ID: ALA4100224

Max Phase: Preclinical

Molecular Formula: C23H25N5O2

Molecular Weight: 403.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Cn1c2ccccc2c2nc3ccccc3nc21)NCCCN1CCOCC1

Standard InChI:  InChI=1S/C23H25N5O2/c29-21(24-10-5-11-27-12-14-30-15-13-27)16-28-20-9-4-1-6-17(20)22-23(28)26-19-8-3-2-7-18(19)25-22/h1-4,6-9H,5,10-16H2,(H,24,29)

Standard InChI Key:  ZUESPZVOZJFJJD-UHFFFAOYSA-N

Associated Targets(non-human)

CV-1 316 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vaccinia virus 4609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vesicular stomatitis virus 4460 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: 403.49Molecular Weight (Monoisotopic): 403.2008AlogP: 2.58#Rotatable Bonds: 6
Polar Surface Area: 72.28Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.00CX LogP: 2.15CX LogD: 2.00
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.50Np Likeness Score: -1.58

References

1. Klimenko K, Lyakhov S, Shibinskaya M, Karpenko A, Marcou G, Horvath D, Zenkova M, Goncharova E, Amirkhanov R, Krysko A, Andronati S, Levandovskiy I, Polishchuk P, Kuz'min V, Varnek A..  (2017)  Virtual screening, synthesis and biological evaluation of DNA intercalating antiviral agents.,  27  (16): [PMID:28666733] [10.1016/j.bmcl.2017.06.035]

Source