
Picrasidine Q
CAS No. 101219-61-8
Picrasidine Q( —— )
Catalog No. M31232 CAS No. 101219-61-8
Picrasidine Q has the capacity of anti-cell transformation and anti-cancer, it might be a chemopreventive and chemotherapeutic agent by direct targeting FGFR2 and inhibiting cell proliferation of ESCC cells.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
10MG | 380 | In Stock |
![]() ![]() |
50MG | Get Quote | In Stock |
![]() ![]() |
100MG | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NamePicrasidine Q
-
NoteResearch use only, not for human use.
-
Brief DescriptionPicrasidine Q has the capacity of anti-cell transformation and anti-cancer, it might be a chemopreventive and chemotherapeutic agent by direct targeting FGFR2 and inhibiting cell proliferation of ESCC cells.
-
DescriptionPicrasidine Q has the capacity of anti-cell transformation and anti-cancer, it might be a chemopreventive and chemotherapeutic agent by direct targeting FGFR2 and inhibiting cell proliferation of ESCC cells.
-
In VitroPicrasidine Q (0~60 μM; 3 hours; ESCC cells) suppresses downstream signaling of FGFR2 in ESCC cells.Picrasidine Q (0~60 μM; 48 and 72 hours; ESCC cells) induces cell cycle arrest and apoptosis.Picrasidine Q (0~60 μM; 24~72 hours; ESCC cells) suppresses the growth of ESCC cells.Picrasidine Q (0~60 μM; 30 minutes; JB6Cl41 cells) inhibits proliferation by inhibition of G1/S cell cycle transition.Picrasidine Q (12.5, 25 or 50 μM) can inhibit the FGFR2 kinase activity in a dose-dependent manner. Western Blot Analysis Cell Line:ESCC cells Concentration:0~60 μM Incubation Time:3 hours Result:Suppressed downstream signaling of FGFR2 in ESCC cells.Apoptosis Analysis Cell Line:ESCC cells Concentration:0~60 μM Incubation Time:48 and 72 hours Result:Induced cell cycle arrest and apoptosis.Cell Cytotoxicity Assay Cell Line:ESCC cells Concentration:0~60 μM Incubation Time:24~72 hours Result:Suppressed the growth of ESCC cells.Cell Cycle Analysis Cell Line:JB6Cl41 cells Concentration:0~60 μM Incubation Time:30 minutes Result:Inhibited proliferation by inhibition of G1/S cell cycle transition.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number101219-61-8
-
Formula Weight266.3
-
Molecular FormulaC15H10N2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog



related products
-
Rel-TREM2 agonist-2
rel-5-(4-Chloro-2-fluorophenyl)-2,3-dimethyl-7-[(2R,4S)-tetrahydro-2-(1-methyl-1H-pyrazol-4-yl)-2H-pyran-4-yl]pyrido[3,4-b] The EC50 value of pyrazine against TREM2 was ≤ 0.05 μM and the E.max value was > 250 μM.
-
Gardoside methyl est...
The herbs of Duranta repens.
-
Lirequinil
Lirequinil (Ro 41-3696) is a small molecule GABAA receptor agonist utilized in the study of neurological disorders.