Norethindrone ['68-22-4]
Referencia M2887-1g
embalaje : 1g
Marca : AbMole Bioscience
All AbMole products are for research use only, cannot be used for human consumption.

Norethisterone
Quality Control & Documentation
Biological Activity
Norethindrone is a synthetic progestin, which mimic the actions of the endogenous ovarian hormone progesterone.
Customer Product Validations & Biological Datas
![]() | Source | J Clin Pharmacol (2012). Figure 1. Norethindrone |
Method | PK and Pharmacodynamic (PD) Assessments | |
Cell Lines | ||
Concentrations | 0.5 mg/kg | |
Incubation Time | 1, 7, 14, 21, 22, 28, 35, 42, 49, 50, and 56 days | |
Results | Mean steady-state Cmax, AUC, and Cmin and their 90% CIs of their GLSMRs fell within the no-effect limit boundary of 0.80 to 1.25. |
Protocol (for reference only)
Cell Experiment | |
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Cell lines | Human epithelial cervical cancer cells |
Preparation method | Thereafter, the cells were incubated with serum-free, phenol-free DMEM for 2 hrs, before treatment with 100 nM DEX, MPA, P4 and NET-A for 1 hr. Cells were crosslinked for 10 min at 37°C with1% formaldehyde and the reaction was stopped with 0.1 mM glycine for 5 min, shaking at room temperature. |
Concentrations | 100 nM |
Incubation time | 1 h |
Animal Experiment | |
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Animal models | Female Sprague-Dawley rats |
Formulation | corn oil |
Dosages | 3 μg/rat/day |
Administration | oral |
Chemical Information
Molecular Weight | 298.42 |
Formula | C20H26O2 |
CAS Number | 68-22-4 |
Form | Solid |
Solubility (25°C) | DMSO 50 mg/mL |
Storage | Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
References
[1] Africander DJ, et al. J Steroid Biochem Mol Biol. A comparative study of the androgenic properties of progesterone and the progestins, medroxyprogesterone acetate (MPA) and norethisterone acetate (NET-A).
[2] Govender Y, et al. PLoS One. The injectable-only contraceptive medroxyprogesterone acetate, unlike norethisterone acetate and progesterone, regulates inflammatory genes in endocervical cells via the glucocorticoid receptor.