(RS)-2-Amino-3-(5,6-dichloro-3',5'-dihydroxybiphenyl-3-yl)-propanoic Acid

ID: ALA3759334

Chembl Id: CHEMBL3759334

PubChem CID: 127024939

Max Phase: Preclinical

Molecular Formula: C15H13Cl2NO4

Molecular Weight: 342.18

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  NC(Cc1cc(Cl)c(Cl)c(-c2cc(O)cc(O)c2)c1)C(=O)O

Standard InChI:  InChI=1S/C15H13Cl2NO4/c16-12-2-7(3-13(18)15(21)22)1-11(14(12)17)8-4-9(19)6-10(20)5-8/h1-2,4-6,13,19-20H,3,18H2,(H,21,22)

Standard InChI Key:  SJULDPMCSFALNL-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3759334

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Associated Targets(non-human)

Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grik1 Glutamate receptor ionotropic kainate 1 (319 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: 342.18Molecular Weight (Monoisotopic): 341.0222AlogP: 3.03#Rotatable Bonds: 4
Polar Surface Area: 103.78Molecular Species: ZWITTERIONHBA: 4HBD: 4
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 1.59CX Basic pKa: 9.53CX LogP: 1.06CX LogD: 1.05
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.68Np Likeness Score: 0.63

References

1. Szymanska E, Frydenvang K, Pickering DS, Krintel C, Nielsen B, Kooshki A, Zachariassen LG, Olsen L, Kastrup JS, Johansen TN..  (2016)  Studies on Aryl-Substituted Phenylalanines: Synthesis, Activity, and Different Binding Modes at AMPA Receptors.,  59  (1): [PMID:26653877] [10.1021/acs.jmedchem.5b01666]

Source