ID: ALA3616999

Max Phase: Preclinical

Molecular Formula: C16H17NO3

Molecular Weight: 271.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C(=O)NCc1ccc(O)c(O)c1)c1ccccc1

Standard InChI:  InChI=1S/C16H17NO3/c1-11(13-5-3-2-4-6-13)16(20)17-10-12-7-8-14(18)15(19)9-12/h2-9,11,18-19H,10H2,1H3,(H,17,20)

Standard InChI Key:  NCHSLAZPCUYEFR-UHFFFAOYSA-N

Associated Targets(Human)

Flap endonuclease 1 12055 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA excision repair protein ERCC-1/DNA repair endonuclease XPF 129 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Deoxyribonuclease-1 73 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: 271.32Molecular Weight (Monoisotopic): 271.1208AlogP: 2.52#Rotatable Bonds: 4
Polar Surface Area: 69.56Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.25CX Basic pKa: CX LogP: 2.69CX LogD: 2.68
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.75Np Likeness Score: -0.38

References

1. Chapman TM, Gillen KJ, Wallace C, Lee MT, Bakrania P, Khurana P, Coombs PJ, Stennett L, Fox S, Bureau EA, Brownlees J, Melton DW, Saxty B..  (2015)  Catechols and 3-hydroxypyridones as inhibitors of the DNA repair complex ERCC1-XPF.,  25  (19): [PMID:26318993] [10.1016/j.bmcl.2015.08.031]

Source