Cart
sales@molnova.com
Trifluoromethyl-tubercidin
CAS No. 1854086-05-7
Trifluoromethyl-tubercidin( —— )
Catalog No. M35960 CAS No. 1854086-05-7
Trifluoromethyl-tubercidin (TFMT) inhibits host MTr1 and suppresses virus replication.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 119 | In Stock |
|
| 5MG | 62 | In Stock |
|
| 10MG | 112 | In Stock |
|
| 25MG | 261 | In Stock |
|
| 50MG | 461 | In Stock |
|
| 100MG | 830 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameTrifluoromethyl-tubercidin
-
NoteResearch use only, not for human use.
-
Brief DescriptionTrifluoromethyl-tubercidin (TFMT) inhibits host MTr1 and suppresses virus replication.
-
DescriptionTrifluoromethyl-tubercidin (TFMT) is a 2'-O-ribose methyltransferase 1 (MTr1) inhibitor through interaction at its S-adenosyl-l-methionine binding pocket to restrict influenza virus replication.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayMicrobiology/Virology
-
TargetInfluenza Virus
-
RecptorInfluenza Virus
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1854086-05-7
-
Formula Weight334.25
-
Molecular FormulaC12H13F3N4O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO[C@H]1[C@H](N2C=3C(C(C(F)(F)F)=C2)=C(N)N=CN3)O[C@H](CO)[C@H]1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Yuta Tsukamoto, et al. Inhibition of cellular RNA methyltransferase abrogates influenza virus capping and replication. Science. 2023 Feb 10;379(6632):586-591.?
molnova catalog
related products
-
Laninamivir
Laninamivir (CS-8958) is a prodrug of the influenza neuraminidase (NA) inhibitor R-125489.
-
Oseltamivir phosphat...
A competitive inhibitor of influenza neuraminidase that prevents new viral particles from being released.
-
Cephaeline
Cephaeline was highly active against protected primary CLL cells (relative IC50's 35nM ) and acted by repressing HIF-1α± and disturbing intracellular redox homeostasis.
