Norethynodrel
Norethynodrel (Enidre) is a 19-nortestosterone derivative to be used as a progestagen. Norethynodrel can be used for researching inhibition of ovulation[1]. Norethynodrel is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Product Specifications
CAS Number
[68-23-5]
Product Name Alternative
Enidrel; SC 4642; NSC 15432
UNSPSC
12352211
Hazard Statement
H302, H312, H332
Target
Endogenous Metabolite
Type
Reference compound
Related Pathways
Metabolic Enzyme/Protease
Applications
Metabolism-protein/nucleotide metabolism
Field of Research
Endocrinology
Assay Protocol
https://www.medchemexpress.com/norethynodrel.html
Purity
90.53
Solubility
DMSO : 1.6 mg/mL (ultrasonic; warming)
Smiles
C#C[C@]1(O)CC[C@@]2([H])[C@]3([H])CCC4=C(CCC(C4)=O)[C@@]3([H])CC[C@]12C
Molecular Formula
C20H26O2
Molecular Weight
298.42
Precautions
H302, H312, H332
References & Citations
[1]D F HAWKINS, et al. 2 - The Clinical Pharmacology of Oestrogens and Progestagens. 1979
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched
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