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

ID: ALA3759390

Chembl Id: CHEMBL3759390

PubChem CID: 127024942

Max Phase: Preclinical

Molecular Formula: C16H15Cl2NO3

Molecular Weight: 340.21

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  NC(Cc1cc(Cl)c(Cl)c(-c2cccc(CO)c2)c1)C(=O)O

Standard InChI:  InChI=1S/C16H15Cl2NO3/c17-13-6-10(7-14(19)16(21)22)5-12(15(13)18)11-3-1-2-9(4-11)8-20/h1-6,14,20H,7-8,19H2,(H,21,22)

Standard InChI Key:  RJANMPORFOUXTF-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3759390

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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: 340.21Molecular Weight (Monoisotopic): 339.0429AlogP: 3.11#Rotatable Bonds: 5
Polar Surface Area: 83.55Molecular Species: ZWITTERIONHBA: 3HBD: 3
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 1.90CX Basic pKa: 9.42CX LogP: 0.90CX LogD: 0.90
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.78Np Likeness Score: 0.38

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