ID: ALA396328

Max Phase: Preclinical

Molecular Formula: C17H18INO2

Molecular Weight: 395.24

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 2-((2-Iodophenoxy)(Phenyl)Methyl)Morpholine
Synonyms from Alternative Forms(1):

    Canonical SMILES:  Ic1ccccc1OC(c1ccccc1)C1CNCCO1

    Standard InChI:  InChI=1S/C17H18INO2/c18-14-8-4-5-9-15(14)21-17(13-6-2-1-3-7-13)16-12-19-10-11-20-16/h1-9,16-17,19H,10-12H2

    Standard InChI Key:  BHMLFPOTZYRDKA-UHFFFAOYSA-N

    Associated Targets(non-human)

    Norepinephrine transporter 2222 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Dopamine transporter 6071 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Serotonin transporter 6087 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

    Properties

    Molecular Weight: 395.24Molecular Weight (Monoisotopic): 395.0382AlogP: 3.40#Rotatable Bonds: 4
    Polar Surface Area: 30.49Molecular Species: NEUTRALHBA: 3HBD: 1
    #RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
    CX Acidic pKa: CX Basic pKa: 7.91CX LogP: 4.01CX LogD: 3.38
    Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.81Np Likeness Score: -0.14

    References

    1. Tamagnan GD, Brenner E, Alagille D, Staley JK, Haile C, Koren A, Early M, Baldwin RM, Tarazi FI, Baldessarini RJ, Jarkas N, Goodman MM, Seibyl JP..  (2007)  Development of SPECT imaging agents for the norepinephrine transporters: [123I]INER.,  17  (2): [PMID:17095215] [10.1016/j.bmcl.2006.10.018]

    Source