ID: ALA4217944

Max Phase: Preclinical

Molecular Formula: C14H16FN3O3S

Molecular Weight: 325.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1cc(OCCNCc2ccc(S(=O)(=O)F)cc2)ccn1

Standard InChI:  InChI=1S/C14H16FN3O3S/c15-22(19,20)13-3-1-11(2-4-13)10-17-7-8-21-12-5-6-18-14(16)9-12/h1-6,9,17H,7-8,10H2,(H2,16,18)

Standard InChI Key:  OJWQOESXUVIZMC-UHFFFAOYSA-N

Associated Targets(non-human)

cya Calmodulin-sensitive adenylate cyclase (164 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 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: 325.36Molecular Weight (Monoisotopic): 325.0896AlogP: 1.49#Rotatable Bonds: 7
Polar Surface Area: 94.31Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.53CX LogP: 1.38CX LogD: -0.27
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.59Np Likeness Score: -0.30

References

1. Jiao GS, Kim S, Moayeri M, Thai A, Cregar-Hernandez L, McKasson L, O'Malley S, Leppla SH, Johnson AT..  (2018)  Small molecule inhibitors of anthrax edema factor.,  28  (2): [PMID:29198864] [10.1016/j.bmcl.2017.11.040]

Source