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Fialuridine

Product Name
Fialuridine
CAS No.
69123-98-4
Chemical Name
Fialuridine
Synonyms
FIAU;DRG-0098;NSC 678514;FIALURIDINE;5-I-2'-F-dU;Fialuridine(FIAU);5-1-Ara-2'-F-2-dU;5-1-Ara-2'-F-2-dU;5-I-Ara-2'-F-2'-dU;Fluoroiodoarauracil
CBNumber
CB4386960
Molecular Formula
C9H10FIN2O5
Formula Weight
372.09
MOL File
69123-98-4.mol
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Fialuridine Property

Melting point:
216-217°C
Density 
2.18±0.1 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMSO: soluble5mg/mL, clear (warmed)
pka
7.94±0.10(Predicted)
form 
powder
color 
white to beige
Merck 
14,4069
InChIKey
IPVFGAYTKQKGBM-BYPJNBLXSA-N
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Safety

Safety Statements 
24/25
WGK Germany 
3
RTECS 
YQ9512500
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0632
Product name
Fialuridine
Purity
≥98% (HPLC)
Packaging
5mg
Price
$123
Updated
2024/03/01
Sigma-Aldrich
Product number
SML0632
Product name
Fialuridine
Purity
≥98% (HPLC)
Packaging
25mg
Price
$496
Updated
2024/03/01
TCI Chemical
Product number
D4200
Product name
1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil
Purity
>98.0%(HPLC)
Packaging
10mg
Price
$190
Updated
2024/03/01
Cayman Chemical
Product number
15867
Product name
Fialuridine
Purity
≥98%
Packaging
1mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
15867
Product name
Fialuridine
Purity
≥98%
Packaging
5mg
Price
$93
Updated
2024/03/01
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Fialuridine Chemical Properties,Usage,Production

Description

Fialuridine (FIAU) is one of a series of 2'-fluoro-substituted arabinosyl pyrimidine nucleosides that have demonstrated potent antiviral activities against a number of clinically important viruses, including hepatitis B virus (HBV). Analogs of FIAU have been shown to inhibit viral replication in the woodchuck and duck models of HBV infection. Although the mechanism of the anti-HBV activity is not well understood, evidence suggests that the triphosphate analog of FIAU is a potent inhibitor of HBV DNA polymerase activity. During early clinical investigation FIAU showed much promise as an antiHBV drug because it markedly reduced the level of HBV DNA in the serum of patients with chronic hepatitis B. However, clinical trials were terminated after adverse events occurred following oral administration of FIAU (0.1 and 0.25 mg/kg of body weight per day) for more than 2 months. The mechanism of the unexpected delayed toxicity is unresolved.

Chemical Properties

Colourless crystals

Uses

An antiviral agent; nucleoside analog with antihepatitis B activity

Uses

Fialuridine has been used in the selection of clones.

General Description

Fialuridine (1-(2-deoxy-2-fluoro-β-d-arabinofuranosyl)-5-iodouracil, or FIAU) is an antiviral agent. It is a thymidine-based nucleoside analogue.

Biochem/physiol Actions

Fialuridine (1-(2-deoxy-2-fluoro-β-d-arabinofuranosyl)-5-iodouracil, or FIAU) and its metabolites blocks DNA polymerase at sites of multiple adjacent analog incorporation, reduces the presence of mtDNA (mitochondrial DNA) and results in mitochondrial structural defects in cultured hepatoblasts. It is considered as an efficient drug against hepatitis B virus (HBV) infection.

Clinical Use

Fialuridine, a nucleoside analog designed for the treatment of hepatitis B virus infection, failed in clinical trials due to fatal hepatotoxicity, occuring after 13 weeks of 0.25 mg/kg qd dosing in HBV infected patients. Both in vitro assays as well as preclinical in vivo tests in mice, rats, dogs, and primates could not predict its hepatotoxic potential. Fialuridine toxicity is thought to be mediated by human-specific impaired mitochondrial function after long-term exposure. We used the micropatterned primary hepatocyte coculture model, HepatoPac™, to assess fialuridine-mediated toxicity in vitro. To confirm the human specific toxicity, also rat, dog and monkey HepatoPac™ were exposed to fialuridine.
Another nucleoside analog, sofosbuvir, which is on the market for the treatment of hepatitis C virus infection and shows no signs of hepatotoxicity in the clinic, was used to study whether this approach would be able to distinguish a nucleoside analog with clinical chronic DILI finding from a nucleoside analog without DILI findings.

in vitro

previous in-vitro data showed that 1-(2-deoxy-2-fluoro-beta-d-arabinofuranosyl)-5-ethyluracil (feau) had activity against herpes simplex virus types 1 and 2 comparable to that of 1-(2-deoxy-2-fluoro-beta-d-arabinofuranosyl)-5-methyluracil (fmau), fialuridine (fiau), and acyclovir (acv). the cellular toxicity of feau was found to be much lower than that of fiau. biochemical experiments indicated that feau had similar affinity toward thymidine kinases encoded by hsv 1 and 2 and a much lower affinity for cellular thymidine kinase than thymidine [1].

in vivo

the in-vivo antiviral efficiency of feau was compared with that of fiau and acv by using the herpes encephalitis mode. moreover, acv and feau could significantly increase the number of survivors at doses of 50 and 100 mg/kg per day, respectively, and fiau showed significant activity at 25 mg/kg per day in the animal model [1].

