ID: ALA247284

Max Phase: Preclinical

Molecular Formula: C18H19IN2O4

Molecular Weight: 454.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=[N+]([O-])c1ccccc1COC(c1cccc(I)c1)C1CNCCO1

Standard InChI:  InChI=1S/C18H19IN2O4/c19-15-6-3-5-13(10-15)18(17-11-20-8-9-24-17)25-12-14-4-1-2-7-16(14)21(22)23/h1-7,10,17-18,20H,8-9,11-12H2

Standard InChI Key:  UHXNRRQHOOUQNZ-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: 454.26Molecular Weight (Monoisotopic): 454.0390AlogP: 3.45#Rotatable Bonds: 6
Polar Surface Area: 73.63Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.10CX LogP: 3.98CX LogD: 3.20
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.41Np Likeness Score: -0.81

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