Weight | 212.248 g/mol |
---|---|
Formula | C14H12O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
2-Benzyloxybenzaldehyde (5896-17-3)
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- Investigation of the cellular mechanism of inhibition of formyl-methionyl-leucyl-phenylalanine-induced superoxide anion generation in rat neutrophils by 2-benzyloxybenzaldehyde (Biochemical Pharmacology, 2003)
- 2-Benzyloxybenzaldehyde inhibits formyl-methionyl-leucyl-phenylalanine stimulation of phospholipase D activation in rat neutrophils. (Biochimica et Biophysica Acta, 2002)
- 2-Benzyloxybenzaldehyde inhibits formyl peptide-stimulated increase in intracellular Ca2+ in neutrophils mainly by blocking Ca2+ entry (Naunyn-schmiedebergs Archives of Pharmacology, 2004)
- In vivo evaluation of the synthesized novel 2-benzyloxybenzaldehyde analog CCY-1a-E2 for the treatment of leukemia in the BALB/c mouse WEHI-3 allograft model (Oncology Letters, 2013)
- 2-Benzyloxybenzaldehyde dialkyl acetals, their preparation and use. (1990)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)COC2=CC=CC=C2C=O
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InChIKeyPBEJTRAJWCNHRS-UHFFFAOYSA-N
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