ID: ALA2443333

Max Phase: Preclinical

Molecular Formula: C18H14N2O3S2

Molecular Weight: 370.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(S(=O)(=O)n2ccc3ccnc(-c4cccs4)c32)cc1

Standard InChI:  InChI=1S/C18H14N2O3S2/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:  VLQQKULGYCFLGJ-UHFFFAOYSA-N

Associated Targets(Human)

Tubulin 5180 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MKN-45 2102 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HT-29 80576 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

KB 17409 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: 370.46Molecular Weight (Monoisotopic): 370.0446AlogP: 4.01#Rotatable Bonds: 4
Polar Surface Area: 61.19Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.08CX LogP: 3.44CX LogD: 3.44
Aromatic Rings: 4Heavy Atoms: 25QED Weighted: 0.54Np Likeness Score: -1.35

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