ID: ALA1644519

Max Phase: Preclinical

Molecular Formula: C11H15BrFN3

Molecular Weight: 207.25

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Br.NCC[C@H]1CNC(c2ccccc2F)=N1

Standard InChI:  InChI=1S/C11H14FN3.BrH/c12-10-4-2-1-3-9(10)11-14-7-8(15-11)5-6-13;/h1-4,8H,5-7,13H2,(H,14,15);1H/t8-;/m0./s1

Standard InChI Key:  UOBWBCOLYXBTNQ-QRPNPIFTSA-N

Associated Targets(non-human)

Nischarin 241 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Adrenergic receptor alpha-2 3313 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: 207.25Molecular Weight (Monoisotopic): 207.1172AlogP: 0.89#Rotatable Bonds: 3
Polar Surface Area: 50.41Molecular Species: BASEHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.54CX LogP: 0.69CX LogD: -1.55
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.77Np Likeness Score: -0.08

References

1. Treder AP, Andruszkiewicz R, Zgoda W, Walkowiak A, Ford C, Hudson AL..  (2011)  New imidazoline/α(2)-adrenoceptors affecting compounds-4(5)-(2-aminoethyl)imidazoline (dihydrohistamine) derivatives. Synthesis and receptor affinity studies.,  19  (1): [PMID:21159515] [10.1016/j.bmc.2010.11.039]

Source