ID: ALA4074094

Max Phase: Preclinical

Molecular Formula: C24H28O5

Molecular Weight: 396.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=CC(C)(C)c1cc2cc3c(cc2oc1=O)O[C@@H](C(C)(C)OC(=O)C=C(C)C)C3

Standard InChI:  InChI=1S/C24H28O5/c1-8-23(4,5)17-11-15-10-16-12-20(24(6,7)29-21(25)9-14(2)3)27-18(16)13-19(15)28-22(17)26/h8-11,13,20H,1,12H2,2-7H3/t20-/m1/s1

Standard InChI Key:  BBVKJQDXUKGIMY-HXUWFJFHSA-N

Associated Targets(Human)

P3HR-1 52 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human gammaherpesvirus 4 1538 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: 396.48Molecular Weight (Monoisotopic): 396.1937AlogP: 4.85#Rotatable Bonds: 5
Polar Surface Area: 65.74Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 5.36CX LogD: 5.36
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.31Np Likeness Score: 2.01

References

1. Lin Y, Wang Q, Gu Q, Zhang H, Jiang C, Hu J, Wang Y, Yan Y, Xu J..  (2017)  Semisynthesis of (-)-Rutamarin Derivatives and Their Inhibitory Activity on Epstein-Barr Virus Lytic Replication.,  80  (1): [PMID:28093914] [10.1021/acs.jnatprod.6b00415]

Source