146 Results for "

testosterone

" in MedChemExpress (MCE) Product Catalog:
Products (146)

146 Results for "testosterone" in MCE Product Catalog:

Cat. No.: HY-N20647
CAS No.: 124902-18-7
Jioglutolide is a cyclopentane monoterpene and weak testosterone 5α-reductase inhibitor. Jioglutolide is isolated from steamed roots of Rehmannia glutinosa var. hueichingensis. Jioglutolide is applicable to research on allergies, anemia, diabetes, and menopause-related conditions .
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Cat. No.: HY-117671
CAS No.: 121242-02-2
Research Areas:  

Metabolic Disease

KS IV is a cyclolignan derivative and antigonadotropic agent. KS IV exhibits activity against pregnant mare serum gonadotropin (PMSG) but shows no activity against luteinizing hormone (LH). KS IV abolishes the stimulatory effect of PMSG on testosterone release from isolated mouse Leydig cells. KS IV can be used in studies on gonadotropin-regulated endocrine functions .
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Cat. No.: HY-P83683
Synonyms: Ts, andrusol, sustanon, teslen, testicular hormone, virosterone

Host:  

Mouse

Application:  

ELISA

Reactivity:  

Species independent

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Cat. No.: HY-N14632
CAS No.: 171784-03-5
Louisianin A is a non-steroidal growth inhibitor of testosterone-responsive SC 115 cells .
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Cat. No.: HY-N14633
CAS No.: 1192169-18-8
Louisianin B is a non-steroidal growth inhibitor of testosterone-responsive SC 115 cells .
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Cat. No.: HY-N14634
CAS No.: 171784-05-7
Louisianin C is a non-steroidal growth inhibitor of testosterone-responsive SC 115 cells .
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Cat. No.: HY-W421914
CAS No.: 500-28-7
Target:  

Insecticide

Research Areas:  

Infection

Chlorthion is an organic phosphorothionate insecticide. Chlorthion inhibits liver microsomal hydroxylation of testosterone .
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Cat. No.: HY-119436
CAS No.: 201654-12-8
Target:  

Androgen Receptor

Research Areas:  

Metabolic Disease

LG-120907 is a selective androgen receptor (AR) antagonist with a Ki value of 26 nM. LG-120907 inhibits Testosterone-induced increases in ventral prostate (VP) tissue weight and seminal vesicles (SV) tissue weight in vivo .
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Cat. No.: HY-L239
71 compounds

Steroid hormones (also known as steroidal hormones) are a class of tetracyclic aliphatic hydrocarbon compounds derived from cholesterol. Typical representatives of steroid hormones include cortisol, aldosterone, testosterone, estradiol, among others. These hormones serve diverse regulatory functions within the body. For instance, aldosterone helps maintain the homeostasis of extracellular fluid volume and circulating blood volume; testosterone and estradiol primarily promote the development and maturation of male and female reproductive organs and regulate reproductive functions.

MCE designs a unique collection of 71 steroid hormones. This library can be used for research related to metabolic or immune diseases, investigations into the mechanisms of action of nuclear receptor signaling pathways, as well as identification and quantitative analysis in metabolomics studies.

Cat. No.: HY-E71704
Research Areas:  

Others

3-Hydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione monooxygenase (EC 1.14.14.12) participates in the degradation of several steroids, including cholesterol and testosterone, and can use either FADH or FMNH2 as flavin cofactor.
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Cat. No.: HY-116219
CAS No.: 16386-65-5
Target:  

Androgen Receptor

Research Areas:  

Endocrinology Cancer

WB2838 is a non-steroidal androgen-receptor antagonist (IC50: 0.8 μM for partially purified rat prostate cytosol receptor). WB2838 exhibits anti-cancer activity against androgen-responsive breast cancer. WB2838 also shows the inhibitory activity against the growth of the ventral prostate induced by Testosterone propionate .
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Cat. No.: HY-164032
CAS No.: 366472-45-9
Synonyms: 7α,11β-Dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Dimethandrolone undecanoate (7α,11β-Dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate) exhibits withrogens and progesterone activity. Dimethandrolone undecanoate inhibits production of gonadotropins, suppresses testosterone production, and thus inhibits sperm production. Dimethandrolone undecanoate is potent for development of male hormone contraceptives .
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Cat. No.: HY-123037
CAS No.: 43121-43-3
Purity:  98.12%
Triadimefon is an orally active fungicide. Triadimefon significantly reduces the phosphorylation of AKT1 and ERK1/2. Triadimefon significantly increases pAMPK levels, but does not affect total AMPK levels. Triadimefon inhibits the growth of Saccharomyces cerevisiae, disrupts hormone homeostasis (affecting the synthesis of testosterone, etc.), inhibits fetal adrenal development in rats, induces metabolic shifts in hepatocytes, and impairs spatial learning and memory .
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Cat. No.: HY-180409
CAS No.: 262295-11-4
Target:  

