Cart
sales@molnova.com
tafamidis meglumine
CAS No. 951395-08-7
tafamidis meglumine( Fx-1006A )
Catalog No. M21003 CAS No. 951395-08-7
Tafamidis meglumine is a Potent and Selective Transthyretin Kinetic Stabilizer That Inhibits the Amyloid Cascade.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 42 | Get Quote |
|
| 10MG | 72 | Get Quote |
|
| 25MG | 140 | Get Quote |
|
| 50MG | 215 | Get Quote |
|
| 100MG | 332 | Get Quote |
|
| 500MG | 782 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product Nametafamidis meglumine
-
NoteResearch use only, not for human use.
-
Brief DescriptionTafamidis meglumine is a Potent and Selective Transthyretin Kinetic Stabilizer That Inhibits the Amyloid Cascade.
-
DescriptionTafamidis meglumine is a Potent and Selective Transthyretin Kinetic Stabilizer That Inhibits the Amyloid Cascade.
-
In Vitro——
-
In Vivo——
-
SynonymsFx-1006A
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research AreaNeurological Disease
-
IndicationAmyloid polyneuropathy; Cardiomyopathies
Chemical Information
-
CAS Number951395-08-7
-
Formula Weight503.33
-
Molecular FormulaC21H24Cl2N2O8
-
Purity>98% (HPLC)
-
SolubilityDMSO:12.5 mg/mL (24.83 mM)
-
SMILESCNCC(O)C(O)C(O)C(O)CO.O=C(O)c1ccc2nc(-c3cc(Cl)cc(Cl)c3)oc2c1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Bulawa C E Connelly S Devit M et al. Tafamidis a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade[J]. Proceedings of the National Academy of Sciences of the United States of America 2012 109(24):p.9629-9634.
molnova catalog
related products
-
Difenoconazole
Difenoconazole is a broad-spectrum triazole fungicide that inhibits ergosterol biosynthesis via inhibition of the cytochrome P450-dependent 14α-demethylation of lanosterol which results in disruption of the fungal cell membrane and cell death.
-
BMS-929075
BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokinetic parameters.BMS-929075 shows cytotoxicity.
-
Ubiquitination-IN-1
Ubiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
