146 Results for "

testosterone

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

146 Results for "testosterone" in MCE Product Catalog:

Cat. No.: HY-P2191
CAS No.: 872717-97-0
Target:  

Kisspeptin Receptor

Research Areas:  

Endocrinology

KISS1-305, the Metastin/Kisspeptin analog, is a prototype peptide and a chemical probe. KISS1-305 has suboptimal KISS1R agonistic activity, and resists plasma protease degradation .
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Cat. No.: HY-W411296
CAS No.: 847674-32-2
Target:  

Androgen Receptor

Research Areas:  

Metabolic Disease

6α-Chloro testosterone is an anabolic androgenic steroid.
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Cat. No.: HY-108409
CAS No.: 302-97-6
Synonyms: Etienic acid; testosterone-17β-carboxylic acid; 3-Oxoandrost-4-ene-17β-carboxylic acid
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease Cancer

Progesterone carboxylic acid (Testosterone-17β-carboxylic acid) is an androstenedione analogue. Progesterone carboxylic acid can conjugate with 20-mer peptide nucleic acid (PNA) and the conjugate has superior binding capacity on complementary DNA. Progesterone carboxylic acid can be used for cancers and type 2 diabetes (T2D) research .
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Cat. No.: HY-P4689
CAS No.: 215510-06-8
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease

Prolactin-Releasing Peptide (1-31) (rat) is a UHR-1/GRP10 receptor ligand. Prolactin-Releasing Peptide (1-31) (rat) reduces fasting-induced food intake, increases plasma levels of LH, FSH, and testosterone in rats .
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Cat. No.: HY-105122
CAS No.: 107000-34-0
Synonyms: WIN 49596
Target:  

Androgen Receptor

Research Areas:  

Endocrinology Cancer

Zanoterone is an orally active antagonist of the androgen receptor (AR) with a Ki of 2.2 μM. Zanoterone blocks the binding of androgens such as testosterone and dihydrotestosterone (DHT), inhibiting the androgen signaling pathway, thereby reducing androgen-dependent prostate hyperplasia and prostate cancer growth .
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Cat. No.: HY-N13215
Research Areas:  

Metabolic Disease

Tongkat Ali Extract is the extract of Tongkat Ali, a testosterone modulator. Tongkat Ali Extract activates CYP17 enzyme to enhance conversion of pregnenolone and progesterone to dehydroepiandrosterone, androstenedione, and testosterone. Tongkat Ali Extract demonstrates antimalarial, antimicrobial, anticancer, and antidiabetic activity. Tongkat Ali Extract can be used for the research of diabetic and male infertility .
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Cat. No.: HY-NP186
Helix pomatia Agglutinin is a N-acetylgalactosamine (GalNAc) binding lectin, found in the reproductive gland of a Roman snail. Helix pomatia Agglutinin binds with high affinity (kD = 1.9-2.4 μM) steroid hormones: testosterone and progesterone. Helix pomatia Agglutinin interacts with adenine (kD = 5.4 μM) and arylaminonaphthalene sulfonate TNS (kD = 12 μM). Helix pomatia Agglutinin is commonly used for characterizing, imaging, or targeting glycoconjugates, and is also a very useful tool for glycomics analysis . Helix pomatia Agglutinin can be used for cancer prognosis study .
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Cat. No.: HY-P2161A
Target:  

Kisspeptin Receptor

Research Areas:  

Cancer

TAK-683 TFA is a potent full KISS1 receptor (KISS1R) agonist (IC50=170 pM) with improved metabolic stability. TAK-683 TFA is a nonapeptide metastin analog, exhibits agonistic activities to KISS1R with EC50 values of 0.96 nM and 1.6 nM for human and rat, respectively . TAK-683 TFA depletes GnRH in the hypothalamus and reduces plasma FSH, LH, and testosterone levels in vivo, it has the potential for the study of hormone-dependent prostate cancer .
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Cat. No.: HY-P10248
CAS No.: 89139-53-7
Target:  

Androgen Receptor

Research Areas:  

Endocrinology

Atriopeptin I rat, mouse is an atrial natriuretic peptide, which stimulates the testosterone production with half-maximum stimulation of 38 nM .
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Cat. No.: HY-123247
CAS No.: 112959-07-6
Target:  

Cytochrome P450

Research Areas:  

