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FIAC

FIAC structure

FIAC 

structure
  • CAS No:

    69123-90-6

  • Formula:

    C9H11FIN3O4

  • Chemical Name:

    FIAC

  • Synonyms:

    2(1H)-Pyrimidinone,4-amino-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodo-;4-Amino-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodo-2(1H)-pyrimidinone;1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)-5-iodocytosine;1-β-D-2′-Fluoroarabino-5-iodocytosine;2′-Fluoro-5-iodo-1-β-D-arabinofuranosylcytosine;FIAC;Fiacitabine;FOAC;NSC 382097

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

Fiacitabine(NSC 382097; FIAC; FOAC) is a selective inhibitior of DNA replication of herpes simplex virus(HSV) with IC50 values of 2.5 nM and 12.6 nM for HSV1 and HSV2, respectively. IC50 value: 2.5/12.6 nM (HSV1/2) [2]Target: HSVFIAC suppressed by 90% the replication of various strains of herpes simplex virus types 1 and 2 at concentrations of 0.0025 to 0.0126 microM. Cytotoxicity was minimal, as determined by trypan blue dye exclusion with norman Vero, WI-38, and NC-37 cell proliferatio


Fiacitabine has been used in trials studying the treatment of HIV Infections and Cytomegalovirus Infections.|Fiacitabine is a pyrimidine nucleoside analog with activity against various herpesviruses. Fiacitabine is converted to its triphosphate form in vivo and inhibits viral DNA polymerase.

FIAC Basic Attributes

371.1

371.10

4058H365ZB

DTXSID8057807

C73202

Characteristics

108

-0.27

2.4±0.1 g/cm3

524.6±60.0 °C at 760 mmHg

271.1±32.9 °C

1.791

Drug Information

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)|Substances that inhibit or prevent the proliferation of NEOPLASMS. (See all compounds classified as Antineoplastic Agents.)

1-(2-fluoro-2-deoxy-beta-D-arabinofuranosyl)-5-iodocytosine

FIAC Use and Manufacturing

Antiviral.

Computed Properties

Molecular Weight:371.10
XLogP3:-0.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:370.97783
Monoisotopic Mass:370.97783
Topological Polar Surface Area:108
Heavy Atom Count:18
Complexity:430
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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