Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H23NO3 |
Molecular Weight | 325.4015 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCC(CC1)OC(=O)C(O)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=UGYPGJCVNPPUPE-UHFFFAOYSA-N
InChI=1S/C20H23NO3/c1-21-14-12-18(13-15-21)24-19(22)20(23,16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-11,18,23H,12-15H2,1H3
Molecular Formula | C20H23NO3 |
Molecular Weight | 325.4015 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Cloned M1 muscarinic receptors mediate both adenylate cyclase inhibition and phosphoinositide turnover. | 1988 Oct |
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Evaluation of novel PET ligands (+)N-[11C]methyl-3-piperidyl benzilate ([11C](+)3-MPB) and its stereoisomer [11C](-)3-MPB for muscarinic cholinergic receptors in the conscious monkey brain: a PET study in comparison with. | 2001 Feb |
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Age-related changes in muscarinic cholinergic receptors in the living brain: a PET study using N-[11C]methyl-4-piperidyl benzilate combined with cerebral blood flow measurement in conscious monkeys. | 2001 Oct 19 |
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Discrepancy between cell injury and benzodiazepine receptor binding after transient middle cerebral artery occlusion in rats. | 2004 Sep 15 |
|
Binding kinetics of 11C-N-methyl piperidyl benzilate (11C-NMPB) in a rhesus monkey brain using the cerebellum as a reference region. | 2005 Sep |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:51:44 UTC 2023
by
admin
on
Fri Dec 15 17:51:44 UTC 2023
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Record UNII |
QWK86805EB
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID20189664
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77157
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222-774-0
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