GW604714X?
CAS No. 853953-65-8
GW604714X?( 2,4-Thiazolidinedione, 5-[[5-[6-(4-acetyl-1-piperazinyl)-3-nitro-2-pyridinyl]-2-fluorophenyl]methylene]- )
Catalog No. M24847 CAS No. 853953-65-8
GW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 227 | In Stock |
|
| 10MG | 364 | In Stock |
|
| 25MG | 620 | In Stock |
|
| 50MG | 830 | In Stock |
|
| 100MG | 1144 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameGW604714X?
-
NoteResearch use only, not for human use.
-
Brief DescriptionGW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate.
-
DescriptionGW604714X were found to be potent inhibitors of mitochondrial respiration supported by pyruvate.
-
In VitroGW604714X inhibits the mitochondrial pyruvate carrier (MPC) with?Ki?value <0.1 μM in direct measurement of pyruvate transport into rat liver and yeast?mitochondria.Inhibitor?titrations?of pyruvate-dependent respiration by heart mitochondria gave values for the concentration of inhibitor binding sites and their?Ki?(nM) of 56.0 nM and 0.057 nM for the GW604714X.GW604714X inhibits the transport of 0.5 mM [14C]-l-lactate into rat red blood cells, mediated by the monocarboxylate transporter MCT1. GW604714X at 10 μM reduces the initial rate of uptake to 30% of control values.
-
In Vivo——
-
Synonyms2,4-Thiazolidinedione, 5-[[5-[6-(4-acetyl-1-piperazinyl)-3-nitro-2-pyridinyl]-2-fluorophenyl]methylene]-
-
PathwayOthers
-
TargetOther Targets
-
RecptorMitochondrial Metabolism
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number853953-65-8
-
Formula Weight471.46
-
Molecular FormulaC21H18FN5O5S
-
Purity>98% (HPLC)
-
SolubilityDMF:5mg/ml(10.61mM; need ultrasonic)
-
SMILESO=C(NC1=O)SC1=CC2=CC(C3=NC(N4CCN(C(C)=O)CC4)=CC=C3[N+]([O-])=O)=CC=C2F
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
WRW4 TFA(878557-55-2...
Selective antagonist of formyl peptide receptor 2 (FPR2) signaling. Inhibits WKYMVm binding to FPR2 (IC50 = 0.23 μM) and inhibits intracellular calcium release induced by WKYMVm, MMK 1, amyloid β42, and F peptide. Also inhibits FPR2-mediated signaling in human neutrophils; blocks chemotactic migration and superoxide generation by amyloid β42 peptide.
-
Ganoderenic acid A
Ganoderenic acid A has a potent hepatoprotective, and cytotoxic effects, it shows inhibitory activity on human aldose reductase in vitro.From the acidic fraction, potent human aldose reductase inhibitors, ganoderic acid C2 (1) and Ganoderenic acid A (2), were isolated together with three related compounds.
-
Ebeiedinone
Ebeiedinone, a steroidal alkaloid from Fritillaria species, inhibits the bioactivity of human whole blood cholinesterase (ChE) at the concentration of 0.1 mM, with the inhibitory effects of 69.0%.
Cart
sales@molnova.com