D-64131
Tocris Bioscience | Catalog # 1643
Key Product Details
Description
Product Description
D-64131 is a novel inhibitor of tubulin polymerization; cytotoxic and inhibits tumor cell proliferation in vitro (IC50 = 74 nM). Prevents growth of tumor models in mice following oral administration in vivo.
Product Specifications for D-64131
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 25.13 | 100 | |
| Ethanol | 5.03 | 20 |
Preparing Stock Solutions for D-64131
The following data is based on the product molecular weight 251.28.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.98 mL | 19.90 mL | 39.80 mL |
| 5 mM | 0.80 mL | 3.98 mL | 7.96 mL |
| 10 mM | 0.40 mL | 1.99 mL | 3.98 mL |
| 50 mM | 0.08 mL | 0.40 mL | 0.80 mL |
Calculators
Background References
References are publications that support the biological activity of the product.
- Mahboobi Synthetic 2-aroylindole derivatives as a new class of potent tubulin-inhibitory, antimitotic agents. J.Med.Chem. 2001 PMID: 11741473
- Beckers 2-aroylindoles, a novel class of potent, orally active small molecule tubulin inhibitors. Cancer Res. 2002 PMID: 12036922
Product Documents for D-64131
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for D-64131
For research use only
Related Research Areas
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Species: HumanVerified Customer | Posted 12/23/2019The antitumoral efficacy of D-64131 in comparison to paclitaxel and vincristine was evaluated in resistance mediated by the MRP and in human tumor cells with resistance to cisplatin, the topoisomerase I inhibitor SN-38 (7-ethyl-10-hydroxycamptothecin) and the thymidylate synthase inhibitors 5-fluorouracil and raltitexed.
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