ZINC69391
CAS No. 303094-67-9
ZINC69391( ZINC-69391 | N'-(4,6-dimethylpyrimidin-2-yl)-N-[2-(trifluoromethyl)phenyl]guanidine )
Catalog No. M27796 CAS No. 303094-67-9
ZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 192 | Get Quote |
|
| 10MG | 312 | Get Quote |
|
| 25MG | 530 | Get Quote |
|
| 50MG | 758 | Get Quote |
|
| 100MG | 1044 | Get Quote |
|
| 500MG | 2097 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameZINC69391
-
NoteResearch use only, not for human use.
-
Brief DescriptionZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.
-
DescriptionZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.(In Vitro):In U-87 MG and LN229 cells, ZINC69391 (0-125 μM) reduces cell proliferation of human glioma cells. ZINC69391 (50-100 μM) triggers cell cycle arrest. ZINC69391 inhibits the growth of U937, HL-60, KG1A, and Jurkat cells (IC50s = 41-54 μM). In HL-60, U937, and KG1A cell lines, ZINC69391 (50 μM) triggers an increase in apoptotic cells. In LN229 cells, ZINC69391 (50 and 100 μM) augments the enzymatic activity of caspase 3 and increases the percentage of cells in the sub-G0/G1 phase in a concentration-dependent manner.(In Vivo):In specific pathogen-free female BALB/c inbred mice (bearing F3II cells), ZINC69391 (25 mg/kg; i.p) impairs metastatic lung colonization and reduces by about 60% the formation of total metastatic lung colonies.
-
In VitroZINC69391 inhibits growth of U937, HL-60, KG1A and Jurkat cells with IC50s ranging from 41 to 54 μM.ZINC69391 (50-100 μM; 24 hours) augments the enzymatic activity of caspase 3 in a concentration dependent manner.ZINC69391 (0-125 μM; 72h) reduces cell proliferation of human glioma cells.ZINC69391 (50-100 μM; 48 hours) triggers cell cycle arrest.ZINC69391 (50 μM; 24 hours) triggers apoptosis on human acute leukemic cells. Cell Proliferation Assay Cell Line:U-87 MG, LN229 cells Concentration:0-125μM Incubation Time:72 hours Result:Reduced cell proliferation in a concentration-dependent manner.Cell Cycle Analysis Cell Line:LN229 cells Concentration:50, 100 μM Incubation Time:48 hours Result:Resulted in a significant increased percentage of cells in the sub-G0/G1 phase in a concentration dependent manner.Apoptosis Analysis Cell Line:HL-60, U937 and KG1A cell lines Concentration:50 μM Incubation Time:24 hours Result:Led to a significant increase in apoptotic cells.
-
In VivoZINC69391 (25 mg/kg; i.p; daily for 21 days) impairs metastatic lung colonization in a syngeneic animal model. Animal Model:Specific pathogen-free female BALB/c inbred mice (bearing F3II cells)Dosage:25 mg/kg body weight Administration:I.p; daily for 21 days Result:Significantly reduced by about 60% the formation of total metastatic lung colonies.
-
SynonymsZINC-69391 | N'-(4,6-dimethylpyrimidin-2-yl)-N-[2-(trifluoromethyl)phenyl]guanidine
-
PathwayApoptosis
-
TargetApoptosis
-
RecptorEGFR|EGFR (L858R)|EGFR (L858R/T790M)|EGFR (L858R/T790M/C797S)
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number303094-67-9
-
Formula Weight309.296
-
Molecular FormulaC14H14F3N5
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 25 mg/mL (80.83 mM)
-
SMILESCc1cc(C)nc(NC(=N)Nc2ccccc2C(F)(F)F)n1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
3-O-Methylgallic aci...
3,4-Dihydroxy-5-methoxybenzoic acid reduces cell proliferation in Caco-2 cells(IC50 = 24.1 μM) more effectively than anthocyanins and may offer protection against colon cancer after its formation in the gut. 3,4-Dihydroxy-5-methoxybenzoic acid inhibits transcription factors NF-κB, AP-1, STAT-1, and OCT-1 which are known to be activated in colorectal cancer.
-
5-Benzylidene-3-ethy...
5-Benzylidene-3-ethyl rhodanine(BTR-1) is an active anti-cancer agent. BTR-1 activates apoptosis and induces cell death.
-
Exisulind
Exisulind induces apoptosis through the activation of protein kinase G (PKG). Exisulind exhibits antineoplastic activity in solid tumour and haematological cancer cell lines and is an inhibitor of tumour growth in rodent models of colon, prostate, bladder, mammary and lung cancer.
Cart
sales@molnova.com