ID: ALA2443324

Max Phase: Preclinical

Molecular Formula: C20H16N2O4S

Molecular Weight: 380.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(S(=O)(=O)n2ccc3ccnc(-c4ccc(O)cc4)c32)cc1

Standard InChI:  InChI=1S/C20H16N2O4S/c1-26-17-6-8-18(9-7-17)27(24,25)22-13-11-15-10-12-21-19(20(15)22)14-2-4-16(23)5-3-14/h2-13,23H,1H3

Standard InChI Key:  QUYSARHLBUKCRH-UHFFFAOYSA-N

Associated Targets(Human)

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: 380.43Molecular Weight (Monoisotopic): 380.0831AlogP: 3.65#Rotatable Bonds: 4
Polar Surface Area: 81.42Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.49CX Basic pKa: 3.24CX LogP: 3.36CX LogD: 3.35
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.58Np Likeness Score: -0.57

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