Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H12O2 |
| Molecular Weight | 152.1904 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCCC1=CC=C(O)C=C1
InChI
InChIKey=NJCVPQRHRKYSAZ-UHFFFAOYSA-N
InChI=1S/C9H12O2/c10-7-1-2-8-3-5-9(11)6-4-8/h3-6,10-11H,1-2,7H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Autoradiographic analysis of mouse brain kinin B1 and B2 receptors after closed head trauma and ability of Anatibant mesylate to cross the blood-brain barrier. | 2006-05 |
|
| Evidence of a new biotransformation pathway of p-coumaric acid into p-hydroxybenzaldehyde in Pycnoporus cinnabarinus. | 2001-12 |
|
| Potent inhibition of CYP2D6 by haloperidol metabolites: stereoselective inhibition by reduced haloperidol. | 2001-01 |
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1DJM7P148S
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DTXSID80144638
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10210-17-0
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233-511-4
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82452
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SUBSTANCE RECORD
