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Nestoron

Nestoron Structure
CAS No.
7759-35-5
Chemical Name:
Nestoron
Synonyms
ST 1435;NESTORON;NESTORONE;Elcometrine;Nestorone Acetate;Nestoron (ST-1435);Norgestone acetate;Segesterone Acetate;ELCOMETRINE;NESTORONE;ST-1435;ST1435;ELCOMETRINE; NESTORONE; ST-1435; ST 1435; ST1435
CBNumber:
CB31011778
Molecular Formula:
C23H30O4
Molecular Weight:
370.48
MOL File:
7759-35-5.mol
Modify Date:
2024/1/4 15:13:51

Nestoron Properties

Melting point 178-179°
alpha D21 -105° (c = 1.2 in chloroform)
Boiling point 420.37°C (rough estimate)
Density 1.0550 (rough estimate)
refractive index 1.4433 (estimate)
storage temp. 2-8°C
solubility DMSO: soluble5mg/mL, clear
form powder
color white to beige
InChIKey CKFBRGLGTWAVLG-GOMYTPFNSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H351-H361
Precautionary statements  P201-P202-P281-P308+P313-P405-P501-P201-P202-P281-P308+P313-P405-P501
WGK Germany  3

Nestoron price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML0550 Nestorone ≥97% (HPLC) 7759-35-5 10MG ₹9277.03 2022-06-14 Buy
Sigma-Aldrich(India) SML0550 Nestorone ≥97% (HPLC) 7759-35-5 50MG ₹37530.28 2022-06-14 Buy
Product number Packaging Price Buy
SML0550 10MG ₹9277.03 Buy
SML0550 50MG ₹37530.28 Buy

Nestoron Chemical Properties,Uses,Production

Uses

Segesterone Acetate has been used to study the: comparison of androgenic and estrogenic properties of progestins used in contraception and hormone therapy; impact on hepatic estrogen-sensitive proteins by 1-yr contraceptive vaginal ring delivering Nestorone and ethinyl estradiol.

Pharmacokinetics

Elcometrine is a member of the 19-norprogesterone class of pr ogestins. when administered subcuta neously (implant), intravaginally (vaginal ring), or transdermally, elcometrine is an exceptionally potent progestin. It is 100-fold more potent when administered subcutaneously than when delivered orally. Its oral bioavaiability is only 10%,with a half life of just 1 to 2 hours because of rapid metabolism. The C16 methylene functionality substantially increases its affinity for the progesterone receptor.

Clinical Use

Because of its antiestrogenic action, elcometrine also can be administered transdermally along with estradiol as a treatment for menopausal symptoms .

Nestoron Preparation Products And Raw materials

Raw materials

Preparation Products

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Nestoron Spectrum

ST 1435 NESTORONE NESTORON 17-Hydroxy-16-methylene-19-norpregn-4-ene-3,20-dione acetate Elcometrine 17-(ACETYLOXY)-16-METHYLENE-19-NORPREGN-4-ENE-20-DIONE 16-Methylene-17-hydroxy-19-norpregn-4-ene-3,20-dione acetate 16-Methylene-17-alpha-acetoxy-19-nor-4-pregnene-3,20-dione 19-Norpregn-4-ene-3,20-dione, 17-(acetyloxy)-16-methylene- (9ci) 19-Norpregn-4-ene-3,20-dione, 17-hydroxy-16-methylene-, acetate Nestoron (ST-1435) 17-(Acetyloxy)-16-methylene-19-norpregn-4-ene-3,20-dione ELCOMETRINE;NESTORONE;ST-1435;ST1435 Segesterone Acetate (8R,9S,10R,13S,14S,17R)-17-acetyl-13-methyl-16-methylene-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate ELCOMETRINE; NESTORONE; ST-1435; ST 1435; ST1435 19-Norpregn-4-ene-3,20-dione, 17-(acetyloxy)-16-methylene- Estr-4-en-3-one,17-acetyl-17-(acetyloxy)-16-methylene-,(17α)- Norgestone acetate ST 1435,Inhibitor,Nestoron,ST1435,inhibit,Progesterone Receptor,NR3C3 Nestorone Acetate 7759-35-5 API