6'-fluoro-1'-[[5-methylsulfonyl-1-(4,4,4-trifluorobutyl)benzimidazol-2-yl]methyl]spiro[cyclopropane-1,3'-indoline]-2'-one

ID: ALA4873987

PubChem CID: 164627839

Max Phase: Preclinical

Molecular Formula: C23H21F4N3O3S

Molecular Weight: 495.50

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CS(=O)(=O)c1ccc2c(c1)nc(CN1C(=O)C3(CC3)c3ccc(F)cc31)n2CCCC(F)(F)F

Standard InChI:  InChI=1S/C23H21F4N3O3S/c1-34(32,33)15-4-6-18-17(12-15)28-20(29(18)10-2-7-23(25,26)27)13-30-19-11-14(24)3-5-16(19)22(8-9-22)21(30)31/h3-6,11-12H,2,7-10,13H2,1H3

Standard InChI Key:  NSZSVFLNKNEXKI-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4873987

    ---

Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human orthopneumovirus (392 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F Fusion glycoprotein F0 (67 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: 495.50Molecular Weight (Monoisotopic): 495.1240AlogP: 4.50#Rotatable Bonds: 6
Polar Surface Area: 72.27Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 3.07CX LogP: 3.38CX LogD: 3.38
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.47Np Likeness Score: -1.55

References

1. Cockerill GS, Angell RM, Bedernjak A, Chuckowree I, Fraser I, Gascon-Simorte J, Gilman MSA, Good JAD, Harland R, Johnson SM, Ludes-Meyers JH, Littler E, Lumley J, Lunn G, Mathews N, McLellan JS, Paradowski M, Peeples ME, Scott C, Tait D, Taylor G, Thom M, Thomas E, Villalonga Barber C, Ward SE, Watterson D, Williams G, Young P, Powell K..  (2021)  Discovery of Sisunatovir (RV521), an Inhibitor of Respiratory Syncytial Virus Fusion.,  64  (7.0): [PMID:33729773] [10.1021/acs.jmedchem.0c01882]

Source