Evidence & regulatory context
- Mechanism
- ChEMBL compound_search for 'LP-211' returned 0 records (explicit negative result, not an omission). LP-211 is a research-grade selective 5-HT7 receptor agonist with no INN/USAN name and no ChEMBL entity. ClinicalTrials.gov searched for 'LP-211 OR 5-HT7 receptor agonist': 0 hits. No human trial administers LP-211 or any selective 5-HT7 agonist.
- Target
- Not recorded
- Injury models
- Spinal cord injury
- Reported indication
- Not recorded
- First approval
- Not recorded
- Development stage
- Not recorded
- ChEMBL record
- Not recorded
- ChEMBL max phase
- Not recorded
- Synonyms
- Not recorded
- Note
- Not recorded
Clinical trials 0
0 linked trials carry an injury-indication flag. These flags support record-level exploration and sit alongside the stringent aggregate counts described in Methods.
No linked human trial in this dataset.
Preclinical evidence 1
1 studies reported at therapy level; 1 evidence entries itemised.
RatSpinal cord injuryCompressionWistar albinoMalen = 60 rats in total, six groups of tenIntraperitoneal0.003 to 0.3 mg/kgCommenced two weeks after spinal cord injury
Model: Extradural aneurysm clip compression of the spinal cord at T10 (Yasargil FE 760 clip, 180 g closing force, 1 min) after T9-T11 laminectomy
LP-211 lowered serum sodium and raised serum potassium and magnesium in spinal cord-injured rats, producing hyponatraemia, hyperkalaemia and hypermagnesaemia. The authors concluded LP-211 may not be a potential electroprotective agent for spinal cord injury.
Extraction: extract · Subtype source: rule · Supplied extraction confidence: 0.9. Machine-extracted fields require source verification.