9-(2-Oxoindolin-5-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2(1H)-one

ID: ALA4540379

PubChem CID: 118077886

Max Phase: Preclinical

Molecular Formula: C27H16F3N3O2

Molecular Weight: 471.44

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  O=C1Cc2cc(-c3ccc4ncc5ccc(=O)n(-c6cccc(C(F)(F)F)c6)c5c4c3)ccc2N1

Standard InChI:  InChI=1S/C27H16F3N3O2/c28-27(29,30)19-2-1-3-20(13-19)33-25(35)9-6-17-14-31-23-8-5-16(11-21(23)26(17)33)15-4-7-22-18(10-15)12-24(34)32-22/h1-11,13-14H,12H2,(H,32,34)

Standard InChI Key:  WLHRPFMHTLEVQT-UHFFFAOYSA-N

Molfile:  

 
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M  END

Associated Targets(Human)

RD (1212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MTOR Tclin mTORC1 (330 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Enterovirus A71 (1246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 471.44Molecular Weight (Monoisotopic): 471.1195AlogP: 5.72#Rotatable Bonds: 2
Polar Surface Area: 63.99Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.18CX Basic pKa: 3.46CX LogP: 4.90CX LogD: 4.90
Aromatic Rings: 5Heavy Atoms: 35QED Weighted: 0.34Np Likeness Score: -1.09

References

1. Hao T, Li Y, Fan S, Li W, Wang S, Li S, Cao R, Zhong W..  (2019)  Design, synthesis and pharmacological evaluation of a novel mTOR-targeted anti-EV71 agent.,  175  [PMID:31082764] [10.1016/j.ejmech.2019.04.048]

Source