ID: ALA4208162

Max Phase: Preclinical

Molecular Formula: C15H13ClN2O6

Molecular Weight: 352.73

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N[C@H](Cc1cc(-c2cc(O)ccc2O)c(Cl)c([N+](=O)[O-])c1)C(=O)O

Standard InChI:  InChI=1S/C15H13ClN2O6/c16-14-10(9-6-8(19)1-2-13(9)20)3-7(4-11(17)15(21)22)5-12(14)18(23)24/h1-3,5-6,11,19-20H,4,17H2,(H,21,22)/t11-/m1/s1

Standard InChI Key:  XSAWTCPSWFHFII-LLVKDONJSA-N

Associated Targets(non-human)

Glutamate receptor ionotropic, AMPA 2 249 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Glutamate receptor ionotropic, AMPA 3 147 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: 352.73Molecular Weight (Monoisotopic): 352.0462AlogP: 2.28#Rotatable Bonds: 5
Polar Surface Area: 146.92Molecular Species: ZWITTERIONHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.33CX Basic pKa: 9.47CX LogP: 0.40CX LogD: 0.38
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.37Np Likeness Score: 0.47

References

1. Szymańska E, Nielsen B, Johansen TN, Cuñado Moral AM, Pickering DS, Szczepańska K, Mickowska A, Kieć-Kononowicz K..  (2017)  Pharmacological characterization and binding modes of novel racemic and optically active phenylalanine-based antagonists of AMPA receptors.,  138  [PMID:28738307] [10.1016/j.ejmech.2017.07.007]

Source