Evidence & regulatory context
- Mechanism
- Botanical extract (Ocimum gratissimum aqueous leaf extract); not a ChEMBL entity; no matching trial identified
- Target
- Not recorded
- Injury models
- Chemical/toxin
- 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.
RatChemical/toxinWistarMalen = 32 rats in total, 8 per group across 4 groupsOral0.2 mg/kg body weightConcurrent with CCl4 dosing across the 12-week period
Model: Carbon tetrachloride (CCl4) induced hepatic injury, intraperitoneal CCl4 twice weekly for 12 weeks
OGAE significantly increased serum catalase and DPPH scavenging and significantly reduced hepatic HSP70, iNOS, MMP-9/MMP-2 ratio, uPA, phosphorylated ERK and phosphorylated p65 compared with CCl4 alone, with effects comparable to silymarin. No numerical effect sizes were reported.
Extraction: extract · Supplied extraction confidence: 0.8. Machine-extracted fields require source verification.