| MDL | MFCD26792570 |
|---|---|
| Molecular Weight | 415.49 |
| Molecular Formula | C27H21N5 |
| SMILES | C1(C2=NC=CC=C2)=NC(NCC3=CC=C(C4=CC=CC=C4)C=C3)=C(C5=CC=CC=C5)N=N1 |
EC50: 1 μM (HIF) [1]
ML228 (CID-46742353) represents a novel chemotype available to the research community for the study of HIF activation and its therapeutic potential. Not only is the compound substantially different in structure from known HIF activators, ML228 lacks the acidic functional group almost universally present in PHD inhibitors, which may be important for certain disease applications [1] [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
ML228 (injection; 1 µg/kg; 7 days) treatments following spinal cord injury (SCI) improves the local hypoxic ischemia environment, reduce SCI secondary injury and promote the recovery of neurological function
[3]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
| Animal Model: | SD rat [3] |
| Dosage: | 1 µg/kg |
| Administration: | injection; 7 days |
| Result: | Alleviated SCI of the central nervous system and relieve associated symptoms. |
Solid
Room temperature in continental US; may vary elsewhere.
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
DMSO : ≥ 35 mg/mL ( 84.24 mM )
* "≥" means soluble, but saturation unknown.
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.4068 mL | 12.0340 mL | 24.0680 mL |
| 5 mM | 0.4814 mL | 2.4068 mL | 4.8136 mL |
| 10 mM | 0.2407 mL | 1.2034 mL | 2.4068 mL |