ID: ALA1824115

Max Phase: Preclinical

Molecular Formula: C24H22N2O5S

Molecular Weight: 450.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1(C)C=Cc2cc(CN(c3ccccc3)S(=O)(=O)c3ccc([N+](=O)[O-])cc3)ccc2O1

Standard InChI:  InChI=1S/C24H22N2O5S/c1-24(2)15-14-19-16-18(8-13-23(19)31-24)17-25(20-6-4-3-5-7-20)32(29,30)22-11-9-21(10-12-22)26(27)28/h3-16H,17H2,1-2H3

Standard InChI Key:  PQBZWKNGVRLLPK-UHFFFAOYSA-N

Associated Targets(Human)

Hypoxia inducible factors; HIF-1-alpha, HIF-2-alpha 820 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: 450.52Molecular Weight (Monoisotopic): 450.1249AlogP: 5.17#Rotatable Bonds: 6
Polar Surface Area: 89.75Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.25CX LogD: 5.25
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.38Np Likeness Score: -0.57

References

1. Tan C, de Noronha RG, Devi NS, Jabbar AA, Kaluz S, Liu Y, Mooring SR, Nicolaou KC, Wang B, Van Meir EG..  (2011)  Sulfonamides as a new scaffold for hypoxia inducible factor pathway inhibitors.,  21  (18): [PMID:21831638] [10.1016/j.bmcl.2011.06.099]
2. Mun J, Jabbar AA, Devi NS, Liu Y, Van Meir EG, Goodman MM..  (2012)  Structure-activity relationship of 2,2-dimethyl-2H-chromene based arylsulfonamide analogs of 3,4-dimethoxy-N-[(2,2-dimethyl-2H-chromen-6-yl)methyl]-N-phenylbenzenesulfonamide, a novel small molecule hypoxia inducible factor-1 (HIF-1) pathway inhibitor and anti-cancer agent.,  20  (14): [PMID:22682301] [10.1016/j.bmc.2012.04.064]

Source