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Deferoxamin

Deferoxamine Struktur
70-51-9
CAS-Nr.
70-51-9
Bezeichnung:
Deferoxamin
Englisch Name:
Deferoxamine
Synonyma:
DESFEROXAMINE;dfoa;taone;entaone;ba33112;desferin;desferex;desferan;ba-29837;ba-33112
CBNumber:
CB8506290
Summenformel:
C25H48N6O8
Molgewicht:
560.69
MOL-Datei:
70-51-9.mol

Deferoxamin Eigenschaften

Schmelzpunkt:
139°C
Siedepunkt:
627.9°C (rough estimate)
Dichte
1.2216 (rough estimate)
Brechungsindex
1.5540 (estimate)
storage temp. 
-20°C
Aggregatzustand
Solid
pka
9.08±0.50(Predicted)
Farbe
White to off-white
Major Application
pharmaceutical
InChIKey
UBQYURCVBFRUQT-UHFFFAOYSA-N
SMILES
C(=O)(N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN)CCC(=O)NCCCCCN(O)C(=O)C
EPA chemische Informationen
Deferoxamine (70-51-9)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
WGK Germany  WGK 3
Speicherklasse 11 - Combustible Solids
Giftige Stoffe Daten 70-51-9(Hazardous Substances Data)
Toxizit?t LD50 oral in mouse: 1340mg/kg
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P261 Einatmen von Staub vermeiden.
P272 Kontaminierte Arbeitskleidung nicht au?erhalb des Arbeitsplatzes tragen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P352 BEI BERüHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckm??ig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P321 Besondere Behandlung
P333+P313 Bei Hautreizung oder -ausschlag: ?rztlichen Rat einholen/?rztliche Hilfe hinzuziehen.
P363 Kontaminierte Kleidung vor erneutem Tragen waschen.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Deferoxamin Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Deferoxamine was introduced in the 1960s for chelation of iron. It is synthesized by removing a central iron molecule from ferrioxamine B, a compound obtained from the microorganism Streptomyces pilosus. Deferoxamine binds to iron from ferritin and forms ferrioxamine, a very stable and water-soluble chelate with a characteristic reddish color.

Verwenden

Deferoxamine is used for the treatment of both acute iron intoxication and chronic iron overload due to transfusiondependent anemias. It has also been used in trials for malaria treatment and for aluminum chelation in hemodialysis patients. Studies of a rat model of intracerebral hemorrhage have noted that deferoxamine treatment reduced oxidative stress from iron release, indicating a possible role in preventing damage associated with hemorrhagic strokes.

Environmental Fate

Localized infusion or injection site reactions may occur with deferoxamine administration, such as pain, urticaria and flushing of the skin. Hypersensitivity reactions have been documented with both acute and chronic administration of deferoxamine. Some of the more serious side effects include infusion rate-related hypotension, renal insufficiency, neurotoxicity, growth retardation, pulmonary toxicity, and infections. Deferoxamine may induce venous dilation when given at doses greater than 15 mg kg-1 h-1 leading to poor venous return, depressed cardiac output, and eventually hypotension. Increased levels of histamine have been noted during hypotensive episodes, although pretreatment with antihistamines has not been shown to stop the reaction. An acute decrease in glomerular filtration rate and renal plasma flow secondary to hypotension is the possible mechanism underlying the nephrotoxicity induced by deferoxamine. Depletion of iron, translocation of copper, and chelation of other trace elements including zinc may interfere with critical iron-dependent enzymes, causing oxidative damage within various tissues. These are possible mechanisms thought to be responsible for deferoxamineinduced neurotoxicity, growth retardation, and pulmonary toxicity. In vitro studies have shown that deferoxamine inhibits the synthesis of prostaglandin, hemoglobin, ferritin, collagen, and DNA. The iron–deferoxamine complex, ferrioxamine, is a growth factor for many bacteria and fungi. Deferoxamine has been associated with Yersinia enterocolitica overgrowth and fatal cases of mucormycosis with prolonged therapy.

