Sanguinarine
CAS No. 2447-54-3
Sanguinarine( Synthetic thyrotropin-releasing factor | TSH-RF | pGlu-His-Pro-NH2 )
Catalog No. M18300 CAS No. 2447-54-3
Sanguinarine is a specific inhibitor of Rac1b with anti-microbial, anti-oxidant and anti-inflammatory properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 156 | In Stock |
|
| 10MG | 232 | In Stock |
|
| 25MG | 393 | In Stock |
|
| 50MG | 565 | In Stock |
|
| 100MG | 800 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSanguinarine
-
NoteResearch use only, not for human use.
-
Brief DescriptionSanguinarine is a specific inhibitor of Rac1b with anti-microbial, anti-oxidant and anti-inflammatory properties.
-
DescriptionSanguinarine is a specific inhibitor of Rac1b with anti-microbial, anti-oxidant and anti-inflammatory properties.
-
In VitroSanguinarine (SANG)-induced apoptosis is associated with the activation of JNK and NF-κB signal pathways.To determine the effects of Sanguinarine on cell viability, 22B-cFluc cells are stimulated with different concentrations of Sanguinarine for 24 h, and then a CKK-8 assay is performed. The treatment with Sanguinarine decreases the proliferation of 22B cells in a dose-dependent manner. Meanwhile, the cytosolic extracts of 22B-cFluc cells treated with different dose of Sanguinarine are measured to detect cellular caspase-3 activity using Ac-DEVD-pNA, which is a validated caspase-3 substrate. The absorbance at 450 nm increases in a dose-dependent manner, indicating increased caspase-3 activity stimulated by Sanguinarine.
-
In VivoTo evaluate the apoptosis induced by Sanguinarine (SANG) in vivo, 22B-cFluc cells are inoculated subcutaneously into one flank of nude mice and xenograft models are allowed to establish. Mice are treated intravenously with 10 mg/kg of Sanguinarine. At 24, 48 and 72 h after treatment, bioluminescent imaging is performed after i.p. injection of mice with 150 mg/kg of D-luciferin substrate. Sanguinarine treatment induces an obvious increase of luminescent signal as early as 48 h after initial treatment. A sustained bioluminescent imaging (BLI) intensity increased is observed throughout the course of experiment. At 72 h after treatment, the tumors are collected and subjected to TUNEL staining for evaluating apoptosis. Compared with the control tumors, the group treated with Sanguinarine exhibits significantly more cell apoptosis, indicated by the increased green signals from the sporadic apoptotic cells.
-
SynonymsSynthetic thyrotropin-releasing factor | TSH-RF | pGlu-His-Pro-NH2
-
PathwayOthers
-
TargetOther Targets
-
RecptorAntioxidant
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number2447-54-3
-
Formula Weight332.33
-
Molecular FormulaC20H14NO4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC[n+]1c2c(c3ccc4c(c3c1)OCO4)ccc1cc3c(cc21)OCO3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Mehra P, et al. Indian J Exp Biol. 2013 Oct;51(10):823-7.
molnova catalog
related products
-
MFCD28987368
MFCD28987368 is a chemical compound.
-
α-Neoendorphin 1-8
α-Neoendorphin (1-8) is a 8-amino acid peptide derived from the N-terminal of α-Neoendorphin. α-Neoendorphin is an endogenous opioid peptide and is a part for the neoendorphins which are a group of endogenous opioid peptides derived from the proteolytic cleavage of prodynorphin isolated from procine hypothalmus and pituitary.
-
Cyclo(Pro-Ala)
Cyclo(Pro-Ala) is a natural product.
Cart
sales@molnova.com