12 Results for "

aldosteronism

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "aldosteronism" in MCE Product Catalog:

Cat. No.: HY-113151
CAS No.: 2410-60-8
Purity:  98.21%
18-Oxocortisol is a derivative of cortisol that is produced by aldosterone synthase (CYP11B2). 18-Oxocortisol is a naturally occurring mineralocorticoid agonist. 18-Oxocortisol is a biomarker in adrenal vein sampling .
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Cat. No.: HY-113986
CAS No.: 102676-87-9
Purity:  98.75%
Synonyms: (R)-Fadrozole; (R)-CGS 16949A free base; FAD286
Target:  

Cytochrome P450

Research Areas:  

Cardiovascular Disease

Dexfadrostat ((R)-Fadrozole) is an orally active and selective aromatase inhibitor, with human aromatase IC50 values of 6.4 nM. Dexfadrostat suppresses estrogen synthesis, reduces circulating estradiol levels and suppresses aldosterone production. Dexfadrostat can be used for the research of breast cancer, primary aldosteronism, and hypertension .
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Cat. No.: HY-B0237
CAS No.: 125-84-8
Synonyms: DL-Aminoglutethimide
Target:  

Cytochrome P450

Aminoglutethimide (DL-Aminoglutethimide) is an orally active anticonvulsant with various endocrine-related side effects. Aminoglutethimide blocks multiple steroid hormone synthesis pathways by inhibiting several cytochrome P-450-dependent hydroxylases, such as aromatase, cholesterol side-chain cleavage enzyme, 11-hydroxylase, and 18-hydroxylase, with IC50 values of 0.3, 3.5, 120, and 20 μM, respectively. Aminoglutethimide reduces cortisol levels. Aminoglutethimide can be used in research on Cushing's syndrome, breast cancer, and other conditions .
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Cat. No.: HY-P2618
CAS No.: 2237216-30-5
Target:  

Kallikrein

Research Areas:  

Others

Pro-Phe-Arg-AMC acetate is a substrate for human glandular kallikrein 2. Pro-Phe-Arg-AMC acetate can be used for the quantitative detection of enzyme activity .
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Cat. No.: HY-112705
CAS No.: 1286725-49-2
Purity:  99.81%
Target:  

Potassium Channel

VU0529331 is a homomeric GIRK channel activator, with an EC50 value of 5.1 μM for human GIRK2 and an EC50 value of 22.3 μM for GIRK4. VU0529331 serves as a starting point for the development of non-GIRK1/X channel probes and also acts as a tool for studying homomeric GIRK channels. VU0529331 is applicable to research related to addiction, primary aldosteronism and delayed-onset obesity .
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Cat. No.: HY-137199
CAS No.: 65147-21-9
Target:  

Kallikrein

Research Areas:  

Others

Pro-Phe-Arg-AMC is a substrate for human glandular kallikrein 2. Pro-Phe-Arg-AMC can be used for the quantitative detection of enzyme activity .
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Cat. No.: HY-162574
CAS No.: 2241573-22-6
Target:  

Cytochrome P450

Research Areas:  

Cancer

CYP11B2-IN-2 (Compound 10k) is an inhibitor for enzyme aldosterone synthase CYP11B2 with an IC50 of 0.3 nM. CYP11B2-IN-2 CYP11B-IN-2 is labeled with 18F and can be used as a positron emission tomography (PET) tracer for the diagnosis of primary aldosteronism .
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Cat. No.: HY-113249
CAS No.: 3604-86-2
Target:  

Drug Metabolite

Aldosterone 18-glucuronide is a urinary metabolite of Aldosterone (HY-113313). It exhibits 100% specificity in distinguishing primary aldosteronism from essential hypertension, but has relatively low overall sensitivity. There is no difference in sensitivity of Aldosterone 18-glucuronide between hypokalemic and normokalemic primary aldosteronism. Aldosterone 18-glucuronide can be used for the research of primary aldosteronism .
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Cat. No.: HY-180533
CAS No.: 1356479-94-1
AldoView (Compound 3) is an intermediate. AldoView can be labeled with fluorine-18 to synthesize [ 18F]AldoView. [ 18F]AldoView is a highly selective aldosterone synthase PET imaging agent. AldoView can be used in imaging studies of primary aldosteronism .
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Cat. No.: HY-165401
CAS No.: 22785-18-8
Target:  

DNA/RNA Synthesis

Research Areas:  

Endocrinology

SC 19886 is an inhibitor of Aldosterone (HY-113313) synthesis. SC 19886 blocks Aldosterone-induced DNA-dependent RNA synthesis. SC 19886 can be used in studies related to primary aldosteronism [1] [2].
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Cat. No.: HY-113986C
CAS No.: 131863-75-7
Synonyms: (R)-Fadrozole hydrochloride; (R)-CGS 16949A; FAD286 hydrochloride
Target:  

Cytochrome P450

Research Areas:  

Cardiovascular Disease Cancer

Dexfadrostat ((R)-Fadrozole) hydrochloride is an orally active and selective aromatase inhibitor, with human aromatase IC50 values of 6.4 nM. Dexfadrostat hydrochloride suppresses estrogen synthesis, reduces circulating estradiol levels and suppresses aldosterone production. Dexfadrostat hydrochloride can be used for the research of breast cancer, primary aldosteronism, and hypertension .
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Cat. No.: HY-115425
CAS No.: 23734-88-5
Synonyms: DL-Aminoglutethimide phosphate
Target:  

Cytochrome P450

Aminoglutethimide phosphate (DL-Aminoglutethimide phosphate) is an orally active anticonvulsant with various endocrine-related side effects. Aminoglutethimide phosphate blocks multiple steroid hormone synthesis pathways by inhibiting several cytochrome P-450-dependent hydroxylases, such as aromatase, cholesterol side-chain cleavage enzyme, 11-hydroxylase, and 18-hydroxylase, with IC50 values of 0.3, 3.5, 120, and 20 μM, respectively. Aminoglutethimide phosphate reduces cortisol levels. Aminoglutethimide phosphate can be used in research on Cushing's syndrome, breast cancer, and other conditions .
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