Mifepristone

Mifepristone Struktur
84371-65-3
CAS-Nr.
84371-65-3
Englisch Name:
Mifepristone
Synonyma:
RU486;Mifeprestone;Mifepristone INN;C-1073;r38486;ru486-6;VGX 410;MIFEGYNE;RU-38486;Mifeprex
CBNumber:
CB6351940
Summenformel:
C29H35NO2
Molgewicht:
429.6
MOL-Datei:
84371-65-3.mol

Mifepristone Eigenschaften

Schmelzpunkt:
195-198°C
alpha 
D20 +138.5° (c = 0.5 in chloroform)
Siedepunkt:
544.13°C (rough estimate)
Dichte
1.0731 (rough estimate)
Brechungsindex
1.6290 (estimate)
storage temp. 
2-8°C
Löslichkeit
Soluble in DMSO (up to 40 mg/ml) or in Ethanol (up to 20 mg/ml).
Aggregatzustand
Yellow solid
pka
12.94±0.60(Predicted)
Farbe
Yellow
Wasserlöslichkeit
474.8ug/L(22.5 ºC)
Merck 
14,6186
Stabilität:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
InChIKey
VKHAHZOOUSRJNA-GCNJZUOMSA-N
CAS Datenbank
84371-65-3(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T
R-Sätze: 60-61
S-Sätze: 53-22-36/37/39-45
WGK Germany  3
RTECS-Nr. KG2955000
HS Code  29372900
Giftige Stoffe Daten 84371-65-3(Hazardous Substances Data)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H360 Kann die Fruchtbarkeit beeinträchtigen oder das Kind im Mutterleib schädigen. Fertility (Fruchtbarkeit) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" />
Sicherheit
P201 Vor Gebrauch besondere Anweisungen einholen.
P308+P313 BEI Exposition oder falls betroffen: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.

Mifepristone Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R60:Kann die Fortpflanzungsfähigkeit beeinträchtigen.
R61:Kann das Kind im Mutterleib schädigen.

S-Sätze Betriebsanweisung:

S53:Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.
S22:Staub nicht einatmen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).

Beschreibung

Mifepristone is an orally-active progesterone and glucocorticoid receptor antagonist indicated for use as a post-coital contraceptive. In addition to being an abortifacient, mifepristone is reported to be effective in the treatment of ocular hypertension; its potential therapeutic effect in hormone-dependent tumors is currently under investigation.

Chemische Eigenschaften

Pale Yellow Solid

Verwenden

Mifepristone is a progesterone receptor antagonist with partial agonist activity. Abortifacient.

Indications

Mifepristone is a progesterone receptor antagonist that has a high affinity for glucocorticoid receptors and little agonist effect.This drug has recently been approved for use in the United States for the treatment of hypercortisolism. At high doses, mifepristone blocks negative feedback of the hypothalamic–pituitary axis, thereby increasing endogenous corticotrophin and cortisol levels. Because mifepristone exerts its effects at the receptor level and not by altering glucocorticoid production, elevated serum cortisol and corticotrophin levels may not accurately reflect the effectiveness of the therapeutic regimen. Mifepristone does not inhibit cortisol binding to the mineralocorticoid receptor, so that the resulting corticotrophin disinhibition may cause potassium depletion. Thus, administration of a mineralocorticoid receptor antagonist such as spironolactone may be indicated with mifepristone. Hypoadrenalism, nausea, and drowsiness have been reported during prolonged administration of mifepristone.

Weltgesundheitsorganisation (WHO)

Mifepristone, an antiprogesterone used in combination with a prostaglandin for the termination of early pregnancy, was introduced in 1990. Use of the combination has been associated with episodes of coronary spasm that are attributed to administration of the prostaglandin and which have resulted in several cases of cardiac infarction and ventricular fibrillation. At least one of these incidents has been fatal.

Biologische Aktivität

Selective antagonist at progesterone (PR) and glucocorticoid (GR) receptors in vitro and in vivo . Is a silent antagonist at PR and has a higher affinity than progesterone. Has higher affinity for GR than dexamethasone.

Pharmakokinetik

Following oral administration, mifepristone is rapidly absorbed, with a peak plasmaconcentration in approximately 90 minutes , an oral bioavailability of approximately 70%, and a term inal elimination half-life of 18 hours. It is 98% protein bound, primarily to album in and α1-acid glycoprotein. Mifepristone is metabolized primarily via CYP3A4 pathways involving mono- and di-N-demethylation and terminal hydroxylation of the 17-propynyl chain. The fact that approximately 83% of the drug is recovered in the feces and 9% in the urine suggests a biliary route of elimination. Mifepristone also demonstrates antiglucocorticoid activity.

Clinical Use

An antiprogestin is a substance that competes with progesterone for its receptor and, ultimately, prevents progesterone from binding to and activating its receptor. Because progesterone is integral to the continuation of an early pregnancy, it is expected that antipro-gestins will interfere with pregnancy maintenance. In 1982, the first antiproges tin, mifepristone (RU 486), was reported. Mifepristone was shown to interrupt early stages of implantation and pregnancy in humans.

