Esaxerenone
- Product Name
- Esaxerenone
- CAS No.
- 1632006-28-0
- Chemical Name
- Esaxerenone
- Synonyms
- cs3150;cs-3150;CS-2614;XL-550);Esaxerenone;5G,100G,500G;Esaxerenone(CS-3150);CS-3150 (Esaxerenone;Esaxerenone, 10 mM in DMSO;CS-3150; CS 3150; CS3150; XL-550; XL550; XL 550.
- CBNumber
- CB33159937
- Molecular Formula
- C22H21F3N2O4S
- Formula Weight
- 466.48
- MOL File
- 1632006-28-0.mol
Esaxerenone Property
- Boiling point:
- 581.3±50.0 °C(Predicted)
- Density
- 1.35±0.1 g/cm3(Predicted)
- solubility
- DMSO:100.0(Max Conc. mg/mL);214.37(Max Conc. mM)
- pka
- 12.76±0.70(Predicted)
- form
- Solid
- color
- White to light yellow
- InChI
- InChI=1S/C22H21F3N2O4S/c1-14-18(21(29)26-15-7-9-16(10-8-15)32(2,30)31)13-27(11-12-28)20(14)17-5-3-4-6-19(17)22(23,24)25/h3-10,13,28H,11-12H2,1-2H3,(H,26,29)
- InChIKey
- NOSNHVJANRODGR-UHFFFAOYSA-N
- SMILES
- C(N1C=C(C(=O)NC2C=CC(S(=O)(=O)C)=CC=2)C(C)=C1C1C=CC=CC=1C(F)(F)F)CO
N-Bromosuccinimide Price
- Product number
- E888295
- Product name
- Esaxerenone
- Packaging
- 10mg
- Price
- $270
- Updated
- 2021/12/16
- Product number
- CS-8044
- Product name
- Esaxerenone
- Purity
- 99.84%
- Packaging
- 5mg
- Price
- $396
- Updated
- 2021/12/16
- Product number
- CS-8044
- Product name
- Esaxerenone
- Purity
- 99.84%
- Packaging
- 10mg
- Price
- $600
- Updated
- 2021/12/16
- Product number
- CS-8044
- Product name
- Esaxerenone
- Purity
- 99.84%
- Packaging
- 50mg
- Price
- $1800
- Updated
- 2021/12/16
- Product number
- CS-8044
- Product name
- Esaxerenone
- Purity
- 99.84%
- Packaging
- 100mg
- Price
- $2520
- Updated
- 2021/12/16
Esaxerenone Chemical Properties,Usage,Production
Uses
Esaxerenone, is a novel, highly potent and selective non-steroidal mineralocorticoid receptor antagonist.
Biological Activity
Esaxerenone exerts its antihypertensive effect by blocking excessive activation of the mineralocorticoid receptor by endogenous ligands (such as aldosterone), has a mineralocorticoid receptor selectivity at least 1000-fold greater than other steroid hormone receptors, a long half-life, high oral bioavailability, and has a more significant antihypertensive effect than spironolactone or eplerenone.
Synthesis
below shows the synthesis route of Esaxerenone
in vivo
After single oral administration of Esaxerenone at 0.1, 0.3, 1, and 3?mg/kg, maximum plasma concentration (Cmax) and the area under the plasma concentration versus time curve (AUC) are increased with dose. Time to reach the maximum plasma concentration (Tmax) of Esaxerenone ranges from 2.0 to 4.5?h. After intravenous administration of Esaxerenone at 0.1, 0.3, 1, and 3?mg/kg, the total body clearance (CL) and distribution volume at steady state (Vss) are 3.53 to 6.69?mL/min/kg and 1.47 to 2.49?L/kg, respectively, in rats, and 2.79 to 3.69?mL/min/kg and 1.34 to 1.54?L/kg, respectively, in cynomolgus monkeys. Up to 168?h after administration, 3.9% and 91.4% of dosed radioactivity are excreted in rat urine and feces, respectively, and 95.2% in total. In monkeys, the excreted radioactivity up to 168?h is 11.5% in urine, 82.3% in feces, and 93.9% in total[1].
Esaxerenone Preparation Products And Raw materials
Raw materials
Preparation Products
Esaxerenone Suppliers
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View Lastest Price from Esaxerenone manufacturers
- Product
- Esaxerenone 1632006-28-0
- Price
- US $0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1000kg
- Release date
- 2025-06-07