ID: ALA4874099

Max Phase: Preclinical

Molecular Formula: C30H30N3O7P

Molecular Weight: 575.56

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(C)C(NC(=O)Cn1cccc(NC(=O)Oc2ccccc2)c1=O)P(=O)(Oc1ccccc1)Oc1ccccc1

Standard InChI:  InChI=1S/C30H30N3O7P/c1-22(2)28(41(37,39-24-15-8-4-9-16-24)40-25-17-10-5-11-18-25)32-27(34)21-33-20-12-19-26(29(33)35)31-30(36)38-23-13-6-3-7-14-23/h3-20,22,28H,21H2,1-2H3,(H,31,36)(H,32,34)

Standard InChI Key:  QCRLFRZMKZDITK-UHFFFAOYSA-N

Associated Targets(Human)

Leukocyte elastase 8173 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HEp-2 3859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Probable periplasmic serine endoprotease DegP-like 58 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Chlamydia trachomatis 699 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Chlamydia pecorum 35 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: 575.56Molecular Weight (Monoisotopic): 575.1821AlogP: 5.91#Rotatable Bonds: 11
Polar Surface Area: 124.96Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.19CX Basic pKa: CX LogP: 5.20CX LogD: 5.20
Aromatic Rings: 4Heavy Atoms: 41QED Weighted: 0.21Np Likeness Score: -0.80

References

1. Hwang J, Strange N, Phillips MJA, Krause AL, Heywood A, Gamble AB, Huston WM, Tyndall JDA..  (2021)  Optimization of peptide-based inhibitors targeting the HtrA serine protease in Chlamydia: Design, synthesis and biological evaluation of pyridone-based and N-Capping group-modified analogues.,  224  [PMID:34265463] [10.1016/j.ejmech.2021.113692]

Source