83 Results for "

benign

" in MedChemExpress (MCE) Product Catalog:
Products (83)

83 Results for "benign" in MCE Product Catalog:

9
Terazosin hydrochloride
Terazosin hydrochloride
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9 Publications Verification
Cat. No.: HY-B0371F
CAS No.: 63074-08-8
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease Metabolic Disease Endocrinology

Terazosin hydrochloride is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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9
Terazosin
Terazosin
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9 Publications Verification
Cat. No.: HY-B0371
CAS No.: 63590-64-7
Category:  

Disease Research Fields Endocrinology

Target:  

Adrenergic Receptor

Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin works by relaxing blood vessels and the opening of the bladder. Terazosin has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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9
Terazosin hydrochloride dihydrate
Terazosin hydrochloride dihydrate
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9 Publications Verification
Cat. No.: HY-B0371A
CAS No.: 70024-40-7
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease Metabolic Disease Endocrinology

Terazosin hydrochloride dihydrate is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride dihydrate works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride dihydrate has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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5
Ulipristal acetate
Ulipristal acetate
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5 Cited Publications
Cat. No.: HY-16508
CAS No.: 126784-99-4
Synonyms: CDB-2914
Target:  

Progesterone Receptor Autophagy

Research Areas:  

Metabolic Disease Cancer

Ulipristal acetate (CDB-2914) is an orally active, selective progesterone receptor modulator (SPRM). Ulipristal acetate stimulates the autophagic response selectively in leiomyoma cells. Ulipristal acetate has the potential for benign gynecological conditions treatment, such as uterine myoma .
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4
Finasteride
Finasteride
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4 Cited Publications
Cat. No.: HY-13635
CAS No.: 98319-26-7
Purity:  99.97%
Synonyms: MK-906
Target:  

Environmental Pollutants 5 alpha Reductase

Research Areas:  

Cancer

Finasteride (MK-906) is an orally active 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 .
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2
Alfuzosin
Alfuzosin
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2 Cited Publications
Cat. No.: HY-B0192
CAS No.: 81403-80-7
Synonyms: SL 77499
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

Alfuzosin (SL 77499-10) is an orally active, selective and competitive α1-adrenoceptor antagonist. Alfuzosin relaxes the muscles of the prostate and bladder neck, aiding in urination. Alfuzosin can be used in study of benign prostatic hyperplasia (BPH) .
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2
Alfuzosin hydrochloride
Alfuzosin hydrochloride
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2 Cited Publications
Cat. No.: HY-B0192A
CAS No.: 81403-68-1
Synonyms: SL 77499-10
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

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) .
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1
Zinc sulphate
Zinc sulphate
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1 Cited Publications
Cat. No.: HY-B1820
CAS No.: 7733-02-0
Target:  

Environmental Pollutants Biochemical Assay Reagents Glutathione Reductase (GR) Tyrosinase

Research Areas:  

Metabolic Disease Inflammation/Immunology

Zinc sulphate is an orally active inhibitor of tyrosinase and glutathione reductase. Zinc sulphate enhances the activity of dopachrome tautomerase. Zinc sulphate delays anagen-related eumelanin production, induces hair hypopigmentation in mice, and accelerates wound healing. Zinc sulphate can be used in research related to benign gastric ulcers. Zinc sulphate can be used in research related to rheumatoid arthritis .
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1
Quercetin 5-O-β-D-glucopyranoside
Quercetin 5-O-β-D-glucopyranoside
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1 Cited Publications
Cat. No.: HY-N13015
CAS No.: 34199-21-8
Category:  

Flavonols Flavonoids Animals

Target:  

Endogenous Metabolite

Quercetin 5-O-β-D-glucopyranoside is a glycosylated flavonoid metabolite and flavonoid compound. Quercetin 5-O-β-D-glucopyranoside can be produced by microbial transformation of Quercetin (HY-18085) via Mucor hiemalis. Quercetin 5-O-β-D-glucopyranoside can be used in studies related to benign prostatic hyperplasia .
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Tinlorafenib
Tinlorafenib
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Cat. No.: HY-147405
CAS No.: 2573781-75-4
Purity:  98.20%
Synonyms: PF-07284890; ARRY-461
Target:  

Raf ERK

Research Areas:  

Cancer

Tinlorafenib (PF-07284890) is the orally active inhibitor for BRAF and CRAF with IC50s of 5.8 nM and 4.1 nM. Tinlorafenib (Compound 10) inhibits V600E mutated BRAF and V600K mutanted BRAF with IC50s of 4.25 nM and 2.7 nM. Tinlorafenib can cross the blood brain barrier. Tinlorafenib demonstrates CNS penetration and can be used in the research of BRAF-associated malignant and benign tumors of the CNS as well as extracranial malignancies .
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Monomethyl phthalate
Monomethyl phthalate
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Cat. No.: HY-Y1097
CAS No.: 4376-18-5
Synonyms: 2-(Methoxycarbonyl)benzoic acid
Category:  

