ID: ALA460104

Max Phase: Preclinical

Molecular Formula: C16H11ClO4S

Molecular Weight: 334.78

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=S(=O)(c1ccc(Cl)cc1)c1cc(O)c2ccccc2c1O

Standard InChI:  InChI=1S/C16H11ClO4S/c17-10-5-7-11(8-6-10)22(20,21)15-9-14(18)12-3-1-2-4-13(12)16(15)19/h1-9,18-19H

Standard InChI Key:  SXWUEZFUYNUEML-UHFFFAOYSA-N

Associated Targets(non-human)

Beta-ketoacyl-ACP-synthase III 71 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

3-oxoacyl-[acyl-carrier-protein] synthase III 179 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium falciparum 966862 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: 334.78Molecular Weight (Monoisotopic): 334.0067AlogP: 3.74#Rotatable Bonds: 2
Polar Surface Area: 74.60Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.96CX Basic pKa: CX LogP: 4.56CX LogD: 4.00
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.70Np Likeness Score: -0.71

References

1. Alhamadsheh MM, Waters NC, Sachdeva S, Lee P, Reynolds KA..  (2008)  Synthesis and biological evaluation of novel sulfonyl-naphthalene-1,4-diols as FabH inhibitors.,  18  (24): [PMID:18996691] [10.1016/j.bmcl.2008.10.097]

Source