ID: ALA4163633

Max Phase: Preclinical

Molecular Formula: C19H26Cl2N4O2

Molecular Weight: 340.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=N)NCc1cccc(CNC(=O)[C@@H](N)Cc2ccc(O)cc2)c1.Cl.Cl

Standard InChI:  InChI=1S/C19H24N4O2.2ClH/c1-13(20)22-11-15-3-2-4-16(9-15)12-23-19(25)18(21)10-14-5-7-17(24)8-6-14;;/h2-9,18,24H,10-12,21H2,1H3,(H2,20,22)(H,23,25);2*1H/t18-;;/m0../s1

Standard InChI Key:  OOQNOBCRTYFLII-NTEVMMBTSA-N

Associated Targets(non-human)

Nitric-oxide synthase, endothelial 692 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nitric oxide synthase, inducible 3573 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: 340.43Molecular Weight (Monoisotopic): 340.1899AlogP: 1.67#Rotatable Bonds: 7
Polar Surface Area: 111.23Molecular Species: BASEHBA: 4HBD: 5
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.52CX Basic pKa: 12.16CX LogP: 0.59CX LogD: -1.88
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.39Np Likeness Score: 0.23

References

1. Maccallini C, Di Matteo M, Gallorini M, Montagnani M, Graziani V, Ammazzalorso A, Amoia P, De Filippis B, Di Silvestre S, Fantacuzzi M, Giampietro L, Potenza MA, Re N, Pandolfi A, Cataldi A, Amoroso R..  (2018)  Discovery of N-{3-[(ethanimidoylamino)methyl]benzyl}-l-prolinamide dihydrochloride: A new potent and selective inhibitor of the inducible nitric oxide synthase as a promising agent for the therapy of malignant glioma.,  152  [PMID:29689474] [10.1016/j.ejmech.2018.04.027]

Source