[go: up one dir, main page]

Ötvös et al., 1995 - Google Patents

Synthesis of high specific activity [15, 16‐3H2] buprenorphine

Ötvös et al., 1995

Document ID
8571386947524086286
Author
Ötvös F
Hosztafi S
Simon C
Tóth G
Publication year
Publication venue
Journal of Labelled Compounds and Radiopharmaceuticals

External Links

Snippet

Tritium labelling of buprenorphine, a mixed agonist‐antagonist opioid ligand, was performed with a specific activity of 2.35 TBq/mmol (63.6 Ci/mmol) starting with 15, 16‐ didehydrobuprenorphine. Labels at positions 15 and 16 of the morphine skeleton proved to …
Continue reading at analyticalsciencejournals.onlinelibrary.wiley.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D489/00Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
    • C07D489/06Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with a hetero atom directly attached in position 14
    • C07D489/08Oxygen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2103/00Systems containing at least three condensed rings
    • C07C2103/02Ortho- or ortho- and peri-condensed systems
    • C07C2103/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2103/06Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2103/10Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof

Similar Documents

Publication Publication Date Title
Pert et al. Properties of opiate-receptor binding in rat brain
AU668721B2 (en) Biologically active tropane derivatives
US4775759A (en) Synthesis and utilization of 17-methyl and 17-cyclopropylmethyl-3,14-dihydroxy-4,5α-epoxy 6β-fluoromorphinans (foxy and cyclofoxy) as (18F)-labeled opioid ligands for position emission transaxial tomography (PETT)
Maryanoff et al. Potential affinity labels for the opiate receptor based on fentanyl and related compounds
Ötvös et al. Synthesis of high specific activity [15, 16‐3H2] buprenorphine
FI75337B (en) FOERFARANDE FOR FRAMSTAELLNING AV 9- (3-ISOPROPYLAMINOPROPYL) -9-CARBAMOYLFLUOREN, SAMT NY MELLANPRODUKT.
Wyrick et al. Tritium labelled (±)‐7‐chloro‐8‐hydroxy‐3‐methyl‐1‐phenyl‐2, 3, 4, 5‐tetrahydro‐1H‐3‐benzazepine (SCH23390)
CN114438532A (en) Method for synthesizing di-deuterated hydrocarbon by using de-deuterated aldehyde ketone
WO2016014864A1 (en) Hydroxy-(r)-2,2&#39;-bismethylnal trexones and uses thereof
Zlotos et al. Bisquaternary dimers of strychnine and brucine. A new class of potent enhancers of antagonist binding to muscarinic M2 receptors
Lever et al. Radiosynthesis of a photoaffinity probe for the cocaine receptor of the dopamine transporter: 3β‐(p‐chlorophenyl) tropan‐2β‐carboxylic acid m‐([125I]‐iodo)‐p‐azidophenethyl ester ([125I]‐RTI‐82)
Kolb et al. Synthesis and pharmacological characterization of fluorescent opioid receptor probes
CN101845047B (en) Method for preparing methylnaltrexone bromide
Vichard et al. Synthesis, X-ray structure and chemical properties of 17α-ferrocenylestradiol
Liu et al. Synthesis and characterization of thienorphine and its glucuronide conjugate
Paquette et al. Synthesis and dynamic behavior of (1, 5) cyclooctatetraenophanes. Effect of distal atom bridging on racemization rates and electrochemical reducibility
Terrier et al. Relative acidifying effects of tricarbonylchromium (0) and p-nitro groups upon di-and triphenylmethanes
Toth et al. Tritium Labelling of Naltrindole, a δ‐Receptor‐Selective Opioid Antagonist via 1‐Bromonaltrexone
Johansson et al. C3-Methylated 5-hydroxy-2-(dipropylamino) tetralins: Conformational and steric parameters of importance for central dopamine receptor activation
Bagley et al. Synthesis and conformational analysis of isomeric 3‐propananilidotropanes
Finch et al. Synthesis of 1, 3, 4, 5, 6, 7, 8, 8a-octahydro-2-methyl-4a-phenylisoquinolin-6-ols. Novel fragments of the morphine molecule
Mathews et al. Synthesis of N1′‐([18F] fluoroethyl) naltrindole ([18F] FEtNTI): a radioligand for positron emission tomographic studies of delta opioid receptors
Iorio et al. Synthesis, stereochemistry, and biological activity of the 1-(1-phenyl-2-methylcyclohexyl) piperidines and the 1-(1-phenyl-4-methylcyclohexyl) piperidines. Absolute configuration of the potent trans-(-)-1-(1-phenyl-2-methylcyclohexyl) piperidine
Tamura et al. Stereochemistry and base-catalyzed rearrangement of 9-phenylthioxanthene-N-(p-toluenesulfonyl) sulfilimine
Zecca et al. Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: A potential in vivo tracer for benzodiazepine receptors