Ketones, Aldehydes, Acids Endogenous metabolite Disease Research Fields Cancer

Target:  

Endogenous Metabolite Reactive Oxygen Species (ROS)

Monomethyl phthalate is an orally active metabolite of phthalic acid. Monomethyl phthalate, as a urine biomarker after exposure to phthalate, can be used as a detection indicator for thyroid cancer and benign nodules. Monomethyl phthalate reduces the survival rate of young frogs. Monomethyl phthalate induces oxidative damage to red blood cells in rats .
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ONO-0300302
ONO-0300302
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Cat. No.: HY-115450
CAS No.: 856689-51-5
Purity:  99.43%
Target:  

LPL Receptor

Research Areas:  

Endocrinology Cancer

ONO-0300302 is an orally active and potent LPA1 (lysophosphatidic acid receptor 1) antagonist, with an IC50 of 0.086 μM. ONO-0300302 is a slow tight binding inhibitor, and its binding affinity increases with time, with Kd of 0.34 nM (37 °C, 2 h). ONO-0300302 can be used for benign prostatic hyperplasia (BPH) research .
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H-Tyr-Phe-OH
H-Tyr-Phe-OH
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Cat. No.: HY-W011258
CAS No.: 17355-11-2
Synonyms: L-Tyrosyl-L-phenylalanine
Target:  

Xanthine Oxidase Angiotensin-converting Enzyme (ACE)

Research Areas:  

Inflammation/Immunology Cancer

H-Tyr-Phe-OH (L-Tyrosyl-L-phenylalanine) is an orally active inhibitor of Angiotensin converting enzyme (ACE), with an inhibiton rate of 48% at 50 μM. H-Tyr-Phe-OH can be used as an biomarker for differentiating benign thyroid nodules (BTN) from thyroid cancer (TC). H-Tyr-Phe-OH exhibits xanthine oxidase inhibition (uric acid lowering) activity and serves as regulator in IL-8 production in neutrophil-like cells .
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Monomethyl phthalate-d4
Monomethyl phthalate-d4
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Cat. No.: HY-Y1097S
CAS No.: 1276197-40-0
Synonyms: 2-(Methoxycarbonyl)benzoic acid-d4
Monomethyl phthalate-d4 (2-(Methoxycarbonyl)benzoic acid-d4) is the deuterium labeled Monomethyl phthalate. Monomethyl phthalate is a phthalate metabolite. Monomethyl phthalate acts as a urinary biomarker of phthalates exposure and can be used as a standard for the determination of thyroid cancer and benign nodule .
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Fexapotide
Fexapotide
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Cat. No.: HY-P3501
CAS No.: 492447-54-8
Synonyms: NX-1207
Target:  

Apoptosis

Research Areas:  

Cancer

Fexapotide (NX-1207) 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 .
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FA2 glycan (G0F)
FA2 glycan (G0F)
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Cat. No.: HY-158498
Synonyms: FA2 N-linked oligosaccharide; F(6)A2 glycan
FA2 glycan (G0F) (FA2 N-linked oligosaccharide; F(6)A2 glycan) is a core-fucosylated biantennary N-linked oligosaccharide that serves as a prostate cancer biomarker. The level of FA2 glycan (G0F) is higher in prostate cancer than in benign prostatic hyperplasia, and it is further elevated in advanced prostate cancer with a Gleason score ≥8 compared with both benign prostatic hyperplasia and low-/intermediate-risk prostate cancer. FA2 glycan (G0F) can be used in prostate cancer research .
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RS100329 hydrochloride
RS100329 hydrochloride
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Cat. No.: HY-103204
CAS No.: 1215654-26-4
Purity:  99.57%
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

RS100329 hydrochloride is a potent and selective α1A-adrenoceptor antagonist with pKi values of 9.6, 7.9 and 7.5 for α1A, α1D, and α1B, respectively. RS100329 hydrochloride inhibits reflex urethral contractions. RS100329 hydrochloride can be used in research of benign prostatic hyperplasia .
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2,4-Dimethoxybenzaldehyde
2,4-Dimethoxybenzaldehyde
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Cat. No.: HY-Y1356
CAS No.: 613-45-6
Target:  

Biochemical Assay Reagents

Research Areas:  

Cancer

2,4-Dimethoxybenzaldehyde is a tumor initiator with genotoxic property. 2,4-Dimethoxybenzaldehyde can induce benign papilloma development and converse to squamous cell carcinoma in the skin of susceptible mouse models. 2,4-Dimethoxybenzaldehyde can be used for skin cancer research .
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Angelol G
Angelol G
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Cat. No.: HY-N8850
CAS No.: 83199-38-6
Category:  

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