ID: ALA4566399

Max Phase: Preclinical

Molecular Formula: C15H12FN3O2S

Molecular Weight: 317.35

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NNC(=S)NC(=O)c1ccccc1)c1ccc(F)cc1

Standard InChI:  InChI=1S/C15H12FN3O2S/c16-12-8-6-11(7-9-12)14(21)18-19-15(22)17-13(20)10-4-2-1-3-5-10/h1-9H,(H,18,21)(H2,17,19,20,22)

Standard InChI Key:  CTBBUJAYQKQBKC-UHFFFAOYSA-N

Associated Targets(non-human)

Synechocystis sp. PCC 6803 30 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fructose-bisphosphate aldolase class 2 38 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 317.35Molecular Weight (Monoisotopic): 317.0634AlogP: 1.77#Rotatable Bonds: 2
Polar Surface Area: 70.23Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.76CX Basic pKa: CX LogP: 2.78CX LogD: 2.77
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.58Np Likeness Score: -2.02

References

1. Xiao S, Wei L, Hong Z, Rao L, Ren Y, Wan J, Feng L..  (2019)  Design, synthesis and algicides activities of thiourea derivatives as the novel scaffold aldolase inhibitors.,  27  (5): [PMID:30711311] [10.1016/j.bmc.2019.01.023]

Source