ChemicalBook--->CAS DataBase List--->58691-88-6

58691-88-6

58691-88-6 Structure

58691-88-6 Structure
IdentificationBack Directory
[Name]

Nomegestrol
[CAS]

58691-88-6
[Synonyms]

Monaco
TherMex
Nomegestrol
Nomegestrel
MELEGESTROL ACETATE
NOMEGESTROL ACETATE
Nomegestrol USP/EP/BP
Nomegestrol###58691-88-6
17-Hydroxy-6-methyl-19-nor-4,6-pregnadiene-3,20-dione
17-Hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione
19-Norpregna-4,6-diene-3,20-dione,17-hydroxy-6-Methyl-
17ALPHA-ACETOXY-6ALPHA-METHYL-19-NOR-PREGN-4,6-DIEN-3,20-DIONE
(8S,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,13-dimethyl-1,2,8,9,10,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
(8S,9S,10R,13S,14S,17R)-17-ethanoyl-17-hydroxy-6,13-dimethyl-1,2,8,9,10,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C21H28O3
[MDL Number]

MFCD00941390
[MOL File]

58691-88-6.mol
[Molecular Weight]

328.45
Chemical PropertiesBack Directory
[Boiling point ]

502.6±50.0 °C(Predicted)
[density ]

1.17±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Chloroform: soluble,DMSO: slightly soluble,Methanol: slightly soluble
[form ]

A solid
[pka]

12.99±0.60(Predicted)
Hazard InformationBack Directory
[Description]

Nomegestrol acetate is the 19-nor derivative of megestrol acetate, useful in the treatment of gynecological conditions associated with luteal deficiency.
[Originator]

Theramex (Monaco)
[Uses]

A progestogen, derivatives of which are used in contraceptives and hormone therapies.
[Uses]

Progetin used in implantable hormone replacement therapies.
[Definition]

ChEBI: Nomegestrol is a corticosteroid hormone.
[Brand name]

LUTENYL
[General Description]

Nomegestrol acetate, 17-hydroxy-6-methyl-19-norpregna-4,6-diene-3,20-dione acetate,is being investigated as the progestin component of anew oral contraceptive, in combination with the estrogenestradiol. This new combination, NOMAC/E2, is in phaseIII trials and would be the first oral contraceptive to utilizeestradiol itself as the estrogenic component. Structurally,NOMAC is considered a nor-progesterone derivative thatlacks the C19 methyl group in megestrol acetate.
[References]

[1] J BOTELLA. Structure-activity and structure-affinity relationships of 19-nor-progesterone derivatives in rat uterus.[J]. Journal of Endocrinological Investigation, 1990, 13 11: 905-910. DOI: 10.1007/bf03349652
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