N-methyl-4-homoisotwistane-3-carboxamide

ID: ALA3276692

Chembl Id: CHEMBL3276692

Cas Number: 58432-99-8

PubChem CID: 516775

Max Phase: Preclinical

Molecular Formula: C13H21NO

Molecular Weight: 207.32

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CNC(=O)C12CCCC3CC(CCC31)C2

Standard InChI:  InChI=1S/C13H21NO/c1-14-12(15)13-6-2-3-10-7-9(8-13)4-5-11(10)13/h9-11H,2-8H2,1H3,(H,14,15)

Standard InChI Key:  HJMRXYVXEPANLV-UHFFFAOYSA-N

Associated Targets(non-human)

Newcastle disease virus (78 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

Calculated Properties

Molecular Weight: 207.32Molecular Weight (Monoisotopic): 207.1623AlogP: 2.34#Rotatable Bonds: 1
Polar Surface Area: 29.10Molecular Species: NEUTRALHBA: 1HBD: 1
#RO5 Violations: HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 0.24CX LogP: 2.24CX LogD: 2.24
Aromatic Rings: Heavy Atoms: 15QED Weighted: 0.70Np Likeness Score: 1.12

References

1. Aigami K, Inamoto Y, Takaishi N, Fujikura Y..  (1976)  Biologically active polycycloalkanes. 2. Antiviral 4-homoisotwistane derivatives.,  19  (4): [PMID:1263206] [10.1021/jm00226a018]

Source