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Fluorocytosine
CAS No. 2022-85-7
Fluorocytosine( Ancobon | Ancotil | 5-FC | NSC 103805 | Ro 2-9915 )
Catalog No. M13149 CAS No. 2022-85-7
Flucytosine is a Nucleoside Analog Antifungal. The chemical classification of flucytosine is Nucleoside Analog.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1G | 43 | In Stock |
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Biological Information
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Product NameFluorocytosine
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NoteResearch use only, not for human use.
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Brief DescriptionFlucytosine is a Nucleoside Analog Antifungal. The chemical classification of flucytosine is Nucleoside Analog.
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DescriptionFlucytosine is a Nucleoside Analog Antifungal. The chemical classification of flucytosine is Nucleoside Analog.
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In Vitro——
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In Vivo——
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SynonymsAncobon | Ancotil | 5-FC | NSC 103805 | Ro 2-9915
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PathwayCell Cycle/DNA Damage
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TargetDNA/RNA Synthesis
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RecptorDNA synthesis
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number2022-85-7
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Formula Weight129.09
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Molecular FormulaC4H4FN3O
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Purity>98% (HPLC)
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SolubilityWater: 5 mg/mL (38.73 mM); DMSO: 8 mg/mL (61.97 mM)
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SMILESO=C1N=CC(F)=C(N)N1
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Chemical Name6-amino-5-fluoro-1H-pyrimidin-2-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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1,4-Dideoxy-1,4-epit...
1,4-Dideoxy-1,4-epithio-D-ribitol is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and possesses a broad spectrum of antitumor activity.1,4-Dideoxy-1,4-epithio-D-ribitol induces apoptosis through inhibition of DNA synthesis.
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AS-136A
AS-136A is an orally active measles virus RNA-dependent RNA polymerase (RdRp) inhibitor with antiviral activity that inhibits measles virus and blocks viral RNA synthesis.
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NSAH?
NSAH is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively.A unique nonnucleoside small-molecule hRR inhibitor, naphthyl salicylic acyl hydrazone (NSAH), using virtual screening, binding affinity, inhibition, and cell toxicity assays.?NSAH binds to hRRM1 with an apparent dissociation constant of 37 μM, and steady-state kinetics reveal a competitive mode of inhibition.?
