ID: ALA4751659

Max Phase: Preclinical

Molecular Formula: C28H28BrNO4S

Molecular Weight: 554.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc2c(Oc3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(Br)cc3)[s+]([O-])c2c1

Standard InChI:  InChI=1S/C28H28BrNO4S/c1-32-24-13-14-25-26(19-24)35(31)28(20-5-7-21(29)8-6-20)27(25)34-23-11-9-22(10-12-23)33-18-17-30-15-3-2-4-16-30/h5-14,19H,2-4,15-18H2,1H3

Standard InChI Key:  DTSJMKXTEZOGKV-UHFFFAOYSA-N

Associated Targets(non-human)

Zaire ebolavirus 77 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Marburgvirus 118 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: 554.51Molecular Weight (Monoisotopic): 553.0922AlogP: 7.66#Rotatable Bonds: 8
Polar Surface Area: 53.99Molecular Species: BASEHBA: 5HBD: 0
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 8.78CX LogP: 5.11CX LogD: 3.72
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.21Np Likeness Score: -0.62

References

1. Cooper L,Schafer A,Li Y,Cheng H,Medegan Fagla B,Shen Z,Nowar R,Dye K,Anantpadma M,Davey RA,Thatcher GRJ,Rong L,Xiong R.  (2020)  Screening and Reverse-Engineering of Estrogen Receptor Ligands as Potent Pan-Filovirus Inhibitors.,  63  (19.0): [PMID:32886512] [10.1021/acs.jmedchem.0c01001]

Source