CID 797718
CID 797718 Basic information
- Product Name:
- CID 797718
- Synonyms:
-
- 9-HYDROXY-3,4-DIHYDRO-1H-CHROMENO[3,4-B]PYRIDIN-5(2H)-ONE
- CID 797718
- CID 797718, >=98%
- CID-797718;CID797718
- CS-1341
- CID 797718, 370586-05-3
- 9-HYDROXY-1,2,3,4-TETRAHYDROCHROMENO[3,4-B]PYRIDIN-5-ONE
- 9-Hydroxy-1H,2H,3H,4H-chromeno[3,4-b]pyridin-5-one
- CAS:
- 370586-05-3
- MF:
- C12H11NO3
- MW:
- 217.22
- Product Categories:
-
- Inhibitors
- Mol File:
- 370586-05-3.mol
CID 797718 Chemical Properties
- Melting point:
- 213-216 °C(Solv: isopropanol (67-63-0))
- Boiling point:
- 517.6±50.0 °C(Predicted)
- Density
- 1.43±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: 30 mg/ml; DMSO: 20 mg/ml; Ethanol: 1 mg/ml
- form
- A crystalline solid
- pka
- 9.39±0.20(Predicted)
- color
- Light brown to brown
CID 797718 Usage And Synthesis
Description
CID797718 is a protein kinase D1 (PKD1) inhibitor (IC50 = 7 μM). It also inhibits CDK activating kinase (CAK) and polo-like kinase 1 (PLK1) but has no activity at AKT (IC50s = 8.4, 21.9, and >50 μM, respectively). CID797718 inhibits PKD1 activity in LNCaP cells with an IC50 value of 0.21 μM. CID797718 is a byproduct in the synthesis of CID755673 .
Uses
CID-797718 is a compound with ambiguous properties.
References
[1] ELIZABETH R SHARLOW. Potent and selective disruption of protein kinase D functionality by a benzoxoloazepinolone.[J]. The Journal of Biological Chemistry, 2008, 283 48: 33516-33526. DOI: 10.1074/jbc.m805358200
[2] COURTNEY R LAVALLE. Novel protein kinase D inhibitors cause potent arrest in prostate cancer cell growth and motility.[J]. BMC chemical biology, 2010, 10: 5. DOI: 10.1186/1472-6769-10-5
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