ID: ALA4857177

Max Phase: Preclinical

Molecular Formula: C36H33N3O7

Molecular Weight: 619.67

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C(OC[C@H]2O[C@@H](n3cc4c(nc3=O)Nc3ccccc3O4)C[C@@H]2O)(c2ccccc2)c2ccc(OC)cc2)cc1

Standard InChI:  InChI=1S/C36H33N3O7/c1-42-26-16-12-24(13-17-26)36(23-8-4-3-5-9-23,25-14-18-27(43-2)19-15-25)44-22-32-29(40)20-33(46-32)39-21-31-34(38-35(39)41)37-28-10-6-7-11-30(28)45-31/h3-19,21,29,32-33,40H,20,22H2,1-2H3,(H,37,38,41)/t29-,32+,33+/m0/s1

Standard InChI Key:  YJFRFVQDQPYFKL-PHCUSUGSSA-N

Associated Targets(non-human)

Tick-borne encephalitis virus 132 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: 619.67Molecular Weight (Monoisotopic): 619.2319AlogP: 5.77#Rotatable Bonds: 9
Polar Surface Area: 113.30Molecular Species: NEUTRALHBA: 10HBD: 2
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.99CX Basic pKa: CX LogP: 5.36CX LogD: 5.36
Aromatic Rings: 5Heavy Atoms: 46QED Weighted: 0.19Np Likeness Score: 0.14

References

1. Kozlovskaya LI, Volok VP, Shtro AA, Nikolaeva YV, Chistov AA, Matyugina ES, Belyaev ES, Jegorov AV, Snoeck R, Korshun VA, Andrei G, Osolodkin DI, Ishmukhametov AA, Aralov AV..  (2021)  Phenoxazine nucleoside derivatives with a multiple activity against RNA and DNA viruses.,  220  [PMID:33894564] [10.1016/j.ejmech.2021.113467]

Source