ID: ALA2288422

Max Phase: Preclinical

Molecular Formula: C13H18N4

Molecular Weight: 230.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCc1cc(CC)n(-c2nc(C)cc(C)n2)n1

Standard InChI:  InChI=1S/C13H18N4/c1-5-11-8-12(6-2)17(16-11)13-14-9(3)7-10(4)15-13/h7-8H,5-6H2,1-4H3

Standard InChI Key:  USIVEVYVKFUVOJ-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: 230.31Molecular Weight (Monoisotopic): 230.1531AlogP: 2.40#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: 2.19CX LogP: 2.63CX LogD: 2.63
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.81Np Likeness Score: -1.52

References

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

Source