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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T19186 | Aldosterone | Others | |
Aldosterone is the primary mineralocorticoid. Aldosterone is synthesized and secreted in response to renin-angiotensin system activation or high dietary potassium by the zona glomerulosa of the adrenal cortex. | |||
T19185 | Aldosterone-d8 | Aldosterone D8 | Others |
Aldosterone D8, a deuterium-labeled variant of Aldosterone produced in the adrenal zona glomerulosa, regulates blood pressure. | |||
T36381 | Aldosterone 21-sulfate (sodium salt) | ||
Aldosterone 21-sulfate is a metabolite of the steroid hormone aldosterone .1It reduces the sodium-to-potassium ratio in rat urine when administered at doses ranging from 10 to 100 μg, indicating mineralocorticoid activit... | |||
T29852 | Aldosterone-3-(O-carboxymethyl)oximino-(2-iodohistamine) | ||
Aldosterone-3-(O-carboxymethyl)oximino-(2-iodohistamine) is a biochemical. | |||
T4316 | ML365 | Potassium Channel | |
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3). | |||
T0293 | Metyrapone | NSC-25265,Su-4885 | Others , P450 , Dehydrogenase , Autophagy |
Metyrapone (NSC-25265) is an inhibitor of the enzyme STEROID 11-BETA-MONOOXYGENASE. It is used as a test of the feedback hypothalamic-pituitary mechanism in the diagnosis of CUSHING SYNDROME. | |||
T1410 | Torsemide | AC-4464,JDL-464,Torasemide | Na-K-Cl cotransporter |
Torsemide (AC-4464) is an anilinopyridine sulfonylurea belonging to the class of loop diuretics. Torsemide has a prolonged duration of action compared to other loop diuretics, is extensively protein bound in plasma and h... | |||
T0083 | Eplerenone | Epoxymexrenone,CGP 30083,SC-66110 | Glucocorticoid Receptor |
Eplerenone (CGP 30083) is an aldosterone receptor antagonist and potassium-sparing diuretic used in the therapy of hypertension. Eplerenone therapy has been associated with transient elevations in serum aminotransferase ... | |||
T3033 | Deoxycorticosterone acetate | DOC acetate,Cortexone acetate,11-Deoxycorticosterone acetate | Glucocorticoid Receptor , Endogenous Metabolite , Adrenergic Receptor |
Deoxycorticosterone acetate (Cortexone acetate) is the 21-acetate derivative of desoxycorticosterone, used for intramuscular injection for replacement therapy of the adrenocortical steroid. | |||
T4277 | Osilodrostat | LCI699 | Glucocorticoid Receptor , Others , Hydroxylase |
Osilodrostat (LCI699) (LCI699) is an effective inhibitor of human 11β-hydroxylase (IC50: 2.5 nM) and aldosterone synthase (IC50: 0.7 nM). | |||
T0354 | Canrenone | 6,7-Dehydro-7α-desthioacetylspironolactone,SC9376,Aldadiene,RP-11614,SC14266 | Glucocorticoid Receptor , Endogenous Metabolite |
Canrenone (SC14266) is an aldosterone antagonist with potassium-sparing diuretic activity. | |||
T0476 | Spironolactone | SC9420,Abbolactone | Glucocorticoid Receptor , Androgen Receptor , Autophagy |
Spironolactone (SC9420) is an Aldosterone Antagonist. The mechanism of action of spironolactone is as an Aldosterone Antagonist. | |||
T13881 | Dicirenone | SC26304 | ATPase , Glucocorticoid Receptor |
Dicirenone (SC26304) inhibits the Mineralocorticoid receptor (MR), aldosterone regulation of the urinary K+:Na+ ratio, and aldosterone binding to renal cytoplasmic and nuclear receptors. | |||
T61373 | Baxdrostat | Others | |
Baxdrostat is an aldosterone synthase inhibitor. | |||
T20302 | Deoxycorticosterone | Desoxycorticosterone,Desoxycorticosteronum,Desoxycortone | Endogenous Metabolite |
Deoxycorticosterone (Desoxycortone) is a steroid metabolite produced by the adrenal gland. Deoxycorticosterone is an aldosterone precursor and possesses mineralocorticoid activity. | |||
T71664 | Mespirenone | Others | |
Mespirenone is a spironolactone derivative and aldosterone antagonist with diuretic effects. | |||
T3096 | Canrenoate potassium | Potassium aldadiene,Canrenoic acid potassium salt,Potassium canrenoate,Soldactone | Glucocorticoid Receptor |
Canrenoate potassium (Soldactone) is a synthetic pregnadiene derivative with anti-aldosterone activity. | |||
T6262 | Evacetrapib | LY2484595 | CETP |
Evacetrapib (LY2484595) (LY2484595) is a potent and selective inhibitor of CETP with IC50 of 5.5 nM, elevates HDL cholesterol without increases in aldosterone or blood pressure. Phase 3. | |||
T1866 | AT-56 | Others , PGE Synthase | |
AT56, a specific inhibitor of prostaglandin D2 synthase enzymatic activity, blunted adipogenic aldosterone effects. | |||
T7040 | Angiotensin II human | DRVYIHPF,Angiotensin II,Hypertensin II,Ang II | Apoptosis , RAAS |
Angiotensin II human (Ang II) is a biologically active peptide, a vasoconstrictor. Angiotensin II interacts with AT1R and AT2R to regulate blood pressure, stimulate sympathetic nerves, and increase aldosterone biosynthes... |