ID: ALA2272052

Max Phase: Preclinical

Molecular Formula: C15H19NO3

Molecular Weight: 261.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(C)c(C2=C(O)C(C)(C)N(O)C2=O)c(C)c1

Standard InChI:  InChI=1S/C15H19NO3/c1-8-6-9(2)11(10(3)7-8)12-13(17)15(4,5)16(19)14(12)18/h6-7,17,19H,1-5H3

Standard InChI Key:  WMHMIUNXKLATSJ-UHFFFAOYSA-N

Associated Targets(non-human)

Cucumis sativus 803 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Oryza sativa 2923 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Myzus persicae 1112 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nilaparvata lugens 786 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: 261.32Molecular Weight (Monoisotopic): 261.1365AlogP: 2.89#Rotatable Bonds: 1
Polar Surface Area: 60.77Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.80CX Basic pKa: CX LogP: 2.81CX LogD: 2.65
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.76Np Likeness Score: 0.27

References

1. Ito M, Okui H, Nakagawa H, Mio S, Kinoshita A, Obayashi T, Miura T, Nagai J, Yokoi S, Ichinose R, Tanaka K, Kodama S, Iwasaki T, Miyake T, Takashio M, Iwabuchi J..  (2002)  Synthesis and insecticidal activity of N-oxydihydropyrroles: 4-hydroxy-3-mesityl-5,5-dimethyl derivatives with various substituents at the 1-position.,  66  (11): [PMID:12506980] [10.1271/bbb.66.2406]

Source