Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 35 checked references that resolve
resolves10.1016/S0022-3565(24)37585-8Stimulation of Guanosine-5′-O-(3-[35S]Thio)Triphosphate Binding by Endogenous Opioids Acting at a Cloned Mu Receptor
resolves10.1007/BF02245071Differential effects of systemically administered nor-binaltorphimine (nor-BNI) on κ-opioid agonists in the mouse writhing assay
resolves10.1016/S0022-3565(25)32103-8Pharmacological studies with an alkylating narcotic agonist, chloroxymorphamine, and antagonist, chlornaltrexamine.
resolves10.1016/0006-2952(73)90196-2Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
resolves10.1111/j.1476-5381.1991.tb12239.xAlkylation with β‐funaltrexamine suggests differences between μ‐opioid receptor systems in guinea‐pig brain and myenteric‐plexus
resolves10.1111/j.1476-5381.1985.tb11112.xDetermination of the receptor selectivity of opioid agonists in the guinea‐pig ileum and mouse vas deferens by use of β‐funaltrexamine
resolves10.1016/S0022-3565(25)38586-15 beta-Methyl-14 beta-(p-nitrocinnamoylamino)-7,8-dihydromorphinone and its corresponding N-cyclopropylmethyl analog, N-cyclopropylmethylnor-5 beta-methyl-14 beta-(p-nitrocinnamoylamino)- 7,8-dihydromorphinone: mu-selective irreversible opioid antagonists.
resolves10.1016/S0022-3565(25)39535-2Effects of intracerebroventricular administration of beta-funaltrexamine on [3H]DAMGO binding to rat brain sections.
resolves10.1016/S0022-3565(25)24539-6Alkylation of mu opioid receptors by beta-funaltrexamine in vivo: comparison of the effects on in situ binding and heroin self-administration in rats.
resolves10.1038/383819a0Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the µ-opioid-receptor gene
resolves10.1016/S0022-3565(24)38137-6Nitrocinnamoyl and Chlorocinnamoyl Derivatives of Dihydrocodeinone: In Vivo and In Vitro Characterization of μ-Selective Agonist and Antagonist Activity
resolves10.1016/S0022-3565(25)20248-8Characteristics of dose-dependent antagonism by beta-funaltrexamine of the antinociceptive effects of intrathecal mu agonists.
resolves10.3727/10715699581956356414ß-CINNAMOYLAMIDOMORPHINONES AND CODEINONES. ANALOGS OF THE SELECTIVE IRREVERSIBLE ANTAGONIST CLOCINNAMOX.
resolves10.3727/107156995819563122MOLECULAR MODELLING OF FUMARAMIDO AND CINNAMOYLAMIDO DERIVATIVES IN EPOXY-MORPHINANS. CORRELATION WITH PHARMACOLOGICAL PROFILES.
resolves10.1021/jm00177a002A novel opioid receptor site directed alkylating agent with irreversible narcotic antagonistic and reversible agonistic activities
resolves10.1021/jm00016a010Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 11. 3-Hydroxycyprodime and Analogs: Opioid Antagonist Profile in Comparison to Cyprodime
resolves10.1016/0014-2999(81)90355-1The irreversible narcotic antagonistic and reversible agonistic properties of the fumaramate methyl ester derivative of naltrexone
resolves10.1016/S0022-3565(25)39259-1Evidence for the interaction of morphine with kappa and delta opioid receptors to induce analgesia in beta-funaltrexamine-treated mice.
resolves10.1016/S0022-3565(25)23584-4Reversible and irreversible binding of beta-funaltrexamine to mu, delta and kappa opioid receptors in guinea pig brain membranes.
resolves10.1016/S0022-3565(24)35214-0Ring-Constrained Orvinols as Analogs of Buprenorphine: Differences in Opioid Activity Related to Configuration of C20 Hydroxyl Group
resolves10.1016/S0026-895X(25)08634-1Modulation by mu-opioid agonists of guanosine-5'-O-(3-[35S]thio)triphosphate binding to membranes from human neuroblastoma SH-SY5Y cells.
resolves10.1016/0014-2999(82)90083-8Pharmacological profiles of β-funaltrexamine (β-FNA) and β-chlornaltrexamine (β-CNA) on the mouse vas deferens preparation
resolves10.1037/1064-1297.3.4.323Opioid agonist effects on mouse writhing after irreversible mu receptor blockade with clocinnamox.
resolves10.1016/S0022-3565(25)20932-6Mechanism of clocinnamox blockade of opioid receptors: evidence from in vitro and ex vivo binding and behavioral assays.
resolves10.1016/S0022-3565(25)38710-0In vivo determination of mu opioid receptor turnover in rhesus monkeys after irreversible blockade with clocinnamox.
resolves10.1016/S0022-3565(24)36877-6Activation of the Cloned Human Kappa Opioid Receptor by Agonists Enhances [35S]GTPγS Binding to Membranes: Determination of Potencies and Efficacies of Ligands
resolves10.1016/S0022-5347(25)00270-8Use of beta-funaltrexamine to determine mu opioid receptor involvement in the analgesic activity of various opioid ligands.
The 5 references without a DOI — listed, not checked
no DOI — not checked10.1016/S0022-3565(24)39155-4_bib12
no DOI — not checkedNew 14-aminomorphinones and codeinones.
no DOI — not checked10.1016/S0022-3565(24)39155-4_bib28
no DOI — not checkedStandard binding and functional assays related to medications development division testing for potential cocaine and opiate narcotic treatment medications.
no DOI — not checkedCharacterization of [3H]clocinnamox binding in mouse brain membranes.
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