ID: ALA3392615

Max Phase: Preclinical

Molecular Formula: C20H17ClFN3O4S

Molecular Weight: 449.89

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOc1ccccc1NC(=O)c1nc(S(=O)(=O)Cc2ccccc2F)ncc1Cl

Standard InChI:  InChI=1S/C20H17ClFN3O4S/c1-2-29-17-10-6-5-9-16(17)24-19(26)18-14(21)11-23-20(25-18)30(27,28)12-13-7-3-4-8-15(13)22/h3-11H,2,12H2,1H3,(H,24,26)

Standard InChI Key:  ZCCMVUNZUGZJAF-UHFFFAOYSA-N

Associated Targets(Human)

Mothers against decapentaplegic homolog 3 68039 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosyl-DNA phosphodiesterase 1 345557 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Thioredoxin reductase 1, cytoplasmic 45279 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

ATP-dependent Clp protease proteolytic subunit 20705 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: 449.89Molecular Weight (Monoisotopic): 449.0612AlogP: 3.89#Rotatable Bonds: 7
Polar Surface Area: 98.25Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.91CX Basic pKa: CX LogP: 3.87CX LogD: 3.87
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.55Np Likeness Score: -2.25

References

1. PubChem BioAssay data set, 

Source

Source(1):