ID: ALA3314426

Max Phase: Preclinical

Molecular Formula: C15H14F2N2

Molecular Weight: 260.29

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C)c1ccc(/C=C/c2c(F)cccc2F)cn1

Standard InChI:  InChI=1S/C15H14F2N2/c1-19(2)15-9-7-11(10-18-15)6-8-12-13(16)4-3-5-14(12)17/h3-10H,1-2H3/b8-6+

Standard InChI Key:  YDOGFUMHYSQPOM-SOFGYWHQSA-N

Associated Targets(Human)

S-adenosylmethionine synthase isoform type-2 713 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 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: 260.29Molecular Weight (Monoisotopic): 260.1125AlogP: 3.60#Rotatable Bonds: 3
Polar Surface Area: 16.13Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.16CX LogP: 4.08CX LogD: 4.06
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.84Np Likeness Score: -1.34

References

1. Sviripa VM, Zhang W, Balia AG, Tsodikov OV, Nickell JR, Gizard F, Yu T, Lee EY, Dwoskin LP, Liu C, Watt DS..  (2014)  2',6'-Dihalostyrylanilines, pyridines, and pyrimidines for the inhibition of the catalytic subunit of methionine S-adenosyltransferase-2.,  57  (14): [PMID:24950374] [10.1021/jm5004864]

Source