental cardiovascular drug
2-Hydroxyestradiol→2-Methoxyestradiol 2-Hydroxyestrone→2-Methoxyestrone 4-Hydroxyestradiol→4-Methoxyestradiol 4-Hydroxyestrone→4-Methoxyestrone Inhibitors: 2-Hydroxyestradiol
Zamicastat
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Pregnanediol_glucuronide
Chemical compound
(BANTooltip British Approved Name), also known as 16β-epiestriol or simply 16-epiestriol, as well as 16β-hydroxy-17β-estradiol, is a minor and weak endogenous
Epiestriol
Selective estrogen receptor modulator
years, 7.5% of women who took only tamoxifen had a recurrence, compared with 16% who took either paroxetine, fluoxetine or sertraline, drugs considered to
Tamoxifen
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
21-Deoxycortisone
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Androsterone_glucuronide
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
11β-Methoxyestradiol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Broparestrol
Chemical compound
properties of star anise (Illicium verum Hook. f.)". Phytotherapy Research. 16 (1): 94–95. doi:10.1002/ptr.989. PMID 11807977. S2CID 27196549. Kubo, I.;
Anethole
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
21-Hydroxypregnenolone
Chemical compound
Huh MM, Bradlow HL, Fishman J (April 1984). "Antiestrogen action of 2-hydroxyestrone on MCF-7 human breast cancer cells". J. Biol. Chem. 259 (8): 4840–5
Quinalizarin
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Estriol_sulfate
Combination drug
ISBN 978-92-832-1272-0. Archived from the original (PDF) on 28 August 2021. Retrieved 16 September 2018. "Farmaco SOLUNA 150 + 10 registrado en Perú". "Unijab Dosage
Estradiol benzoate butyrate/algestone acetophenide
Estradiol_benzoate_butyrate/algestone_acetophenide
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Bolandiol
Chemical compound
16-Ketoestradiol (16-keto-E2, 16-oxoestradiol, or 16-oxo-E2) is an endogenous estrogen related to 16-ketoestrone. 16-Ketoestrone is a very weak estrogen
16-Ketoestradiol
Chemical compound
original (PDF) on 16 March 2018. Retrieved 17 April 2017. Dinnendahl V, Fricke U, eds. (2000). Arzneistoff-Profile (in German). Vol. 4 (16 ed.). Eschborn
Entacapone
Class of chemical compounds
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Steroid_sulfate
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
3α-Etiocholanediol
Chemical compound
StatPearls. PMID 32491566. Archived from the original on 21 April 2023. Retrieved 16 July 2023. Auchus RJ (November 2004). "The backdoor pathway to dihydrotestosterone"
5α-Pregnan-17α-ol-3,20-dione
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
3β-Hydroxytibolone
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Β-Zearalenol
Chemical compound
2-Hydroxyestradiol→2-Methoxyestradiol 2-Hydroxyestrone→2-Methoxyestrone 4-Hydroxyestradiol→4-Methoxyestradiol 4-Hydroxyestrone→4-Methoxyestrone Inhibitors: 2-Hydroxyestradiol
Meciadanol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Trestolone
Chemical compound
Estratetraenol, also known as estra-1,3,5(10),16-tetraen-3-ol, is an endogenous steroid found in women that has been described as having pheromone-like
Estratetraenol
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
27-Hydroxycholesterol
Xenoestrogens produced by fungi
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Mycoestrogen
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
5α-Dihydrocortisol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Estrobin
Chemical compound
inhibition of dopamine biosynthesis by 2-hydroxyestradiol because 2-hydroxyestrone, which inhibits tyrosine hydroxylase similarly to 2-hydroxyestradiol
2-Hydroxyestradiol
Chemical compound
estriol (which is 16α-hydroxy-17β-estradiol). It is formed from 16α-hydroxyestrone. In contrast to other endogenous estrogens like estradiol, 17α-epiestriol
17α-Epiestriol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Estradiol_hexahydrobenzoate
Chemical compound
2-Hydroxyestradiol→2-Methoxyestradiol 2-Hydroxyestrone→2-Methoxyestrone 4-Hydroxyestradiol→4-Methoxyestradiol 4-Hydroxyestrone→4-Methoxyestrone Inhibitors: 2-Hydroxyestradiol
Sercloremine
Chemical compound
Fishman J, Martucci C (September 1980). "Biological properties of 16 alpha-hydroxyestrone: implications in estrogen physiology and pathophysiology". The
Estetrol
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
16β,17α-Epiestriol
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
O-Desmethylangolensin
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Estradiol_monopropionate
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Α-Zearalenol
Chemical compound
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
4-Hydroxyestriol
Chemical compound
"Bioidentical hormone therapy: a review of the evidence". J Women's Health (Larchmt). 16 (5): 600–31. doi:10.1089/jwh.2006.0311. PMID 17627398. Sittig M (1 January
Estradiol_cypionate
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Pentafluranol
Class of chemical compounds
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Lipoidal_estradiol
Class of drugs
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Nonsteroidal_estrogen
Herbicide
Protection Agency. 2007-04-24. Archived from the original (PDF) on 2012-03-16. Xu J, Stucki JW, Wu J, Kostka J, Sims GK (2001). "Fate of atrazine and alachlor
Atrazine
Chemical compound
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Finrozole
Class of steroid hormones
2-Hydroxyestrone 4-Hydroxyestradiol 4-Hydroxyestriol 4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 16α-Hydroxyestrone 16β-Hydroxyestrone 16-Ketoestradiol
Corticosteroid
Combined oral contraceptive medication
15α-Hydroxyestradiol 16-Ketoestradiol 16-Ketoestrone 16α-Fluoroestradiol 16α-Hydroxy-DHEA 16α-Hydroxyestrone 16α-Iodoestradiol 16α-LE2 16β-Hydroxyestrone 16β,17α-Epiestriol
Mestranol/noretynodrel
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE
16 HYDROXYESTRONE