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Chemical compound
15α-hydroxy-DHEA or 15α-OH-DHEA, is an endogenous metabolite of dehydroepiandrosterone (DHEA). Both 15α-OH-DHEA and its 3β-sulfate ester, 15α-OH-DHEA-S
15α-Hydroxy-DHEA
Chemical compound
15α-Hydroxydehydroepiandrosterone sulfate, abbreviated as 15α-hydroxy-DHEA sulfate or 15α-OH-DHEA-S, also known as 15α-hydroxy-17-oxoandrost-5-en-3β-yl sulfate, is an endogenous
15α-Hydroxy-DHEA_sulfate
Chemical compound
7α-Hydroxydehydroepiandrosterone (7α-hydroxy-DHEA; 7α-OH-DHEA), also known as 3β,7α-dihydroxyandrost-5-ene-17-one, is an endogenous, naturally occurring
7α-Hydroxy-DHEA
Chemical compound
Agency (WADA) lists 7-keto-DHEA as a prohibited anabolic agent. List of investigational anxiolytics 7α-Hydroxy-DHEA 7β-Hydroxy-DHEA 7α-Hydroxyepiandrosterone
7-Keto-DHEA
Chemical compound
7β-Hydroxydehydroepiandrosterone (7β-hydroxy-DHEA; 7β-OH-DHEA), also known as 3β,7β-dihydroxyandrost-5-ene-17-one, is an endogenous, naturally occurring
7β-Hydroxy-DHEA
Chemical compound
16α-Hydroxydehydroepiandrosterone sulfate (16α-OH-DHEA-S), also known as 16α-hydroxy-17-oxoandrost-5-en-3β-yl sulfate, is an endogenous, naturally occurring
16α-Hydroxy-DHEA_sulfate
Chemical compound
thereby extending the duration of DHEA. Metabolites of DHEA include DHEA-S, 7α-hydroxy-DHEA, 7β-hydroxy-DHEA, 7-keto-DHEA, 7α-hydroxyepiandrosterone, and
Dehydroepiandrosterone
Chemical compound
Dehydroepiandrosterone sulfate, abbreviated as DHEA sulfate or DHEA-S, also known as androstenolone sulfate, is an endogenous androstane steroid that is
Dehydroepiandrosterone sulfate
Dehydroepiandrosterone_sulfate
Chemical compound
4-Dehydroepiandrosterone (4-DHEA) or 4-Andro is a steroid that is an isomer of 5-dehydroepiandrosterone. 4-DHEA has been prepared by laboratory synthesis
4-Dehydroepiandrosterone
Chemical compound
(16α-hydroxy-DHEA or 16α-OH-DHEA) is an endogenous metabolite of dehydroepiandrosterone (DHEA). Both 16α-OH-DHEA and its 3β-sulfate ester, 16α-OH-DHEA-S
16α-Hydroxy-DHEA
Chemical compound
dehydroepiandrosterone (DHEA) that is formed by the enzyme CYP7B1 in tissues such as the liver and brain. 7β-Hydroxyepiandrosterone 7α-Hydroxy-DHEA 7β-Hydroxy-DHEA 7-Oxo-DHEA
7α-Hydroxyepiandrosterone
Chemical compound
1-Dehydroepiandrosterone (also known as 1-Andro, 1-DHEA, 1-androsterone or 5α-androst-1-en-3β-ol-17-one) is a synthetic, orally active anabolic-androgenic
1-Dehydroepiandrosterone
Chemical compound
19-Nordehydroepiandrosterone (19-nor-DHEA), or 19-nor-5-dehydroepiandrosterone (19-nor-5-DHEA), is an estrane (19-norandrostane) steroid which was never
19-Nordehydroepiandrosterone
Chemical compound
1982. In addition, cyprosterone acetate and its main metabolite, 15β-hydroxy acetate, as well as the newly isolated free alcohol of the main metabolite
15β-Hydroxycyproterone acetate
15β-Hydroxycyproterone_acetate
Medical usage of the prasterone compound
Prasterone, also known as dehydroepiandrosterone (DHEA) and sold under the brand name Intrarosa among others, is a medication as well as over-the-counter
Prasterone
Mammalian pheromone also found in truffles
analogous to the biosynthesis of 3α-androstanediol from dehydroepiandrosterone (DHEA). Androstenol may also be synthesized in the adrenal glands and the ovaries
Androstenol
Chemical compound
pregnancy. It is produced from dehydroepiandrosterone (DHEA), which is converted into 16α-hydroxy-DHEA sulfate, then desulfated and aromatized into 16α-hydroxyestrone
16α-Hydroxyandrostenedione
Chemical compound
Epiandrosterone, or isoandrosterone, also known as 3β-androsterone, 3β-hydroxy-5α-androstan-17-one, or 5α-androstan-3β-ol-17-one, is a steroid hormone
Epiandrosterone
Combination drug
Testosterone propionate/testosterone cypionate/prasterone (TP/TC/DHEA), sold under the brand name Sten, is an injectable combination medication of testosterone
Testosterone propionate/testosterone cypionate/prasterone
