4-(4-bromophenyl)-4-fluoro-N-(3-fluoro-5-(trifluoromethyl)phenyl)piperidine-1-carboxamide

ID: ALA3618194

Chembl Id: CHEMBL3618194

PubChem CID: 122190862

Max Phase: Preclinical

Molecular Formula: C19H16BrF5N2O

Molecular Weight: 463.24

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1cc(F)cc(C(F)(F)F)c1)N1CCC(F)(c2ccc(Br)cc2)CC1

Standard InChI:  InChI=1S/C19H16BrF5N2O/c20-14-3-1-12(2-4-14)18(22)5-7-27(8-6-18)17(28)26-16-10-13(19(23,24)25)9-15(21)11-16/h1-4,9-11H,5-8H2,(H,26,28)

Standard InChI Key:  RCVXYEFHAASDEC-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3618194

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Associated Targets(Human)

S1PR2 Tchem Sphingosine 1-phosphate receptor Edg-5 (1593 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsome (8277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatocyte (2737 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

S1pr2 Sphingosine 1-phosphate receptor 2 (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsome (4459 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: 463.24Molecular Weight (Monoisotopic): 462.0366AlogP: 6.10#Rotatable Bonds: 2
Polar Surface Area: 32.34Molecular Species: NEUTRALHBA: 1HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.68CX Basic pKa: CX LogP: 4.97CX LogD: 4.97
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.54Np Likeness Score: -1.56

References

1. Kusumi K, Shinozaki K, Yamaura Y, Hashimoto A, Kurata H, Naganawa A, Ueda H, Otsuki K, Matsushita T, Sekiguchi T, Kakuuchi A, Seko T..  (2015)  Discovery of novel S1P2 antagonists. Part 2: Improving the profile of a series of 1,3-bis(aryloxy)benzene derivatives.,  25  (20): [PMID:26384288] [10.1016/j.bmcl.2015.09.022]

Source