Evidence & regulatory context
- Mechanism
- ADTM, a danshensu/tetramethylpyrazine hybrid derivative (antithrombotic/antioxidant).
- Target
- Not recorded
- Injury models
- Ischaemia-reperfusion
- 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.
MixedIschaemia-reperfusionCardiacC57BL/6Male12 to 24 mg/kg in mice; 50 to 200 microM in zebrafish; 200…Treatment given after myocardial infarction for 14 days
Model: Experimental myocardial infarction
ADTM at 12 to 24 mg/kg for 14 days significantly reduced myocardial infarct size and increased peri-infarct vessel density, and 24 mg/kg raised serum VEGF (P < 0.05). ADTM rescued chemical-induced vessel loss in zebrafish and increased VEGF in A7r5 cells, and at 200 microM inhibited L-type calcium…
Extraction: extract · Subtype source: rule · Supplied extraction confidence: 0.6. Machine-extracted fields require source verification.