ID: ALA2286192

Max Phase: Preclinical

Molecular Formula: C18H18ClFN4O

Molecular Weight: 360.82

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1nc2nccnc2c(NCC(C)C)c1-c1c(F)cccc1Cl

Standard InChI:  InChI=1S/C18H18ClFN4O/c1-10(2)9-23-15-14(13-11(19)5-4-6-12(13)20)18(25-3)24-17-16(15)21-7-8-22-17/h4-8,10H,9H2,1-3H3,(H,22,23,24)

Standard InChI Key:  XUUKCPOQYGOTML-UHFFFAOYSA-N

Associated Targets(non-human)

Zymoseptoria tritici 367 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Puccinia triticina 278 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pyricularia grisea 1253 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: 360.82Molecular Weight (Monoisotopic): 360.1153AlogP: 4.56#Rotatable Bonds: 5
Polar Surface Area: 59.93Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.99CX LogP: 3.95CX LogD: 3.95
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.72Np Likeness Score: -1.10

References

1. Crowley PJ, Lamberth C, Müller U, Wendeborn S, Nebel K, Williams J, Sageot OA, Carter N, Mathie T, Kempf HJ, Godwin J, Schneiter P, Dobler MR..  (2010)  Synthesis and fungicidal activity of tubulin polymerisation promoters. Part 1: pyrido[2,3-b]pyrazines.,  66  (2): [PMID:19795441] [10.1002/ps.1852]

Source