CID 755673
Tocris Bioscience | Catalog # 3327
Key Product Details
Description
Product Description
CID 755673 is a selective protein kinase D (PKD) inhibitor (IC50 values are 0.182, 0.280, 0.227, >10, 15.3, 20.3, 40.5 and >50 μM at PKD1, PKD2, PKD3, PKC, CAK, PLK1, CAMKIIα and Akt respectively). Blocks PKD-mediated protein transport and inhibits prostate cancer cell proliferation, migration and invasion in vitro.
Product Specifications for CID 755673
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 | 21.72 | 100 |
Preparing Stock Solutions for CID 755673
The following data is based on the product molecular weight 217.22.
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 | 4.60 mL | 23.02 mL | 46.04 mL |
| 5 mM | 0.92 mL | 4.60 mL | 9.21 mL |
| 10 mM | 0.46 mL | 2.30 mL | 4.60 mL |
| 50 mM | 0.09 mL | 0.46 mL | 0.92 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 40 publications citing the usage of this product.
- Sharlow Potent and selective disruption of protein kinase D functionality by benzoxoloazepinolone. J.Biol.Chem. 2008 PMID: 18829454
Product Documents for CID 755673
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 CID 755673
For research use only
Citations for CID 755673
Customer Reviews for CID 755673 (1)
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Customer Images
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Species: HumanVerified Customer | Posted 01/16/2020Effect of CID 755673 on PKD has been under observation. Changes in the FRET ratio from COS-7 cells expressing the kinase activity reporter, DKAR, following activation of endogenous PKD (light blue diamonds) or overexpressed PKD (dark blue diamonds) via 200 nM PDBu treatment and subsequent PKD inhibition with the non-competitive CID 755673 (50 μM).
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