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2-Fluoroadenosine

2-Fluoroadenosine Struktur
146-78-1
CAS-Nr.
146-78-1
Englisch Name:
2-Fluoroadenosine
Synonyma:
2-fas;2-far;nsc30605;2-Fluorodenosine;2-FLUOROADENOSINE;2-fluoro-adenosin;Adenosine, 2-fluoro-;2-Fluoroadenosine>2-Fluoroadenosine USP/EP/BP;2-Fluoroadenosine, 10 mM in DMSO
CBNumber:
CB6306915
Summenformel:
C10H12FN5O4
Molgewicht:
285.23
MOL-Datei:
146-78-1.mol

2-Fluoroadenosine Eigenschaften

Schmelzpunkt:
240 °C (D)(lit.)
Siedepunkt:
747.3±70.0 °C(Predicted)
Dichte
2.17±0.1 g/cm3(Predicted)
Brechungsindex
-72 ° (C=0.1, EtOH)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
L?slichkeit
DMSO (Slightly, Sonicated), Methanol (Slightly, Heated, Sonicated)
Aggregatzustand
Solid
pka
13.05±0.70(Predicted)
Farbe
Off-White
InChI
InChI=1S/C10H12FN5O4/c11-10-14-7(12)4-8(15-10)16(2-13-4)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,14,15)/t3-,5-,6-,9-/m1/s1
InChIKey
HBUBKKRHXORPQB-UUOKFMHZSA-N
SMILES
OC[C@H]1O[C@@H](N2C3C(=C(N=C(F)N=3)N)N=C2)[C@H](O)[C@@H]1O
CAS Datenbank
146-78-1(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22-36/37/38
S-S?tze: 26
WGK Germany  3
RTECS-Nr. AU7386000
HS Code  29349990
Speicherklasse 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Toxizit?t mouse,LD10,unreported,1000ug/kg (1mg/kg),Progress in Medical Chemistry. Vol. 7, Pg. 69, 1970.
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t 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-Toxizit?t (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 zweckm??ig, 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 M?glichkeit entfernen. Weiter spülen.

2-Fluoroadenosine Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

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

S-S?tze Betriebsanweisung:

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

Beschreibung

2-Fluoroadenosine (F-Ado) was developed at Southern Research Institute in 1957 as a potential anticancer drug. 2-Fluoroadenosine is not deaminated by adenosine deaminase but metabolized to triphosphate as shown in vitro. The drug was also shown to be a potent inhibitor of lymphocyte-mediated cytolysis.

Verwenden

2-Fluoroadenosine is a fluorinated analog of Adenoside nucleotide. It is used as an intermediate for the drug fludarabine. Fludarabine is a purine analogue and antineoplastic agent. It is a chemotherapy medication used in the treatment of leukemia and lymphoma.

Biologische Funktion

2-Fluoroadenosine (F-Ado) was synthesized by Montgomery and his co-workers. This compound has been found to suppress the growth of H.Ep. No. 2 cells growing in culture. Bennett and Smithers have shown that in the same cells, the synthesis of 5-phosphoribosylamine was markedly inhibited by both 2- fluoroadenine and F-Ado. The compound was found to inhibit the incorporation of variously labeled precursors into ribonucleic acid in whole Ehrlich ascites cells. Upon incubation with ascites cells, the nucleoside was readily converted to the 5’-mono-, 5’-di-, and 5’-triphosphates.In addition, striking potentiation of the inhibition of human platelet aggregation by combinations of forskolin with PGE 1 or F-Ado [1-2].

Synthese

A novel method for the introduction of fluorine in the purine 2-position is described and employed in the synthesis of a potential antimycobacterial compound. Also 2-fluoroadenosine has been synthesized for the first time from adenosine with perbenzoylated 2-nitroadenosine as a key intermediate. Mild reaction conditions are employed and few synthetic steps are required. The novel synthesis of fluoroadenosine can be regarded as a formal synthesis of the antileukemic drug fludarabine phosphate.
[1] MORTEN BRNDVANG L. G. A Novel Method for the Introduction of Fluorine into the Purine 2-Position: Synthesis of 2-Fluoroadenosine and a Formal Synthesis of the Antileukemic Drug Fludarabine[J]. Synthesis-Stuttgart, 2006, 87 1: 2993-2995. DOI:10.1055/S-2006-942544.

2-Fluoroadenosine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2-Fluoroadenosine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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146-78-1()Verwandte Suche:


  • 6-amino-2-fluoro-9-beta-d-ribofuranosyl-purin
  • 6-amino-2-fluoro-9-beta-d-ribofuranosylpurine
  • nsc30605
  • 2-FLUOROADENOSINE
  • 2-FLUOROADENOSINE(FLUDARABINE INTERMEDIATE)
  • 2-Fluorodenosine
  • 2-Fluoro-9-β-D-ribofuranosyl-9H-purin-6-amine
  • (2R,3R,4S,5R)-2-(6-aMino-2-fluoro-9H-purin-9-yl)-5-(hydroxyMethyl)oxolane-3,4-diol
  • (2R,3R,4S,5R)-2-(6-AMino-2-fluoro-9H-purin-9-yl)-5-(hydroxyMethyl)tetrahydrofuran-3,4-diol
  • 2-far
  • 2-fas
  • 2-fluoro-adenosin
  • Adenosine, 2-fluoro-
  • 2-Fluoroadenosine>
  • 2-Fluoroadenosine USP/EP/BP
  • (2R,3R,4S,5R)-2-(6-amino-2-fluoropurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
  • 2-Fluoroadenosine, 10 mM in DMSO
  • 146-78-1
  • 145-78-1
  • C10H12FN5O4
  • Oligonucleotide Synthesis
  • Nucleosides
  • Specialty Synthesis
  • Biochemistry
  • Nucleosides and their analogs
  • Nucleosides, Nucleotides & Related Reagents
  • Nucleosides
  • Oligonucleotide Synthesis
  • Specialty Synthesis
  • Miscellaneous Biochemicals
  • API intermediates
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