48 Results for "

Steroid 5α- reductase

" in MedChemExpress (MCE) Product Catalog:
Products (48)

48 Results for "Steroid 5α- reductase" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-135794
CAS No.: 32694-37-4
Purity:  ≥98.0%
Synonyms: 11-KDHT; -Dihydro-11-keto testosterone
Target:  

Androgen Receptor

Research Areas:  

Endocrinology

11-Ketodihydrotestosterone (11-KDHT; -Dihydro-11-keto testosterone) is an endogenous steroid and a metabolite of 11β-Hydroxyandrostenedione. 11-Ketodihydrotestosterone is an active androgen and is also a potent androgen receptor (AR) agonist with a Ki of 20.4 nM and an EC50 of 1.35 nM for human AR. 11-Ketodihydrotestosterone drives gene regulation, protein expression and cell growth in androgen-dependent prostate cancer cells .
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Cat. No.: HY-107819
CAS No.: 80-97-7
Purity:  99.92%
Synonyms: Dihydrocholesterol; -Cholestanol; NSC 18188
-Cholestan-3β-ol is a derivitized steroid compound.
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Cat. No.: HY-N2489
CAS No.: 56786-63-1
Synonyms: BrassinoSteroid BB 16; DI 31
Research Areas:  

Others

-Hydroxy-laxogenin (Brassinosteroid BB 16; DI 31) is a derivative of laxogenin, a spirostane-type steroid. -Hydroxy-laxogenin serves as a plant-derived anabolic agent and is used as a dietary supplement .
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Cat. No.: HY-E70558
Target:  

5 alpha Reductase

Research Areas:  

Metabolic Disease

-reductase, Rat (Sprague-Dawley) Liver is an enzyme involved in steroid metabolism and participates in the androgen metabolic pathway. -reductase, Rat (Sprague-Dawley) Liver catalyzes the conversion of testosterone to -dihydrotestosterone (DHT). DHT plays important roles in the development of male sex organs, hair growth, prostate function, and other aspects .
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Cat. No.: HY-W677042
CAS No.: 1153-51-1
Synonyms: -Androst-16-en-3α-ol
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

α-Androstenol (-Androst-16-en-3α-ol) is a steroid pheromone that has been found in boar testes and male axillary sweat. α-Androstenol is also a positive allosteric modulator of GABAA receptors, which enhances GABA-activated currents in primary mouse cerebellar granule cells (EC50 of 0.4 μM). α-Androstenol produces anxiolytic-like, antidepressant-like, and anticonvulsant effects in mice. α-Androstenol can be used for the research of seizures .
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Cat. No.: HY-133970
CAS No.: 481-21-0
Purity:  99.34%
-Cholestane is a steroidal hydrocarbon and fecal stanol, and is used as an internal standard for gas chromatographic sterol analysis. -Cholestane is the parent steroidal skeleton of polyhydroxylated brassinosteroids of plant origin. It is used as an internal standard for GC-FID and GC-MS analysis of fecal sterols in urine and sludge samples. -Cholestane can be used in studies of age- or disease-related skeletal muscle atrophy .
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Cat. No.: HY-135794S
CAS No.: 2479914-02-6
Purity:  99.00%
Synonyms: 11-KDHT-d3; -Dihydro-11-keto testosterone-d3
11-Ketodihydrotestosterone-d3 is the deuterium labeled 11-Ketodihydrotestosterone. 11-Ketodihydrotestosterone (11-KDHT; -Dihydro-11-keto testosterone) is an endogenous steroid and a metabolite of 11β-Hydroxyandrostenedione. 11-Ketodihydrotestosterone is an active androgen and is also a potent androgen receptor (AR) agonist with a Ki of 20.4 nM and an EC50 of 1.35 nM for human AR. 11-Ketodihydrotestosterone drives gene regulation, protein expression and cell growth in androgen-dependent prostate cancer cells .
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Cat. No.: HY-113364
CAS No.: 600-63-5
Synonyms: -THB
-Tetrahydrocorticosterone (-HB), an endogenous steroid, is a glucocorticoid receptor (GR) agonist and a metabolite of Corticosterone (HY-B1618). -Tetrahydrocorticosterone is an effective topical anti-inflammatory agent in vivo. -Tetrahydrocorticosterone reduces metabolites that bind to GR-Corticosterone and its -reduced metabolites in rat hepatocytes, with a Kd of 268 nM. -Tetrahydrocorticosterone can be used for research on inflammatory skin diseases .
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Cat. No.: HY-103245
CAS No.: 188589-66-4
Purity:  99.64%
Target:  

Androgen Receptor

Research Areas:  

Cancer

Cl-4AS-1, a potent steroidal androgen receptor (AR) agonist (IC50 = 12 nM), is also an inhibitor of -reductase types I and II (IC50 = 6 and 10 nM, respectively) .
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Cat. No.: HY-W010934
CAS No.: 1253-84-5
3β,5α,6β-Trihydroxycholestane is a steroid that occurs naturally in the body and is also found in certain foods. It belongs to a class of compounds known as cholestanes, which are closely related to the better known cholesterol. This particular compound is formed from cholesterol through a series of enzymatic reactions in the liver and other organs. It has been studied for its potential health benefits, including its ability to reduce inflammation and oxidative stress in the body. Some research suggests that it may also play a role in regulating blood sugar levels and improving insulin sensitivity. Despite these potential benefits, 3β,5α,6β-Trihydroxycholestane is not widely used as a supplement or medicine due to its relatively low content, focus on natural resources and limited research. However, researchers continue to investigate its potential uses and effects on human health.
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Cat. No.: HY-152094
CAS No.: 2279077-93-7
Purity:  99.82%
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

