F16
CAS No. 36098-33-6
F16( (E)-4-(3-indolylvinyl)-N-methylpyridinium iodide )
Catalog No. M26683 CAS No. 36098-33-6
F16 inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 27 | Get Quote |
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| 10MG | 42 | Get Quote |
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| 25MG | 87 | Get Quote |
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| 50MG | 159 | Get Quote |
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| 100MG | 232 | Get Quote |
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| 200MG | 350 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameF16
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NoteResearch use only, not for human use.
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Brief DescriptionF16 inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.
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DescriptionF16 inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.(In Vitro):F16 arrests the cell cycle and increases apoptosis in F16-sensitive EpH4-A6 cells. F16 (3 μM) influences growth in human and mice cancer cell lines. F16 shows mitochondriotoxic property and triggers apoptosis or necrosis depending on the genetic background of the target carcinoma cell.
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In VitroF16 (3 μM; 3 days/7 days) affects growth in several mouse and human cancer cell lines.F16 arrests cell cycle and increases apoptosis in F16-sensitive EpH4-A6 cells. Cell Proliferation Assay Cell Line:MDA-MB231, MDA-MB435, MDA-MB436, MDA-MB453, MDA-MB-468, SKBR-3, MCF-7, T47D, ZR-75-1 cells and mouse mammary epithelial cell line NMuMGConcentration:3 μM Incubation Time:3 days/7 days Result:Displayed antiproliferative activity against both mouse and human breast cancer cells. The growth of the mouse fibrosarcoma cell lines derived from ras-transgenic mice was not affected.
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In Vivo——
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Synonyms(E)-4-(3-indolylvinyl)-N-methylpyridinium iodide
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PathwayOthers
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TargetOther Targets
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RecptorIGF-1R| P-Akt (S473)| P-Akt (T308)| S6 Kinase
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Research Area——
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Indication——
Chemical Information
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CAS Number36098-33-6
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Formula Weight362.21
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Molecular FormulaC16H15IN2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 31 mg/mL (85.59 mM)
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SMILES[I-].C[n+]1ccc(\C=C\c2c[nH]c3ccccc23)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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R121919
R121919 (NBI30775) is a potent small molecule antagonist of the adrenocorticotropic hormone-releasing factor receptor 1 (CRF1), demonstrating antidepressant and anxiolytic activity, and inhibiting the CRF1 receptor, CRF2 receptor, and CRF-binding proteins.
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DPPS
DPPS (12-Dipalmitoyl-sn-glycero-3-PS sodium salt) is an anionic diacyl-phospholipid, a form of phosphatidylserine (PS), which is a negatively charged phospholipid located in the lobules of cell membranes. DPPS are used to make cationic vesicles and liposomes.
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Isothymusin
Isothymusin( MIC= 200 microg/mL) exhibits inhibition activity against Mycobacterium tuberculosis. It ( IC50=7.7 microg/mL ) exhibits antioxidant activity against the radical scavenging ability of DPPH.
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