ID: ALA2288281

Max Phase: Preclinical

Molecular Formula: C14H18N4

Molecular Weight: 242.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=CCc1c(C)nn(-c2nc(C)cc(C)n2)c1C

Standard InChI:  InChI=1S/C14H18N4/c1-6-7-13-11(4)17-18(12(13)5)14-15-9(2)8-10(3)16-14/h6,8H,1,7H2,2-5H3

Standard InChI Key:  RRCVASHRQBWBFF-UHFFFAOYSA-N

Associated Targets(non-human)

Pyricularia oryzae 1832 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nakataea oryzae 97 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: 242.33Molecular Weight (Monoisotopic): 242.1531AlogP: 2.62#Rotatable Bonds: 3
Polar Surface Area: 43.60Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.20CX LogP: 2.51CX LogD: 2.51
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.78Np Likeness Score: -1.50

References

1. KONISHI K, KURAGANO T.  (1990)  Fungicidal Activity of Pyrazolylpyrimidines,  15  (1): [10.1584/jpestics.15.13]

Source