Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H26F2N2O2S |
| Molecular Weight | 420.516 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=O)[C@H](CN1CCC2(CC1)OCCC3=C2SC(F)=C3)CC4=CC=CC=C4F
InChI
InChIKey=MZBCQWLYUQJXKA-KRWDZBQOSA-N
InChI=1S/C22H26F2N2O2S/c1-25-21(27)17(12-15-4-2-3-5-18(15)23)14-26-9-7-22(8-10-26)20-16(6-11-28-22)13-19(24)29-20/h2-5,13,17H,6-12,14H2,1H3,(H,25,27)/t17-/m0/s1
| Molecular Formula | C22H26F2N2O2S |
| Molecular Weight | 420.516 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
11C-NOP-1A is a new radioligand for thenociceptin/orphanin FQ peptide (NOP) receptor, with high affinity (Ki, 0.15 nM) and appropriate lipophilicity (measured logD, 3.4) for PET brain imaging. 11C-NOP-1A is the the first successful radioligand to image NOP receptors in rat and monkey brain. 11C-NOP-1A is a selective antagonist at the NOP receptor and has high affinity and appropriate lipophilicity for blood–brain barrier permeability. 11C-NOP-1A imaging in rhesus monkeys showed high brain uptake and a large receptor-specific signal and could be quantified with the gold standard method of compartmental modeling. In humans 1C-NOP-1A reliably quantified NOP receptors in human brain both in large brain regions and at a voxelwise level using parametric imaging. The radiation absorbed dose in humans was similar to that observed with other 11C-labeled ligands and would allow multiple scans of a single subject. Thus, 11C-NOP-1A is a promising radioligand for reliably quantifying NOP receptors in human brain.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nociceptin Receptors Upregulated in Cocaine Use Disorder: A Positron Emission Tomography Imaging Study Using [11C]NOP-1A. | 2019-06-01 |
|
| Retest imaging of [11C]NOP-1A binding to nociceptin/orphanin FQ peptide (NOP) receptors in the brain of healthy humans. | 2014-02-15 |
|
| Brain and whole-body imaging of nociceptin/orphanin FQ peptide receptor in humans using the PET ligand 11C-NOP-1A. | 2012-03 |
|
| Brain and whole-body imaging in rhesus monkeys of 11C-NOP-1A, a promising PET radioligand for nociceptin/orphanin FQ peptide receptors. | 2011-10 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22312136
After intravenous injection of 11C-NOP-1A, 7 healthy subjects underwent brain PET for 2 h and serial sampling of radial arterial blood to measure parent radioligand concentrations. The radioligand was obtained with high radiochemical purity (>99%) and aspecific activity of 213 ± 100 GBq/umol at the time of injection. The injected mass dose of 11C-NOP-1A was 53 ± 36 pmol/kg. The effective dose of 11C-NOP-1A (4.3 uSv/MBq) estimated from whole-body scans inhumans was similar to previous estimates (5 uSv/MBq) from monkey studies and tothose of 34 other 11C-radioligands used for brain imaging, which ranged from 3 to 16 uSv/MBq.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21880575
11C-NOP-1A is a new radioligand for the nociceptin/orphanin FQ peptide (NOP) receptor, with high affinity (Ki, 0.15 nM) and appropriate lipophilicity (measured logD, 3.4) for PET brain imaging.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:53:09 GMT 2025
by
admin
on
Mon Mar 31 21:53:09 GMT 2025
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| Record UNII |
DQY244459T
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| Record Status |
Validated (UNII)
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| Record Version |
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