NCT-504
CAS No. 1222765-97-0
NCT-504( —— )
Catalog No. M35051 CAS No. 1222765-97-0
NCT-504, a selective allosteric inhibitor of PIP4Kγ, exhibits an IC50 value of 15.8 μM. It holds promise for the investigation of Huntington's disease.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 98 | In Stock |
|
| 5MG | 90 | In Stock |
|
| 10MG | 144 | In Stock |
|
| 25MG | 236 | In Stock |
|
| 50MG | 328 | In Stock |
|
| 100MG | 452 | In Stock |
|
| 200MG | 603 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNCT-504
-
NoteResearch use only, not for human use.
-
Brief DescriptionNCT-504, a selective allosteric inhibitor of PIP4Kγ, exhibits an IC50 value of 15.8 μM. It holds promise for the investigation of Huntington's disease.
-
DescriptionNCT-504 is a selective allosteric inhibitor of PIP4Kγ, with an IC50 of 15.8 μM. NCT-504 is potential for the research of Huntington's disease.
-
In VitroNCT-504 dose not impair the intrinsic ATP-hydrolytic activity of PIP4Kγ in the absence of PI5P substrate.NCT-504 does not inhibit PIP4Kbeta and weakly inhibits PIP4Kalpha phosphorylation of PI5P .NCT-504 dose not inhibit PIP4Kbeta or PIP4Kalpha (IC50 between 50 μM and 100 μM) at 50 μM concentration.NCT-504 elevates the levels of PI(3,5)P2, PI3P and PI5P in MEFs.NCT-504 (10 μM; 12 hours) does not affect cell viability in MEFs.NCT-504 (5 μM, 10 μM; 2 hours, 6 hours) elevates both the induction of autophagy as well as the rate of turnover of autophagic cargo.NCT-504 treatment causes a robust increase in the formation of autolysosomes with only a modest elevation in autophagosomes.NCT-504 increases autophagy flux and decreases huntingtin protein in 293A cells.NCT-504 reduces mHtt protein levels in immortalized striatal cells from knock-in HD mice.Western Blot Analysis Cell Line:HEK293T cells Concentration:5 μM, 10 μM Incubation Time:2 hours, 6 hours Result:Induced autophagosome formation.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1222765-97-0
-
Formula Weight404.49
-
Molecular FormulaC15H12N6O2S3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (309.03 mM; Ultrasonic )
-
SMILESCn1nnnc1Sc1ncnc2scc(-c3cccc(c3)S(C)(=O)=O)c12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
PTD-p65-P1 Peptide
PTD-p65-P1 Peptide is a nuclear transcription factor NF-kappaB inhibitor, composed of a membrane-translocating peptide sequence generated from antennapedia (PTD) conjugated with p65-P1, which selectively inhibits activation induced by various inflammatory stimuli. PTD-p65-P1 suppressed NF-kappaB activation induced by lipopolysaccharide, interleukin-1, okadaic acid, phorbol 12-myristate 13-acetate, H(2)O(2), and cigarette smoke condensate as well as that induced by TNF.
-
Mucic Acid
Mucic acid is an aldaric acid obtained by nitric acid oxidation of galactose or galactose-containing compounds such as lactose, dulcite, quercite, and most varieties of gum.
-
GSK-626616
GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50: 0.7 nM). It inhibits other members of the DYRK family with similar potency. GSK-626616 is a potential therapy for the treatment of anemia.
Cart
sales@molnova.com