ID: ALA2443321

Max Phase: Preclinical

Molecular Formula: C21H19N3O4S

Molecular Weight: 409.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(Nc2nccc3ccn(S(=O)(=O)c4ccc(OC)cc4)c23)cc1

Standard InChI:  InChI=1S/C21H19N3O4S/c1-27-17-5-3-16(4-6-17)23-21-20-15(11-13-22-21)12-14-24(20)29(25,26)19-9-7-18(28-2)8-10-19/h3-14H,1-2H3,(H,22,23)

Standard InChI Key:  RIVMWYLRKBDGLS-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: 409.47Molecular Weight (Monoisotopic): 409.1096AlogP: 4.03#Rotatable Bonds: 6
Polar Surface Area: 82.45Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.29CX LogP: 3.50CX LogD: 3.50
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.52Np Likeness Score: -1.00

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