Testosterone_propionate/testosterone_cypionate/prasterone
Chemical compound
activity into 16α-hydroxy-DHEA-S (16α-OH-DHEA-S) in the fetal liver and to a limited extent in the fetal adrenal glands. 16α-OH-DHEA-S is then taken up
Estriol
Chemical compound
Sandra N, Ester P, Marie-Agnès P, Robert M, Olivier H (2012). "The DHEA metabolite 7β-hydroxy-epiandrosterone exerts anti-estrogenic effects on breast cancer
7β-Hydroxyepiandrosterone
Chemical compound
progesterone to their 17α-hydroxy derivatives by its 17α-hydroxylase activity, and (b) the subsequent formation of dehydroepiandrosterone (DHEA) and androstenedione
Orteronel
Combination drug
Estradiol valerate/prasterone enanthate (EV/DHEA-E), sold under the brand name Gynodian Depot among others, is an injectable combination medication of
Estradiol valerate/prasterone enanthate
Estradiol_valerate/prasterone_enanthate
Chemical compound
steroid is dehydroepiandrosterone sulfate (DHEA-S), which is the C3β sulfate ester of dehydroepiandrosterone (DHEA). Harteneck C (2013). "Pregnenolone sulfate:
Pregnenolone_sulfate
Chemical compound
5α-Pregnan-17α-ol-3,20-dione, also known as 17α-hydroxy-dihydroprogesterone (17-OH-DHP) is an endogenous steroid, a metabolite of 17α-hydroxyprogesterone
5α-Pregnan-17α-ol-3,20-dione
Chemical compound
Hydroxy-α-sanshool (/-sænʃoʊ.ɒl/), also known as simply sanshool is a molecule found in plants from the genus Zanthoxylum. It is believed to be responsible
Hydroxy-α-sanshool
Chemical compound
is considered a prohormone in the formation of dehydroepiandrosterone (DHEA), itself a prohormone of the sex steroids. This conversion is mediated by
17α-Hydroxypregnenolone
Chemical compound
glands as a metabolite of dehydroepiandrosterone (DHEA). It is believed to have similar effects as DHEA and androstenediol. A study in rodents found that
Androstenetriol
Dietary supplement used for bodybuilding
example, nandrolone (19-nortestosterone). Dehydroepiandrosterone (DHEA), DHEA sulfate (DHEA-S), and androstenedione may all be considered proandrogens of
Bodybuilding_supplement
Chemical compound
3β-Androstanediol 4-Androstenedione 5-Androstenediol DHEA DHEA sulfate 7-Keto-DHEA 7α-Hydroxy-DHEA 16α-Hydroxy-DHEA Metabolites: 2-Methoxyestradiol 2-Methoxyestrone
Tetrahydrocortisone
Chemical compound
intermediate in the biosynthesis of testosterone from dehydroepiandrosterone (DHEA). It is closely related to androstenedione (androst-4-ene-3,17-dione). Androstenediol
Androstenediol
Combination formulation of aclobifene and prasterone
selective estrogen receptor modulator, and prasterone (dehydroepiandrosterone; DHEA), an androgen, estrogen, and neurosteroid, which is under development by
Acolbifene/prasterone
Chemical compound
conversion of tamoxifen and N-desmethyltamoxifen into norendoxifen (4-hydroxy-N,N-desmethyltamoxifen), an active metabolite of tamoxifen. Sanchez-Spitman
N,N-Didesmethyltamoxifen
Chemical compound
progesterone to their 17α-hydroxy derivatives by its 17α-hydroxylase activity, and (b) the subsequent formation of dehydroepiandrosterone (DHEA) and androstenedione
Abiraterone_acetate
Chemical compound
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Α-Zearalenol
Chemical compound
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
2-Phenyl-1-benzothiophene
Steroidal antiandrogen and antimineralocorticoid
metabolites of spironolactone are 7α-thiomethylspironolactone (7α-TMS), 6β-hydroxy-7α-thiomethylspironolactone (6β-OH-7α-TMS), and canrenone
Spironolactone
Anticonvulsant drug
γ-Amino-β-hydroxybutyric acid (GABOB), also known as β-hydroxy-γ-aminobutyric acid (β-hydroxy-GABA), sold under the brand name Gamibetal among others,
Γ-Amino-β-hydroxybutyric_acid
Human hormone
dysfunction, loss of libido, and reduced ejaculate volume, may occur in 3.4 to 15.8% of men treated with finasteride or dutasteride. A small increase in the
Dihydrotestosterone
Chemical compound
