7-[(4-Fluoro-3-((methylamino)methyl)phenoxy)methyl]quinolin-2-amine dihydrochloride

ID: ALA3735022

Chembl Id: CHEMBL3735022

PubChem CID: 127036483

Max Phase: Preclinical

Molecular Formula: C18H20Cl2FN3O

Molecular Weight: 311.36

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CNCc1cc(OCc2ccc3ccc(N)nc3c2)ccc1F.Cl.Cl

Standard InChI:  InChI=1S/C18H18FN3O.2ClH/c1-21-10-14-9-15(5-6-16(14)19)23-11-12-2-3-13-4-7-18(20)22-17(13)8-12;;/h2-9,21H,10-11H2,1H3,(H2,20,22);2*1H

Standard InChI Key:  UQCIKNKGXSVWJL-UHFFFAOYSA-N

Associated Targets(non-human)

Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos1 Nitric-oxide synthase, brain (2987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NOS3 Nitric-oxide synthase, endothelial (692 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: 311.36Molecular Weight (Monoisotopic): 311.1434AlogP: 3.25#Rotatable Bonds: 5
Polar Surface Area: 60.17Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 8.45CX LogP: 3.16CX LogD: 2.07
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.76Np Likeness Score: -0.79

References

1. Cinelli MA, Li H, Pensa AV, Kang S, Roman LJ, Martásek P, Poulos TL, Silverman RB..  (2015)  Phenyl Ether- and Aniline-Containing 2-Aminoquinolines as Potent and Selective Inhibitors of Neuronal Nitric Oxide Synthase.,  58  (21): [PMID:26469213] [10.1021/acs.jmedchem.5b01330]

Source