(S)-9-Methoxy-12b-methyl-1,2,3,12b-tetrahydro-5-oxa-benzo[k]acephenanthrylene-6,8,11-trione

ID: ALA344243

Chembl Id: CHEMBL344243

PubChem CID: 10497902

Max Phase: Preclinical

Molecular Formula: C21H16O5

Molecular Weight: 348.35

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COC1=CC(=O)c2cc3c(cc2C1=O)C(=O)c1occ2c1[C@@]3(C)CCC2

Standard InChI:  InChI=1S/C21H16O5/c1-21-5-3-4-10-9-26-20(17(10)21)19(24)13-6-12-11(7-14(13)21)15(22)8-16(25-2)18(12)23/h6-9H,3-5H2,1-2H3/t21-/m0/s1

Standard InChI Key:  RGVWNPNSTILHHK-NRFANRHFSA-N

Associated Targets(Human)

HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

XRS6 (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Top2 DNA topoisomerase II (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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

Calculated Properties

Molecular Weight: 348.35Molecular Weight (Monoisotopic): 348.0998AlogP: 3.38#Rotatable Bonds: 1
Polar Surface Area: 73.58Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.81CX LogD: 2.81
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.79Np Likeness Score: 2.37

References

1. Concepción GP, Foderaro TA, Eldredge GS, Lobkovsky E, Clardy J, Barrows LR, Ireland CM..  (1995)  Topoisomerase II-mediated DNA cleavage by adocia- and xestoquinones from the Philippine sponge Xestospongia sp.,  38  (22): [PMID:7473578] [10.1021/jm00022a016]

Source