ID: ALA2286188

Max Phase: Preclinical

Molecular Formula: C19H19F3N4O

Molecular Weight: 376.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1nc2nccnc2c(N[C@H](C)C(C)C)c1-c1c(F)cc(F)cc1F

Standard InChI:  InChI=1S/C19H19F3N4O/c1-9(2)10(3)25-16-15(14-12(21)7-11(20)8-13(14)22)19(27-4)26-18-17(16)23-5-6-24-18/h5-10H,1-4H3,(H,24,25,26)/t10-/m1/s1

Standard InChI Key:  LYUCDQCOHCTJIV-SNVBAGLBSA-N

Associated Targets(non-human)

Puccinia triticina 278 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pyricularia grisea 1253 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Zymoseptoria tritici 367 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: 376.38Molecular Weight (Monoisotopic): 376.1511AlogP: 4.57#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: 1.91CX LogP: 4.05CX LogD: 4.05
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.71Np Likeness Score: -0.80

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