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Ibutilide fumarate

Ibutilide fumarate Struktur
122647-32-9
CAS-Nr.
122647-32-9
Englisch Name:
Ibutilide fumarate
Synonyma:
D00648;Corvert (tn);Corvert Fumarate;Ibutilide fumarate;IBUTILIDE FUMRTATE;Ibutibide Fumarate;Ibulitide fumarate;Ibutilide 1/2Fumarate;Ibutilide hemifumarate;IbutilideHemifumarate>
CBNumber:
CB2511478
Summenformel:
(C20H36N2O3S)2.C4H4O4
Molgewicht:
885.24
MOL-Datei:
122647-32-9.mol

Ibutilide fumarate Eigenschaften

Schmelzpunkt:
112-117?C
RTECS-Nr.
PB0475700
storage temp. 
2-8°C
L?slichkeit
H2O: >20mg/mL
Aggregatzustand
solid
Farbe
off-white to tan
Wasserl?slichkeit
H2O: >20mg/mL
maximale Wellenl?nge (λmax)
267nm(EtOH)(lit.)
Merck 
14,4883
CAS Datenbank
122647-32-9(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22
WGK Germany  1
HS Code  2935904000
Toxizit?t rat,LD,oral,> 500mg/kg (500mg/kg),Teratology, The International Journal of Abnormal Development. Vol. 49, Pg. 406, 1994.
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P202 Vor Gebrauch alle Sicherheitshinweise lesen und verstehen.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P308+P313 BEI Exposition oder falls betroffen: ?rztlichen Rat einholen/?rztliche Hilfe hinzuziehen.

Ibutilide fumarate Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Covert was launched in the US and UK for treatment of atrial fibrillation and flutter and can be synthesized in three steps from N-phenyl rnethanesulfonamide. While ibutilide has an asymmetric center, it has been determined that the racemate is equipotent with either enantiomer. The antiarrhythmic action is derived from the compounds ability to prolong the action potential duration and lengthen the refractory period of myocardial tissue. Class Ⅲ antiarrhythrnic agents accomplish this by blocking outward potassium channels, however, ibutilide elicits the same effect by activation of slow inward sodium channels. Recent evidence indicates that it also is a potent blocker of the rapidly acting delayed rectifier potassium current (lkr)and may block the ATP-inhibited potassium channel.

Chemische Eigenschaften

White to Off-White Solid

Verwenden

A methanesulfonanilide antiarrhythmic agent; prologns myocardial action potential duration, predominantly by activation of slow inward sodium current. Antiarrhythmic (class III).

Clinical Use

Ibutilide (Corvert) is a structural analog of sotalol and produces cardiac electrophysiological effects similar to those of the antiarrhythmic agents in class III.
Ibutilide is approved for the chemical cardioversion of recent-onset atrial fibrillation and atrial flutter. Ibutilide appears to be more effective in terminating atrial flutter than atrial fibrillation. It can also lower the defibrillation threshold for atrial fibrillation resistant to chemical cardioversion.

Nebenwirkungen

The major adverse effect associated with the use of ibutilide is the risk of torsades de pointes due to QT prolongation. Other reported adverse cardiovascular events (all 2%) include hypotension and hypertension, bradycardia and tachycardia, and varying degrees of A-V block. The incidence of noncardiac adverse events with the exception of nausea does not differ from that of placebo.

Arzneimittelwechselwirkung

Ibutilide has significant drug interactions.

Vorsichtsma?nahmen

Contraindications to the use of ibutilide include baseline prolongation of the QT interval, use of other QTprolonging drugs, history of torsades de pointes, hypersensitivity to ibutilide, uncorrected hypokalemia or hypomagnesemia, and pregnancy or breast-feeding.

Ibutilide fumarate Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ibutilide fumarate Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 250)Lieferanten
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122647-32-9()Verwandte Suche:


  • Ibutibide Fumarate
  • IBUTILIDE FUMRTATE
  • Ibutilide fumarate
  • N-[4-[4-(ethyl-heptyl-amino)-1-hydroxy-butyl]phenyl]methanesulfonamide fumarate
  • Corvert (tn)
  • D00648
  • Ibutilide fumarate (usan)
  • Ibutilide heMifuMarate salt, 99%
  • N-[4-[4-(ethylheptylamino)-1-hydroxybutyl]phenyl]-methanesulfonamide, (2E)-2-butenedioate (2:1)
  • (±)-N-[4-[4-(Ethylheptylamino)-1-hydroxybutyl]phenyl]-methanesulfonamide hemifumarate salt
  • Ibutilide Fumarate Licensed by Pfizer
  • Ibutilide hemifumarate
  • Ibutilide fumarate, >=99%
  • (±)-N-[4-[4-(Ethylheptylamino)-1-hydroxybutyl]phenyl]methanesulfonamide hemifumarate
  • Ibulitide fumarate
  • IbutilideHemifumarate>
  • Corvert Fumarate
  • Ibutilidehemifumaratesalt,99%
  • Ibutilide fumarate USP/EP/BP
  • Ibutilide Fumarate (U70226E)
  • Ibutilide Fumarate (1335610)
  • Ibutilide 1/2Fumarate
  • Ibutilide fumarate (mM/ml), sodium channel activator
  • Ibutilide Fumarate, 10 mM in DMSO
  • 122647-32-9
  • C20H36N2O3S2C4H4O4
  • C22H38N2O5S
  • C20H36N2O3SC4H4O4
  • C20H36N2O3Ssup1sup2C4H4O4
  • C24H40N2O7S
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
  • Medicine intermediate
  • Inhibitors
  • Antiarrhythmic
  • Cardiovascular APIs
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