ID: ALA5172797

Max Phase: Preclinical

Molecular Formula: C22H20N2O5

Molecular Weight: 392.41

Associated Items:

Representations

Canonical SMILES:  CNC(=O)C1=C(C)N(c2cccc(OC)c2)C(=O)/C1=C\c1ccc(C(=O)O)cc1

Standard InChI:  InChI=1S/C22H20N2O5/c1-13-19(20(25)23-2)18(11-14-7-9-15(10-8-14)22(27)28)21(26)24(13)16-5-4-6-17(12-16)29-3/h4-12H,1-3H3,(H,23,25)(H,27,28)/b18-11-

Standard InChI Key:  ALTRNRFZLBLKEX-WQRHYEAKSA-N

Associated Targets(Human)

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 392.41Molecular Weight (Monoisotopic): 392.1372AlogP: 2.84#Rotatable Bonds: 5
Polar Surface Area: 95.94Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.08CX Basic pKa: CX LogP: 1.79CX LogD: -1.32
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.76Np Likeness Score: -0.93

References

1. Satoh H, Ochi S, Mizuno K, Saga Y, Ujita S, Toyoda M, Nishiyama Y, Tada K, Matsushita Y, Deguchi Y, Suzuki K, Tanaka Y, Ueda H, Inaba T, Hosoi Y, Morita A, Aoki S..  (2022)  Design, synthesis and biological evaluation of 2-pyrrolone derivatives as radioprotectors.,  67  [PMID:35635928] [10.1016/j.bmc.2022.116764]

Source