Evidence & regulatory context
- Mechanism
- Not recorded
- 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.
MouseIschaemia-reperfusionRenalBALB/c (in vivo); TCMK-1 (mouse) and HK-2 (human) renal tubular epithelial cell lines used in vitroMalen = In vivo: n=6 mice per group per time point; in vitro: at le…Intraperitoneal injection (CHBP, in vivo); tail vein injection (TRPM7 siRNA, in vivo); direct addition to culture medium (in vitro)CHBP 8 nmol/kg (in vivo, intraperitoneal) or 30 nM (in vitr…CHBP administered at the onset of reperfusion; TRPM7 siRNA administered 2 h bef…
Model: Renal ischemia-reperfusion injury: bilateral renal pedicle clamping for 30 min ischemia followed by reperfusion for 12 h to 7 days in mice; complemented by in vitro hypoxia (12-24 h) followed by 2-24 h reoxygenation in TCMK-1/HK-2 cells
CHBP reversed the ischemia-reperfusion-induced upregulation of TRPM7 expression and TRPM7-like current, and reduced downstream inflammation (HMGB1) and apoptosis (caspase-3, Bax/Bcl-2 ratio) in both hypoxia-reoxygenation-treated tubular cells and mouse IR kidneys. TRPM7 knockdown by siRNA similarly…
Extraction: extract · Subtype source: rule · Supplied extraction confidence: 0.85. Machine-extracted fields require source verification.