(3R,4R,5S)-4-acetamido-5-amino-N-((1-(4-cyanobenzyl)-1H-1,2,3-triazol-4-yl)methyl)-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxamide

ID: ALA4456723

Chembl Id: CHEMBL4456723

PubChem CID: 155526160

Max Phase: Preclinical

Molecular Formula: C25H33N7O3

Molecular Weight: 479.59

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CCC(CC)O[C@@H]1C=C(C(=O)NCc2cn(Cc3ccc(C#N)cc3)nn2)C[C@H](N)[C@H]1NC(C)=O

Standard InChI:  InChI=1S/C25H33N7O3/c1-4-21(5-2)35-23-11-19(10-22(27)24(23)29-16(3)33)25(34)28-13-20-15-32(31-30-20)14-18-8-6-17(12-26)7-9-18/h6-9,11,15,21-24H,4-5,10,13-14,27H2,1-3H3,(H,28,34)(H,29,33)/t22-,23+,24+/m0/s1

Standard InChI Key:  ZHTWIMKGCCBYIL-RBZQAINGSA-N

Alternative Forms

  1. Parent:

    ALA4456723

    ---

Associated Targets(non-human)

NA Neuraminidase (1107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NA Neuraminidase (149 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

Calculated Properties

Molecular Weight: 479.59Molecular Weight (Monoisotopic): 479.2645AlogP: 1.55#Rotatable Bonds: 10
Polar Surface Area: 147.95Molecular Species: BASEHBA: 8HBD: 3
#RO5 Violations: HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 13.59CX Basic pKa: 9.11CX LogP: 1.28CX LogD: -0.42
Aromatic Rings: 2Heavy Atoms: 35QED Weighted: 0.47Np Likeness Score: -0.74

References

1. Ju H, Xiu S, Ding X, Shang M, Jia R, Huang B, Zhan P, Liu X..  (2020)  Discovery of novel 1,2,3-triazole oseltamivir derivatives as potent influenza neuraminidase inhibitors targeting the 430-cavity.,  187  [PMID:31835169] [10.1016/j.ejmech.2019.111940]

Source