![](../../files/images/goods/700-49-2.png)
2-Fluoroadenine
CAS No. 700-49-2
2-Fluoroadenine ( NSC 27364;2- Fluoro-6-Aminopurine )
Catalog No. M27216 CAS No. 700-49-2
2-Fluoroadenine has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.
Purity : >98% (HPLC)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
Size | Price / USD | Stock | Quantity |
100MG | 37 | In Stock |
![]() ![]() |
200MG | 49 | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product Name2-Fluoroadenine
-
NoteResearch use only, not for human use.
-
Brief Description2-Fluoroadenine has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.
-
Description2-Fluoroadenine has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.(In Vitro):In Balb-3T3 cells, 2-Fluoroadenine (0.22, 2.2 and 22 μM; 30 hours) inhibits protein, RNA, and DNA syntheses. In CEM cells, 2-Fluoroadenine (2 μM; 4 hours) inhibits CEM cell growth by targeting one or more enzymes involved in either RNA or protein synthesis. In nonproliferating MRC-5 cells, 2-Fluoroadenine (0-1000 μM; 96 hours) exhibits cytotoxicity.
-
SynonymsNSC 27364;2- Fluoro-6-Aminopurine
-
PathwayCell Cycle/DNA Damage
-
TargetDNA/RNA Synthesis
-
RecptorSARS-CoV
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number700-49-2
-
Formula Weight153.1
-
Molecular FormulaC5H4FN5
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESNc1[nH]c(F)nc2ncnc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
![](/themes/theme/en/images/ct.png)
![](/themes/theme/en/images/ct2.png)
-
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.?
-
Methylbenactyzine Br...
Dimethadione is an anticonvulsant that is the active metabolite of trimethadione.
-
Fosifloxuridine nafa...
NUC-3373 (Fosifloxuridine nafalbenamide), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor.NUC-3373 has anticancer activity.