Thalidomide-O-C6-NH2 hydrochloride
CAS No. 2245697-88-3
Thalidomide-O-C6-NH2 hydrochloride ( 4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride )
Catalog No. M28271 CAS No. 2245697-88-3
Thalidomide-O-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 35 | Get Quote |
|
10MG | 58 | Get Quote |
|
25MG | 110 | Get Quote |
|
50MG | 160 | Get Quote |
|
100MG | 241 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameThalidomide-O-C6-NH2 hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionThalidomide-O-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate.
-
DescriptionThalidomide-O-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate.
-
Synonyms4-((6-aminohexyl)oxy)-2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione hydrochloride
-
PathwayOthers
-
TargetOther Targets
-
RecptorNLRP3
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2245697-88-3
-
Formula Weight409.9
-
Molecular FormulaC19H24ClN3O5
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC=C3OCCCCCCN)=O.[H]Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Gary Glick, et al. Substituted imidazo-quinolines as nlrp3 modulators. WO2018152396A1.
molnova catalog
related products
-
Dihydroevocarpine
Dihydroevocarpine shows potent anti-Helicobacter pylori activity with the minimum inhibitory concentration (MIC) value of 10-20 microg/ml. Dihydroevocarpine is a moderate modulator of p-glycoprotein (p-gp) activity; it shows more potent inhibitory effects against MAO-B compared to MAO-A.
-
(S)-(+)-Carvone
(S)-(+)-Carvone is the main constituent of caraway oil and pineapple seed oil.
-
Geranylacetone
Geranylacetone has trypanostatic activity and could protect animals against the T. congolense-induced anaemia through the inhibition of sialidase and/or the protection of the parasite-induced hepatosplenomegaly.