References

[1] mansuri, m. m.,ghazzouli, i.,chen, m.s., et al. 1-(2-deoxy-2-fluoro-β-d-arabinofuranosyl)-5-ethyluracil. a highly selective antiherpes simplex agent. journal of medicinal chemistry 30(5), 867-871 (1987).
[2] mckenzie r et al. hepatic failure and lactic acidosis due to fialuridine (fiau), an investigational nucleoside analogue for chronic hepatitis b. n engl j med. 1995 oct 26;333(17):1099-105.

Fialuridine Preparation Products And Raw materials

Raw materials

Preparation Products

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Fialuridine Suppliers

Panaishen (Henan) Pharmaceutical Science and Technology Co. , Ltd.
Tel
0371-65325800 13700860222
Email
haifeng.zhang@pannacean.com
Country
China
ProdList
539
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58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
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76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6005
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61
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
T&W GROUP
Tel
021-61551611 13296011611
Fax
+86 21-50676805
Email
contact@trustwe.com
Country
China
ProdList
9895
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58
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28387
Advantage
80
TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23671
Advantage
75
TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23653
Advantage
75
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View Lastest Price from Fialuridine manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Fialuridine 69123-98-4
Price
US $0.00-0.00/g
Min. Order
5g
Purity
98%min
Supply Ability
1000g
Release date
2021-08-30
Career Henan Chemical Co
Product
Fialuridine 69123-98-4
Price
US $5.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1ton
Release date
2019-08-05

69123-98-4, FialuridineRelated Search:


  • 1-(2-deoxy-2-fluoro-beta-d-arabinofuranosyl)-5-iodouracil
  • 2,4(1h,3h)-pyrimidinedione,1-(2-deoxy-2-fluoro-beta-d-arabinofuranosyl)-5-io
  • 2’-fluoro-5-iodo-1-beta-d-arabinofuranosyluracil
  • 2'-Deoxy-2'-fluoro-5-iodo-D-uridine
  • 5-IODO-2'-FLUORO-2'-DEOXY-1-BETA-D-ARABINOFURANOSYLURACIL
  • 2,4(1H,3H)-PYRIMIDINEDIONE, 1-(2-DEOXY-2-FLUORO-BETA-D-ARABINOFURANOSYL)-5-IODO-
  • 2'-FLUORO-5-IODOURACIL
  • 2'-FLUORO 2'-DEOXY-5-IODOURACIL-BETA-D-ARABINOFURANOSIDE
  • 1-(2'FLUORO-2'-DEOXYARABINOFURANOSYL)-5-IODOURACIL
  • 1-(2-DEOXY-2-FLUORO-B-D-ARABINOFURANOSYL)-5-IODOURACIL
  • FIALURIDINE
  • FIAU
  • 1-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodo-1,2,3,4-tetrahydropyrimidine-2,4-dione
  • 5-I-Ara-2'-F-2'-dU
  • 1-[(2R,3S,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidine-2,4-dione
  • Fialuridine(FIAU)
  • 5-Iodo-2'-fluoro-deoxyuridine
  • 1-(2-deoxy-2-fluoro-beta-d-arabinofuranosyl)-5-iodo-uraci
  • 2,4(1H,3H)-Pyrimidinedione, 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodo-
  • 1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil 5-Iodo-2'-fluoroarauracil
  • Fluoroiodoarauracil
  • NSC 678514
  • 1-(2-Deoxy-2-fluoro--D-arabinofuranosyl)-5-iodo-2,4(1H,3H)-pyrimidinedione
  • 1-(2'-Deoxy-2'-fluoro--D-arabinofuranosyl)-5-iodouracil
  • 5-Iodo-2'-fluoroarauracil
  • 5-Iodo-1-(2-fluoro-2-deoxy-β-D-arabinofuranosyl)uracil
  • 2'-Deoxy-2'-fluoro-5-iodouridine
  • 5-Iodo-2'-fluoro-2'-deoxy-ara-uridine
  • 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodo-
  • Fialuridine FIAU 2'-Fluoro-5-iodoarauracil
  • 5-Iodo-2'-deoxy-2'-fluoro-beta-D-arabinouridine
  • 5-I-2'-F-dU
  • 1-(2-Deoxy-2-fluoro--D-arabinofuranosyl)-5-iodouracil (FIAU
  • 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil&gt
  • DRG-0098
  • 5-Iodo-2’-deoxy-2’-fluoro-beta-D-arabinouridine, FIAU, Fiauridine
  • 5-Iodo-2’-deoxy-2’-fluoro-β-D-arabinouridine
  • 69123-98-4 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
  • 2'-Fluoro-5-iodoarauracil
  • Fialuridine USP/EP/BP
  • 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodouracil
  • 1-((2R,3S,4R,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-iodopyrimidine-2,4(1H,3H)-dione
  • 5-Iodo-2’-deoxy-2’-fluoro-arabinouridine
  • 5-1-Ara-2'-F-2-dU
  • Fluoroiodoarauridine
  • 5-Iodo-2’-deoxy-2’-fluoro-arabinouridine
  • 5-1-Ara-2'-F-2-dU
  • 69123-98-4
  • C9H10FIN2O5
  • Anti-virals
  • Bases & Related Reagents
  • Intermediates & Fine Chemicals
  • Nucleotides
  • Pharmaceuticals