ID: ALA3217991

Max Phase: Preclinical

Molecular Formula: C23H32O6

Molecular Weight: 404.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)c2c(c1)[C@@H](CCCC[C@H]1CCC[C@]3(CC[C@H](C)O3)O1)OC2=O

Standard InChI:  InChI=1S/C23H32O6/c1-15-10-12-23(28-15)11-6-8-16(29-23)7-4-5-9-19-18-13-17(25-2)14-20(26-3)21(18)22(24)27-19/h13-16,19H,4-12H2,1-3H3/t15-,16-,19+,23+/m0/s1

Standard InChI Key:  VSZPANPQXDVROZ-NBZRVGKJSA-N

Associated Targets(non-human)

Helicobacter pylori 3113 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: 404.50Molecular Weight (Monoisotopic): 404.2199AlogP: 4.94#Rotatable Bonds: 7
Polar Surface Area: 63.22Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.64CX Basic pKa: CX LogP: 4.48CX LogD: 4.48
Aromatic Rings: 1Heavy Atoms: 29QED Weighted: 0.47Np Likeness Score: 1.53

References

1. Dimitrov I, Furkert DP, Fraser JD, Radcliff FJ, Finch O, Brimble MA.  (2012)  Synthesis and anti-Helicobacter pylori activity of analogues of spirolaxine methyl ether,  (8): [10.1039/C2MD00314G]

Source