ID: ALA4516434

Max Phase: Preclinical

Molecular Formula: C20H24N2O5S

Molecular Weight: 404.49

Molecule Type: Unknown

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C20H24N2O5S/c1-14-6-8-17(22-10-4-3-5-11-22)16(12-14)21-28(25,26)19-13-15(20(23)24)7-9-18(19)27-2/h6-9,12-13,21H,3-5,10-11H2,1-2H3,(H,23,24)

Standard InChI Key:  FUPPCZKANSXYHA-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: 404.49Molecular Weight (Monoisotopic): 404.1406AlogP: 3.49#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: 3.92CX Basic pKa: 4.64CX LogP: 2.53CX LogD: -0.14
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.77Np Likeness Score: -1.59

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