76 Results for "

Prostate Hyperplasia

" in MedChemExpress (MCE) Product Catalog:
Products (76)

76 Results for "Prostate Hyperplasia" in MCE Product Catalog:

Cat. No.: HY-13635R
CAS No.: 98319-26-7
Synonyms: MK-906 (Standard)
Research Areas:  

Cancer

Finasteride (Standard) is the analytical standard of Finasteride. This product is intended for research and analytical applications. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
loading...
    loading...
Cat. No.: HY-105173
CAS No.: 151272-78-5
Synonyms: EP 24332
Research Areas:  

Endocrinology Cancer

Teverelix (EP 24332) is a GnRH antagonist. Teverelix binds competitively and reversibly to GnRH receptors, thereby suppressing the release of LH and FSH. Teverelix can be used in the research of prostatic hyperplasia, endometriosis, and prostate cancer .
loading...
    loading...
Cat. No.: HY-165478
CAS No.: 155651-56-2
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

FCE 28260 is an orally active 4-azacyclic 5α-reductase (5αR) inhibitor. FCE 28260 exhibits IC₅₀ values for human 5αR type 1 and 5αR type 2 of 36 and 3.3 nM, respectively, and for human and rat prostates with IC₅₀ values of 16 and 15 nM, respectively. FCE 28260 simultaneously blocks the production of dihydrotestosterone (DHT) in the prostate and peripheral tissues. FCE 28260 can significantly inhibit the induction of prostatic and seminal vesicle hyperplasia by testosterone (T) in rat models, without inhibiting the growth of the prostate in DHT implantation models. FCE 28260 can be used for the studies DHT-dependent diseases such as benign prostatic hyperplasia (BPH) .
loading...
    loading...
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 5α-reductase inhibitor, used to inhibit the conversion of testosterone to dihydrotestosterone, with potential effects in inhibiting benign prostatic hyperplasia.
loading...
    loading...
Cat. No.: HY-106174
CAS No.: 142139-60-4
Purity:  ≥99.0%
Synonyms: CS 891
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

Lapisteride (CS 891) is an orally active 5α-reductase inhibitor. Lapisteride can inhibit 5α-reductaseactivity in the hair follicles (HF). Lapisteride can be used in prostatic hyperplasia and androgenic alopecia research .
loading...
    loading...
Cat. No.: HY-B0192AR
CAS No.: 81403-68-1
Synonyms: SL 77499-10 (Standard)
Research Areas:  

Endocrinology

Alfuzosin (hydrochloride) (Standard) is the analytical standard of Alfuzosin (hydrochloride). This product is intended for research and analytical applications. Alfuzosin (SL 77499-10) hydrochloride is an orally active, selective and competitive α1-adrenoceptor antagonist. Alfuzosin hydrochloride relaxes the muscles of the prostate and bladder neck, aiding in urination. Alfuzosin hydrochloride can be used in study of benign prostatic hyperplasia (BPH) .
loading...
    loading...
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 .
loading...
    loading...
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) .
loading...
    loading...
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 .
loading...
    loading...
Cat. No.: HY-B0661AS1
CAS No.: 2518100-55-3
Synonyms: (R)-(-)-YM12617-d4; LY253351-d4
Tamsulosin-d4 (hydrochloride) is deuterium labeled Tamsulosin (hydrochloride). Tamsulosin hydrochloride ((R)-(-)-YM12617) is an inhibitor of α1-adrenergic receptor. Tamsulosin hydrochloride is used for the research of prostatic hyperplasia. Tamsulosin hydrochloride attenuates abdominal aortic aneurysm growth in animal models .
loading...
    loading...
Cat. No.: HY-19268
CAS No.: 179535-60-5
Synonyms: GW 1818
Target:  

Adrenergic Receptor

Research Areas:  

Metabolic Disease

GG-818 (GW 1818) is a potent and selective α1 adrenoceptor antagonist, with pKi values of 9.7 for α1a, 7.8 for α1b, and 7.6 for α1d. GG-818 (GW 1818) can be used for benign prostatic hyperplasia research .
loading...
    loading...
Cat. No.: HY-17019
CAS No.: 194674-19-6
Target:  

Adrenergic Receptor

Research Areas:  

Inflammation/Immunology

SL-89.0591 is a uroselective α1-adrenoceptor antagonist. SL-89.0591 exhibits a more potent blocking effect on urethral receptors than on vascular receptors in anesthetized rabbits, with a lower risk of orthostatic hypotension. SL-89.0591 can be used in research related to benign prostatic hyperplasia .
loading...
    loading...
Cat. No.: HY-B0391A
CAS No.: 57149-08-3
Synonyms: KT-611 dihydrochloride; BM-15275 dihydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cancer

Naftopidil dihydrochloride (KT-611 dihydrochloride) is a selective alpha1-adrenoceptor antagonist, with Kis of 3.7 nM, 20 nM and 1.2 nM for the cloned human α1a-, α1b- and α1d-adrenoceptor subtypes, respectively. Naftopidil dihydrochloride has antiproliferative effects. Naftopidil dihydrochloride can be used for the research of prostate hyperplasia .
loading...
    loading...
Cat. No.: HY-P3501A
Synonyms: NX-1207 TFA
Target:  

Apoptosis

Research Areas:  

Cancer

Fexapotide (NX-1207) TFA induces apoptosis selectively, reducing prostate volume at a cellular level. Fexapotide can be used in lower urinary tract symptoms (LUTS) and benign prostatic hyperplasia (BPH) research .
loading...
    loading...
Cat. No.: HY-103202
CAS No.: 157066-77-8
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

SNAP5089 (hydrochloride) is a selective α1A adrenergic receptor antagonist. SNAP5089 (hydrochloride) can be used in the research of hypertension and benign prostatic hyperplasia .
loading...
    loading...
Cat. No.: HY-134632
CAS No.: 175870-21-0
Synonyms: KMD-3241
Target:  

Adrenergic Receptor

Research Areas:  

Cancer

Dehydro silodosin (KMD-3241) is a selective α1A-adrenoceptor antagonist used in the study of benign prostatic hyperplasia .
loading...
    loading...
Cat. No.: HY-B0192AS
CAS No.: 1216383-97-9
Synonyms: SL 77499-10-d3
Alfuzosin-d3 hydrochloride is the deuterium labeled Alfuzosin hydrochloride. Alfuzosin hydrochloride is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH).
loading...
    loading...
Cat. No.: HY-B0192AS1
CAS No.: 1276197-14-8
Synonyms: SL 77499-10-d7
Alfuzosin-d7 (hydrochloride) is the deuterium labeled Alfuzosin hydrochloride. Alfuzosin hydrochloride is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH).
loading...
    loading...
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 .
loading...
    loading...
Cat. No.: HY-123710
CAS No.: 185739-21-3
Target:  

Endogenous Metabolite

Research Areas:  

Others

GYKI-16084 is a new compound that can be isolated from dog and rat urine. GYKI-16084 can be used in the research of benign prostatic hyperplasia .
loading...
    loading...