ID: ALA3741101

Max Phase: Preclinical

Molecular Formula: C24H19NO3

Molecular Weight: 369.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)c1cccc(NC(c2ccccc2)c2ccc3ccccc3c2O)c1

Standard InChI:  InChI=1S/C24H19NO3/c26-23-20-12-5-4-7-16(20)13-14-21(23)22(17-8-2-1-3-9-17)25-19-11-6-10-18(15-19)24(27)28/h1-15,22,25-26H,(H,27,28)

Standard InChI Key:  TUHAYLBLXPNFBE-UHFFFAOYSA-N

Associated Targets(Human)

Prenyl protein specific protease 365 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CAAX prenyl protease 1 homolog 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein farnesyltransferase 3470 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: 369.42Molecular Weight (Monoisotopic): 369.1365AlogP: 5.45#Rotatable Bonds: 5
Polar Surface Area: 69.56Molecular Species: ACIDHBA: 3HBD: 3
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.76CX Basic pKa: 2.03CX LogP: 5.30CX LogD: 2.69
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.44Np Likeness Score: -0.63

References

1. Mohammed I, Hampton SE, Ashall L, Hildebrandt ER, Kutlik RA, Manandhar SP, Floyd BJ, Smith HE, Dozier JK, Distefano MD, Schmidt WK, Dore TM..  (2016)  8-Hydroxyquinoline-based inhibitors of the Rce1 protease disrupt Ras membrane localization in human cells.,  24  (2): [PMID:26706114] [10.1016/j.bmc.2015.11.043]

Source