Fangchinoline
CAS No. 436-77-1
Fangchinoline( —— )
Catalog No. M17509 CAS No. 436-77-1
Fangchinoline is extracted from Stephania tetrandra S. Moore.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 39 | Get Quote |
|
| 10MG | 56 | Get Quote |
|
| 25MG | 87 | Get Quote |
|
| 50MG | 133 | Get Quote |
|
| 100MG | 200 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameFangchinoline
-
NoteResearch use only, not for human use.
-
Brief DescriptionFangchinoline is extracted from Stephania tetrandra S. Moore.
-
DescriptionFangchinoline is extracted from Stephania tetrandra S. Moore.(In Vitro):Fangchinoline (2.5-40 μM; 24-96 hours) inhibits both T24 and 5637 cells in dose-dependent manner, the IC50 values of Fangchinoline in T24 cells are 19.0 μM (24 h), 12.0 μM (48 h) and 7.57 μM (72 h), and 11.9 μM (24 h), 9.92 μM (48 h) and 7.13 μM (72 h) in 5637 cells.Fangchinoline (5 μM; 24 hours) induces a significant increase in the LC3-II/LC3-I ratio and a decrease in p62 in both T24 and 5637 cells, and causes a significant increase in the cleavage of caspase-3.
-
In VitroFangchinoline (2.5-40 μM; 24-96 hours) inhibits both T24 and 5637 cells in dose-dependent manner, the IC50 values of Fangchinoline in T24 cells are 19.0 μM (24 h), 12.0 μM (48 h) and 7.57 μM (72 h), and 11.9 μM (24 h), 9.92 μM (48 h) and 7.13 μM (72 h) in 5637 cells.Fangchinoline (5 μM; 24 hours) induces a significant increase in the LC3-II/LC3-I ratio and a decrease in p62 in both T24 and 5637 cells, and causes a significant increase in the cleavage of caspase-3. Cell Viability AssayCell Line:T24 and 5637 cells Concentration:2.5 μM; 5 μM; 10 μM; 20 μM; 30 μM; 40 μM Incubation Time:24 hours; 48 hours; 96 hours Result:Inhibited both T24 and 5637 cells proliferation.Western Blot Analysis Cell Line:T24 and 5637 cells Concentration:5 μM Incubation Time:24 hours Result:Incresed LC3-II/LC3-I ratio and the cleavage of caspase-3.
-
In Vivo——
-
Synonyms——
-
PathwayNeuroscience
-
TargetGluR
-
RecptorFAK
-
Research AreaOthers-Field
-
Indication——
Chemical Information
-
CAS Number436-77-1
-
Formula Weight608.72
-
Molecular FormulaC37H40N2O6
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 50 mg/mL (82.14 mM)
-
SMILESO1c2c3[C@@H](N(CCc3cc(OC)c2O)C)Cc2cc(Oc3ccc(C[C@@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Guo B, et al. J Drug Target. 2015 Apr;23(3):266-74.
molnova catalog
related products
-
cis-PDA
cis-PDA is a general ionotropic receptor antagonist. cis-PDA acts by blocking NMDA, AMPA, and kainate-mediated responses.
-
CBiPES hydrochloride
CBiPES hydrochloride (CBiPES HCl) is a potent orthosteric modulator of the mGlu2 receptor with an EC50 value of 92.8 nM.CBiPES hydrochloride blocks the action of WT and mGlu(3) receptors.
-
VU0650786
VU0650786 is a selective and potent CNS penetrant negative allosteric modulator of metabotropic glutamate receptor subtype 3 (mGlu3 NAM) (IC50: 392 nM).
Cart
sales@molnova.com