ID: ALA2386145

Max Phase: Preclinical

Molecular Formula: C16H16N2

Molecular Weight: 236.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)c1ccc(-c2ccc(C#N)cn2)cc1

Standard InChI:  InChI=1S/C16H16N2/c1-16(2,3)14-7-5-13(6-8-14)15-9-4-12(10-17)11-18-15/h4-9,11H,1-3H3

Standard InChI Key:  AWPJMIQUTCBORO-UHFFFAOYSA-N

Associated Targets(Human)

Cytochrome P450 3A4/3A5 100 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver microsomes 16955 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus 775804 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Liver microsomes 8692 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

Properties

Molecular Weight: 236.32Molecular Weight (Monoisotopic): 236.1313AlogP: 3.92#Rotatable Bonds: 1
Polar Surface Area: 36.68Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 0.73CX LogP: 4.19CX LogD: 4.19
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.75Np Likeness Score: -1.71

References

1. Barnes-Seeman D, Jain M, Bell L, Ferreira S, Cohen S, Chen XH, Amin J, Snodgrass B, Hatsis P..  (2013)  Metabolically Stable tert-Butyl Replacement.,  (6): [PMID:24900702] [10.1021/ml400045j]

Source