Androgen Receptor

Research Areas:  

Cancer

YM580 is a potent, orally active and selective Androgen Receptor (AR) antagonist (IC50 = 0.11 μM, hAR Ki = 4.6 nM, rAR Ki = 6.2 nM). YM580 exhibits good selectivity over PR, GR, and ERα (Kis > 3300 nM). YM580 decreases ventral prostate weight in mature intact rats dose-dependently without affecting serum testosterone levels. YM580 can be used for the research of prostate cancer .
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Cat. No.: HY-B1095R
CAS No.: 302-22-7
Chlormadinone acetate (Standard) is the analytical standard of Chlormadinone acetate (HY-B1095). This product is intended for research and analytical applications. Chlormadinone acetate is a progestogen with potent progestogenic activity and antiandrogenic effects. Chlormadinone acetate acts on glucocorticoid receptor, progesterone receptor, androgen receptor, and GABAA receptor. Chlormadinone acetate induces endometrial proliferation in estrogen-pretreated rabbits, inhibits testosterone-stimulated growth of the prostate and seminal vesicles in castrated rats, and reduces the thymus and adrenal weights in juvenile rats. Chlormadinone acetate is applicable to research related to diseases such as depression and reproductive metabolic disorders.
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Cat. No.: HY-B1095S1
Chlormadinone acetate-d6-1 is deuterium labeled Chlormadinone acetate (HY-B1095). Chlormadinone acetate is a progestogen with potent progestogenic activity and antiandrogenic effects. Chlormadinone acetate acts on glucocorticoid receptor, progesterone receptor, androgen receptor, and GABAA receptor. Chlormadinone acetate induces endometrial proliferation in estrogen-pretreated rabbits, inhibits testosterone-stimulated growth of the prostate and seminal vesicles in castrated rats, and reduces the thymus and adrenal weights in juvenile rats. Chlormadinone acetate is applicable to research related to diseases such as depression and reproductive metabolic disorders .
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Cat. No.: HY-B1095S2
Chlormadinone acetate-d3 is the deuterium labeled Chlormadinone acetate (HY-B1095). Chlormadinone acetate is a progestogen with potent progestogenic activity and antiandrogenic effects. Chlormadinone acetate acts on glucocorticoid receptor, progesterone receptor, androgen receptor, and GABAA receptor. Chlormadinone acetate induces endometrial proliferation in estrogen-pretreated rabbits, inhibits testosterone-stimulated growth of the prostate and seminal vesicles in castrated rats, and reduces the thymus and adrenal weights in juvenile rats. Chlormadinone acetate is applicable to research related to diseases such as depression and reproductive metabolic disorders .
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Cat. No.: HY-P10413
Target:  

Androgen Receptor

Research Areas:  

Metabolic Disease Endocrinology

SHBG 141-161 is a GPRC6A receptor agonist. SHBG 141-161 mimics the action of GPRC6A endogenous agonist uncarboxylated osteocalcin by binding to GPRC6A and promoting downstream signaling to increase testosterone and insulin secretion. SHBG 141-161 also reduces the affinity of GPRC6A to GDP protein by binding to the outer cell domain of GPRC6A thus affecting the dynamics of signal transduction. SHBG 141-161 can be used to study GPRC6A in energy metabolism and endocrine regulation .
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Cat. No.: HY-W673613
CAS No.: 1067191-08-5
Research Areas:  

Endocrinology

ADX68692 is an orally active FSHR negative allosteric regulator, with an IC50 value of 140 nM against hFSHR. ADX68692 antagonizes hCG (HY-107953)-mediated cAMP production, β-arrestin 2 recruitment, and the LH/CGR signaling pathway. ADX68692 partially inhibits testosterone synthesis. ADX68692 blocks follicle growth, disrupts the estrous cycle in rats, and reduces the pregnancy rate in rats. ADX68692 can be used in research related to contraception and endometriosis .
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Cat. No.: HY-19599
CAS No.: 129731-10-8
Synonyms: (+)-Vorozole; R83842
Target:  

Cytochrome P450

Research Areas:  

Cancer

Vorozole is a potent and selective, orally active non-steroidal aromatase inhibitor . Vorozole shows antitumor activity in vivo. Vorozole has the potential for the research of mammary cancer .
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