3β-Androstanediol 4-Androstenedione 5-Androstenediol DHEA DHEA sulfate 7-Keto-DHEA 7α-Hydroxy-DHEA 16α-Hydroxy-DHEA Metabolites: 2-Methoxyestradiol 2-Methoxyestrone
18-Hydroxycortisol
Chemical compound
4-Hydroxynonenal, or 4-hydroxy-2E-nonenal or 4-hydroxy-2-nonenal or 4-HNE or HNE, (C9H16O2), is an α,β-unsaturated hydroxyalkenal that is produced by
4-Hydroxynonenal
Chemical compound
androgens like testosterone, dihydrotestosterone (DHT), dehydroepiandrosterone (DHEA), and androstenedione. It is the C5 epimer of etiocholanedione (5β-androstanedione)
Androstanedione
Chemical compound
Other positional isomers: Isovanillin ortho-Vanillin 2-Hydroxy-5-methoxybenzaldehyde 2-Hydroxy-4-methoxybenzaldehyde Benzaldehyde Protocatechuic aldehyde
Vanillin
Chemicals that can interfere with endocrine or hormonal systems
Pesticides: the Wildlife / Human Connection". Toxicol Ind Health. 15 (1–2): 1–5. Bibcode:1999ToxIH..15....1.. doi:10.1191/074823399678846547. Diamanti-Kandarakis
Endocrine_disruptor
Drug class
estrone and DHEA into hormonally inactive steroid sulfates. Although hormonally inactive, some steroid sulfates, such as pregnenolone sulfate and DHEA sulfate
Steroidogenesis_inhibitor
Polycyclic organic compound having sterane as a core structure
the oxidation state of the rings. Sterols are forms of steroids with a hydroxy group at position three and a skeleton derived from cholestane. Steroids
Steroid
Chemical compound
Hydroxycitronellal (7-hydroxy-3,7-dimethyloctanal) is an odorant used in perfumery. Its molecular formula is C10H20O2. It derives from a citronellal. 7-Hydroxy-3, 7-dimethyloctanal
Hydroxycitronellal
Corticosteroid precursor and metabolite of cortisol
Receptors and Transporters. CRC Press. p. 248–286. doi:10.1201/9780203299388-15. ISBN 978-0-429-09545-0. Retrieved 18 May 2026. Johnston GA (1996). "GABAA
Cortisone
Endogenous weak androgen
biosynthesis of estrone and of testosterone from dehydroepiandrosterone (DHEA). It is closely related to androstenediol (androst-5-ene-3β,17β-diol). Androstenedione
Androstenedione
sources. In postmenopausal women, circulating levels of estradiol are below 15 pg/mL. During normal human pregnancy, estrogen production increases progressively
Pharmacokinetics_of_estradiol
Chemical compound
androgens like testosterone, dihydrotestosterone, dehydroepiandrosterone (DHEA), and androstenedione. It is the C5 epimer of androstanedione (5α-androstanedione)
Etiocholanedione
Chemical compound
synthesis of estrone from cholesterol by way of dehydroepiandrosterone (DHEA) was developed by Hans Herloff Inhoffen and Walter Hohlweg in 1939 or 1940
Estrone
Chemical used in plastics, xenoestrogen
of organisms. Its half life in water has been estimated at between 4.5 and 15 days, degradation in the air is faster than this, while soil samples degrade
Bisphenol_A
Chemical compound
polyprenyl diphosphate and 4-hydroxybenzoate to produce diphosphate and 4-hydroxy-3-polyprenylbenzoate. This enzyme participates in ubiquinone biosynthesis
4-Hydroxybenzoic_acid
Chemical compound
configuration of the chirality of the hydroxy functional group at carbon position 15. Its 15(R) enantiomer is designated 15(R)-hydroxy-5Z,8Z,11Z,13E-eicosatetraenoic
15-Hydroxyeicosatetraenoic acid
15-Hydroxyeicosatetraenoic_acid
Mechanisms of action
metabolites of spironolactone include 7α-thiospironolactone (7α-TS), 6β-hydroxy-7α-thiomethylspironolactone (6β-OH-7α-TMS), and a number of others. Aside
Pharmacodynamics of spironolactone
Pharmacodynamics_of_spironolactone
Chemical compound
Prasterone enanthate, also known as dehydroepiandrosterone enanthate (DHEA-E) and sold in combination with estradiol valerate under the brand name Gynodian
Prasterone_enanthate
Chemical compound
3β-Androstanediol 4-Androstenedione 5-Androstenediol DHEA DHEA sulfate 7-Keto-DHEA 7α-Hydroxy-DHEA 16α-Hydroxy-DHEA Metabolites: 2-Methoxyestradiol 2-Methoxyestrone
11β-Hydroxyandrostenedione
Compounds from outside the body that mimic estrogen