Einzelnachweise

https://pubchem.ncbi.nlm.nih.gov/compound/mifepristone#section=Top
https://www.drugbank.ca/drugs/DB00834
https://www.drugs.com/cdi/mifepristone-tablets.html

Mifepristone Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Mifepristone Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 539)Lieferanten
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84371-65-3()Verwandte Suche:


  • ra-4,9-dien-3-one
  • ru486-6
  • MIFEGYNE
  • MIFEPRISTONE
  • RU-38486
  • 11BETA-[4-(DIMETHYLAMINO)PHENYL]-17BETA-HYDROXY-17-(1-PROPYNYL)ESTRA-4,9-DIEN-3-ONE
  • (11BETA,17BETA)-11-(4-(DIMETHYLAMINO)PHENYL)-17-HYDROXY-17-(1-PROPYNYL)ESTRA-4,9-DIEN-3-ONE
  • (11B,17 B)-11-[4-(DIMETHYLAMINO)PHENYL]-17-HYDROXY-17-(1-PROPYNYL)-ESTRA-4,9-DIEN-3-ONE
  • 11b-[p-(dimethylamino)phenyl]-17b-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one
  • 4,9-ESTRADIEN-17-ALPHA-PROPYNYL, 11-BETA-[4-DIMETHYNYLAMINO]PHENYL-17-BETA-OL-3-ONE
  • Mifepriston Dianhydride
  • MifepristoneTablets/Mifeprex/(Ru-486)
  • RU-486, RU-38486, Mifegyne,
  • Mifepristone(Mifeprex)
  • Mifepristone (200 mg)
  • Mifepristone-D6
  • Mifepriston
  • (10S,11S,14S,15S,17R)-17-[4-(diMethylaMino)phenyl]-14-hydroxy-15-Methyl-14-(prop-1-yn-1-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1,6-dien-5-one
  • C-1073
  • Mifepristone 11b-[p-(Dimethylamino)phenyl]-17b-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one
  • Mifepristone, >=99%
  • 11-(4-(dimethylamino)phenyl)-17-hydroxy-17-(1-propynyl)-estra-9-dien-3-one
  • 11beta-[4-(n,n-dimethylamino)phenyl]-17alpha-(prop-1-ynyl)-delta4,9-estradiene
  • 17-beta)-(11-bet
  • 17beta)-11-[4-(dimethylamino)-phenyl]-17-hydroxy-17-(1-propynyl)estra-(11bet
  • 17-beta-hydroxy-11-beta-(4-dimethylaminophenyl-1)-17-alpha-(prop-1-ynyl)oest
  • -17beta-ol-3-one
  • 4,9-dien-3-one
  • r38486
  • 11β-(4-dimethyl-amino)-phenyl-17β-hydroxy-17-(1-propynyl)-estra-4,9-dien-3-one
  • 11β -[4-(N,N-dimethylaminyl)]-phenyl-17β -hydroxy-17α-(1-propynyl)-estra-4,9-diene-3-one
  • 11b-(4-Dimethyl amino) phenyl-17b-hydroxy-17-(1-propynyl) estra-4,9-dien-3-one
  • 17-beta-Hydroxy-11-beta-(4-dimethylaminophenyl-1)-17-alpha-(prop-1-ynyl)oestra-4,9-dien-3-one
  • Estra-4,9-dien-3-one, 11-(4-(dimethylamino)phenyl)-17-hydroxy-17-(1-propynyl)-, (11-beta, 17-beta)
  • 11-(4-Dimethylaminophenyl)-17-hydroxy-13-methyl-17-prop-1-ynyl-1,2,6,7,8,11,12,13,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • (11β,17β)-11-[4-(Dimethylamino)phenyl]-17-hydroxy-17-(1-propynyl)-estra-4,9-dien-3-one
  • Mifepristone,11β-(4-Dimethyl-amino)-phenyl-17β-hydroxy-17-(1-propynyl)-estra-4,9-dien-3-one, RU-38486, RU-486
  • (11,17)-11-[4-(Dimethylamino)phenyl]-17-hydroxy-17-(1-propyn-1-yl)estra-4,9-dien-3-one
  • Mifeprex
  • Mifestone
  • VGX 410
  • RU-38486, RU-486, 11β-(4-Dimethylamino)phenyl-17β-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one
  • (1lβ,17β)-11-[4- (Dimethylamino)phenyl]-17-hydroxy-17-(1-propynyl)estra-4,9-dien-3-one
  • 11β-(p-Dimethylaminophenyl)-17β-hydroxy-17α-(1-propynyl)estra-4,9-dien-3-one
  • RU486, RU 38486
  • Mifepristone - CAS 84371-65-3 - Calbiochem
  • 11-[4-(dimethylamino)phenyl]-17-hydroxy-17-(1-propyn-1-yl)estra-4,9-dien-3-one
  • (8S,11R,13S,14S,17S)-11-[4-(dimethylamino)phenyl]-17-hydroxy-13-methyl-17-prop-1-ynyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
  • Mifepristone>
  • Mifepristone Solution
  • Mifepristone Mifepristone
  • Estra-4,9-dien-3-one, 11-[4-(dimethylamino)phenyl]-17-hydroxy-17-(1-propyn-1-yl)-, (11β,17β)-
  • (8S,11R,13S,14S,17S)-11-(4-(Dimethylamino)phenyl)-17-hydroxy-13-methyl-17-(prop-1-yn-1-yl)-1,2,6,7,8,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one
  • Mifepristone USP/EP/BP
  • MifepristoneQ: What is Mifepristone Q: What is the CAS Number of Mifepristone Q: What is the storage condition of Mifepristone
  • Mifepristone D3Q: What is Mifepristone D3 Q: What is the CAS Number of Mifepristone D3
  • (11β,17β)-11-[4-(Dimethylamino)phenyl]-17-hydroxy-17-(1-propyn-1-yl)estra-4,9-dien-3-one
  • Mifepristone (1443759)
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