ID: ALA4863303

Max Phase: Preclinical

Molecular Formula: C24H31NO6

Molecular Weight: 429.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ncc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O

Standard InChI:  InChI=1S/C24H31NO6/c1-15-21(9-8-18(22(15)27)20(26)13-24(3,4)5)31-11-7-6-10-30-17-12-19(23(28)29)16(2)25-14-17/h8-9,12,14,27H,6-7,10-11,13H2,1-5H3,(H,28,29)

Standard InChI Key:  HXFYIHVUJKIJBT-UHFFFAOYSA-N

Associated Targets(non-human)

Metabotropic glutamate receptor 3 981 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Metabotropic glutamate receptor 2 1326 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 429.51Molecular Weight (Monoisotopic): 429.2151AlogP: 4.96#Rotatable Bonds: 10
Polar Surface Area: 105.95Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 2.71CX Basic pKa: 4.54CX LogP: 3.69CX LogD: 1.41
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.41Np Likeness Score: -0.24

References

1. Yamada Y, Gilliland K, Xiang Z, Haymer D, Crocker KE, Loch MT, Schulte ML, Rodriguez AL, Niswender CM, Jeffrey Conn P, Lindsley CW, Melancon BJ..  (2021)  Positive allosteric modulators (PAMs) of the group II metabotropic glutamate receptors: Design, synthesis, and evaluation as ex-vivo tool compounds.,  50  [PMID:34461178] [10.1016/j.bmcl.2021.128342]

Source