Fiacitabine
CAS No. 69123-90-6
Fiacitabine( NSC-382097 | FIAC )
Catalog No. M15648 CAS No. 69123-90-6
A synthesized pyrimidine analog that is a potent and selective anti-herpesvirus agent; suppresses various strains of HSV1 and HSV2 with IC90 of 2.5 nM and 12.6 nM, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 218 | In Stock |
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| 2MG | 128 | In Stock |
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| 5MG | 198 | In Stock |
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| 10MG | 283 | In Stock |
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| 25MG | 454 | In Stock |
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| 50MG | 603 | In Stock |
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| 100MG | 809 | In Stock |
|
| 200MG | 1088 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameFiacitabine
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NoteResearch use only, not for human use.
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Brief DescriptionA synthesized pyrimidine analog that is a potent and selective anti-herpesvirus agent; suppresses various strains of HSV1 and HSV2 with IC90 of 2.5 nM and 12.6 nM, respectively.
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DescriptionA synthesized pyrimidine analog that is a potent and selective anti-herpesvirus agent; suppresses various strains of HSV1 and HSV2 with IC90 of 2.5 nM and 12.6 nM, respectively, shows minimal cytotoxicity; more potent than arabinosylcytosine, iododeoxyuridine, and arabinosyladenine.HSV Infection Phase 2 Discontinued.
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In Vitro——
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In Vivo——
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SynonymsNSC-382097 | FIAC
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PathwayMicrobiology/Virology
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TargetHSV
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RecptorHSV
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Research AreaInfection
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IndicationHSV Infection
Chemical Information
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CAS Number69123-90-6
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Formula Weight371.1042
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Molecular FormulaC9H11FIN3O4
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 37 mg/mL
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SMILESO=C1N=C(N)C(I)=CN1[C@H]2[C@@H](F)[C@@H]([C@@H](CO)O2)O
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Chemical Name2(1H)-Pyrimidinone, 4-amino-1-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)-5-iodo-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Lopez C, et al. Antimicrob Agents Chemother. 1980 May;17(5):803-6.
2. Allaudeen HS, et al. J Biol Chem. 1982 Oct 25;257(20):11879-82.
3. Schinazi RF, et al. Antimicrob Agents Chemother. 1983 Jul;24(1):95-103.
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