ID: ALA2402029

Max Phase: Preclinical

Molecular Formula: C18H19NO6

Molecular Weight: 345.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc2c(c1)oc(=O)n2Cc1cc(OC)c(OC)c(OC)c1

Standard InChI:  InChI=1S/C18H19NO6/c1-21-12-5-6-13-14(9-12)25-18(20)19(13)10-11-7-15(22-2)17(24-4)16(8-11)23-3/h5-9H,10H2,1-4H3

Standard InChI Key:  PUORVQNHIQNFOG-UHFFFAOYSA-N

Associated Targets(Human)

MDA-MB-231 73002 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

PC-3 62116 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Tubulin 1327 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: 345.35Molecular Weight (Monoisotopic): 345.1212AlogP: 2.68#Rotatable Bonds: 6
Polar Surface Area: 72.06Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.29CX LogD: 2.29
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.68Np Likeness Score: -0.68

References

1. Sun Y, Pandit B, Chettiar SN, Etter JP, Lewis A, Johnsamuel J, Li PK..  (2013)  Design, synthesis and biological studies of novel tubulin inhibitors.,  23  (15): [PMID:23790539] [10.1016/j.bmcl.2013.04.078]

Source