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Norethindrone - 10mM in DMSO, high purity , CAS No.68-22-4(DMSO), Progesterone receptor agonist

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Item Number
N407798
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N407798-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$349.90

Potent synthetic progestin

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Compound libraries (12325)

Basic Description

Synonyms Norethisterone | 19-Norpregn-4-en-20-yn-3-one, 17-hydroxy-, (17α)-
Specifications & Purity Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms Norethindrone (Norethisterone) is a synthetic progestin, which mimic the actions of the endogenous ovarian hormone progesterone.
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type AGONIST
Mechanism of action Progesterone receptor agonist
Product Description

Information

Norethindrone (Norethisterone) is a synthetic progestin, which mimic the actions of the endogenous ovarian hormone progesterone.
In vitro

Norethisterone, or, is a 19-nortestosterone derivative, that lacks a C19 methyl group and possesses C17 ethinyl substitution, and primarily displays progestational activity rather than androgenic activity and, to a lesser extent, has oestrogenic and anti-oestrogenic activity. NET shows five- to eight-fold weaker progesterone receptor binding and transactivation activities than the Org 2058 (100%) and two-fold stronger than progesterone. Binding and transactivation activities of NET for androgen receptor (5α-dihydrotestosterone 100%) are 3.2 and 1.1%, respectively, for estrogen receptor none (estradiol 100%) and for glucocorticoid receptor below 1% (dexamethasone 100%). Norethisterone (1 nM) inhibits serum-stimulated or oestradiol (0.1 nM)-induced proliferation of MCF-7 by 41% and 34%, respectively. Norethisterone (50 nM) induces significant effects on rat osteoblast proliferation, differentiation, and mineralization processes, mimicking the effects of estradiol, which is mediated by estrogen receptor.

In vivo

Norethisterone displays hormonal properties in vivo. Mean active dose (MAD) of Norethisterone s.c. in progestagenic test (McPhail), androgenic test (Hershberger), estrogenic test (Allen–Doisy), and in a progestagenic and estrogenic test (ovulation inhibition test) is 0.63 mg/kg, 2.5 mg/kg, 4 mg/kg, and 0.235 mg/kg, respectively, and the MAD for orally administration is 0.25 mg/kg, 20 mg/kg, 8 mg/kg, and 12 mg/kg, respectively. Norethisterone influences bone formation and resorption. Norethisterone (80 μg/day) decreased bone resorption in SO and OVX mice, while enhances estradiol-stimulated endosteal bone formation. Norethisterone at the dose which is used in hormonal therapy for prevention of osteoporosis has a slight protective effect against bone mineral loss in castrated mice.
Cell Data

cell lines:BON-1 cells and NCI-H727 cells

Concentrations:0.1 nM - 1 mM

Incubation Time:7 days

Powder Purity:≥99%

Product Properties

ALogP 4.315
hba_count 1

Associated Targets(Human)

SHBG Tchem Sex hormone-binding globulin (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
PGR Tclin Progesterone receptor (5 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)

Names and Identifiers

Smiles CC12CCC3C(CCC4=CC(=O)CCC34)C1CCC2(O)C#C
Molecular Weight 298.42
Reaxy-Rn 2664607
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2664607&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility 60
DMSO(mM) Max Solubility 201.06
Water(mg / mL) Max Solubility <1

Citations of This Product

1. Haoyu Long, Yanhao Jiang, Yanjuan Liu, Yuefei Zhang, Wei Chen, Sheng Tang.  (2023)  Chromatographic separation performance of silica microspheres surface-modified with triazine-containing imine-linked covalent organic frameworks.  TALANTA,  260  (124589). 
2. Qianyu Li, Guoliang Li, Lihua Fan, Yanxin Yu, Jin Liu.  (2022)  Click reaction triggered turn-on fluorescence strategy for highly sensitive and selective determination of steroid hormones in food samples.  FOOD CHEMISTRY,  374  (131565). 

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