SRD5A1-IN-1 (Compound 4) is a competitive and covalent steroid -reductase type 1 (SRD5A1) inhibitor with an IC50 of 1.44 µM. SRD5A1-IN-1 modulates SRD5A1 function, leading to a lower level of dihydrotestosterone (DHT) production and SRD5A1 protein suppression .
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Cat. No.: HY-107819S
CAS No.: 2260669-14-3
Purity:  99.18%
Synonyms: Dihydrocholesterol-d5; -Cholestanol-d5; NSC 18188-d5
5α-Cholestan-3β-ol-d5 is the deuterium labeled -Cholestan-3β-ol. -Cholestan-3β-ol is a derivitized steroid compound .
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Cat. No.: HY-106129
CAS No.: 176975-26-1
Synonyms: LY 320236
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology Cancer

Izonsteride (Compound LY320236) is an inhibitor of 5α-reductase (IC50 = 11.6 nM for type I; 7.37 nM for type II). LY320236 inhibits the activity of steroid -reductase, preventing the conversion of testosterone (T) to dihydrotestosterone (DHT). LY320236 can significantly inhibit the growth of LNCaP tumors in thymic mice without exhibiting obvious host toxicity .
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Cat. No.: HY-W741872
CAS No.: 516-41-6
Synonyms: -DHF
-Dihydrocortisol (-DHF), a metabolite of Hydrocortisone (Cortisol) (HY-N0583), is a steroid hormone. -Dihydrocortisol can enhance the mineralocorticoid activity of aldosterone .
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Cat. No.: HY-123323
CAS No.: 134067-56-4
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

MK-0434 is an orally active steroid 5α-reductase inhibitor. MK-0434 specifically inhibits steroid 5α-reductase, thereby reducing the level of dihydrotestosterone (DHT) in the body. MK-0434 can be used in the study of benign prostatic hyperplasia .
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Cat. No.: HY-19144
CAS No.: 119347-91-0
Target:  

5 alpha Reductase

Research Areas:  

Others

ONO-3805 is an early lead compound of a non-steroidal -reductase inhibitor, used to inhibit the conversion of testosterone to dihydrotestosterone, with potential effects in inhibiting benign prostatic hyperplasia.
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Cat. No.: HY-106363
CAS No.: 103497-68-3
Synonyms: L 654066
Target:  

5 alpha Reductase

Research Areas:  

Others

MK-0963 is a steroidal 5α-reductase inhibitor. MK-0963 reduces serum dihydrotestosterone (DHT) concentrations in a dose-dependent manner. MK-0963 can be used for the study of dihydrotestosterone-related diseases such as benign prostate hyperplasia (BPH) .
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Cat. No.: HY-106614
CAS No.: 105149-00-6
Research Areas:  

Endocrinology

Osaterone acetate is an orally active steroid anti-androgen agent, mainly used for benign prostatic hyperplasia (BPH) in dogs. Osaterone acetate competitively antagonizes androgen receptor and inhibits 5α-reductase, reducing the concentration of dihydrotestosterone (DHT) while blocking the growth-stimulating effects of testosterone and DHT on prostate cells. Osaterone acetate can rapidly alleviate the symptoms of BPH in dogs without affecting the fertility of breeding dogs .
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Cat. No.: HY-B1734
CAS No.: 979-02-2
Synonyms: 16-DPA
16-Dehydropregnenolone acetate (16-DPA), a sterols compound, is an orally active 17α-hydroxylase and 5α-reductase inhibitor. 16-Dehydropregnenolone is also a potent bile acid receptor (BAR)/farnesoid X receptor (FXR) antagonist. 16-Dehydropregnenolone hypolipidemic and anticancer effects. 16-Dehydropregnenolone acetate (16-DPA) is the drug intermediate that can be used for synthesis of Dexamethasone (HY-14648) and related other steroidal pharmacophores .
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Cat. No.: HY-135794R
CAS No.: 32694-37-4
Synonyms: 11-KDHT (Standard); -Dihydro-11-keto testosterone (Standard)
Research Areas:  

Endocrinology

11-Ketodihydrotestosterone (Standard) is the analytical standard of 11-Ketodihydrotestosterone. This product is intended for research and analytical applications. 11-Ketodihydrotestosterone (11-KDHT; -Dihydro-11-keto testosterone) is an endogenous steroid and a metabolite of 11β-Hydroxyandrostenedione. 11-Ketodihydrotestosterone is an active androgen and is also a potent androgen receptor (AR) agonist with a Ki of 20.4 nM and an EC50 of 1.35 nM for human AR. 11-Ketodihydrotestosterone drives gene regulation, protein expression and cell growth in androgen-dependent prostate cancer cells .
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