ID: ALA3217985

Max Phase: Preclinical

Molecular Formula: C23H33NO4

Molecular Weight: 387.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)c2ccn(CCCC[C@H]3CCC[C@]4(CC[C@H](C)O4)O3)c2c1

Standard InChI:  InChI=1S/C23H33NO4/c1-17-9-12-23(27-17)11-6-8-18(28-23)7-4-5-13-24-14-10-20-21(24)15-19(25-2)16-22(20)26-3/h10,14-18H,4-9,11-13H2,1-3H3/t17-,18-,23+/m0/s1

Standard InChI Key:  OLBCIQVOCOCECS-IUKKYPGJSA-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: 387.52Molecular Weight (Monoisotopic): 387.2410AlogP: 5.29#Rotatable Bonds: 7
Polar Surface Area: 41.85Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.74CX LogD: 4.74
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.61Np Likeness Score: 0.43

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