ID: ALA4876106

Max Phase: Preclinical

Molecular Formula: C30H28O10

Molecular Weight: 548.54

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COC1=C2c3c4c5c(c(O)cc(OC)c5c5c(OC)cc(O)c(c35)C1=O)C(=O)[C@@H](OC)[C@@]41C[C@](C)(O)[C@@H]2[C@@]1(C)O

Standard InChI:  InChI=1S/C30H28O10/c1-28(35)9-30-22-19-15(24(34)27(30)40-6)11(32)8-13(38-4)17(19)16-12(37-3)7-10(31)14-18(16)20(22)21(25(39-5)23(14)33)26(28)29(30,2)36/h7-8,26-27,31-32,35-36H,9H2,1-6H3/t26-,27-,28+,29-,30-/m1/s1

Standard InChI Key:  BZSUJBKWSNVUAD-CMPUJJQDSA-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: 548.54Molecular Weight (Monoisotopic): 548.1682AlogP: 2.96#Rotatable Bonds: 4
Polar Surface Area: 151.98Molecular Species: NEUTRALHBA: 10HBD: 4
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.98CX Basic pKa: CX LogP: 1.97CX LogD: 1.86
Aromatic Rings: 3Heavy Atoms: 40QED Weighted: 0.36Np Likeness Score: 2.10

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