Pesticides: the Wildlife / Human Connection". Toxicol Ind Health. 15 (1–2): 1–5. Bibcode:1999ToxIH..15....1.. doi:10.1191/074823399678846547. Kase NG, Speroff L
Xenoestrogen
Any steroid hormone that promotes male characteristics
precursors), and the subset includes dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulfate (DHEA-S), androstenedione (A4), and androstenediol (A5). Besides
Androgen
Chemical compound
estradiol for the ER, respectively. The affinity of another metabolite, 4-hydroxy-N-desmethyltoremifene, was not assessed. 4-Hydroxytoremifene showed about
Toremifene
Index of lists with the same name
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
List_of_steroid_esters
Chemical compound
increasing its plasma concentrations. Lovastatin is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), an enzyme that
Lovastatin
Xenoestrogens produced by fungi
3 β-hydroxy steroid dehydrogenase (HSD). CYP450 enzymes will then catalyze aromatic hydroxylation at the 13 or 15 position resulting in 13- or 15- catechols
Mycoestrogen
Chemical compound
steroid hormone and a metabolite of androgens like dehydroepiandrosterone (DHEA) and dihydrotestosterone (DHT). 3β-Androstanediol is a selective, high-affinity
3β-Androstanediol
Chemical compound
Gingerol Names Preferred IUPAC name (5S)-5-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)decan-3-one Other names [6]-Gingerol; 6-Gingerol Identifiers CAS Number
Gingerol
Chemical compound
converts estriol to its glucuronide by adding a sugar acid at the phenolic hydroxy group, with uridine diphosphate (UDP) as byproduct: estriol + UDP-glucuronate
Estriol_3-glucuronide
Chemical compound
A chemical synthesis of methyltestosterone from dehydroepiandrosterone (DHEA) with methandriol as an intermediate proceeds as follows: A newer synthesis
Methyltestosterone
Medication
Astenile, Mylis, Teloin, others), also known as dehydroepiandrosterone sulfate (DHEA-S), is a naturally occurring androstane steroid which is marketed and used
Prasterone_sulfate
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
List of sex-hormonal medications available in the United States
List_of_sex-hormonal_medications_available_in_the_United_States
Combination drug
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Ethinylestradiol/megestrol acetate
Ethinylestradiol/megestrol_acetate
Dietary supplement and medication
A review of efficacy and safety". Experimental Dermatology. 28 (Suppl 1): 15–22. doi:10.1111/exd.13819. PMID 30698874. "Nicotinamide Safety Concerns".
Nicotinamide
Chemical compound
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Testosterone_cypionate
Androstenediol (A5; 5-androstenediol) Boldenone (δ1-T)* Dehydroepiandrosterone (DHEA; prasterone, 5-androstenolone) Dihydrotestosterone (DHT; androstanolone,
List of androgens and anabolic steroids
List_of_androgens_and_anabolic_steroids
Infertility treatment for women
of 4-hydroxy-N-desethylclomiphenewas 15 hours. Individuals with the CYP2D6*10 allele showed longer half-lives for 4-hydroxyclomifene and 4-hydroxy-N-desethylclomiphene
Clomifene
Chemical compound
Simonitsch E, Roth L, Hagen AA, Diczfalusy E (November 1967). "Isolation of 15-alpha-hydroxy-oestriol from pregnancy urine and from the urine of newborn infants"
Estetrol
the ERα/ERβ antagonist fulvestrant (ICI-182,780) and the GPER antagonist G-15. ER-X GPER (GPR30) Gq-mER Estrogen receptor Kampa M, Notas G, Pelekanou V
ERx
Combination drug
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Estradiol diundecylate/hydroxyprogesterone heptanoate/testosterone cyclohexylpropionate
Estradiol_diundecylate/hydroxyprogesterone_heptanoate/testosterone_cyclohexylpropionate
Chemical compound
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Enclomifene
of tamoxifen), elacestrant, enclomifene ((E)-clomifene), endoxifen (4-hydroxy-N-desmethyltamoxifen; metabolite of tamoxifen), and zuclomifene ((Z)-clomifene)
List of selective estrogen receptor modulators
List_of_selective_estrogen_receptor_modulators
