ID: ALA4587278

Max Phase: Preclinical

Molecular Formula: C19H21FN2O5S

Molecular Weight: 408.45

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C(=O)O)cc1S(=O)(=O)Nc1cc(F)ccc1N1CCCCC1

Standard InChI:  InChI=1S/C19H21FN2O5S/c1-27-17-8-5-13(19(23)24)11-18(17)28(25,26)21-15-12-14(20)6-7-16(15)22-9-3-2-4-10-22/h5-8,11-12,21H,2-4,9-10H2,1H3,(H,23,24)

Standard InChI Key:  UBKLNIFGBDJHPL-UHFFFAOYSA-N

Associated Targets(Human)

Endoplasmic reticulum aminopeptidase 2 387 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Endoplasmic reticulum aminopeptidase 1 581 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Interleukin-1 receptor antagonist protein 23 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: 408.45Molecular Weight (Monoisotopic): 408.1155AlogP: 3.32#Rotatable Bonds: 6
Polar Surface Area: 95.94Molecular Species: ACIDHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.19CX Basic pKa: 3.47CX LogP: 2.64CX LogD: -0.60
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.76Np Likeness Score: -1.76

References

1. Maben Z, Arya R, Rane D, An WF, Metkar S, Hickey M, Bender S, Ali A, Nguyen TT, Evnouchidou I, Schilling R, Stratikos E, Golden J, Stern LJ..  (2020)  Discovery of Selective Inhibitors of Endoplasmic Reticulum Aminopeptidase 1.,  63  (1): [PMID:31841350] [10.1021/acs.jmedchem.9b00293]

Source