Cloxacepride
Cloxacepride is an orally active and potent antiallergic agent. Cloxacepride is a CaM (calmodulin) antagonist. Cloxacepride has anti-PCA (passive cutaneous anaphylaxis) activity.
For research use only. We do not sell to patients.
- CAS No.: 65569-29-1
- Formula: C22H27Cl2N3O4
- Molecular Weight:468.37
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Cloxacepride (10-50 μM) shows inhibitory effect on Compound 48/80 (HY-115768)-induced histamine and serotonin release from rat mesenterial mast cells. The IC50 is determined to 21 μM (histamine) and 19 μM (serotonin)[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Cloxacepride has anti-PCA activity when administered orally 15 or 60 min before antigenic challenge[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 65569-29-1
-
Molecular Weight 468.37
-
Formula C22H27Cl2N3O4
-
SMILES
O=C(C1=CC(Cl)=C(NC(COC2=CC=C(C=C2)Cl)=O)C=C1OC)NCCN(CC)CC
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Metz G, et al. Cloxacepride and related compounds: a new series of orally active antiallergic compounds. J Med Chem. 1983 Jul;26(7):1065-70. [Content Brief]
[2]. Gigl G, et al. Calmodulin antagonism: a pharmacological approach for the inhibition of mediator release from mast cells. Cell Calcium. 1987 Oct;8(5):327-44. [Content Brief]
[3]. Friedrich G, et al. Inhibitory effect of cloxacepride on compound 48/80-induced histamine and serotonin release from rat mast cells. Arch Int Pharmacodyn Ther. 1984 Feb;267(2):264-8. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)