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2-Fluoroadenosine

CAS No.
146-78-1
Chemical Name:
2-Fluoroadenosine
Synonyms
2-fas;2-far;nsc30605;2-Fluorodenosine;2-FLUOROADENOSINE;2-fluoro-adenosin;Adenosine, 2-fluoro-;2-Fluoroadenosine>2-Fluoroadenosine USP/EP/BP;2-FLUOROADENOSINE(FLUDARABINE INTERMEDIATE)
CBNumber:
CB6306915
Molecular Formula:
C10H12FN5O4
Molecular Weight:
285.23
MDL Number:
MFCD00866394
MOL File:
146-78-1.mol
MSDS File:
SDS
Last updated:2024-03-25 09:26:41

2-Fluoroadenosine Properties

Melting point 240 °C (D)(lit.)
Boiling point 747.3±70.0 °C(Predicted)
Density 2.17±0.1 g/cm3(Predicted)
refractive index -72 ° (C=0.1, EtOH)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly, Sonicated), Methanol (Slightly, Heated, Sonicated)
form Solid
pka 13.05±0.70(Predicted)
color 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 DataBase Reference 146-78-1(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 0S67290CRJ

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26
WGK Germany  3
RTECS  AU7386000
HS Code  29349990
Toxicity mouse,LD10,unreported,1000ug/kg (1mg/kg),Progress in Medical Chemistry. Vol. 7, Pg. 69, 1970.
NFPA 704
1
2 0

2-Fluoroadenosine price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 656402 2-Fluoroadenosine 97% 146-78-1 250mg $85.2 2024-03-01 Buy
Sigma-Aldrich 656402 2-Fluoroadenosine 97% 146-78-1 1g $679 2024-03-01 Buy
TCI Chemical F0656 2-Fluoroadenosine >96.0%(HPLC)(T) 146-78-1 1g $283 2024-03-01 Buy
TCI Chemical F0656 2-Fluoroadenosine >96.0%(HPLC)(T) 146-78-1 200mg $71 2024-03-01 Buy
Alfa Aesar H27412 2-Fluoroadenosine, 97% 146-78-1 250mg $150 2021-12-16 Buy
Product number Packaging Price Buy
656402 250mg $85.2 Buy
656402 1g $679 Buy
F0656 1g $283 Buy
F0656 200mg $71 Buy
H27412 250mg $150 Buy

2-Fluoroadenosine Chemical Properties,Uses,Production

Description

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.

Uses

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.

Definition

ChEBI: 2-fluoroadenosine is a member of adenosines and an organofluorine compound.

Biological Functions

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].

Synthesis

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 BR?NDVANG 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.

References

[1] H T Shigeura. “Metabolism of 2-fluoroadenosine by Ehrlich ascites cells.” Archives of biochemistry and biophysics 111 3 (1965): 713–9.
[2] Kailash C. Agarwal, Robert E. Parks Jr. “Synergistic inhibition of platelet aggregation by forskolin plus PGE1 or 2-fluoroadenosine: Effects 2′,5′-dideoxyadenosine and 5′-methylthioadenosine.” Biochemical pharmacology 31 22 (1982): Pages 3713-3716.

2-Fluoroadenosine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 204)Suppliers
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View Lastest Price from 2-Fluoroadenosine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Fluoroadenosine pictures 2022-02-22 2-Fluoroadenosine
146-78-1
US $0.00 / KG 1KG 99.3% 100 tons Honest Joy Holdings Limited
	2-Fluoroadenosine pictures 2019-07-06 2-Fluoroadenosine
146-78-1
US $7.00 / KG 1KG 99% 100kg Career Henan Chemical Co

2-Fluoroadenosine Spectrum

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 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