ID: ALA206163

Max Phase: Preclinical

Molecular Formula: C15H16O6

Molecular Weight: 292.29

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Oc1cccc2c(O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)cccc12

Standard InChI:  InChI=1S/C15H16O6/c16-10-5-1-4-9-8(10)3-2-6-12(9)21-15-14(19)13(18)11(17)7-20-15/h1-6,11,13-19H,7H2/t11-,13+,14-,15+/m1/s1

Standard InChI Key:  WKRVPJCKVWCWGJ-BEAPCOKYSA-N

Associated Targets(Human)

HFL1 (586 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T-24 (2342 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

BALB/3T3 (534 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SV3T3 (134 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: 292.29Molecular Weight (Monoisotopic): 292.0947AlogP: 0.36#Rotatable Bonds: 2
Polar Surface Area: 99.38Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.50CX Basic pKa: CX LogP: 0.72CX LogD: 0.71
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.64Np Likeness Score: 1.39

References

1. Jacobsson M, Ellervik U, Belting M, Mani K..  (2006)  Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.,  49  (6): [PMID:16539380] [10.1021/jm0512488]

Source