Metyrapon

METYRAPONE Struktur
54-36-4
CAS-Nr.
54-36-4
Bezeichnung:
Metyrapon
Englisch Name:
METYRAPONE
Synonyma:
Metapyron;Metyrapon;Metopirone;Metapirone;Metapyrone;Methapyrapone;Methopirapone;Methopyrapone;Methopyrinine;Methbipyranone
CBNumber:
CB8329426
Summenformel:
C14H14N2O
Molgewicht:
226.27
MOL-Datei:
54-36-4.mol

Metyrapon Eigenschaften

Schmelzpunkt:
52-55 °C(lit.)
Siedepunkt:
367.89°C (rough estimate)
Dichte
1.0852 (rough estimate)
Brechungsindex
1.6419 (estimate)
Flammpunkt:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
Löslichkeit
H2O: soluble (sparingly)
Aggregatzustand
solid
pka
4.61±0.10(Predicted)
Farbe
White
Merck 
13,6181
BRN 
163023
Stabilität:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 2 months.
InChI
InChI=1S/C14H14N2O/c1-14(2,12-6-4-8-16-10-12)13(17)11-5-3-7-15-9-11/h3-10H,1-2H3
InChIKey
FJLBFSROUSIWMA-UHFFFAOYSA-N
SMILES
C(C1=CC=CN=C1)(=O)C(C)(C1=CC=CN=C1)C
EPA chemische Informationen
Metyrapone (54-36-4)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22-36/37/38
S-Sätze: 26
WGK Germany  3
RTECS-Nr. UC3050000
HS Code  2933399090
Speicherklasse 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Giftige Stoffe Daten 54-36-4(Hazardous Substances Data)
Toxizität A well-known inhibitor of monooxygenase reactions and can also, under some circumstances, stimulate metabolism of xenobiotics in vitro. In either case, the effect is non-competitive, in that the KM does not change whereas Vmax does, decreasing in the case of inhibition and increasing in the case of stimulation.
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.

Metyrapon Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R22:Gesundheitsschädlich beim Verschlucken.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

Verwenden

Metyrapone acts as a glucocorticoid synthesis inhibitor, maintaining stress-hormone levels.

Biologische Aktivität

Cytochrome P450 inhibitor. Blocks glucocorticoid synthesis via inhibition of steroid 11- β hydroxylase (CYP11B1) activity (IC 50 = 7.83 μ M). Also inhibits CYP3A4 and cytochrome P450-mediated ω / ω -1 hydroxylase activity.

Mechanism of action

Metyrapone (Metopirone) produces its primary pharmacological effect by inhibiting 11-β-hydroxylase, thereby causing diminished production and release of cortisol. The resulting reduction in the negative feedback of cortisol on the hypothalamus and pituitary causes an increase in corticotrophin release and in the secretion of precursor 11-deoxysteroids.

Clinical Use

Metyrapone is used in the differential diagnosis of both adrenocortical insufficiency and Cushing’s syndrome (hypercortisolism). The drug tests the functional competence of the hypothalamic–pituitary axis when the adrenals are able to respond to corticotrophin; that is, when primary adrenal insufficiency has been ruled out.
After metyrapone administration, a patient with a disease of pituitary origin cannot achieve a compensatory increase in the urinary excretion of 17-hydroxycorticosteroids or 11-deoxysteroids. Moreover, if pituitary corticotrophin is suppressed by an autonomously secreting adrenal carcinoma, there will be no increase in response to metyrapone. On the other hand, if pituitary corticotrophin secretion is maintained, as occurs in adrenal hyperplasia, the inhibition of corticoid synthesis produced by metyrapone will stimulate corticotrophin secretion and the release of metabolites of precursor urinary steroids, which can be measured as 17-hydroxycorticosteroids. Metyrapone is now used less frequently in the differential diagnosis of Cushing’s syndrome because of the ability to measure plasma corticotrophin directly.
The steroid-inhibiting properties of metyrapone have also been used in the treatment of Cushing’s syndrome, and it remains one of the more effective drugs used to treat this syndrome. However, the compensatory rise in corticotrophin levels in response to falling cortisol levels tends to maintain adrenal activity.This requires that glucocorticoids be administered concomitantly to suppress hypothalamic–pituitary activity. Although metyrapone interferes with 11β- and 18- hydroxylation reactions and thereby inhibits aldosterone synthesis, it may not cause mineralocorticoid deficiency because of the compensatory increased production of 11-desoxycorticosterone.

