ID: ALA2253340

Max Phase: Preclinical

Molecular Formula: C16H13FN6O3

Molecular Weight: 356.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=CCN1C(=O)COc2cc(F)c(-n3nnc4c(cnn4C)c3=O)cc21

Standard InChI:  InChI=1S/C16H13FN6O3/c1-3-4-22-12-6-11(10(17)5-13(12)26-8-14(22)24)23-16(25)9-7-18-21(2)15(9)19-20-23/h3,5-7H,1,4,8H2,2H3

Standard InChI Key:  YJLVIFBRSVZSDT-UHFFFAOYSA-N

Associated Targets(non-human)

Digitaria sanguinalis 1594 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Echinochloa crus-galli 3685 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Amaranthus retroflexus 1838 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Brassica rapa subsp. oleifera 1696 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protoporphyrinogen IX oxidase 35 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: 356.32Molecular Weight (Monoisotopic): 356.1033AlogP: 0.56#Rotatable Bonds: 3
Polar Surface Area: 95.14Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.71CX LogD: 1.71
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.64Np Likeness Score: -2.09

References

1. Li HB, Zhu YQ, Song XW, Hu FZ, Liu B, Li YH, Niu ZX, Liu P, Wang ZH, Song HB, Zou XM, Yang HZ..  (2008)  Novel protoporphyrinogen oxidase inhibitors: 3H-pyrazolo[3,4-d][1,2,3]triazin-4-one derivatives.,  56  (20): [PMID:18808144] [10.1021/jf801774k]

Source