(R)-1-(4-(benzofuran-5-ylmethyl)pyridin-2-yl)-N-(3-fluoro-2-hydroxypropyl)indoline-4-carboxamide

ID: ALA4866543

Chembl Id: CHEMBL4866543

PubChem CID: 122653724

Max Phase: Preclinical

Molecular Formula: C26H24FN3O3

Molecular Weight: 445.49

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(NC[C@@H](O)CF)c1cccc2c1CCN2c1cc(Cc2ccc3occc3c2)ccn1

Standard InChI:  InChI=1S/C26H24FN3O3/c27-15-20(31)16-29-26(32)22-2-1-3-23-21(22)7-10-30(23)25-14-18(6-9-28-25)12-17-4-5-24-19(13-17)8-11-33-24/h1-6,8-9,11,13-14,20,31H,7,10,12,15-16H2,(H,29,32)/t20-/m0/s1

Standard InChI Key:  LIXIVUDDNQRTCC-FQEVSTJZSA-N

Alternative Forms

  1. Parent:

    ALA4866543

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Associated Targets(Human)

GPR52 Tchem Probable G-protein coupled receptor 52 (435 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: 445.49Molecular Weight (Monoisotopic): 445.1802AlogP: 4.17#Rotatable Bonds: 7
Polar Surface Area: 78.60Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 13.76CX Basic pKa: 5.58CX LogP: 3.95CX LogD: 3.94
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.45Np Likeness Score: -0.57

References

1.  (2020)  1-heteroaryl-indoline-4-carboxamides as modulators of gpr52 useful for the treatment or prevention of disorders related thereto, 

Source