ID: ALA4859170

Max Phase: Preclinical

Molecular Formula: C30H24O8

Molecular Weight: 512.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1c2c3c4c(c(OC)c(=O)c5c(O)cc(OC)c(c6c(OC)ccc(c1=O)c63)c54)CC(C)=C2C(C)=O

Standard InChI:  InChI=1S/C30H24O8/c1-11-9-14-20-24-19-13(27(33)30(38-6)26(24)18(11)12(2)31)7-8-16(35-3)22(19)23-17(36-4)10-15(32)21(25(20)23)28(34)29(14)37-5/h7-8,10,32H,9H2,1-6H3

Standard InChI Key:  IYHSYNIZPLPHDX-UHFFFAOYSA-N

Associated Targets(non-human)

Spike glycoprotein 75 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 512.51Molecular Weight (Monoisotopic): 512.1471AlogP: 4.55#Rotatable Bonds: 5
Polar Surface Area: 108.36Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.12CX Basic pKa: 2.89CX LogP: 3.83CX LogD: 3.37
Aromatic Rings: 5Heavy Atoms: 38QED Weighted: 0.27Np Likeness Score: 1.35

References

1. Li YT, Yang C, Wu Y, Lv JJ, Feng X, Tian X, Zhou Z, Pan X, Liu S, Tian LW..  (2021)  Axial Chiral Binaphthoquinone and Perylenequinones from the Stromata of Hypocrella bambusae Are SARS-CoV-2 Entry Inhibitors.,  84  (2.0): [PMID:33560122] [10.1021/acs.jnatprod.0c01136]

Source