ID: ALA2414428

Max Phase: Preclinical

Molecular Formula: C19H28N4

Molecular Weight: 312.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(N)nc(CCCCCCCc2cc(C)cc(N)n2)c1

Standard InChI:  InChI=1S/C19H28N4/c1-14-10-16(22-18(20)12-14)8-6-4-3-5-7-9-17-11-15(2)13-19(21)23-17/h10-13H,3-9H2,1-2H3,(H2,20,22)(H2,21,23)

Standard InChI Key:  FSVLONGGRYPEKX-UHFFFAOYSA-N

Associated Targets(non-human)

Nitric oxide synthase, inducible 3573 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric-oxide synthase, endothelial 692 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric-oxide synthase, brain 2987 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: 312.46Molecular Weight (Monoisotopic): 312.2314AlogP: 3.99#Rotatable Bonds: 8
Polar Surface Area: 77.82Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.47CX LogP: 4.60CX LogD: 2.99
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.72Np Likeness Score: -0.11

References

1. Jing Q, Li H, Fang J, Roman LJ, Martásek P, Poulos TL, Silverman RB..  (2013)  In search of potent and selective inhibitors of neuronal nitric oxide synthase with more simple structures.,  21  (17): [PMID:23867386] [10.1016/j.bmc.2013.06.014]

Source