ID: ALA2408700

Max Phase: Preclinical

Molecular Formula: C16H11FN2O4S

Molecular Weight: 346.34

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1c(C2Nc3ccccc3S(=O)(=O)N2)coc2ccc(F)cc12

Standard InChI:  InChI=1S/C16H11FN2O4S/c17-9-5-6-13-10(7-9)15(20)11(8-23-13)16-18-12-3-1-2-4-14(12)24(21,22)19-16/h1-8,16,18-19H

Standard InChI Key:  AYKFLTDUIZGVBD-UHFFFAOYSA-N

Associated Targets(Human)

5'-nucleotidase 622 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Alkaline phosphatase, tissue-nonspecific isozyme 128 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Intestinal alkaline phosphatase 300 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

5'-nucleotidase 305 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: 346.34Molecular Weight (Monoisotopic): 346.0424AlogP: 2.33#Rotatable Bonds: 1
Polar Surface Area: 88.41Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.20CX Basic pKa: CX LogP: 1.88CX LogD: 1.87
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.71Np Likeness Score: -0.80

References

1. al-Rashida M, Raza R, Abbas G, Shah MS, Kostakis GE, Lecka J, Sévigny J, Muddassar M, Papatriantafyllopoulou C, Iqbal J..  (2013)  Identification of novel chromone based sulfonamides as highly potent and selective inhibitors of alkaline phosphatases.,  66  [PMID:23831808] [10.1016/j.ejmech.2013.06.015]
2. al-Rashida M, Batool G, Sattar A, Ejaz SA, Khan S, Lecka J, Sévigny J, Hameed A, Iqbal J..  (2016)  2-Alkoxy-3-(sulfonylarylaminomethylene)-chroman-4-ones as potent and selective inhibitors of ectonucleotidases.,  115  [PMID:27054295] [10.1016/j.ejmech.2016.02.073]

Source