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(S)-(1'-(azetidin-3-yl)spiro[indoline-3,3'-pyrrolidine]-1-yl)(5-fluoro-1H-indol-2-yl)methanone ID: ALA1933520
Chembl Id: CHEMBL1933520
PubChem CID: 57396879
Max Phase: Preclinical
Molecular Formula: C23H23FN4O
Molecular Weight: 390.46
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C(c1cc2cc(F)ccc2[nH]1)N1C[C@@]2(CCN(C3CNC3)C2)c2ccccc21
Standard InChI: InChI=1S/C23H23FN4O/c24-16-5-6-19-15(9-16)10-20(26-19)22(29)28-14-23(18-3-1-2-4-21(18)28)7-8-27(13-23)17-11-25-12-17/h1-6,9-10,17,25-26H,7-8,11-14H2/t23-/m0/s1
Standard InChI Key: XPHCAEDIXCJNLS-QHCPKHFHSA-N
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: 390.46Molecular Weight (Monoisotopic): 390.1856AlogP: 2.88#Rotatable Bonds: 2Polar Surface Area: 51.37Molecular Species: BASEHBA: 3HBD: 2#RO5 Violations: ┄HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 11.93CX Basic pKa: 9.49CX LogP: 2.35CX LogD: 0.29Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.71Np Likeness Score: -0.71
References 1. Powell NA, Kohrt JT, Filipski KJ, Kaufman M, Sheehan D, Edmunds JE, Delaney A, Wang Y, Bourbonais F, Lee DY, Schwende F, Sun F, McConnell P, Catana C, Chen H, Ohren J, Perrin LA.. (2012) Novel and selective spiroindoline-based inhibitors of Sky kinase., 22 (1): [PMID:22119469 ] [10.1016/j.bmcl.2011.11.036 ]