2-Chloro-N-((3R,4R)-3-fluoro-1-isopropylpiperidin-4-yl)-4-(trifluoromethyl)benzamide

ID: ALA4450131

Chembl Id: CHEMBL4450131

PubChem CID: 155521189

Max Phase: Preclinical

Molecular Formula: C16H19ClF4N2O

Molecular Weight: 366.79

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)N1CC[C@@H](NC(=O)c2ccc(C(F)(F)F)cc2Cl)[C@H](F)C1

Standard InChI:  InChI=1S/C16H19ClF4N2O/c1-9(2)23-6-5-14(13(18)8-23)22-15(24)11-4-3-10(7-12(11)17)16(19,20)21/h3-4,7,9,13-14H,5-6,8H2,1-2H3,(H,22,24)/t13-,14-/m1/s1

Standard InChI Key:  VNYMKPMXOYCTFQ-ZIAGYGMSSA-N

Alternative Forms

  1. Parent:

    ALA4450131

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Associated Targets(non-human)

H5N1 subtype (135 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: 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: 366.79Molecular Weight (Monoisotopic): 366.1122AlogP: 3.91#Rotatable Bonds: 3
Polar Surface Area: 32.34Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.48CX Basic pKa: 7.48CX LogP: 3.53CX LogD: 3.19
Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.82Np Likeness Score: -1.73

References

1. Gaisina IN, Peet NP, Cheng H, Li P, Du R, Cui Q, Furlong K, Manicassamy B, Caffrey M, Thatcher GRJ, Rong L..  (2020)  Optimization of 4-Aminopiperidines as Inhibitors of Influenza A Viral Entry That Are Synergistic with Oseltamivir.,  63  (6): [PMID:32069052] [10.1021/acs.jmedchem.9b01900]

Source