| Name | ganirelix | 
|---|
| Description | Ganirelix is a competitive and selective gonadotropin releasing hormone (GnRH) antagonist. Ganirelix prevents endogenous GnRH from inducing luteinising hormone (LH) and follicle stimulating hormone relea[1]. | 
|---|---|
| Related Catalog | |
| In Vivo | Ganirelix (0.1 mg/kg; s.c.; daily for 14 d) reduces luteinising hormone levels in female rats[2]. Animal Model: Female Sprague-Dawley rats, weighing 225–300 mg[2] Dosage: 0.1 mg/kg Administration: Subcutaneous injection, daily for 14 d Result: Reduced luteinising hormone levels. | 
| References | 
                                 [1]. Gillies PS, et al. Ganirelix. Drugs. 2000 Jan;59(1):107-11; discussion 112-3.  | 
                        
| Density | 1.31 g/cm3 | 
|---|---|
| Molecular Formula | C80H113ClN18O13 | 
| Molecular Weight | 1570.32000 | 
| Exact Mass | 1568.84000 | 
| PSA | 451.49000 | 
| LogP | 7.99260 |