verosudil   

GtoPdb Ligand ID: 8911

Synonyms: AR 12286 | AR-12286
Compound class: Synthetic organic
Comment: Verosudil is an investigational Rho kinase inhibitor.
The INN record for verosudil indicates that this is a racemic mixture. We show the chemical structure without stereochemistry to represent the mixture. The (2S)-isomer is represented in PubChem CID 86270580 and the (2R)-isomer is represented in CID 44198631.
2D Structure
Click here for structure editor
Physico-chemical Properties
Hydrogen bond acceptors 4
Hydrogen bond donors 2
Rotatable bonds 5
Topological polar surface area 93.44
Molecular weight 327.1
XLogP 1.83
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
Canonical SMILES CN(C(c1cscc1)C(=O)Nc1ccc2c(c1)cc[nH]c2=O)C
Isomeric SMILES CN(C(c1cscc1)C(=O)Nc1ccc2c(c1)cc[nH]c2=O)C
InChI InChI=1S/C17H17N3O2S/c1-20(2)15(12-6-8-23-10-12)17(22)19-13-3-4-14-11(9-13)5-7-18-16(14)21/h3-10,15H,1-2H3,(H,18,21)(H,19,22)
InChI Key VDYRZXYYQMMFJW-UHFFFAOYSA-N
Bioactivity Comments
In humans topically applied verosudil is able to reduce intraocular pressure by more than 25% (administering 0.25% drug, twice daily) [1].
We have been unable to find publicly available, peer reviewed data quantifying the direct enzyme inhibitory action of this compound.
Selectivity at enzymes
Key to terms and symbols Click column headers to sort
Target Sp. Type Action Value Parameter Concentration range (M) Reference
Rho associated coiled-coil containing protein kinase 1 Hs Inhibitor Inhibition - - - 1
[1]
Rho associated coiled-coil containing protein kinase 2 Hs Inhibitor Inhibition - - - 1
[1]