Endocrinology

LY113174 is an orally active aromatase inhibitor (IC50 = 24 nM). LY113174 blocks testosterone induced increase in uterine weight in rat, and inhibits ovarian estrogen biosynthesis .
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Cat. No.: HY-N14006
CAS No.: 171784-06-8
Target:  

Others

Louisianin D is a non-steroidal growth inhibitor of Testosterone-responsive SC 115 cells. Louisianin D potently suppresses the tube formation of cultured vascular endothelical cells in vitro.
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Cat. No.: HY-B1405R
CAS No.: 853-23-6
Synonyms: Dehydroepiandrosterone 3-acetate (Standard); DHEA acetate (Standard)
Research Areas:  

Endocrinology Cancer

Dehydroisoandrosterone 3-acetate (Standard) is the analytical standard of Dehydroisoandrosterone 3-acetate. This product is intended for research and analytical applications. Dehydroepiandrosterone 3-acetate is a testosterone/estrogen precursor and known modulator of vertebrate aggression.
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Cat. No.: HY-N2318R
CAS No.: 5947-49-9
Dehydroisoandrosterone 3-acetate (Standard) is the analytical standard of Dehydroisoandrosterone 3-acetate. This product is intended for research and analytical applications. Dehydroepiandrosterone 3-acetate is a testosterone/estrogen precursor and known modulator of vertebrate aggression.
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Cat. No.: HY-N10265
CAS No.: 360765-75-9
Stephacidin B is a fungal metabolite. Stephacidin B shows in vitro cytotoxicity against a panel of human tumor cell lines. Stephacidin B shows the strongest cytotoxicity against testosterone-dependent prostate LNCaP cancer cells .
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Cat. No.: HY-164457
CAS No.: 1429329-63-4
Target:  

Cytochrome P450

Research Areas:  

Cancer

ASN-001 is an orally active CYP-17A1 lyase inhibitor that selectively inhibits testosterone synthesis. ASN-001 has anticancer activity and can be used for research in the field of prostate cancer .
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Cat. No.: HY-B1623R
CAS No.: 2098-66-0
Research Areas:  

Cancer

Cyproterone (Standard) is the analytical standard of Cyproterone. This product is intended for research and analytical applications. Cyproterone is an antiandrogen that suppresses the actions of testosterone via blocking androgen receptors. Cyproterone’s acetate form can be used in the research of hypersexuality and prostate cancer .
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Cat. No.: HY-113320S1
CAS No.: 2687960-82-1
Synonyms: 5β-Androsterone-d2
Etiocholanolone-d2 is the deuterium labeled Etiocholanolone. Etiocholanolone (5β-Androsterone) is the excreted metabolite of testosterone and has anticonvulsant activity . Etiocholanolone is a less potent?neurosteroid positive allosteric modulator?(PAM) of the GABAA?receptor than its?enantiomer form .
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Cat. No.: HY-P0037
CAS No.: 136208-71-4
Synonyms: Org 30850ANT
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Org-30850 is a potent LHRH antagonist designed for treating hormone-dependent disorders. In animal studies, a single subcutaneous dose effectively inhibited ovulation in rats and significantly reduced testosterone levels in male rats for up to 48 hours post-administration. Daily doses of Org-30850 in female rats suppressed estrous cycles, decreased uterine and ovarian weights, and lowered estradiol and FSH serum levels. In male rats, prolonged treatment resulted in reversible reductions in gonadal function and testosterone levels, with almost complete recovery observed after cessation of treatment. Unlike comparable LHRH antagonists, Org-30850 exhibited minimal injection site irritation and no edematous reactions, suggesting a more favorable therapeutic profile .
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Cat. No.: HY-17375R
CAS No.: 432-60-0
Allylestrenol (Standard) is the analytical standard of Allylestrenol. This product is intended for research and analytical applications. Allylestrenol is an orally active synthetic anti-androgen sexualsteroid. Allylestrenol can prevent miscarriage in vivo. Allylestrenol significantly affects testosterone progesterone level in rat model. Allylestrenol can reduce ventral prostate weight in rat model .
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Cat. No.: HY-N1581R
CAS No.: 76-78-8
Synonyms: Nigakilactone D (Standard)
Quassin (Standard) is the analytical standard of Quassin. This product is intended for research and analytical applications. Quassin (Nigakilactone D) is a bioactive triterpenoid from stem bark extract of Quassia amara. Quassin inhibits P. falciparum with an IC50 of 0.15 μM. Quassin possesses reversible antifertility, anti-estrogenic and anti-plasmodial activity .
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