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(E)-N-(3-(2-amino-1H-imidazol-4-yl)allyl)-5-chloro-1H-indole-2-carboxamide ID: ALA4210636
Chembl Id: CHEMBL4210636
PubChem CID: 145967358
Max Phase: Preclinical
Molecular Formula: C15H14ClN5O
Molecular Weight: 315.76
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Nc1nc(/C=C/CNC(=O)c2cc3cc(Cl)ccc3[nH]2)c[nH]1
Standard InChI: InChI=1S/C15H14ClN5O/c16-10-3-4-12-9(6-10)7-13(21-12)14(22)18-5-1-2-11-8-19-15(17)20-11/h1-4,6-8,21H,5H2,(H,18,22)(H3,17,19,20)/b2-1+
Standard InChI Key: KZGCMSHMRDZXCJ-OWOJBTEDSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 315.76Molecular Weight (Monoisotopic): 315.0887AlogP: 2.57#Rotatable Bonds: 4Polar Surface Area: 99.59Molecular Species: BASEHBA: 3HBD: 4#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 0CX Acidic pKa: 13.93CX Basic pKa: 8.52CX LogP: 1.98CX LogD: 0.96Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.60Np Likeness Score: -0.35
References 1. Zidar N, Žula A, Tomašič T, Rogers M, Kirby RW, Tytgat J, Peigneur S, Kikelj D, Ilaš J, Mašič LP.. (2017) Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels., 139 [PMID:28802123 ] [10.1016/j.ejmech.2017.08.015 ]