ID: ALA3742267

Max Phase: Preclinical

Molecular Formula: C14H17ClN4O

Molecular Weight: 292.77

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)Cn1c(C2CC2)c(Cl)nc(-n2cccn2)c1=O

Standard InChI:  InChI=1S/C14H17ClN4O/c1-9(2)8-18-11(10-4-5-10)12(15)17-13(14(18)20)19-7-3-6-16-19/h3,6-7,9-10H,4-5,8H2,1-2H3

Standard InChI Key:  JQPICWWHKCGNNY-UHFFFAOYSA-N

Associated Targets(non-human)

Parastagonospora nodorum 325 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Puccinia triticina 278 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botrytis cinerea 4183 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: 292.77Molecular Weight (Monoisotopic): 292.1091AlogP: 2.62#Rotatable Bonds: 4
Polar Surface Area: 52.71Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.20CX LogP: 2.22CX LogD: 2.22
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.87Np Likeness Score: -1.82

References

1. Taggi AE, Stevenson TM, Bereznak JF, Sharpe PL, Gutteridge S, Forman R, Bisaha JJ, Cordova D, Crompton M, Geist L, Kovacs P, Marshall E, Sheth R, Stavis C, Tseng CP..  (2016)  Tubulin modulating antifungal and antiproliferative pyrazinone derivatives.,  24  (3): [PMID:26386818] [10.1016/j.bmc.2015.08.038]

Source