Biological Activity
Less active enantiomer of the PDE4 inhibitor rolipram (Cat. No. 0905). (R)-(-)-Rolipram (Cat. No. 1349) also available.
Technical Data
M. Wt | 275.35 |
Formula | C16H21NO3 |
Storage | Store at RT |
Purity | ≥99% (HPLC) |
CAS Number | 85416-73-5 |
PubChem ID | 158758 |
InChI Key | HJORMJIFDVBMOB-GFCCVEGCSA-N |
Smiles | O=C1NC[C@H](C2=CC(OC3CCCC3)=C(OC)C=C2)C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 27.54 | 100 |
Preparing Stock Solutions
The following data is based on the product molecular weight 275.35. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.63 mL | 18.16 mL | 36.32 mL |
5 mM | 0.73 mL | 3.63 mL | 7.26 mL |
10 mM | 0.36 mL | 1.82 mL | 3.63 mL |
50 mM | 0.07 mL | 0.36 mL | 0.73 mL |
Molarity Calculator
Reconstitution Calculator
Dilution Calculator
Product Datasheets
References
References are publications that support the products' biological activity.
Ohsawa et al (1998) Inhibitory effects of rolipram on partially purified phosphodiesterase 4 from rat brains. Jpn.J.Pharmacol. 77 147 PMID: 9681571
Owens et al (1997) Human phosphodiesterase 4A: characterization of full-length and truncated enzymes expressed in COS cells. Biochem.J. 326 53 PMID: 9337850
Schneider et al (1986) Stereospecific binding of the antidepressant rolipram to brain protein structures. Eur.J.Pharmacol. 127 105 PMID: 3019721
Keywords: (S)-(+)-Rolipram, supplier, PDE4, inhibitors, inhibits, Phosphodiesterases, Phosphodiesterases, Phosphodiesterases, Tocris Bioscience