Suprafenacine
CAS No. 1477482-50-0
Suprafenacine( N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide )
Catalog No. M27928 CAS No. 1477482-50-0
Suprafenacine is a cell-permeable microtubule destabilizer that induces cell cycle arrest and apoptosis in G2/M phase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 129 | In Stock |
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| 2MG | 78 | In Stock |
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| 5MG | 126 | In Stock |
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| 10MG | 179 | In Stock |
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| 25MG | 321 | In Stock |
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| 50MG | 442 | In Stock |
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| 100MG | 625 | In Stock |
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| 200MG | 826 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameSuprafenacine
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NoteResearch use only, not for human use.
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Brief DescriptionSuprafenacine is a cell-permeable microtubule destabilizer that induces cell cycle arrest and apoptosis in G2/M phase.
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DescriptionSuprafenacine is a cell-permeable microtubule destabilizer that induces cell cycle arrest and apoptosis in G2/M phase. Suprafenacine binds to microtubules and inhibits aggregation at the colchicine junction. Suprafenacine is selective for cancer cells, including drug-resistant cancer cells.
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In Vitro——
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In Vivo——
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SynonymsN'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide
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PathwayCytoskeleton/Cell Adhesion Molecules
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TargetMicrotubule/Tubulin
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Recptorβ2-adrenergic receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number1477482-50-0
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Formula Weight282.347
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Molecular FormulaC16H18N4O
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Purity>98% (HPLC)
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Solubility——
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SMILESCc1ccc(\C=N\NC(=O)c2n[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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Vinflunine ditartrat...
Vinflunine ditartrate is the first fluorinated microtubule inhibitor belonging to the Vinca alkaloids family. Vinflunine ditartrate has anti-angiogenic, vascular-disrupting and anti-metastatic activities.
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Taccalonolide B
Taccalonolide B is effective in vitro against cell lines that overexpress P-glycoprotein (Pgp) and multidrug-resistance protein (MRP7).?Taccalonolide B inhibits growth of SK-OV-3 cells with an IC50 of 208 nM.The structures were elucidated using a combination of spectroscopic methods, including 1D and 2D NMR and HR-ESI-MS.
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ATM-3507
ATM-3507 (ATM3507) is a small molecule inhibitor of Tpm3.1 tropomyosin isoform, disrupts Tpm3.1-containing microfilaments in SK-N-SH cells at 5 uM.
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