Cinromide is an inhibitor of epithelial neutral amino acid transporter B0AT1 (SLC6A19) with IC50 of 0.5 μM. Cinromide (10-100 μM) inhibits 5-HT-induced contractions in rat fundus strips by 46%.
| Molecular Weight | 254.12 |
| Formula | C11H12BrNO |
| CAS Number | 58473-74-8 |
| Solubility (25°C) | DMSO 90 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
| Species | Mouse | Rat | Rabbit | Guinea pig | Hamster | Dog |
| Weight (kg) | 0.02 | 0.15 | 1.8 | 0.4 | 0.08 | 10 |
| Body Surface Area (m2) | 0.007 | 0.025 | 0.15 | 0.05 | 0.02 | 0.5 |
| Km factor | 3 | 6 | 12 | 8 | 5 | 20 |
| Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
| Animal A Km |
For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.
[1] P Chiu, et al. Neuropharmacology. The effect of cinromide on "kindled" seizures in the rat
[3] A J Wilensky, et al. Epilepsia. Cinromide in epilepsy: a pilot study
[4] G H Fromm, et al. Epilepsia. Effect of cinromide on inhibitory and excitatory mechanisms
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