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Protein Inhibitors
- Protein Control Ligand
- Pathway Inhibitors
- Enzyme Inhibitors
- Kinase Inhibitors
- Protease
- Synthase
- p18
- p38
- p53
- p70
- p90
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- Hydroxylases
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- Adenosine Deaminase
- Clathrin
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- p68
- ACE
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- DHFR
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- Reductase
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- Topoisomerase
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- Transporter Inhibitors
- Cell Inhibition
- Synthase
- Receptor Tyrosine Phosphatases (RTP)
- AChE
- Peptidase
- Autophagy
- Toll-Like Receptor (TLR)
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- Function Modulators
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- G Protein-Coupled Receptor Ligands
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- CCK Receptors
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- EAA Receptors
- Ghrelin Receptors
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- Ryanodine receptor
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- Imidazoline receptor
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View larger Quantity Discount Table - Order More To Get More Price Discount
| Quantity | mg | Unit Price ($/mg or $/Unit) | Final Price |
|---|---|---|---|
| 1 | 100 | $36.90 | Total: $3,690.00 |
| 1 | 50 | $42.64 | Total: $2,132.00 |
| 1 | 25 | $50.02 | Total: $1,250.50 |
| 1 | 10 | $59.04 | Total: $590.40 |
| 1 | 5 | $69.70 | Total: $348.50 |
Data sheet
| Molecular Formula | C16H18N4O |
| Molecular Weight | 282.34 |
| CAS Numbers | 1477482-50-0 |
| Storage Condition | 0C Short Term, -20C Long Term |
| Solubility | DMSO |
| Purity | 98% by HPLC |
| SMILES Code | CC1=CC=C(C=NNC(=O)C2=NNC3=C2CCCC3)C=C1 |
| References | Choi BH, Chattopadhaya S, Thanh le N, Feng L, Nguyen QT, Lim CB, Harikishore A, Nanga RP, Bharatham N, Zhao Y, Liu X, Yoon HS. Suprafenacine, an indazole-hydrazide agent, targets cancer cells through microtubule destabilization. PLoS One. 2014 Oct 29;9[10] e110955. |
More info
Suprafenacine (N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide) is a cell-permeable microtubule destabilizer that induces cell cycle arrest and apoptosis in G2M phase. Suprafenacine binds to microtubules and inhibits aggregation at the colchicine junction. Suprafenacine is selective for cancer cells, including drug-resistant cancer cells.