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BioWorld - Tuesday, February 3, 2026
Home » Keywords » pain

Items Tagged with 'pain'

ARTICLES

Neurology/psychiatric

Sea4us patent discloses new oxazolidone-derived compounds for pain

Feb. 2, 2026
Sea4us - Biotecnologia e Recursos Marinhos Lda. has reported oxazolidone-derived compounds potentially useful for the treatment of chronic pain.
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Cancer

EGFR inhibition ameliorates oral cancer-related pain

Feb. 2, 2026
No Comments
Opioids are widely used to relieve the pain associated with oral squamous cell carcinoma (OSCC), but tolerance and undesired effects often limit their use. EGFR is commonly amplified in oral cancer and its involvement in OSCC-associated pain and opioid tolerance was investigated through the sensitization of trigeminal ganglion cells, which are the main sensory neurons that innervate the face and mouth. For this purpose, they used the EGFR inhibitor AG-1478, which was tested in vitro as well as in in vivo in human OSCC and an orthotopic murine models.
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Neurology/psychiatric

Humanwell Pharmaceutical patents new somatostatin SST4 receptor agonists for pain

Jan. 30, 2026
Humanwell Pharmaceutical US Inc. has disclosed prodrugs of somatostatin SST4 receptor agonists described as potentially useful for the treatment of visceral and neuropathic pain.
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The voltage-gated sodium channel in the open conformation (side view)
Neurology/psychiatric

O-Alkylated piperine derivative inhibits Nav1.7, shows antinociceptive effects

Jan. 28, 2026
No Comments
Voltage-gated sodium channels, particularly Nav1.7, are highly expressed in peripheral sensory neurons and are crucial for pain signal conduction and signal transmission in the spinal dorsal horn. Because of their role in triggering pain, these channels are considered critical targets for analgesics. Systemic inhibition of Nav1.7 has been shown to abolish pain perception.
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Neurology/psychiatric

New Nav1.8 blockers disclosed in Jumpcan Pharmaceutical patent

Jan. 5, 2026
Jumpcan Pharmaceutical Group Ltd. has divulged sodium channel protein type 10 subunit α (SCN10A; Nav1.8) blockers reported to be useful for the treatment of pain.
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Neurology/psychiatric

New Nav1.8 blockers disclosed in Chengdu Easton Biopharmaceuticals patent

Dec. 30, 2025
Chengdu Easton Biopharmaceuticals Co. Ltd. has divulged sodium channel protein type 10 subunit α (SCN10A; Nav1.8) blockers reported to be useful for the treatment of pain, arrhythmia, cough, urinary incontinence and multiple sclerosis.
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Art concept for pain
Neurology/psychiatric

Tonix licenses S1R antagonist from Rutgers University

Dec. 17, 2025
No Comments
Tonix Pharmaceuticals Holding Corp. has licensed exclusive worldwide rights to TNX-4900 (formerly PW-507) from Rutgers University. TNX-4900 is a highly selective, small-molecule sigma-1 receptor (S1R) antagonist, which has demonstrated analgesic activity in multiple models of neuropathic pain.
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Neurology/psychiatric

New opioid receptor agonists disclosed in Alphamol Science patent

Dec. 11, 2025
Alphamol Science Ltd. has divulged opioid receptor agonists reported to be useful for the treatment of pain.
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Neurology/psychiatric

New Nav1.8 blockers disclosed in Hengrui patent

Nov. 20, 2025
Jiangsu Hengrui Pharmaceuticals Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have divulged aromatic compounds acting as sodium channel protein type 10 subunit α (SCN10A; Nav1.8) blockers reported to be useful for the treatment of pain.
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Neurology/psychiatric

Yichang Humanwell Pharmaceutical patents new κ-opioid receptor agonists

Nov. 19, 2025
Yichang Humanwell Pharmaceutical Co. Ltd. has disclosed morphinan derivatives acting as κ-opioid receptor agonists reported to be useful for the treatment of pain and pruritus.
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