Molecular Formula | C43H67N11O12S2 |
Molar Mass | 994.19 |
Density | 1.254±0.06 g/cm3(Predicted) |
Melting Point | >165oC (dec.) |
Boling Point | 1469.0±65.0 °C(Predicted) |
Flash Point | 842.2°C |
Solubility | H2O: ≤100mg/mL |
Vapor Presure | 0mmHg at 25°C |
Appearance | solid |
Color | White to Off-White |
pKa | 12.81±0.70(Predicted) |
Storage Condition | -20°C |
Refractive Index | 1.549 |
Physical and Chemical Properties | White crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from synthesis. |
In vitro study | Atosiban inhibits the oxytocin-mediated release of IP3 from the myometrial cell membrane. There is reduced release of intracellular, stored calcium from the sacroplasmic reticulum of myometrial cells, and reduced influx of Ca 2+ from the extracellular space through voltage gated channels. In addition, Atosiban suppresses oxytocin-mediated release of PGE and PGF from the decidua. |
In vivo study | The posterior pituitary hormones, oxytocin and arginine vasopressin, differ in structure by only two amino acids, and Atosiban influences physiological effects of arginine vasopressin on the feto-maternal cardiovascular and renal systems. In late-gestation sheep, the administration of Atosiban for 1 hour fails to induce fetomaternal cardiovascular changes. Atosiban blocks the activation of oxytocin-receptor-expressing neurons in the parabrachial nucleus of mice. |
WGK Germany | 3 |
RTECS | RS7590000 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.006 ml | 5.029 ml | 10.058 ml |
5 mM | 0.201 ml | 1.006 ml | 2.012 ml |
10 mM | 0.101 ml | 0.503 ml | 1.006 ml |
5 mM | 0.02 ml | 0.101 ml | 0.201 ml |