ID: ALA5198204

Max Phase: Preclinical

Molecular Formula: C28H35N7O2

Molecular Weight: 501.64

Associated Items:

Representations

Canonical SMILES:  CC(C)c1nnc2ccc(O[C@@H]3CC[C@H](NC(=O)Nc4cc(C(C)(C)C)nn4C)c4ccccc43)cn12

Standard InChI:  InChI=1S/C28H35N7O2/c1-17(2)26-32-31-24-14-11-18(16-35(24)26)37-22-13-12-21(19-9-7-8-10-20(19)22)29-27(36)30-25-15-23(28(3,4)5)33-34(25)6/h7-11,14-17,21-22H,12-13H2,1-6H3,(H2,29,30,36)/t21-,22+/m0/s1

Standard InChI Key:  FBVITWOBMBQCDO-FCHUYYIVSA-N

Associated Targets(Human)

MAP kinase p38 alpha 12866 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: 501.64Molecular Weight (Monoisotopic): 501.2852AlogP: 5.66#Rotatable Bonds: 5
Polar Surface Area: 98.37Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.95CX Basic pKa: 2.84CX LogP: 4.56CX LogD: 4.56
Aromatic Rings: 4Heavy Atoms: 37QED Weighted: 0.37Np Likeness Score: -1.41

References

1. Armani E, Capaldi C, Bagnacani V, Saccani F, Aquino G, Puccini P, Facchinetti F, Martucci C, Moretto N, Villetti G, Patacchini R, Civelli M, Hurley C, Jennings A, Alcaraz L, Bloomfield D, Briggs M, Daly S, Panchal T, Russell V, Wicks S, Finch H, Fitzgerald M, Fox C, Delcanale M..  (2022)  Design, Synthesis, and Biological Characterization of Inhaled p38α/β MAPK Inhibitors for the Treatment of Lung Inflammatory Diseases.,  65  (10.0): [PMID:35546685] [10.1021/acs.jmedchem.2c00115]

Source