ID: ALA2288419

Max Phase: Preclinical

Molecular Formula: C12H16N4

Molecular Weight: 216.29

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C12H16N4/c1-5-11-7-10(4)16(15-11)12-13-8(2)6-9(3)14-12/h6-7H,5H2,1-4H3

Standard InChI Key:  ICVOYIISIONDSH-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: 216.29Molecular Weight (Monoisotopic): 216.1375AlogP: 2.15#Rotatable Bonds: 2
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: 2.24CX LogP: 2.11CX LogD: 2.11
Aromatic Rings: 2Heavy Atoms: 16QED Weighted: 0.77Np Likeness Score: -2.02

References

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

Source