ID: ALA5271501

Max Phase: Preclinical

Molecular Formula: C19H26N2O2

Molecular Weight: 314.43

Associated Items:

Representations

Canonical SMILES:  CC12CN3CC(C)(CN(C1)C3C1=CC(=O)[C@H]3C[C@@H]1C3(C)C)C2=O

Standard InChI:  InChI=1S/C19H26N2O2/c1-17(2)12-6-13(17)14(22)5-11(12)15-20-7-18(3)8-21(15)10-19(4,9-20)16(18)23/h5,12-13,15H,6-10H2,1-4H3/t12-,13+,15?,18?,19?/m0/s1

Standard InChI Key:  OUGZNEFXXKBMDR-VXRSPYDMSA-N

Associated Targets(non-human)

MDCK 10148 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Influenza A virus 11224 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 314.43Molecular Weight (Monoisotopic): 314.1994AlogP: 1.71#Rotatable Bonds: 1
Polar Surface Area: 40.62Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.67CX LogP: 2.67CX LogD: 2.66
Aromatic Rings: 0Heavy Atoms: 23QED Weighted: 0.74Np Likeness Score: 1.06

References

1. Suslov E, Zarubaev VV, Slita AV, Ponomarev K, Korchagina D, Ayine-Tora DM, Reynisson J, Volcho K, Salakhutdinov N..  (2017)  Anti-influenza activity of diazaadamantanes combined with monoterpene moieties.,  27  (19): [PMID:28886889] [10.1016/j.bmcl.2017.08.062]

Source