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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

(2S)-N-2-methoxy-2-phenylethyl-6,7-benzomorphan compound (2S-LP2): Discovery of a biased mu/delta opioid receptor agonist
Lorella Pasquinucci, Rita Turnaturi, Girolamo Calò, et al.
European Journal of Medicinal Chemistry (2019) Vol. 168, pp. 189-198
Open Access | Times Cited: 19

Showing 19 citing articles:

Pathology of pain and its implications for therapeutic interventions
Bo Cao, Qixuan Xu, Yajiao Shi, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 15
Biased Opioid Ligands
Abdelfattah Faouzi, Balázs R. Varga, Susruta Majumdar
Molecules (2020) Vol. 25, Iss. 18, pp. 4257-4257
Open Access | Times Cited: 105
Structural Assessment of Agonist Efficacy in the μ-Opioid Receptor: Morphine and Fentanyl Elicit Different Activation Patterns
Adrián Ricarte, James A. R. Dalton, Jesús Giraldo
Journal of Chemical Information and Modeling (2021) Vol. 61, Iss. 3, pp. 1251-1274
Open Access | Times Cited: 46
Simultaneous Activation of Mu and Delta Opioid Receptors Reduces Allodynia and Astrocytic Connexin 43 in an Animal Model of Neuropathic Pain
Nunzio Vicario, Lorella Pasquinucci, Federica Maria Spitale, et al.
Molecular Neurobiology (2019) Vol. 56, Iss. 11, pp. 7338-7354
Closed Access | Times Cited: 44
Comprehensive overview of biased pharmacology at the opioid receptors: biased ligands and bias factors
Jolien De Neve, Thomas Barlow, Dirk Tourwé, et al.
RSC Medicinal Chemistry (2021) Vol. 12, Iss. 6, pp. 828-870
Open Access | Times Cited: 34
Intercellular communication and ion channels in neuropathic pain chronicization
Nunzio Vicario, Rita Turnaturi, Federica Maria Spitale, et al.
Inflammation Research (2020) Vol. 69, Iss. 9, pp. 841-850
Closed Access | Times Cited: 34
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia
Andrea Angeli, Laura Micheli, Rita Turnaturi, et al.
European Journal of Medicinal Chemistry (2023) Vol. 260, pp. 115783-115783
Closed Access | Times Cited: 11
Mu and Delta Opioid Receptor Targeting Reduces Connexin 43-Based Heterocellular Coupling during Neuropathic Pain
Nunzio Vicario, Simona Denaro, Rita Turnaturi, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 5864-5864
Open Access | Times Cited: 17
Progress in the development of more effective and safer analgesics for pain management
Rita Turnaturi, Santina Chiechio, Loredana Salerno, et al.
European Journal of Medicinal Chemistry (2019) Vol. 183, pp. 111701-111701
Closed Access | Times Cited: 28
Novel N-normetazocine Derivatives with Opioid Agonist/Sigma-1 Receptor Antagonist Profile as Potential Analgesics in Inflammatory Pain
Rita Turnaturi, Santina Chiechio, Lorella Pasquinucci, et al.
Molecules (2022) Vol. 27, Iss. 16, pp. 5135-5135
Open Access | Times Cited: 10
LP1 and LP2: Dual-Target MOPr/DOPr Ligands as Drug Candidates for Persistent Pain Relief
Lorella Pasquinucci, Carmela Parenti, Zafiroula Georgoussi, et al.
Molecules (2021) Vol. 26, Iss. 14, pp. 4168-4168
Open Access | Times Cited: 11
Historical perspectives and recent advances in small molecule ligands of selective/biased/multi-targeted μ/δ/κ opioid receptor (2019–2022)
Ye He, Qian Peter Su, Liyun Zhao, et al.
Bioorganic Chemistry (2023) Vol. 141, pp. 106869-106869
Closed Access | Times Cited: 4
Exploiting the Power of Stereochemistry in Drug Action: 3-[(2S,6S,11S)-8-Hydroxy-6,11-dimethyl-1,4,5,6-tetrahydro-2,6-methano-3-benzazocin-3(2H)-yl]-N-phenylpropanamide as Potent Sigma-1 Receptor Antagonist
Rita Turnaturi, Lorella Pasquinucci, Santina Chiechio, et al.
ACS Chemical Neuroscience (2020) Vol. 11, Iss. 7, pp. 999-1005
Closed Access | Times Cited: 11
Novel N-Substituted Benzomorphan-Based Compounds: From MOR-Agonist/DOR-Antagonist to Biased/Unbiased MOR Agonists
Lorella Pasquinucci, Carmela Parenti, M. Carmen Ruiz‐Cantero, et al.
ACS Medicinal Chemistry Letters (2020) Vol. 11, Iss. 5, pp. 678-685
Open Access | Times Cited: 9
New Insights into the Opioid Analgesic Profile of cis-(−)-N-Normetazocine-derived Ligands
Giuliana Costanzo, Rita Turnaturi, Carmela Parenti, et al.
Molecules (2023) Vol. 28, Iss. 12, pp. 4827-4827
Open Access | Times Cited: 3
A Novel Multi-Target Mu/Delta Opioid Receptor Agonist, HAGD, Produced Potent Peripheral Antinociception with Limited Side Effects in Mice and Minimal Impact on Human Sperm Motility In Vitro
Fangfang Li, Feng Yue, Wei Zhang, et al.
Molecules (2023) Vol. 28, Iss. 1, pp. 427-427
Open Access | Times Cited: 1
Asymmetric synthesis of (1R,5S)‐2‐methyl‐6,7‐benzomorphan via Aza‐Prins reaction
José A. Gálvez, Ramón Badorrey, Alejandro Mahía, et al.
Chirality (2021) Vol. 33, Iss. 9, pp. 543-548
Open Access | Times Cited: 2
Solid Lipid Nanoparticles as Carriers for the Synthetic Opioid LP2: Characterization and In Vitro Release
Angelo Spadaro, Lorella Pasquinucci, Miriam Lorenti, et al.
Applied Sciences (2021) Vol. 11, Iss. 21, pp. 10250-10250
Open Access | Times Cited: 1
A Novel Multitarget Mu- and Delta-Opioid Receptors Agonist HAGD Has Peripherally Restrictive Potent Analgesia with Less Side Effects in Mice and Minimal Impact on Human Sperm Motility
Fangfang Li, Yue Feng, Wei Zhang, et al.
Research Square (Research Square) (2021)
Open Access
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