ID: ALA2234471

Max Phase: Preclinical

Molecular Formula: C56H46O6

Molecular Weight: 814.98

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1CC(c2ccccc2)CC2=C1C(c1cccc(C3C4=C(CC(c5ccccc5)CC4=O)OC4=C3C(=O)CC(c3ccccc3)C4)c1)C1=C(CC(c3ccccc3)CC1=O)O2

Standard InChI:  InChI=1S/C56H46O6/c57-43-25-39(33-14-5-1-6-15-33)29-47-53(43)51(54-44(58)26-40(30-48(54)61-47)34-16-7-2-8-17-34)37-22-13-23-38(24-37)52-55-45(59)27-41(35-18-9-3-10-19-35)31-49(55)62-50-32-42(28-46(60)56(50)52)36-20-11-4-12-21-36/h1-24,39-42,51-52H,25-32H2

Standard InChI Key:  VWGQOFKAKODZTG-UHFFFAOYSA-N

Associated Targets(non-human)

Aspergillus niger 16508 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhodotorula mucilaginosa 339 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Proteus vulgaris 5823 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nocardia canis 47 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus epidermidis 22802 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus cereus 7522 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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: 814.98Molecular Weight (Monoisotopic): 814.3294AlogP: 11.52#Rotatable Bonds: 6
Polar Surface Area: 86.74Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 9.16CX LogD: 9.16
Aromatic Rings: 5Heavy Atoms: 62QED Weighted: 0.17Np Likeness Score: -0.08

References

1. Kaya M, Basar E, Colak F.  (2011)  Synthesis and antimicrobial activity of some bisoctahydroxanthene-1,8-dione derivatives,  20  (8): [10.1007/s00044-010-9459-2]

Source