ID: ALA553726

Max Phase: Preclinical

Molecular Formula: C12H15ClN2O2

Molecular Weight: 218.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cccc2c1OC(C1=NCCN1)C2.Cl

Standard InChI:  InChI=1S/C12H14N2O2.ClH/c1-15-9-4-2-3-8-7-10(16-11(8)9)12-13-5-6-14-12;/h2-4,10H,5-7H2,1H3,(H,13,14);1H

Standard InChI Key:  AFETZMJAWPHWRE-UHFFFAOYSA-N

Associated Targets(non-human)

Alpha-2 adrenergic receptor 120 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Adrenergic receptor alpha-1 5652 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: 218.26Molecular Weight (Monoisotopic): 218.1055AlogP: 1.00#Rotatable Bonds: 2
Polar Surface Area: 42.85Molecular Species: BASEHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.10CX LogP: 0.98CX LogD: -0.65
Aromatic Rings: 1Heavy Atoms: 16QED Weighted: 0.80Np Likeness Score: 0.49

References

1. Chapleo CB, Myers PL, Butler RC, Davis JA, Doxey JC, Higgins SD, Myers M, Roach AG, Smith CF, Stillings MR..  (1984)  Alpha-adrenoreceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on alpha-adrenoreceptor activity.,  27  (5): [PMID:6143826] [10.1021/jm00371a003]

Source