Norethisterone Enanthate
Norethisterone Enanthate (CAS No.: 3836-23-5) is a synthetic steroidal progestin ester and a long acting progestogenic research molecule that is commonly classified within endocrine modulation and reproductive biology tool compounds, with experimental utility in studies of steroid hormone signaling, gonadotropic axis regulation, and structure activity relationships of progesterone receptor modulators; in biomedical research contexts it is generally understood to function primarily through progesterone receptor agonistic activity with downstream transcriptional reprogramming of progesterone responsive genes and secondary antigonadotropic effects on hypothalamic pituitary gonadal signaling, while additional exploratory use has been reported in chemical biology settings where derivatized alkyne containing forms are employed as click chemistry compatible probes for copper catalyzed azide alkyne ligation workflows to enable conjugation, tracking, or mechanistic assay development; as a lipophilic ester prodrug type within the norethisterone class, it is frequently used as a comparator in hormone dependent cell systems and in vivo endocrine models to examine receptor dependent phenotypes, feedback regulation, and pharmacodynamic persistence, and although compound specific potency values are not uniformly reported across standardized assay panels, activity for related progestin receptor driven endpoints is typically characterized in the nanomolar to micromolar range depending on assay format, receptor context, and exposure duration, with concentrations or doses used in experiments typically depending on specific experimental designs and research objectives; overall, this molecule is best positioned as a research reagent for mechanistic endocrinology, pathway interrogation, and screening workflows focused on steroid receptor biology rather than any non research use.
| Storage | -20°C for 3 years |
| M.Wt | 410.59 |
| Cas No. | 3836-23-5 |
| Formula | C27H38O3 |
| Synonyms | Norigest |
| Canonical SMILES | C#C[C@]1(OC(CCCCCC)=O)CC[C@@]2([H])[C@]3([H])CCC4=CC(CC[C@]4([H])[C@@]3([H])CC[C@]12C)=O |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |






