ID: ALA5285500

Max Phase: Preclinical

Molecular Formula: C15H14N2O5S

Molecular Weight: 334.35

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C)c(S(=O)(=O)NC(=O)c2cc(C(=O)O)ccn2)c1

Standard InChI:  InChI=1S/C15H14N2O5S/c1-9-3-4-10(2)13(7-9)23(21,22)17-14(18)12-8-11(15(19)20)5-6-16-12/h3-8H,1-2H3,(H,17,18)(H,19,20)

Standard InChI Key:  WXOVOSNHBREVJB-UHFFFAOYSA-N

Associated Targets(Human)

FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALKBH2 Tbio DNA oxidative demethylase ALKBH2 (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALKBH3 Tchem Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALKBH5 Tchem RNA demethylase ALKBH5 (134 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 334.35Molecular Weight (Monoisotopic): 334.0623AlogP: 1.52#Rotatable Bonds: 4
Polar Surface Area: 113.43Molecular Species: ACIDHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.41CX Basic pKa: 0.16CX LogP: 2.27CX LogD: -2.02
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.88Np Likeness Score: -1.27

References

1. Perry GS, Das M, Woon ECY..  (2021)  Inhibition of AlkB Nucleic Acid Demethylases: Promising New Epigenetic Targets.,  64  (23.0): [PMID:34792334] [10.1021/acs.jmedchem.1c01694]

Source