ID: ALA2443332

Max Phase: Preclinical

Molecular Formula: C18H14N2O4S

Molecular Weight: 354.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(S(=O)(=O)n2ccc3ccnc(-c4ccco4)c32)cc1

Standard InChI:  InChI=1S/C18H14N2O4S/c1-23-14-4-6-15(7-5-14)25(21,22)20-11-9-13-8-10-19-17(18(13)20)16-3-2-12-24-16/h2-12H,1H3

Standard InChI Key:  IZAAPPPGNNSEMR-UHFFFAOYSA-N

Associated Targets(Human)

Tubulin 5180 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

KB 17409 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HT-29 80576 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HUVEC 11049 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MKN-45 2102 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 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: 354.39Molecular Weight (Monoisotopic): 354.0674AlogP: 3.54#Rotatable Bonds: 4
Polar Surface Area: 74.33Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.25CX LogP: 2.72CX LogD: 2.72
Aromatic Rings: 4Heavy Atoms: 25QED Weighted: 0.56Np Likeness Score: -1.12

References

1. Lee HY, Pan SL, Su MC, Liu YM, Kuo CC, Chang YT, Wu JS, Nien CY, Mehndiratta S, Chang CY, Wu SY, Lai MJ, Chang JY, Liou JP..  (2013)  Furanylazaindoles: potent anticancer agents in vitro and in vivo.,  56  (20): [PMID:24106982] [10.1021/jm4011115]

Source