4-[6-(4-cyanoanilino)-1,3-dioxo-2,3-dihydro-1H-5-isoindolylamino]benzonitrile

ID: ALA267869

Chembl Id: CHEMBL267869

PubChem CID: 10407341

Max Phase: Preclinical

Molecular Formula: C22H13N5O2

Molecular Weight: 379.38

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  N#Cc1ccc(Nc2cc3c(cc2Nc2ccc(C#N)cc2)C(=O)NC3=O)cc1

Standard InChI:  InChI=1S/C22H13N5O2/c23-11-13-1-5-15(6-2-13)25-19-9-17-18(22(29)27-21(17)28)10-20(19)26-16-7-3-14(12-24)4-8-16/h1-10,25-26H,(H,27,28,29)

Standard InChI Key:  KQTHJPWPAZKUSZ-UHFFFAOYSA-N

Associated Targets(Human)

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRKD3 Tchem Protein kinase C (PKC) (1010 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

cAMP-dependent protein kinase alpha-catalytic subunit (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 379.38Molecular Weight (Monoisotopic): 379.1069AlogP: 3.80#Rotatable Bonds: 4
Polar Surface Area: 117.81Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 8.73CX Basic pKa: CX LogP: 3.29CX LogD: 3.27
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.59Np Likeness Score: -0.68

References

1. Trinks U, Buchdunger E, Furet P, Kump W, Mett H, Meyer T, Müller M, Regenass U, Rihs G, Lydon N..  (1994)  Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinase.,  37  (7): [PMID:8151612] [10.1021/jm00033a019]

Source