ID: ALA4218248

Max Phase: Preclinical

Molecular Formula: C39H64N12O4

Molecular Weight: 765.02

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(CC)c1ccc(/N=N/c2ccc(C(=O)N[C@@H](CC(N)=O)C(=O)NCCCCCCCCCNCCCNC(=O)[C@@H](N)CCCNC(=N)N)cc2)cc1

Standard InChI:  InChI=1S/C39H64N12O4/c1-3-51(4-2)32-21-19-31(20-22-32)50-49-30-17-15-29(16-18-30)36(53)48-34(28-35(41)52)38(55)46-25-11-9-7-5-6-8-10-23-44-24-13-27-45-37(54)33(40)14-12-26-47-39(42)43/h15-22,33-34,44H,3-14,23-28,40H2,1-2H3,(H2,41,52)(H,45,54)(H,46,55)(H,48,53)(H4,42,43,47)/b50-49+/t33-,34-/m0/s1

Standard InChI Key:  OQXFUYHFWLMALK-ZAHVXGADSA-N

Associated Targets(non-human)

Glutamate receptor ionotropic, AMPA 1 398 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: 765.02Molecular Weight (Monoisotopic): 764.5173AlogP: 3.46#Rotatable Bonds: 29
Polar Surface Area: 258.30Molecular Species: BASEHBA: 10HBD: 9
#RO5 Violations: 2HBA (Lipinski): 16HBD (Lipinski): 12#RO5 Violations (Lipinski): 3
CX Acidic pKa: CX Basic pKa: 12.20CX LogP: 2.54CX LogD: -3.47
Aromatic Rings: 2Heavy Atoms: 55QED Weighted: 0.03Np Likeness Score: -0.30

References

1. Nørager NG, Poulsen MH, Strømgaard K..  (2018)  Controlling Ca2+ Permeable α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA) Receptors with Photochromic Ion Channel Blockers.,  61  (17): [PMID:30125106] [10.1021/acs.jmedchem.8b00756]

Source