Grossamide
CAS No. 80510-06-1
Grossamide( —— )
Catalog No. M31110 CAS No. 80510-06-1
Grossamide possesses potential anti-inflammatory effects, it also has potential anti-neuroinflammatory effects against lipopolysaccharide (LPS)-induced inflammatory response in BV2 microglia cells. Cis-Grossamide K exerts a particularly strong anti-melanogenic activity on the cells without high cell toxicity.
Grossamide possesses potential anti-inflammatory effects, it also has potential anti-neuroinflammatory effects against lipopolysaccharide (LPS)-induced inflammatory response in BV2 microglia cells. Cis-Grossamide K exerts a particularly strong anti-melanogenic activity on the cells without high cell toxicity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 565 | In Stock |
|
50MG | Get Quote | In Stock |
|
100MG | Get Quote | In Stock |
|
Biological Information
-
Product NameGrossamide
-
NoteResearch use only, not for human use.
-
Brief DescriptionGrossamide possesses potential anti-inflammatory effects, it also has potential anti-neuroinflammatory effects against lipopolysaccharide (LPS)-induced inflammatory response in BV2 microglia cells. Cis-Grossamide K exerts a particularly strong anti-melanogenic activity on the cells without high cell toxicity.
-
DescriptionGrossamide possesses potential anti-inflammatory effects, it also has potential anti-neuroinflammatory effects against lipopolysaccharide (LPS)-induced inflammatory response in BV2 microglia cells. Cis-Grossamide K exerts a particularly strong anti-melanogenic activity on the cells without high cell toxicity.
-
In VitroGrossamide downregulates LPS-mediated production of inflammatory molecules.Grossamide (0-20 μM, 1 h) inhibits the mRNA levels of TNF-α and IL-6 in a dose-dependent manner, inhibits LPS-induced NF-κB activation, and inhibits LPS-induced TLR4 and MyD88 expression without cytotoxicity. RT-PCR Cell Line:BV-2 microglia cell Concentration:0, 10, 15, and 20 μM Incubation Time:1 h and co-cultured with LPS (100 ng/mL) for another 6 h Result:Inhibited the mRNA levels of TNF-α and IL-6 in a dose-dependent manner.Western Blot Analysis Cell Line:BV-2 microglia cell Concentration:0, 10, 15, and 20 μM Incubation Time:1 h followed by LPS (100 ng/mL) stimulation for 1 h or 24 h Result:Inhibited LPS-induced phosphorylation of IκBα and significantly reduced phosphorylation of NF-κB p65 levels. Dose-dependently decreased the expression of TLR4 and MyD88.Cell Viability Assay Cell Line:BV-2 microglia cell Concentration:0, 10, 15, and 20 μM Incubation Time:1 h and co-cultured in the absence or presence of 100 ng/ mL LPS for 24 hResult:Had no cytotoxicity.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number80510-06-1
-
Formula Weight624.69
-
Molecular FormulaC36H36N2O8
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
PIN1 inhibitor API-1
PIN1 inhibitor API-1 is a specific Pin1 inhibitor (IC50: 72.3 nM). PIN1 inhibitor API-1 retains the active conformation of pXPO5 and restores the ability of pXPO5 to transport pre-miRNAs from the nucleus to cytoplasm, thus up-regulating the anticancer miRNA biogenesis to suppress both in vitro and in vivo hepatocellular carcinoma development.
-
Rosamultin
Rosamultin has antioxidant antiinflammatory/antinociceptive propertiesand has anti-human immunodeficiency virus (HIV) activity.
-
Perflexane
Perflexane was developed as an ultrasound contrast agent.