Chemical compound
and analogue of 5-androstenediol (androst-5-ene-3β,17β-diol) and 16α-hydroxy-DHEA (androst-5-ene-3β,16α-diol-17-one), but showed no androgenic or myotrophic
Cetadiol
Chemical compound
2-hydroxylation into 2-hydroxyestradiol, and by CYP2C9, CYP2C19, and CYP2C8 via 17β-hydroxy dehydrogenation into estrone, with various other cytochrome P450 (CYP)
Estradiol
Chemical compound
hydroxytyrosol within the Mediterranean diet is estimated to be between 0.15 and 30 mg. The EFSA has issued a scientific opinion on health claims in relation
Hydroxytyrosol
Chemical compound
methylhydroxynandrolone (4-hydroxy-17α-methyl-19-nortestosterone) and the 17α- and 19-methylated derivative of oxabolone is oxymesterone (4-hydroxy-17α-methyltestosterone)
Oxabolone
Chemical compound
The chemical shape of coumestrol orients its two hydroxy groups in the same position as the two hydroxy groups in estradiol, allowing it to inhibit the
Coumestrol
Chemical compound
of the National Academy of Sciences. 81 (15): 4899–4902. Bibcode:1984PNAS...81.4899W. doi:10.1073/pnas.81.15.4899. PMC 391599. PMID 6589634. Bonneau,
Androstenone
Drugs acting on the estrogen receptor
binding to ERα and ERβ of the three metabolites 4-hydroxy Ospemifene, 4'-hydroxy Ospemifene and the 4-hydroxy-, side chain carboxylic acid Ospemifene is at
Selective estrogen receptor modulator
Selective_estrogen_receptor_modulator
Chemical compound
3β-Androstanediol 4-Androstenedione 5-Androstenediol DHEA DHEA sulfate 7-Keto-DHEA 7α-Hydroxy-DHEA 16α-Hydroxy-DHEA Metabolites: 2-Methoxyestradiol 2-Methoxyestrone
6β-Hydroxycortisol
Thyroid hormone
Thyroxine Names Other names O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosine, (-)-thyroxine, 3,3′,5,5′-tetraiodo-L-thyronine Identifiers CAS Number
Thyroxine
Cellular molecules that help resolve inflammation
DHA by two serial lipoxygenases, probably a 15-lipoxygenase and ALOX12. 22-Hydroxy-PD1 (also termed 22-hydroxy-NPD1) is formed by the omega oxidation of
Specialized pro-resolving mediators
Specialized_pro-resolving_mediators
Blood pressure medication
Retrieved 23 February 2021. "Telmisartan and amlodipine tablet". DailyMed. 15 December 2023. Retrieved 24 December 2024. Opie LH, Gersh BJ (2009). Drugs
Telmisartan
improving muscle strength and endurance, or "other anabolic agents". Andro, DHEA, stanozolol, testosterone, and nandrolone, or derivates (see below) are banned
List of drugs banned by the World Anti-Doping Agency
List_of_drugs_banned_by_the_World_Anti-Doping_Agency
Progestogens and estrogens systemic contraceptives, sequential preparations
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Ethinylestradiol/desogestrel
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
List_of_steroids
Substance with biological function
1529/biophysj.103.035527. PMC 1304487. PMID 15298886. Rousseau, Guy G. (2013-08-15). "Fifty years ago: The quest for steroid hormone receptors". Molecular and
Steroid_hormone
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
Tissue-selective estrogen complex
Tissue-selective_estrogen_complex
Organic chemical compound
of topical AzA, salicylic acid, nicotinamide, sulfur, zinc, and alpha hydroxy acid, AzA had more high-quality evidence of effectiveness than the rest
Azelaic_acid
Class of corticosteroids
associated with steroid use". Infectious Disease Clinics of North America. 15 (2): 423–432, viii. doi:10.1016/s0891-5520(05)70154-9. PMID 11447704. Henderson
Glucocorticoid
Chemical compound
4-Hydroxyestrone 4-Methoxyestradiol 4-Methoxyestrone 5-Androstenediol 7-Oxo-DHEA 7α-Hydroxy-DHEA 7α-Methylestradiol 7β-Hydroxyepiandrosterone 8,9-Dehydroestradiol
O-Desmethylangolensin
Chemical compound
Combination". Fertility and Sterility. 15 (6): 653–660. doi:10.1016/s0015-0282(16)35411-5. PMID 14236842. Bringer J, Hedon B (15 September 1995). Fertility and
Estradiol_enanthate
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA
15 HYDROXY-DHEA