Deferoxamin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Deferoxamin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 75)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21531 55
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000
marketing@targetmol.com United States 32431 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-17392587031
1059@dideu.com China 9984 58
BOC Sciences
16314854226; +8616314854226
inquiry@bocsci.com United States 19852 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 17705817739
info@dycnchem.com China 52693 58
TargetMol Chemicals Inc.
+1-781-999-5354;
support@targetmol.com United States 38999 58
PT CHEM GROUP LIMITED
+86-85511178; +86-85511178
peter68@ptchemgroup.com China 35405 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490
info@gihichemicals.com China 49859 58
Wuhan Topule Biopharmaceutical Co., Ltd
+86-18327326525
masar@topule.com China 8433 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +86-15965530500
nickzhang@hangyubiotech.com China 9935 58

70-51-9(Deferoxamin)Verwandte Suche:


  • deferoxamideb
  • deferoxamin
  • deferoxamine
  • deferoxamineb
  • deferoxaminum
  • deferrioxamine
  • deferrioxamineb
  • desferan
  • desferex
  • desferin
  • desferral
  • desferriferrioxaminb
  • desferrin
  • desferrioxamineb
  • entaone
  • n-[5-[3-[(5-aminopentyl)hydroxycarbamoyl]propionamido]pentyl]-3-[[5-(n-hydroxy
  • n’-[5-[[4-[[5-(acetylhydroxamino)pentyl]amino]-1,4-dioxobutyl]hydroxyamino]pen
  • n-benzoyl-ferrioxamine
  • n-benzoylferrioxamineb
  • nsc-527604
  • ButanediaMide,N4-[5-[[4-[[5-(acetylhydroxyaMino)pentyl]aMino]-1,4-dioxobutyl]hydroxyaMino]pentyl]-N1-(5-aMinopentyl)-N1-hydroxy-
  • 1-amino-6,17-dihydroxy-7,10,18,21-tetraoxo-27-(n-acetylhydroxylamino)-6,11,17,
  • 22-tetraazaheptaeicosane
  • 3,9,14,20,25-pentaazatriacontane-2,10,13,21,24-pentone,30-amino-3,14,25-trih
  • 3,9,14,20,25-pentaazatriacontane-2,10,13,21,24-pentone,30-amino-3,14,25-trihyd
  • 30-amino-3,14,25-trihydroxy-3,9,14,20,25-pentaazatriacontane-2,10,13,21,24-p
  • 30-amino-3,14,25-trihydroxy-3,9,14,20,25-pentaazatriacontane-2,10,13,21,24-pen
  • acetamido)pentyl]carbamoyl]propionohydroxamicacid
  • ba-29837
  • ba33112
  • ba-33112
  • butanediamide,n’-(5-((4-((5-(acetylhydroxyamino)pentyl)amino)-1,4-dioxobutyl)h
  • pentyl)-3-((5-(n-hydroxyacetamido)pentyl)carbamoyl)-
  • taone
  • tyl]-n-(5-aminopentyl)-n-hydroxybutanediamide
  • ydroxyamino)pentyl)-n-(5-aminopentyl)-n-hydroxy-
  • N-[5-[[4-[5-azanylpentyl(hydroxy)amino]-4-oxo-butanoyl]amino]pentyl]-N'-[5-[ethanoyl(hydroxy)amino]pentyl]-N-hydroxy-butanediamide
  • N'-[5-[acetyl(hydroxy)amino]pentyl]-N-[5-[[4-[5-aminopentyl(hydroxy)amino]-4-keto-butanoyl]amino]pentyl]-N-hydroxy-succinamide
  • N'-[5-[acetyl(hydroxy)amino]pentyl]-N-[5-[[4-[5-aminopentyl(hydroxy)amino]-4-oxobutanoyl]amino]pentyl]-N-hydroxybutanediamide
  • N1-(5-Aminopentyl)-N1-hydroxy-N4-(5-(N-hydroxy-4-((5-(N-hydroxyacetamido)-pentyl)amino)-4-oxobuta
  • DESFERROXAMINE
  • N'-[5-[[4-[[5-(Acetylhydroxyamino)pentyl]amino]-1,4-dioxobutyl]hydroxyamino]pentyl]-N-(5-aminopentyl)-N-hydroxysuccinamide
  • N'-{5-[ACETYL(HYDROXY)AMINO]PENTYL}-N-[5-({4-[(5-AMINOPENTYL)(HYDROXY)AMINO]-4-OXOBUTANOYL}AMINO)PENTYL]-N-HYDROXYSUCCINAMIDE
  • N1-(5-aminopentyl)-N1-hydroxy-N4-(5-(N-hydroxy-4-((5-(N-hydroxyacetamido)pentyl)amino)-4-oxobutanamido)pentyl)succinamide
  • Deferoxamine USP/EP/BP
  • dfoa
  • DESFEROXAMINE
  • Deferoxamine B|||Desferrioxamine B
  • Deferoxamine for peak identification CRS 1
  • 70-51-9
  • C25H48N6O8
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