Nebenwirkungen

Side effects associated with the use of metyrapone include gastrointestinal distress, dizziness, headache, sedation, and allergic rash. The drug should not be used in cases of adrenocortical insufficiency or when hypersensitivity reactions can be expected. When administered to pregnant women during the second or third trimesters, the drug may impair steroid biosynthesis in the fetus. Because metyrapone is relatively nontoxic, it is used in combination therapy with the more toxic aminoglutethimide to reduce its dosage.

Metyrapon Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Metyrapon Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 158)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533
Brad@rongnabiotech.com China 3380 58
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29766 58
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000
marketing@targetmol.com United States 32431 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +86-189 4982 3763
sales@tnjchem.com China 34526 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-17392587031
1059@dideu.com China 9983 58
AFINE CHEMICALS LIMITED
+86-571-85134551 +86-18958018566
info@afinechem.com China 15031 58
BOC Sciences
16314854226; +8616314854226
inquiry@bocsci.com United States 19852 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471
sales@sarms4muscle.com China 10378 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 +8619957148339
market18@leapchem.com China 24569 58
TargetMol Chemicals Inc.
+1-781-999-5354;
support@targetmol.com United States 38999 58

54-36-4(Metyrapon)Verwandte Suche:


  • Methopyrone
  • Metopiron
  • Metopirone
  • Metopyrone
  • Metroprione
  • Su 4885
  • su4885
  • su-4885
  • 1-methyl-1-(3-pyridyl)ethyl 3-pyridyl ketone
  • 1,2-di-3-pyridyl-2-methyl-1-propanon
  • 1,2-di-3-pyridyl-2-methyl-1-propanone
  • 1-Propanone, 2-methyl-1,2-di-3-pyridinyl-
  • 1-Propanone, 2-methyl-1,2-di-3-pyridyl-
  • 1-propanone,2-methyl-1,2-di-3-pyridinyl
  • 2-methyl-1,2-bis(3-pyridyl)-1-propane
  • 2-methyl-1,2-bis(3-pyridyl)-1-propanone
  • 2-Methyl-1,2-di(3-pyridinyl)-1-propanone
  • 2-methyl-1,2-di-3-pyridinyl-1-propanon
  • 2-methyl-1,2-di-3-pyridinyl-1-propanone
  • 2-methyl-1,2-di-3-pyridyl-1-propanon
  • 2-Methyl-1,3-di-3-pyridiyl-1-propanone
  • Mepyrapone
  • 2-methyl-1,2-bis(3-pyridyl)propan-1-one
  • 2-methyl-1,2-di(pyridin-3-yl)propan-1-one
  • 2-Methyl-1,2-di-3-pyridyl-1-propanone,Metyrapone, Su-4885
  • Metyrapone (200 mg)
  • Metyrapone USP
  • 2-METHYL-1,2-DI-3-PYRIDYL-1-PROPANE
  • Metyrapone, Su-4885
  • METYRAPONE
  • 2-METHYL-1,2-DI(3-PYRIDYL)-1-PROPANONE
  • NSC-25265
  • 2-methyl-1, 2-?di-3-pyx idyl-l-propanone
  • METYRAPONE USP/EP/BP
  • Metyrapone (1443001)
  • 3-Methyl-1,2-di-3-pyridyl-1-propanone
  • ETYRAPONE
  • Metyrapone, cytochrome P450 inhibitor. Blocks cortisol synthesis.
  • Metyrapone, 10 mM in DMSO
  • Metapirone
  • Metapyron
  • Metapyrone
  • Methapyrapone
  • Methbipyranone
  • Methopirapone
  • Methopyrapone
  • Methopyrinine
  • Metyrapon
  • 54-36-4
  • C9 to C46
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyridines
  • Cytochrome P450 isozyme
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