ID: ALA4867897

Max Phase: Preclinical

Molecular Formula: C30H34FN3O5S

Molecular Weight: 567.68

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CN(C(=O)c1ccc(N(CCN2CCCCC2)S(=O)(=O)c2ccc(F)cc2)cc1)[C@@H](Cc1ccccc1)C(=O)O

Standard InChI:  InChI=1S/C30H34FN3O5S/c1-32(28(30(36)37)22-23-8-4-2-5-9-23)29(35)24-10-14-26(15-11-24)34(21-20-33-18-6-3-7-19-33)40(38,39)27-16-12-25(31)13-17-27/h2,4-5,8-17,28H,3,6-7,18-22H2,1H3,(H,36,37)/t28-/m0/s1

Standard InChI Key:  XYKMDKGRRHMLPM-NDEPHWFRSA-N

Associated Targets(Human)

Endoplasmic reticulum aminopeptidase 2 387 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: 567.68Molecular Weight (Monoisotopic): 567.2203AlogP: 4.27#Rotatable Bonds: 11
Polar Surface Area: 98.23Molecular Species: ACIDHBA: 5HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.14CX Basic pKa: 7.30CX LogP: 1.98CX LogD: 1.70
Aromatic Rings: 3Heavy Atoms: 40QED Weighted: 0.37Np Likeness Score: -1.28

References

1. Laura M, Ronan G, Vy LB, Valentin G, Omar CA, Virgyl C, Piveteau C, Melissa R, Charlotte F, Sandrine W, Julie C, Julie DR, Damien B, Florence L, Peter VE, Benoit D, Rebecca DP..  (2021)  Modulators of hERAP2 discovered by high-throughput screening.,  211  [PMID:33359953] [10.1016/j.ejmech.2020.113053]

Source